[{"month":"01","publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]},"doi":"10.1002/anie.202211663","language":[{"iso":"eng"}],"main_file_link":[{"url":"https://doi.org/10.1002/anie.202211663","open_access":"1"}],"oa":1,"quality_controlled":"1","extern":"1","article_number":"e202211663","author":[{"full_name":"Lepre, Enrico","last_name":"Lepre","first_name":"Enrico"},{"full_name":"Rat, Sylvain","last_name":"Rat","first_name":"Sylvain"},{"first_name":"Cristian","last_name":"Cavedon","full_name":"Cavedon, Cristian"},{"first_name":"Peter H.","last_name":"Seeberger","full_name":"Seeberger, Peter H."},{"orcid":"0000-0001-8689-388X","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","last_name":"Pieber","first_name":"Bartholomäus","full_name":"Pieber, Bartholomäus"},{"last_name":"Antonietti","first_name":"Markus","full_name":"Antonietti, Markus"},{"last_name":"López‐Salas","first_name":"Nieves","full_name":"López‐Salas, Nieves"}],"date_updated":"2023-08-21T09:18:12Z","date_created":"2023-05-08T08:28:14Z","volume":62,"year":"2023","publication_status":"published","publisher":"Wiley","day":"09","article_processing_charge":"No","scopus_import":"1","keyword":["General Chemistry","Catalysis"],"date_published":"2023-01-09T00:00:00Z","publication":"Angewandte Chemie International Edition","citation":{"chicago":"Lepre, Enrico, Sylvain Rat, Cristian Cavedon, Peter H. Seeberger, Bartholomäus Pieber, Markus Antonietti, and Nieves López‐Salas. “Catalytic Properties of High Nitrogen Content Carbonaceous Materials.” Angewandte Chemie International Edition. Wiley, 2023. https://doi.org/10.1002/anie.202211663.","short":"E. Lepre, S. Rat, C. Cavedon, P.H. Seeberger, B. Pieber, M. Antonietti, N. López‐Salas, Angewandte Chemie International Edition 62 (2023).","mla":"Lepre, Enrico, et al. “Catalytic Properties of High Nitrogen Content Carbonaceous Materials.” Angewandte Chemie International Edition, vol. 62, no. 2, e202211663, Wiley, 2023, doi:10.1002/anie.202211663.","ieee":"E. Lepre et al., “Catalytic properties of high nitrogen content carbonaceous materials,” Angewandte Chemie International Edition, vol. 62, no. 2. Wiley, 2023.","apa":"Lepre, E., Rat, S., Cavedon, C., Seeberger, P. H., Pieber, B., Antonietti, M., & López‐Salas, N. (2023). Catalytic properties of high nitrogen content carbonaceous materials. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202211663","ista":"Lepre E, Rat S, Cavedon C, Seeberger PH, Pieber B, Antonietti M, López‐Salas N. 2023. Catalytic properties of high nitrogen content carbonaceous materials. Angewandte Chemie International Edition. 62(2), e202211663.","ama":"Lepre E, Rat S, Cavedon C, et al. Catalytic properties of high nitrogen content carbonaceous materials. Angewandte Chemie International Edition. 2023;62(2). doi:10.1002/anie.202211663"},"article_type":"original","abstract":[{"text":"The influence of structural modifications on the catalytic activity of carbon materials is poorly understood. A collection of carbonaceous materials with different pore networks and high nitrogen content was characterized and used to catalyze four reactions to deduce structure–activity relationships. The CO2 cycloaddition and Knoevenagel reaction depend on Lewis basic sites (electron-rich nitrogen species). The absence of large conjugated carbon domains resulting from the introduction of large amounts of nitrogen in the carbon network is responsible for poor redox activity, as observed through the catalytic reduction of nitrobenzene with hydrazine and the catalytic oxidation of 3,3′,5,5′-tetramethylbenzidine using hydroperoxide. The material with the highest activity towards Lewis acid catalysis (in the hydrolysis of (dimethoxymethyl)benzene to benzaldehyde) is the most effective for small molecule activation and presents the highest concentration of electron-poor nitrogen species.","lang":"eng"}],"issue":"2","type":"journal_article","oa_version":"Published Version","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"12922","title":"Catalytic properties of high nitrogen content carbonaceous materials","status":"public","intvolume":" 62"},{"article_number":" e202304138","date_created":"2024-01-22T11:54:34Z","date_updated":"2024-01-23T08:48:14Z","volume":62,"author":[{"id":"36336939-eb97-11eb-a6c2-c83f1214ca79","orcid":"0000-0002-6401-5151","first_name":"Lea Marie","last_name":"Becker","full_name":"Becker, Lea Marie"},{"full_name":"Berbon, Mélanie","first_name":"Mélanie","last_name":"Berbon"},{"full_name":"Vallet, Alicia","last_name":"Vallet","first_name":"Alicia"},{"last_name":"Grelard","first_name":"Axelle","full_name":"Grelard, Axelle"},{"full_name":"Morvan, Estelle","last_name":"Morvan","first_name":"Estelle"},{"full_name":"Bardiaux, Benjamin","first_name":"Benjamin","last_name":"Bardiaux"},{"last_name":"Lichtenecker","first_name":"Roman","full_name":"Lichtenecker, Roman"},{"full_name":"Ernst, Matthias","last_name":"Ernst","first_name":"Matthias"},{"full_name":"Loquet, Antoine","first_name":"Antoine","last_name":"Loquet"},{"orcid":"0000-0002-9350-7606","id":"7B541462-FAF6-11E9-A490-E8DFE5697425","last_name":"Schanda","first_name":"Paul","full_name":"Schanda, Paul"}],"related_material":{"link":[{"relation":"translation","url":"https://doi.org/10.1002/ange.202304138"}],"record":[{"relation":"other","status":"public","id":"12675"}]},"publication_status":"published","department":[{"_id":"PaSc"}],"publisher":"Wiley","year":"2023","month":"05","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"language":[{"iso":"eng"}],"doi":"10.1002/anie.202304138","main_file_link":[{"url":"https://doi.org/10.1002/anie.202304138","open_access":"1"}],"oa":1,"abstract":[{"text":"Cover Page","lang":"eng"}],"issue":"19","type":"other_academic_publication","oa_version":"Published Version","status":"public","title":"Cover Picture: The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle‐Spinning NMR spectroscopy of aromatic residues","intvolume":" 62","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"14861","day":"02","article_processing_charge":"No","keyword":["General Chemistry","Catalysis"],"date_published":"2023-05-02T00:00:00Z","publication":"Angewandte Chemie International Edition","citation":{"apa":"Becker, L. M., Berbon, M., Vallet, A., Grelard, A., Morvan, E., Bardiaux, B., … Schanda, P. (2023). Cover Picture: The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle‐Spinning NMR spectroscopy of aromatic residues. Angewandte Chemie International Edition (Vol. 62). Wiley. https://doi.org/10.1002/anie.202304138","ieee":"L. M. Becker et al., Cover Picture: The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle‐Spinning NMR spectroscopy of aromatic residues, vol. 62, no. 19. Wiley, 2023.","ista":"Becker LM, Berbon M, Vallet A, Grelard A, Morvan E, Bardiaux B, Lichtenecker R, Ernst M, Loquet A, Schanda P. 2023. Cover Picture: The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle‐Spinning NMR spectroscopy of aromatic residues, Wiley,p.","ama":"Becker LM, Berbon M, Vallet A, et al. Cover Picture: The Rigid Core and Flexible Surface of Amyloid Fibrils Probed by Magic‐Angle‐Spinning NMR Spectroscopy of Aromatic Residues. Vol 62. Wiley; 2023. doi:10.1002/anie.202304138","chicago":"Becker, Lea Marie, Mélanie Berbon, Alicia Vallet, Axelle Grelard, Estelle Morvan, Benjamin Bardiaux, Roman Lichtenecker, Matthias Ernst, Antoine Loquet, and Paul Schanda. Cover Picture: The Rigid Core and Flexible Surface of Amyloid Fibrils Probed by Magic‐Angle‐Spinning NMR Spectroscopy of Aromatic Residues. Angewandte Chemie International Edition. Vol. 62. Wiley, 2023. https://doi.org/10.1002/anie.202304138.","short":"L.M. Becker, M. Berbon, A. Vallet, A. Grelard, E. Morvan, B. Bardiaux, R. Lichtenecker, M. Ernst, A. Loquet, P. Schanda, Cover Picture: The Rigid Core and Flexible Surface of Amyloid Fibrils Probed by Magic‐Angle‐Spinning NMR Spectroscopy of Aromatic Residues, Wiley, 2023.","mla":"Becker, Lea Marie, et al. “Cover Picture: The Rigid Core and Flexible Surface of Amyloid Fibrils Probed by Magic‐Angle‐Spinning NMR Spectroscopy of Aromatic Residues.” Angewandte Chemie International Edition, vol. 62, no. 19, e202304138, Wiley, 2023, doi:10.1002/anie.202304138."}},{"abstract":[{"text":"The short history of research on Li-O2 batteries has seen a remarkable number of mechanistic U-turns over the years. From the initial use of carbonate electrolytes, that were then found to be entirely unsuitable, to the belief that (su)peroxide was solely responsible for degradation, before the more reactive singlet oxygen was found to form, to the hypothesis that capacity depends on a competing surface/solution mechanism before a practically exclusive solution mechanism was identified. Herein, we argue for an ever-fresh look at the reported data without bias towards supposedly established explanations. We explain how the latest findings on rate and capacity limits, as well as the origin of side reactions, are connected via the disproportionation (DISP) step in the (dis)charge mechanism. Therefrom, directions emerge for the design of electrolytes and mediators on how to suppress side reactions and to enable high rate and high reversible capacity.","lang":"eng"}],"article_number":"e202316476","type":"journal_article","date_created":"2023-12-15T16:10:13Z","date_updated":"2024-02-15T14:43:05Z","oa_version":"Published Version","author":[{"full_name":"Jethwa, Rajesh B","last_name":"Jethwa","first_name":"Rajesh B","orcid":"0000-0002-0404-4356","id":"4cc538d5-803f-11ed-ab7e-8139573aad8f"},{"last_name":"Mondal","first_name":"Soumyadip","id":"d25d21ef-dc8d-11ea-abe3-ec4576307f48","full_name":"Mondal, Soumyadip"},{"last_name":"Pant","first_name":"Bhargavi","id":"50c64d4d-eb97-11eb-a6c2-d33e5e14f112","full_name":"Pant, Bhargavi"},{"orcid":"0000-0003-2902-5319","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","last_name":"Freunberger","first_name":"Stefan Alexander","full_name":"Freunberger, Stefan Alexander"}],"status":"public","title":"To DISP or not? The far‐reaching reaction mechanisms underpinning Lithium‐air batteries","publication_status":"epub_ahead","department":[{"_id":"StFr"},{"_id":"GradSch"}],"publisher":"Wiley","_id":"14687","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","year":"2023","month":"12","day":"14","article_processing_charge":"Yes (via OA deal)","publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]},"keyword":["General Chemistry","Catalysis"],"scopus_import":"1","language":[{"iso":"eng"}],"doi":"10.1002/anie.202316476","date_published":"2023-12-14T00:00:00Z","article_type":"review","quality_controlled":"1","publication":"Angewandte Chemie International Edition","oa":1,"citation":{"ista":"Jethwa RB, Mondal S, Pant B, Freunberger SA. 2023. To DISP or not? The far‐reaching reaction mechanisms underpinning Lithium‐air batteries. Angewandte Chemie International Edition., e202316476.","ieee":"R. B. Jethwa, S. Mondal, B. Pant, and S. A. Freunberger, “To DISP or not? The far‐reaching reaction mechanisms underpinning Lithium‐air batteries,” Angewandte Chemie International Edition. Wiley, 2023.","apa":"Jethwa, R. B., Mondal, S., Pant, B., & Freunberger, S. A. (2023). To DISP or not? The far‐reaching reaction mechanisms underpinning Lithium‐air batteries. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202316476","ama":"Jethwa RB, Mondal S, Pant B, Freunberger SA. To DISP or not? The far‐reaching reaction mechanisms underpinning Lithium‐air batteries. Angewandte Chemie International Edition. 2023. doi:10.1002/anie.202316476","chicago":"Jethwa, Rajesh B, Soumyadip Mondal, Bhargavi Pant, and Stefan Alexander Freunberger. “To DISP or Not? The Far‐reaching Reaction Mechanisms Underpinning Lithium‐air Batteries.” Angewandte Chemie International Edition. Wiley, 2023. https://doi.org/10.1002/anie.202316476.","mla":"Jethwa, Rajesh B., et al. “To DISP or Not? The Far‐reaching Reaction Mechanisms Underpinning Lithium‐air Batteries.” Angewandte Chemie International Edition, e202316476, Wiley, 2023, doi:10.1002/anie.202316476.","short":"R.B. Jethwa, S. Mondal, B. Pant, S.A. Freunberger, Angewandte Chemie International Edition (2023)."},"main_file_link":[{"open_access":"1","url":" https://doi.org/10.1002/anie.202316476"}]},{"date_published":"2023-05-01T00:00:00Z","publication":"Angewandte Chemie International Edition","citation":{"ista":"Becker LM, Berbon M, Vallet A, Grelard A, Morvan E, Bardiaux B, Lichtenecker R, Ernst M, Loquet A, Schanda P. 2023. The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle Spinning NMR of aromatic residues. Angewandte Chemie International Edition. 62(19), e202219314.","apa":"Becker, L. M., Berbon, M., Vallet, A., Grelard, A., Morvan, E., Bardiaux, B., … Schanda, P. (2023). The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle Spinning NMR of aromatic residues. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202219314","ieee":"L. M. Becker et al., “The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle Spinning NMR of aromatic residues,” Angewandte Chemie International Edition, vol. 62, no. 19. Wiley, 2023.","ama":"Becker LM, Berbon M, Vallet A, et al. The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle Spinning NMR of aromatic residues. Angewandte Chemie International Edition. 2023;62(19). doi:10.1002/anie.202219314","chicago":"Becker, Lea Marie, Mélanie Berbon, Alicia Vallet, Axelle Grelard, Estelle Morvan, Benjamin Bardiaux, Roman Lichtenecker, Matthias Ernst, Antoine Loquet, and Paul Schanda. “The Rigid Core and Flexible Surface of Amyloid Fibrils Probed by Magic‐Angle Spinning NMR of Aromatic Residues.” Angewandte Chemie International Edition. Wiley, 2023. https://doi.org/10.1002/anie.202219314.","mla":"Becker, Lea Marie, et al. “The Rigid Core and Flexible Surface of Amyloid Fibrils Probed by Magic‐Angle Spinning NMR of Aromatic Residues.” Angewandte Chemie International Edition, vol. 62, no. 19, e202219314, Wiley, 2023, doi:10.1002/anie.202219314.","short":"L.M. Becker, M. Berbon, A. Vallet, A. Grelard, E. Morvan, B. Bardiaux, R. Lichtenecker, M. Ernst, A. Loquet, P. Schanda, Angewandte Chemie International Edition 62 (2023)."},"article_type":"original","day":"01","article_processing_charge":"Yes (via OA deal)","has_accepted_license":"1","keyword":["General Chemistry","Catalysis"],"oa_version":"Published Version","file":[{"relation":"main_file","file_id":"14072","checksum":"7dd083ed8850faa55c34e411ed390de9","success":1,"date_created":"2023-08-16T12:33:31Z","date_updated":"2023-08-16T12:33:31Z","access_level":"open_access","file_name":"2023_AngewChemInt_Becker.pdf","content_type":"application/pdf","file_size":1422445,"creator":"dernst"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"12675","title":"The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle Spinning NMR of aromatic residues","ddc":["540"],"status":"public","intvolume":" 62","abstract":[{"text":"Aromatic side chains are important reporters of the plasticity of proteins, and often form important contacts in protein--protein interactions. By studying a pair of structurally homologous cross-β amyloid fibrils, HET-s and HELLF, with a specific isotope-labeling approach and magic-angle-spinning (MAS) NMR, we have characterized the dynamic behavior of Phe and Tyr aromatic rings to show that the hydrophobic amyloid core is rigid, without any sign of \"breathing motions\" over hundreds of milliseconds at least. Aromatic residues exposed at the fibril surface have a rigid ring axis but undergo ring flips, on a variety of time scales from ns to µs. Our approach provides direct insight into hydrophobic-core motions, enabling a better evaluation of the conformational heterogeneity generated from a NMR structural ensemble of such amyloid cross-β architecture.","lang":"eng"}],"issue":"19","type":"journal_article","doi":"10.1002/anie.202219314","language":[{"iso":"eng"}],"tmp":{"name":"Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc/4.0/legalcode","image":"/images/cc_by_nc.png","short":"CC BY-NC (4.0)"},"external_id":{"pmid":["36738230"],"isi":["000956919900001"]},"oa":1,"isi":1,"quality_controlled":"1","month":"05","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"author":[{"orcid":"0000-0002-6401-5151","id":"36336939-eb97-11eb-a6c2-c83f1214ca79","last_name":"Becker","first_name":"Lea Marie","full_name":"Becker, Lea Marie"},{"last_name":"Berbon","first_name":"Mélanie","full_name":"Berbon, Mélanie"},{"last_name":"Vallet","first_name":"Alicia","full_name":"Vallet, Alicia"},{"first_name":"Axelle","last_name":"Grelard","full_name":"Grelard, Axelle"},{"full_name":"Morvan, Estelle","last_name":"Morvan","first_name":"Estelle"},{"last_name":"Bardiaux","first_name":"Benjamin","full_name":"Bardiaux, Benjamin"},{"full_name":"Lichtenecker, Roman","first_name":"Roman","last_name":"Lichtenecker"},{"last_name":"Ernst","first_name":"Matthias","full_name":"Ernst, Matthias"},{"full_name":"Loquet, Antoine","last_name":"Loquet","first_name":"Antoine"},{"orcid":"0000-0002-9350-7606","id":"7B541462-FAF6-11E9-A490-E8DFE5697425","last_name":"Schanda","first_name":"Paul","full_name":"Schanda, Paul"}],"related_material":{"record":[{"id":"14861","relation":"other","status":"public"},{"id":"12497","relation":"research_data","status":"public"}],"link":[{"description":"News on ISTA website","relation":"press_release","url":"https://ista.ac.at/en/news/dancing-styles-of-atoms/"}]},"date_created":"2023-02-24T10:45:01Z","date_updated":"2024-02-21T12:14:06Z","volume":62,"acknowledgement":"We thank AlbertA. Smith (Leipzig)for insightful discussions. This work was supported by funding from the European Research Council (StG-2012-311318 to P.S.) and used the platforms of the Grenoble Instruct-ERIC center (ISBG;UMS 3518 CNRS-CEA-UJF-EMBL) within the Grenoble Partnership for Structural Biology(PSB) and facilities and expertiseof the Biophysical and Structural Chemistry platform (BPCS) at IECB,CNRSUAR3033,INSERMUS001 and Bordeaux University.","year":"2023","pmid":1,"publication_status":"published","publisher":"Wiley","department":[{"_id":"GradSch"},{"_id":"PaSc"}],"file_date_updated":"2023-08-16T12:33:31Z","license":"https://creativecommons.org/licenses/by-nc/4.0/","article_number":"e202219314"},{"quality_controlled":"1","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1002/anie.202117738"}],"oa":1,"external_id":{"pmid":["35188714"]},"language":[{"iso":"eng"}],"doi":"10.1002/anie.202117738","month":"05","publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]},"publication_status":"published","publisher":"Wiley","year":"2022","pmid":1,"date_created":"2022-08-24T10:41:25Z","date_updated":"2023-02-21T10:09:11Z","volume":61,"author":[{"full_name":"Traxler, Michael","first_name":"Michael","last_name":"Traxler"},{"full_name":"Gisbertz, Sebastian","first_name":"Sebastian","last_name":"Gisbertz"},{"last_name":"Pachfule","first_name":"Pradip","full_name":"Pachfule, Pradip"},{"full_name":"Schmidt, Johannes","first_name":"Johannes","last_name":"Schmidt"},{"first_name":"Jérôme","last_name":"Roeser","full_name":"Roeser, Jérôme"},{"first_name":"Susanne","last_name":"Reischauer","full_name":"Reischauer, Susanne"},{"full_name":"Rabeah, Jabor","last_name":"Rabeah","first_name":"Jabor"},{"full_name":"Pieber, Bartholomäus","first_name":"Bartholomäus","last_name":"Pieber","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X"},{"first_name":"Arne","last_name":"Thomas","full_name":"Thomas, Arne"}],"article_number":"e202117738","extern":"1","article_type":"original","publication":"Angewandte Chemie International Edition","citation":{"ama":"Traxler M, Gisbertz S, Pachfule P, et al. Acridine‐functionalized covalent organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C−N cross‐coupling. Angewandte Chemie International Edition. 2022;61(21). doi:10.1002/anie.202117738","ista":"Traxler M, Gisbertz S, Pachfule P, Schmidt J, Roeser J, Reischauer S, Rabeah J, Pieber B, Thomas A. 2022. Acridine‐functionalized covalent organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C−N cross‐coupling. Angewandte Chemie International Edition. 61(21), e202117738.","ieee":"M. Traxler et al., “Acridine‐functionalized covalent organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C−N cross‐coupling,” Angewandte Chemie International Edition, vol. 61, no. 21. Wiley, 2022.","apa":"Traxler, M., Gisbertz, S., Pachfule, P., Schmidt, J., Roeser, J., Reischauer, S., … Thomas, A. (2022). Acridine‐functionalized covalent organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C−N cross‐coupling. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202117738","mla":"Traxler, Michael, et al. “Acridine‐functionalized Covalent Organic Frameworks (COFs) as Photocatalysts for Metallaphotocatalytic C−N Cross‐coupling.” Angewandte Chemie International Edition, vol. 61, no. 21, e202117738, Wiley, 2022, doi:10.1002/anie.202117738.","short":"M. Traxler, S. Gisbertz, P. Pachfule, J. Schmidt, J. Roeser, S. Reischauer, J. Rabeah, B. Pieber, A. Thomas, Angewandte Chemie International Edition 61 (2022).","chicago":"Traxler, Michael, Sebastian Gisbertz, Pradip Pachfule, Johannes Schmidt, Jérôme Roeser, Susanne Reischauer, Jabor Rabeah, Bartholomäus Pieber, and Arne Thomas. “Acridine‐functionalized Covalent Organic Frameworks (COFs) as Photocatalysts for Metallaphotocatalytic C−N Cross‐coupling.” Angewandte Chemie International Edition. Wiley, 2022. https://doi.org/10.1002/anie.202117738."},"date_published":"2022-05-16T00:00:00Z","scopus_import":"1","day":"16","article_processing_charge":"No","title":"Acridine‐functionalized covalent organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C−N cross‐coupling","status":"public","intvolume":" 61","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"11955","oa_version":"Published Version","type":"journal_article","abstract":[{"text":"Covalent organic frameworks (COFs) are structurally tuneable, porous and crystalline polymers constructed through the covalent attachment of small organic building blocks as elementary units. Using the myriad of such building blocks, a broad spectrum of functionalities has been applied for COF syntheses for broad applications, including heterogeneous catalysis. Herein, we report the synthesis of a new family of porous and crystalline COFs using a novel acridine linker and benzene-1,3,5-tricarbaldehyde derivatives bearing a variable number of hydroxy groups. With the broad absorption in the visible light region, the COFs were applied as photocatalysts in metallaphotocatalytic C−N cross-coupling. The fully β-ketoenamine linked COF showed the highest activity, due to the increased charge separation upon irradiation. The COF showed good to excellent yields for several aryl bromides, good recyclability and even catalyzed the organic transformation in presence of green light as energy source.","lang":"eng"}],"issue":"21"},{"title":"Intraligand charge transfer enables visible‐light‐mediated Nickel‐catalyzed cross-coupling reactions","status":"public","intvolume":" 61","_id":"12924","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","oa_version":"Published Version","type":"journal_article","abstract":[{"text":"We demonstrate that several visible-light-mediated carbon−heteroatom cross-coupling reactions can be carried out using a photoactive NiII precatalyst that forms in situ from a nickel salt and a bipyridine ligand decorated with two carbazole groups (Ni(Czbpy)Cl2). The activation of this precatalyst towards cross-coupling reactions follows a hitherto undisclosed mechanism that is different from previously reported light-responsive nickel complexes that undergo metal-to-ligand charge transfer. Theoretical and spectroscopic investigations revealed that irradiation of Ni(Czbpy)Cl2 with visible light causes an initial intraligand charge transfer event that triggers productive catalysis. Ligand polymerization affords a porous, recyclable organic polymer for heterogeneous nickel catalysis of cross-coupling reactions. The heterogeneous catalyst shows stable performance in a packed-bed flow reactor during a week of continuous operation.","lang":"eng"}],"issue":"46","article_type":"original","publication":"Angewandte Chemie International Edition","citation":{"short":"C. Cavedon, S. Gisbertz, S. Reischauer, S. Vogl, E. Sperlich, J.H. Burke, R.F. Wallick, S. Schrottke, W. Hsu, L. Anghileri, Y. Pfeifer, N. Richter, C. Teutloff, H. Müller‐Werkmeister, D. Cambié, P.H. Seeberger, J. Vura‐Weis, R.M. van der Veen, A. Thomas, B. Pieber, Angewandte Chemie International Edition 61 (2022).","mla":"Cavedon, Cristian, et al. “Intraligand Charge Transfer Enables Visible‐light‐mediated Nickel‐catalyzed Cross-Coupling Reactions.” Angewandte Chemie International Edition, vol. 61, no. 46, e202211433, Wiley, 2022, doi:10.1002/anie.202211433.","chicago":"Cavedon, Cristian, Sebastian Gisbertz, Susanne Reischauer, Sarah Vogl, Eric Sperlich, John H. Burke, Rachel F. Wallick, et al. “Intraligand Charge Transfer Enables Visible‐light‐mediated Nickel‐catalyzed Cross-Coupling Reactions.” Angewandte Chemie International Edition. Wiley, 2022. https://doi.org/10.1002/anie.202211433.","ama":"Cavedon C, Gisbertz S, Reischauer S, et al. Intraligand charge transfer enables visible‐light‐mediated Nickel‐catalyzed cross-coupling reactions. Angewandte Chemie International Edition. 2022;61(46). doi:10.1002/anie.202211433","ieee":"C. Cavedon et al., “Intraligand charge transfer enables visible‐light‐mediated Nickel‐catalyzed cross-coupling reactions,” Angewandte Chemie International Edition, vol. 61, no. 46. Wiley, 2022.","apa":"Cavedon, C., Gisbertz, S., Reischauer, S., Vogl, S., Sperlich, E., Burke, J. H., … Pieber, B. (2022). Intraligand charge transfer enables visible‐light‐mediated Nickel‐catalyzed cross-coupling reactions. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202211433","ista":"Cavedon C, Gisbertz S, Reischauer S, Vogl S, Sperlich E, Burke JH, Wallick RF, Schrottke S, Hsu W, Anghileri L, Pfeifer Y, Richter N, Teutloff C, Müller‐Werkmeister H, Cambié D, Seeberger PH, Vura‐Weis J, van der Veen RM, Thomas A, Pieber B. 2022. Intraligand charge transfer enables visible‐light‐mediated Nickel‐catalyzed cross-coupling reactions. Angewandte Chemie International Edition. 61(46), e202211433."},"date_published":"2022-11-14T00:00:00Z","keyword":["General Chemistry","Catalysis"],"scopus_import":"1","day":"14","article_processing_charge":"No","publication_status":"published","publisher":"Wiley","year":"2022","date_updated":"2023-05-15T08:27:25Z","date_created":"2023-05-08T08:30:11Z","volume":61,"author":[{"first_name":"Cristian","last_name":"Cavedon","full_name":"Cavedon, Cristian"},{"last_name":"Gisbertz","first_name":"Sebastian","full_name":"Gisbertz, Sebastian"},{"full_name":"Reischauer, Susanne","first_name":"Susanne","last_name":"Reischauer"},{"last_name":"Vogl","first_name":"Sarah","full_name":"Vogl, Sarah"},{"first_name":"Eric","last_name":"Sperlich","full_name":"Sperlich, Eric"},{"last_name":"Burke","first_name":"John H.","full_name":"Burke, John H."},{"full_name":"Wallick, Rachel F.","first_name":"Rachel F.","last_name":"Wallick"},{"first_name":"Stefanie","last_name":"Schrottke","full_name":"Schrottke, Stefanie"},{"full_name":"Hsu, Wei‐Hsin","first_name":"Wei‐Hsin","last_name":"Hsu"},{"full_name":"Anghileri, Lucia","first_name":"Lucia","last_name":"Anghileri"},{"full_name":"Pfeifer, Yannik","first_name":"Yannik","last_name":"Pfeifer"},{"first_name":"Noah","last_name":"Richter","full_name":"Richter, Noah"},{"full_name":"Teutloff, Christian","last_name":"Teutloff","first_name":"Christian"},{"full_name":"Müller‐Werkmeister, Henrike","last_name":"Müller‐Werkmeister","first_name":"Henrike"},{"first_name":"Dario","last_name":"Cambié","full_name":"Cambié, Dario"},{"full_name":"Seeberger, Peter H.","last_name":"Seeberger","first_name":"Peter H."},{"full_name":"Vura‐Weis, Josh","first_name":"Josh","last_name":"Vura‐Weis"},{"full_name":"van der Veen, Renske M.","first_name":"Renske M.","last_name":"van der Veen"},{"last_name":"Thomas","first_name":"Arne","full_name":"Thomas, Arne"},{"first_name":"Bartholomäus","last_name":"Pieber","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X","full_name":"Pieber, Bartholomäus"}],"article_number":"e202211433","extern":"1","quality_controlled":"1","main_file_link":[{"url":"https://doi.org/10.1002/anie.202211433","open_access":"1"}],"oa":1,"language":[{"iso":"eng"}],"doi":"10.1002/anie.202211433","month":"11","publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]}},{"has_accepted_license":"1","article_processing_charge":"No","day":"01","scopus_import":"1","date_published":"2022-08-01T00:00:00Z","citation":{"ista":"Parvizian M, Duràn Balsa A, Pokratath R, Kalha C, Lee S, Van Den Eynden D, Ibáñez M, Regoutz A, De Roo J. 2022. The chemistry of Cu₃N and Cu₃PdN nanocrystals. Angewandte Chemie - International Edition. 61(31), e202207013.","apa":"Parvizian, M., Duràn Balsa, A., Pokratath, R., Kalha, C., Lee, S., Van Den Eynden, D., … De Roo, J. (2022). The chemistry of Cu₃N and Cu₃PdN nanocrystals. Angewandte Chemie - International Edition. Wiley. https://doi.org/10.1002/anie.202207013","ieee":"M. Parvizian et al., “The chemistry of Cu₃N and Cu₃PdN nanocrystals,” Angewandte Chemie - International Edition, vol. 61, no. 31. Wiley, 2022.","ama":"Parvizian M, Duràn Balsa A, Pokratath R, et al. The chemistry of Cu₃N and Cu₃PdN nanocrystals. Angewandte Chemie - International Edition. 2022;61(31). doi:10.1002/anie.202207013","chicago":"Parvizian, Mahsa, Alejandra Duràn Balsa, Rohan Pokratath, Curran Kalha, Seungho Lee, Dietger Van Den Eynden, Maria Ibáñez, Anna Regoutz, and Jonathan De Roo. “The Chemistry of Cu₃N and Cu₃PdN Nanocrystals.” Angewandte Chemie - International Edition. Wiley, 2022. https://doi.org/10.1002/anie.202207013.","mla":"Parvizian, Mahsa, et al. “The Chemistry of Cu₃N and Cu₃PdN Nanocrystals.” Angewandte Chemie - International Edition, vol. 61, no. 31, e202207013, Wiley, 2022, doi:10.1002/anie.202207013.","short":"M. Parvizian, A. Duràn Balsa, R. Pokratath, C. Kalha, S. Lee, D. Van Den Eynden, M. Ibáñez, A. Regoutz, J. De Roo, Angewandte Chemie - International Edition 61 (2022)."},"publication":"Angewandte Chemie - International Edition","article_type":"original","issue":"31","abstract":[{"lang":"eng","text":"The precursor conversion chemistry and surface chemistry of Cu3N and Cu3PdN nanocrystals are unknown or contested. Here, we first obtain phase-pure, colloidally stable nanocubes. Second, we elucidate the pathway by which copper(II) nitrate and oleylamine form Cu3N. We find that oleylamine is both a reductant and a nitrogen source. Oleylamine is oxidized by nitrate to a primary aldimine, which reacts further with excess oleylamine to a secondary aldimine, eliminating ammonia. Ammonia reacts with CuI to form Cu3N. Third, we investigated the surface chemistry and find a mixed ligand shell of aliphatic amines and carboxylates (formed in situ). While the carboxylates appear tightly bound, the amines are easily desorbed from the surface. Finally, we show that doping with palladium decreases the band gap and the material becomes semi-metallic. These results bring insight into the chemistry of metal nitrides and might help the development of other metal nitride nanocrystals."}],"type":"journal_article","file":[{"creator":"dernst","file_size":1303202,"content_type":"application/pdf","access_level":"open_access","file_name":"2022_AngewandteChemieInternat_Parvizian.pdf","success":1,"checksum":"2a3ee0bb59e044b808ebe85cd94ac899","date_created":"2022-07-29T09:29:20Z","date_updated":"2022-07-29T09:29:20Z","file_id":"11696","relation":"main_file"}],"oa_version":"Published Version","user_id":"4359f0d1-fa6c-11eb-b949-802e58b17ae8","_id":"11451","intvolume":" 61","title":"The chemistry of Cu₃N and Cu₃PdN nanocrystals","status":"public","ddc":["540"],"publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"month":"08","doi":"10.1002/anie.202207013","language":[{"iso":"eng"}],"external_id":{"isi":["000811084000001"],"pmid":["35612297"]},"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"oa":1,"quality_controlled":"1","isi":1,"file_date_updated":"2022-07-29T09:29:20Z","license":"https://creativecommons.org/licenses/by/4.0/","article_number":"e202207013","related_material":{"record":[{"status":"public","relation":"research_data","id":"11695"}]},"author":[{"full_name":"Parvizian, Mahsa","first_name":"Mahsa","last_name":"Parvizian"},{"full_name":"Duràn Balsa, Alejandra","first_name":"Alejandra","last_name":"Duràn Balsa"},{"last_name":"Pokratath","first_name":"Rohan","full_name":"Pokratath, Rohan"},{"first_name":"Curran","last_name":"Kalha","full_name":"Kalha, Curran"},{"last_name":"Lee","first_name":"Seungho","orcid":"0000-0002-6962-8598","id":"BB243B88-D767-11E9-B658-BC13E6697425","full_name":"Lee, Seungho"},{"first_name":"Dietger","last_name":"Van Den Eynden","full_name":"Van Den Eynden, Dietger"},{"first_name":"Maria","last_name":"Ibáñez","id":"43C61214-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-5013-2843","full_name":"Ibáñez, Maria"},{"first_name":"Anna","last_name":"Regoutz","full_name":"Regoutz, Anna"},{"first_name":"Jonathan","last_name":"De Roo","full_name":"De Roo, Jonathan"}],"volume":61,"date_updated":"2023-08-03T07:19:12Z","date_created":"2022-06-19T22:01:58Z","pmid":1,"year":"2022","acknowledgement":"J.D.R. and M.P. acknowledge the SNF Eccellenza funding scheme (project number: 194172). We acknowledge DESY (Hamburg, Germany), a member of the Helmholtz Association HGF, for the provision of experimental facilities. Parts of this research were carried out at beamline P21.1, PETRA III. We thank Dr. Soham Banerjee for acquiring the PDF data and helpful advice. A.R. acknowledges the support from the Analytical Chemistry Trust Fund for her CAMS-UK Fellowship. C.K. acknowledges the support from the Department of Chemistry, UCL. The authors acknowledge Dr Stephan Lany from NREL for providing the Cu3N DFT calculations. The authors thank Prof. Raymond Schaak and Dr. Robert William Lord for helpful advice and suggestions regarding the purification procedure. Open access funding provided by Universitat Basel.","department":[{"_id":"MaIb"}],"publisher":"Wiley","publication_status":"published"},{"quality_controlled":"1","isi":1,"project":[{"name":"Bottom-up Engineering for Thermoelectric Applications","grant_number":"M02889","_id":"9B8804FC-BA93-11EA-9121-9846C619BF3A"},{"name":"ISTplus - Postdoctoral Fellowships","call_identifier":"H2020","grant_number":"754411","_id":"260C2330-B435-11E9-9278-68D0E5697425"}],"external_id":{"isi":["000828274200001"]},"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"oa":1,"acknowledged_ssus":[{"_id":"EM-Fac"},{"_id":"NanoFab"}],"language":[{"iso":"eng"}],"doi":"10.1002/anie.202207002","month":"08","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"publication_status":"published","department":[{"_id":"MaIb"},{"_id":"EM-Fac"}],"publisher":"Wiley","year":"2022","acknowledgement":"This research was supported by the Scientific Service Units (SSU) of IST Austria through resources provided by Electron Microscopy Facility (EMF) and the Nanofabrication Facility (NNF). This work was financially supported by IST Austria and the Werner Siemens Foundation. C.C. acknowledges funding from the FWF “Lise Meitner Fellowship” grant agreement M 2889-N. Lise Meitner Project (M2889-N). Y.L. acknowledges funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No. 754411. R.L.B. thanks the National Science Foundation for support under DMR-1904719. MCS acknowledge MINECO Juan de la Cierva Incorporation fellowship (JdlCI 2019) and Severo Ochoa. M.C.S. and J.A. acknowledge funding from Generalitat de Catalunya 2017 SGR 327. ICN2 is supported by the Severo Ochoa program from Spanish MINECO (Grant no. SEV-2017-0706) and is funded by the CERCA Programme/Generalitat de Catalunya. This study was supported by MCIN with funding from European Union NextGenerationEU (PRTR-C17.I1) and Generalitat de Catalunya.","date_created":"2022-07-31T22:01:48Z","date_updated":"2023-08-03T12:23:52Z","volume":61,"author":[{"first_name":"Cheng","last_name":"Chang","id":"9E331C2E-9F27-11E9-AE48-5033E6697425","orcid":"0000-0002-9515-4277","full_name":"Chang, Cheng"},{"orcid":"0000-0001-7313-6740","id":"2A70014E-F248-11E8-B48F-1D18A9856A87","last_name":"Liu","first_name":"Yu","full_name":"Liu, Yu"},{"first_name":"Seungho","last_name":"Lee","id":"BB243B88-D767-11E9-B658-BC13E6697425","orcid":"0000-0002-6962-8598","full_name":"Lee, Seungho"},{"first_name":"Maria","last_name":"Spadaro","full_name":"Spadaro, Maria"},{"full_name":"Koskela, Kristopher M.","first_name":"Kristopher M.","last_name":"Koskela"},{"full_name":"Kleinhanns, Tobias","id":"8BD9DE16-AB3C-11E9-9C8C-2A03E6697425","first_name":"Tobias","last_name":"Kleinhanns"},{"id":"D93824F4-D9BA-11E9-BB12-F207E6697425","orcid":"0000-0001-9732-3815","first_name":"Tommaso","last_name":"Costanzo","full_name":"Costanzo, Tommaso"},{"full_name":"Arbiol, Jordi","first_name":"Jordi","last_name":"Arbiol"},{"full_name":"Brutchey, Richard L.","first_name":"Richard L.","last_name":"Brutchey"},{"first_name":"Maria","last_name":"Ibáñez","id":"43C61214-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-5013-2843","full_name":"Ibáñez, Maria"}],"article_number":"e202207002","file_date_updated":"2023-02-02T08:01:00Z","ec_funded":1,"article_type":"original","publication":"Angewandte Chemie - International Edition","citation":{"mla":"Chang, Cheng, et al. “Surface Functionalization of Surfactant-Free Particles: A Strategy to Tailor the Properties of Nanocomposites for Enhanced Thermoelectric Performance.” Angewandte Chemie - International Edition, vol. 61, no. 35, e202207002, Wiley, 2022, doi:10.1002/anie.202207002.","short":"C. Chang, Y. Liu, S. Lee, M. Spadaro, K.M. Koskela, T. Kleinhanns, T. Costanzo, J. Arbiol, R.L. Brutchey, M. Ibáñez, Angewandte Chemie - International Edition 61 (2022).","chicago":"Chang, Cheng, Yu Liu, Seungho Lee, Maria Spadaro, Kristopher M. Koskela, Tobias Kleinhanns, Tommaso Costanzo, Jordi Arbiol, Richard L. Brutchey, and Maria Ibáñez. “Surface Functionalization of Surfactant-Free Particles: A Strategy to Tailor the Properties of Nanocomposites for Enhanced Thermoelectric Performance.” Angewandte Chemie - International Edition. Wiley, 2022. https://doi.org/10.1002/anie.202207002.","ama":"Chang C, Liu Y, Lee S, et al. Surface functionalization of surfactant-free particles: A strategy to tailor the properties of nanocomposites for enhanced thermoelectric performance. Angewandte Chemie - International Edition. 2022;61(35). doi:10.1002/anie.202207002","ista":"Chang C, Liu Y, Lee S, Spadaro M, Koskela KM, Kleinhanns T, Costanzo T, Arbiol J, Brutchey RL, Ibáñez M. 2022. Surface functionalization of surfactant-free particles: A strategy to tailor the properties of nanocomposites for enhanced thermoelectric performance. Angewandte Chemie - International Edition. 61(35), e202207002.","apa":"Chang, C., Liu, Y., Lee, S., Spadaro, M., Koskela, K. M., Kleinhanns, T., … Ibáñez, M. (2022). Surface functionalization of surfactant-free particles: A strategy to tailor the properties of nanocomposites for enhanced thermoelectric performance. Angewandte Chemie - International Edition. Wiley. https://doi.org/10.1002/anie.202207002","ieee":"C. Chang et al., “Surface functionalization of surfactant-free particles: A strategy to tailor the properties of nanocomposites for enhanced thermoelectric performance,” Angewandte Chemie - International Edition, vol. 61, no. 35. Wiley, 2022."},"date_published":"2022-08-26T00:00:00Z","scopus_import":"1","day":"26","article_processing_charge":"Yes (via OA deal)","has_accepted_license":"1","ddc":["540"],"status":"public","title":"Surface functionalization of surfactant-free particles: A strategy to tailor the properties of nanocomposites for enhanced thermoelectric performance","intvolume":" 61","user_id":"4359f0d1-fa6c-11eb-b949-802e58b17ae8","_id":"11705","oa_version":"Published Version","file":[{"access_level":"open_access","file_name":"2022_AngewandteChemieInternat_Chang.pdf","file_size":4072650,"content_type":"application/pdf","creator":"dernst","relation":"main_file","file_id":"12476","checksum":"ad601f2b9e26e46ab4785162be58b5ed","success":1,"date_created":"2023-02-02T08:01:00Z","date_updated":"2023-02-02T08:01:00Z"}],"type":"journal_article","abstract":[{"lang":"eng","text":"The broad implementation of thermoelectricity requires high-performance and low-cost materials. One possibility is employing surfactant-free solution synthesis to produce nanopowders. We propose the strategy of functionalizing “naked” particles’ surface by inorganic molecules to control the nanostructure and, consequently, thermoelectric performance. In particular, we use bismuth thiolates to functionalize surfactant-free SnTe particles’ surfaces. Upon thermal processing, bismuth thiolates decomposition renders SnTe-Bi2S3 nanocomposites with synergistic functions: 1) carrier concentration optimization by Bi doping; 2) Seebeck coefficient enhancement and bipolar effect suppression by energy filtering; and 3) lattice thermal conductivity reduction by small grain domains, grain boundaries and nanostructuration. Overall, the SnTe-Bi2S3 nanocomposites exhibit peak z T up to 1.3 at 873 K and an average z T of ≈0.6 at 300–873 K, which is among the highest reported for solution-processed SnTe."}],"issue":"35"},{"file":[{"date_created":"2023-01-27T10:28:45Z","date_updated":"2023-01-27T10:28:45Z","success":1,"checksum":"4e8152454d12025d13f6e6e9ca06b5d0","file_id":"12422","relation":"main_file","creator":"dernst","content_type":"application/pdf","file_size":1076715,"file_name":"2022_AngewandteChemieInternat_Xu.pdf","access_level":"open_access"}],"oa_version":"Published Version","title":"Isoxazole nucleosides as building blocks for a plausible proto‐RNA","status":"public","ddc":["540"],"intvolume":" 61","_id":"12228","user_id":"4359f0d1-fa6c-11eb-b949-802e58b17ae8","abstract":[{"text":"The question of how RNA, as the principal carrier of genetic information evolved is fundamentally important for our understanding of the origin of life. The RNA molecule is far too complex to have formed in one evolutionary step, suggesting that ancestral proto-RNAs (first ancestor of RNA) may have existed, which evolved over time into the RNA of today. Here we show that isoxazole nucleosides, which are quickly formed from hydroxylamine, cyanoacetylene, urea and ribose, are plausible precursors for RNA. The isoxazole nucleoside can rearrange within an RNA-strand to give cytidine, which leads to an increase of pairing stability. If the proto-RNA contains a canonical seed-nucleoside with defined stereochemistry, the seed-nucleoside can control the configuration of the anomeric center that forms during the in-RNA transformation. The results demonstrate that RNA could have emerged from evolutionarily primitive precursor isoxazole ribosides after strand formation.","lang":"eng"}],"issue":"45","type":"journal_article","date_published":"2022-11-07T00:00:00Z","article_type":"original","publication":"Angewandte Chemie International Edition","citation":{"apa":"Xu, F., Crisp, A., Schinkel, T., Dubini, R. C. A., Hübner, S., Becker, S., … Carell, T. (2022). Isoxazole nucleosides as building blocks for a plausible proto‐RNA. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202211945","ieee":"F. Xu et al., “Isoxazole nucleosides as building blocks for a plausible proto‐RNA,” Angewandte Chemie International Edition, vol. 61, no. 45. Wiley, 2022.","ista":"Xu F, Crisp A, Schinkel T, Dubini RCA, Hübner S, Becker S, Schelter F, Rovo P, Carell T. 2022. Isoxazole nucleosides as building blocks for a plausible proto‐RNA. Angewandte Chemie International Edition. 61(45), e202211945.","ama":"Xu F, Crisp A, Schinkel T, et al. Isoxazole nucleosides as building blocks for a plausible proto‐RNA. Angewandte Chemie International Edition. 2022;61(45). doi:10.1002/anie.202211945","chicago":"Xu, Felix, Antony Crisp, Thea Schinkel, Romeo C. A. Dubini, Sarah Hübner, Sidney Becker, Florian Schelter, Petra Rovo, and Thomas Carell. “Isoxazole Nucleosides as Building Blocks for a Plausible Proto‐RNA.” Angewandte Chemie International Edition. Wiley, 2022. https://doi.org/10.1002/anie.202211945.","short":"F. Xu, A. Crisp, T. Schinkel, R.C.A. Dubini, S. Hübner, S. Becker, F. Schelter, P. Rovo, T. Carell, Angewandte Chemie International Edition 61 (2022).","mla":"Xu, Felix, et al. “Isoxazole Nucleosides as Building Blocks for a Plausible Proto‐RNA.” Angewandte Chemie International Edition, vol. 61, no. 45, e202211945, Wiley, 2022, doi:10.1002/anie.202211945."},"day":"07","article_processing_charge":"No","has_accepted_license":"1","keyword":["General Chemistry","Catalysis"],"scopus_import":"1","date_created":"2023-01-16T09:49:05Z","date_updated":"2023-08-04T09:32:42Z","volume":61,"author":[{"full_name":"Xu, Felix","first_name":"Felix","last_name":"Xu"},{"last_name":"Crisp","first_name":"Antony","full_name":"Crisp, Antony"},{"last_name":"Schinkel","first_name":"Thea","full_name":"Schinkel, Thea"},{"full_name":"Dubini, Romeo C. A.","first_name":"Romeo C. A.","last_name":"Dubini"},{"last_name":"Hübner","first_name":"Sarah","full_name":"Hübner, Sarah"},{"full_name":"Becker, Sidney","first_name":"Sidney","last_name":"Becker"},{"last_name":"Schelter","first_name":"Florian","full_name":"Schelter, Florian"},{"id":"c316e53f-b965-11eb-b128-bb26acc59c00","orcid":"0000-0001-8729-7326","first_name":"Petra","last_name":"Rovo","full_name":"Rovo, Petra"},{"last_name":"Carell","first_name":"Thomas","full_name":"Carell, Thomas"}],"publication_status":"published","publisher":"Wiley","department":[{"_id":"NMR"}],"acknowledgement":"We thank Stefan Wiedemann for the synthesis of reference compounds and Pia Heinrichs for assistance in the NMR measurements of the oligonucleotides. We also thank Dr. Luis Escobar and Jonas Feldmann for valued discussions. This work was supported by the German Research Foundation (DFG) for financial support via CRC1309 (Project ID 325871075, A04), CRC1361 (Project ID 893547839, P02) and CRC1032 (Project ID 201269156, A5). This project has received funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program under grant agreement No 741912 (EpiR). We are grateful for additional funding from the Volkswagen Foundation (EvoRib). Open Access funding enabled and organized by Projekt DEAL.","year":"2022","file_date_updated":"2023-01-27T10:28:45Z","article_number":"e202211945","language":[{"iso":"eng"}],"doi":"10.1002/anie.202211945","quality_controlled":"1","isi":1,"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"oa":1,"external_id":{"isi":["000866428500001"]},"month":"11","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]}},{"month":"03","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"quality_controlled":"1","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1002/anie.202100164"}],"oa":1,"language":[{"iso":"eng"}],"doi":"10.1002/anie.202100164","extern":"1","publication_status":"published","publisher":"Wiley","year":"2021","date_created":"2022-08-24T10:47:16Z","date_updated":"2023-02-21T10:09:14Z","volume":60,"author":[{"first_name":"Luca","last_name":"Schmermund","full_name":"Schmermund, Luca"},{"first_name":"Susanne","last_name":"Reischauer","full_name":"Reischauer, Susanne"},{"full_name":"Bierbaumer, Sarah","first_name":"Sarah","last_name":"Bierbaumer"},{"last_name":"Winkler","first_name":"Christoph K.","full_name":"Winkler, Christoph K."},{"full_name":"Diaz‐Rodriguez, Alba","first_name":"Alba","last_name":"Diaz‐Rodriguez"},{"first_name":"Lee J.","last_name":"Edwards","full_name":"Edwards, Lee J."},{"full_name":"Kara, Selin","first_name":"Selin","last_name":"Kara"},{"full_name":"Mielke, Tamara","first_name":"Tamara","last_name":"Mielke"},{"full_name":"Cartwright, Jared","first_name":"Jared","last_name":"Cartwright"},{"full_name":"Grogan, Gideon","last_name":"Grogan","first_name":"Gideon"},{"full_name":"Pieber, Bartholomäus","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X","first_name":"Bartholomäus","last_name":"Pieber"},{"full_name":"Kroutil, Wolfgang","last_name":"Kroutil","first_name":"Wolfgang"}],"scopus_import":"1","day":"22","article_processing_charge":"No","article_type":"original","page":"6965-6969","publication":"Angewandte Chemie International Edition","citation":{"ama":"Schmermund L, Reischauer S, Bierbaumer S, et al. Chromoselective photocatalysis enables stereocomplementary biocatalytic pathways. Angewandte Chemie International Edition. 2021;60(13):6965-6969. doi:10.1002/anie.202100164","apa":"Schmermund, L., Reischauer, S., Bierbaumer, S., Winkler, C. K., Diaz‐Rodriguez, A., Edwards, L. J., … Kroutil, W. (2021). Chromoselective photocatalysis enables stereocomplementary biocatalytic pathways. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202100164","ieee":"L. Schmermund et al., “Chromoselective photocatalysis enables stereocomplementary biocatalytic pathways,” Angewandte Chemie International Edition, vol. 60, no. 13. Wiley, pp. 6965–6969, 2021.","ista":"Schmermund L, Reischauer S, Bierbaumer S, Winkler CK, Diaz‐Rodriguez A, Edwards LJ, Kara S, Mielke T, Cartwright J, Grogan G, Pieber B, Kroutil W. 2021. Chromoselective photocatalysis enables stereocomplementary biocatalytic pathways. Angewandte Chemie International Edition. 60(13), 6965–6969.","short":"L. Schmermund, S. Reischauer, S. Bierbaumer, C.K. Winkler, A. Diaz‐Rodriguez, L.J. Edwards, S. Kara, T. Mielke, J. Cartwright, G. Grogan, B. Pieber, W. Kroutil, Angewandte Chemie International Edition 60 (2021) 6965–6969.","mla":"Schmermund, Luca, et al. “Chromoselective Photocatalysis Enables Stereocomplementary Biocatalytic Pathways.” Angewandte Chemie International Edition, vol. 60, no. 13, Wiley, 2021, pp. 6965–69, doi:10.1002/anie.202100164.","chicago":"Schmermund, Luca, Susanne Reischauer, Sarah Bierbaumer, Christoph K. Winkler, Alba Diaz‐Rodriguez, Lee J. Edwards, Selin Kara, et al. “Chromoselective Photocatalysis Enables Stereocomplementary Biocatalytic Pathways.” Angewandte Chemie International Edition. Wiley, 2021. https://doi.org/10.1002/anie.202100164."},"date_published":"2021-03-22T00:00:00Z","type":"journal_article","abstract":[{"lang":"eng","text":"Controlling the selectivity of a chemical reaction with external stimuli is common in thermal processes, but rare in visible-light photocatalysis. Here we show that the redox potential of a carbon nitride photocatalyst (CN-OA-m) can be tuned by changing the irradiation wavelength to generate electron holes with different oxidation potentials. This tuning was the key to realizing photo-chemo-enzymatic cascades that give either the (S)- or the (R)-enantiomer of phenylethanol. In combination with an unspecific peroxygenase from Agrocybe aegerita, green light irradiation of CN-OA-m led to the enantioselective hydroxylation of ethylbenzene to (R)-1-phenylethanol (99 % ee). In contrast, blue light irradiation triggered the photocatalytic oxidation of ethylbenzene to acetophenone, which in turn was enantioselectively reduced with an alcohol dehydrogenase from Rhodococcus ruber to form (S)-1-phenylethanol (93 % ee)."}],"issue":"13","title":"Chromoselective photocatalysis enables stereocomplementary biocatalytic pathways","status":"public","intvolume":" 60","_id":"11956","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","oa_version":"Published Version"},{"main_file_link":[{"url":"https://doi.org/10.1002/anie.202014963","open_access":"1"}],"oa":1,"quality_controlled":"1","doi":"10.1002/anie.202014963","language":[{"iso":"eng"}],"month":"03","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"year":"2021","publication_status":"published","publisher":"Wiley","author":[{"full_name":"Ryssy, Joonas","last_name":"Ryssy","first_name":"Joonas"},{"first_name":"Ashwin K.","last_name":"Natarajan","full_name":"Natarajan, Ashwin K."},{"first_name":"Jinhua","last_name":"Wang","full_name":"Wang, Jinhua"},{"first_name":"Arttu J.","last_name":"Lehtonen","full_name":"Lehtonen, Arttu J."},{"last_name":"Nguyen","first_name":"Minh‐Kha","full_name":"Nguyen, Minh‐Kha"},{"full_name":"Klajn, Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","last_name":"Klajn","first_name":"Rafal"},{"last_name":"Kuzyk","first_name":"Anton","full_name":"Kuzyk, Anton"}],"related_material":{"link":[{"relation":"erratum","url":"https://doi.org/10.1002/anie.202210394"}]},"date_updated":"2023-08-02T07:22:23Z","date_created":"2023-08-01T09:35:06Z","volume":60,"extern":"1","publication":"Angewandte Chemie International Edition","citation":{"ama":"Ryssy J, Natarajan AK, Wang J, et al. Light‐responsive dynamic DNA‐origami‐based plasmonic assemblies. Angewandte Chemie International Edition. 2021;60(11):5859-5863. doi:10.1002/anie.202014963","ista":"Ryssy J, Natarajan AK, Wang J, Lehtonen AJ, Nguyen M, Klajn R, Kuzyk A. 2021. Light‐responsive dynamic DNA‐origami‐based plasmonic assemblies. Angewandte Chemie International Edition. 60(11), 5859–5863.","apa":"Ryssy, J., Natarajan, A. K., Wang, J., Lehtonen, A. J., Nguyen, M., Klajn, R., & Kuzyk, A. (2021). Light‐responsive dynamic DNA‐origami‐based plasmonic assemblies. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202014963","ieee":"J. Ryssy et al., “Light‐responsive dynamic DNA‐origami‐based plasmonic assemblies,” Angewandte Chemie International Edition, vol. 60, no. 11. Wiley, pp. 5859–5863, 2021.","mla":"Ryssy, Joonas, et al. “Light‐responsive Dynamic DNA‐origami‐based Plasmonic Assemblies.” Angewandte Chemie International Edition, vol. 60, no. 11, Wiley, 2021, pp. 5859–63, doi:10.1002/anie.202014963.","short":"J. Ryssy, A.K. Natarajan, J. Wang, A.J. Lehtonen, M. Nguyen, R. Klajn, A. Kuzyk, Angewandte Chemie International Edition 60 (2021) 5859–5863.","chicago":"Ryssy, Joonas, Ashwin K. Natarajan, Jinhua Wang, Arttu J. Lehtonen, Minh‐Kha Nguyen, Rafal Klajn, and Anton Kuzyk. “Light‐responsive Dynamic DNA‐origami‐based Plasmonic Assemblies.” Angewandte Chemie International Edition. Wiley, 2021. https://doi.org/10.1002/anie.202014963."},"article_type":"original","page":"5859-5863","date_published":"2021-03-08T00:00:00Z","scopus_import":"1","keyword":["General Chemistry","Catalysis"],"day":"08","article_processing_charge":"No","_id":"13358","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","title":"Light‐responsive dynamic DNA‐origami‐based plasmonic assemblies","status":"public","intvolume":" 60","oa_version":"Published Version","type":"journal_article","abstract":[{"text":"DNA nanotechnology offers a versatile toolbox for precise spatial and temporal manipulation of matter on the nanoscale. However, rendering DNA-based systems responsive to light has remained challenging. Herein, we describe the remote manipulation of native (non-photoresponsive) chiral plasmonic molecules (CPMs) using light. Our strategy is based on the use of a photoresponsive medium comprising a merocyanine-based photoacid. Upon exposure to visible light, the medium decreases its pH, inducing the formation of DNA triplex links, leading to a spatial reconfiguration of the CPMs. The process can be reversed simply by turning the light off and it can be repeated for multiple cycles. The degree of the overall chirality change in an ensemble of CPMs depends on the CPM fraction undergoing reconfiguration, which, remarkably, depends on and can be tuned by the intensity of incident light. Such a dynamic, remotely controlled system could aid in further advancing DNA-based devices and nanomaterials.","lang":"eng"}],"issue":"11"},{"scopus_import":"1","has_accepted_license":"1","article_processing_charge":"No","day":"07","page":"15913-1591","article_type":"original","citation":{"apa":"Bouchal, R., Li, Z., Bongu, C., Le Vot, S., Berthelot, R., Rotenberg, B., … Fontaine, O. (2020). Competitive salt precipitation/dissolution during free‐water reduction in water‐in‐salt electrolyte. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202005378","ieee":"R. Bouchal et al., “Competitive salt precipitation/dissolution during free‐water reduction in water‐in‐salt electrolyte,” Angewandte Chemie International Edition, vol. 59, no. 37. Wiley, pp. 15913–1591, 2020.","ista":"Bouchal R, Li Z, Bongu C, Le Vot S, Berthelot R, Rotenberg B, Favier F, Freunberger SA, Salanne M, Fontaine O. 2020. Competitive salt precipitation/dissolution during free‐water reduction in water‐in‐salt electrolyte. Angewandte Chemie International Edition. 59(37), 15913–1591.","ama":"Bouchal R, Li Z, Bongu C, et al. Competitive salt precipitation/dissolution during free‐water reduction in water‐in‐salt electrolyte. Angewandte Chemie International Edition. 2020;59(37):15913-1591. doi:10.1002/anie.202005378","chicago":"Bouchal, Roza, Zhujie Li, Chandra Bongu, Steven Le Vot, Romain Berthelot, Benjamin Rotenberg, Fréderic Favier, Stefan Alexander Freunberger, Mathieu Salanne, and Olivier Fontaine. “Competitive Salt Precipitation/Dissolution during Free‐water Reduction in Water‐in‐salt Electrolyte.” Angewandte Chemie International Edition. Wiley, 2020. https://doi.org/10.1002/anie.202005378.","short":"R. Bouchal, Z. Li, C. Bongu, S. Le Vot, R. Berthelot, B. Rotenberg, F. Favier, S.A. Freunberger, M. Salanne, O. Fontaine, Angewandte Chemie International Edition 59 (2020) 15913–1591.","mla":"Bouchal, Roza, et al. “Competitive Salt Precipitation/Dissolution during Free‐water Reduction in Water‐in‐salt Electrolyte.” Angewandte Chemie International Edition, vol. 59, no. 37, Wiley, 2020, pp. 15913–1591, doi:10.1002/anie.202005378."},"publication":"Angewandte Chemie International Edition","date_published":"2020-09-07T00:00:00Z","type":"journal_article","issue":"37","abstract":[{"text":"Water-in-salt electrolytes based on highly concentrated bis(trifluoromethyl)sulfonimide (TFSI) promise aqueous electrolytes with stabilities nearing 3 V. However, especially with an electrode approaching the cathodic (reductive) stability, cycling stability is insufficient. While stability critically relies on a solid electrolyte interphase (SEI), the mechanism behind the cathodic stability limit remains unclear. Here, we reveal two distinct reduction potentials for the chemical environments of 'free' and 'bound' water and that both contribute to SEI formation. Free-water is reduced ~1V above bound water in a hydrogen evolution reaction (HER) and responsible for SEI formation via reactive intermediates of the HER; concurrent LiTFSI precipitation/dissolution establishes a dynamic interface. The free-water population emerges, therefore, as the handle to extend the cathodic limit of aqueous electrolytes and the battery cycling stability. ","lang":"eng"}],"intvolume":" 59","title":"Competitive salt precipitation/dissolution during free‐water reduction in water‐in‐salt electrolyte","ddc":["540","546"],"status":"public","_id":"7847","user_id":"c635000d-4b10-11ee-a964-aac5a93f6ac1","file":[{"file_name":"2020_AngChemieINT_Buchal.pdf","access_level":"open_access","content_type":"application/pdf","file_size":1966184,"creator":"dernst","relation":"main_file","file_id":"8400","date_updated":"2020-09-17T08:57:16Z","date_created":"2020-09-17T08:57:16Z","checksum":"7b6c2fc20e9b0ff4353352f7a7004e2d","success":1}],"oa_version":"Published Version","publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]},"month":"09","isi":1,"quality_controlled":"1","tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"external_id":{"isi":["000541488700001"],"pmid":["32390281"]},"oa":1,"language":[{"iso":"eng"}],"doi":"10.1002/anie.202005378","file_date_updated":"2020-09-17T08:57:16Z","department":[{"_id":"StFr"}],"publisher":"Wiley","publication_status":"published","pmid":1,"year":"2020","volume":59,"date_created":"2020-05-14T21:00:30Z","date_updated":"2023-09-05T16:02:53Z","author":[{"last_name":"Bouchal","first_name":"Roza","full_name":"Bouchal, Roza"},{"full_name":"Li, Zhujie","last_name":"Li","first_name":"Zhujie"},{"full_name":"Bongu, Chandra","last_name":"Bongu","first_name":"Chandra"},{"full_name":"Le Vot, Steven","first_name":"Steven","last_name":"Le Vot"},{"last_name":"Berthelot","first_name":"Romain","full_name":"Berthelot, Romain"},{"last_name":"Rotenberg","first_name":"Benjamin","full_name":"Rotenberg, Benjamin"},{"full_name":"Favier, Fréderic","first_name":"Fréderic","last_name":"Favier"},{"first_name":"Stefan Alexander","last_name":"Freunberger","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","orcid":"0000-0003-2902-5319","full_name":"Freunberger, Stefan Alexander"},{"first_name":"Mathieu","last_name":"Salanne","full_name":"Salanne, Mathieu"},{"last_name":"Fontaine","first_name":"Olivier","full_name":"Fontaine, Olivier"}]},{"article_processing_charge":"No","day":"14","scopus_import":"1","date_published":"2020-12-14T00:00:00Z","citation":{"chicago":"Schlemmer, Werner, Philipp Nothdurft, Alina Petzold, Philipp Frühwirt, Max Schmallegger, Georg Gescheidt-Demner, Roland Fischer, Stefan Alexander Freunberger, Wolfgang Kern, and Stefan Spirk. “2‐methoxyhydroquinone from Vanillin for Aqueous Redox‐flow Batteries.” Angewandte Chemie International Edition. Wiley, 2020. https://doi.org/10.1002/anie.202008253.","mla":"Schlemmer, Werner, et al. “2‐methoxyhydroquinone from Vanillin for Aqueous Redox‐flow Batteries.” Angewandte Chemie International Edition, vol. 59, no. 51, Wiley, 2020, pp. 22943–46, doi:10.1002/anie.202008253.","short":"W. Schlemmer, P. Nothdurft, A. Petzold, P. Frühwirt, M. Schmallegger, G. Gescheidt-Demner, R. Fischer, S.A. Freunberger, W. Kern, S. Spirk, Angewandte Chemie International Edition 59 (2020) 22943–22946.","ista":"Schlemmer W, Nothdurft P, Petzold A, Frühwirt P, Schmallegger M, Gescheidt-Demner G, Fischer R, Freunberger SA, Kern W, Spirk S. 2020. 2‐methoxyhydroquinone from vanillin for aqueous redox‐flow batteries. Angewandte Chemie International Edition. 59(51), 22943–22946.","apa":"Schlemmer, W., Nothdurft, P., Petzold, A., Frühwirt, P., Schmallegger, M., Gescheidt-Demner, G., … Spirk, S. (2020). 2‐methoxyhydroquinone from vanillin for aqueous redox‐flow batteries. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202008253","ieee":"W. Schlemmer et al., “2‐methoxyhydroquinone from vanillin for aqueous redox‐flow batteries,” Angewandte Chemie International Edition, vol. 59, no. 51. Wiley, pp. 22943–22946, 2020.","ama":"Schlemmer W, Nothdurft P, Petzold A, et al. 2‐methoxyhydroquinone from vanillin for aqueous redox‐flow batteries. Angewandte Chemie International Edition. 2020;59(51):22943-22946. doi:10.1002/anie.202008253"},"publication":"Angewandte Chemie International Edition","page":"22943-22946","article_type":"original","issue":"51","abstract":[{"lang":"eng","text":"We show the synthesis of a redox‐active quinone, 2‐methoxy‐1,4‐hydroquinone (MHQ), from a bio‐based feedstock and its suitability as electrolyte in aqueous redox flow batteries. We identified semiquinone intermediates at insufficiently low pH and quinoid radicals as responsible for decomposition of MHQ under electrochemical conditions. Both can be avoided and/or stabilized, respectively, using H 3 PO 4 electrolyte, allowing for reversible cycling in a redox flow battery for hundreds of cycles."}],"type":"journal_article","oa_version":"Published Version","_id":"8329","user_id":"c635000d-4b10-11ee-a964-aac5a93f6ac1","intvolume":" 59","title":"2‐methoxyhydroquinone from vanillin for aqueous redox‐flow batteries","status":"public","publication_identifier":{"issn":["1433-7851"],"eissn":["1521-3773"]},"month":"12","doi":"10.1002/anie.202008253","language":[{"iso":"eng"}],"main_file_link":[{"url":"https://doi.org/10.1002/anie.202008253","open_access":"1"}],"external_id":{"isi":["000576148700001"]},"oa":1,"isi":1,"quality_controlled":"1","related_material":{"record":[{"id":"9780","status":"public","relation":"research_data"}]},"author":[{"full_name":"Schlemmer, Werner","last_name":"Schlemmer","first_name":"Werner"},{"last_name":"Nothdurft","first_name":"Philipp","full_name":"Nothdurft, Philipp"},{"full_name":"Petzold, Alina","last_name":"Petzold","first_name":"Alina"},{"last_name":"Frühwirt","first_name":"Philipp","full_name":"Frühwirt, Philipp"},{"full_name":"Schmallegger, Max","first_name":"Max","last_name":"Schmallegger"},{"full_name":"Gescheidt-Demner, Georg","last_name":"Gescheidt-Demner","first_name":"Georg"},{"full_name":"Fischer, Roland","last_name":"Fischer","first_name":"Roland"},{"full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","last_name":"Freunberger","first_name":"Stefan Alexander"},{"full_name":"Kern, Wolfgang","first_name":"Wolfgang","last_name":"Kern"},{"full_name":"Spirk, Stefan","first_name":"Stefan","last_name":"Spirk"}],"volume":59,"date_updated":"2023-09-05T16:03:47Z","date_created":"2020-09-03T16:10:56Z","acknowledgement":"The Austrian Research Promotion Agency (FFG) is gratefully acknowledged for financial support of the project LignoBatt (860429).","year":"2020","department":[{"_id":"StFr"}],"publisher":"Wiley","publication_status":"published"},{"quality_controlled":"1","external_id":{"pmid":["31050132"]},"language":[{"iso":"eng"}],"doi":"10.1002/anie.201902785","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"month":"07","publisher":"Wiley","publication_status":"published","pmid":1,"year":"2019","volume":58,"date_updated":"2023-02-21T10:09:16Z","date_created":"2022-08-24T10:50:19Z","author":[{"id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X","first_name":"Bartholomäus","last_name":"Pieber","full_name":"Pieber, Bartholomäus"},{"last_name":"Malik","first_name":"Jamal A.","full_name":"Malik, Jamal A."},{"full_name":"Cavedon, Cristian","first_name":"Cristian","last_name":"Cavedon"},{"first_name":"Sebastian","last_name":"Gisbertz","full_name":"Gisbertz, Sebastian"},{"full_name":"Savateev, Aleksandr","last_name":"Savateev","first_name":"Aleksandr"},{"first_name":"Daniel","last_name":"Cruz","full_name":"Cruz, Daniel"},{"last_name":"Heil","first_name":"Tobias","full_name":"Heil, Tobias"},{"first_name":"Guigang","last_name":"Zhang","full_name":"Zhang, Guigang"},{"first_name":"Peter H.","last_name":"Seeberger","full_name":"Seeberger, Peter H."}],"extern":"1","page":"9575-9580","article_type":"letter_note","citation":{"chicago":"Pieber, Bartholomäus, Jamal A. Malik, Cristian Cavedon, Sebastian Gisbertz, Aleksandr Savateev, Daniel Cruz, Tobias Heil, Guigang Zhang, and Peter H. Seeberger. “Semi‐heterogeneous Dual Nickel/Photocatalysis Using Carbon Nitrides: Esterification of Carboxylic Acids with Aryl Halides.” Angewandte Chemie International Edition. Wiley, 2019. https://doi.org/10.1002/anie.201902785.","mla":"Pieber, Bartholomäus, et al. “Semi‐heterogeneous Dual Nickel/Photocatalysis Using Carbon Nitrides: Esterification of Carboxylic Acids with Aryl Halides.” Angewandte Chemie International Edition, vol. 58, no. 28, Wiley, 2019, pp. 9575–80, doi:10.1002/anie.201902785.","short":"B. Pieber, J.A. Malik, C. Cavedon, S. Gisbertz, A. Savateev, D. Cruz, T. Heil, G. Zhang, P.H. Seeberger, Angewandte Chemie International Edition 58 (2019) 9575–9580.","ista":"Pieber B, Malik JA, Cavedon C, Gisbertz S, Savateev A, Cruz D, Heil T, Zhang G, Seeberger PH. 2019. Semi‐heterogeneous dual nickel/photocatalysis using carbon nitrides: Esterification of carboxylic acids with aryl halides. Angewandte Chemie International Edition. 58(28), 9575–9580.","apa":"Pieber, B., Malik, J. A., Cavedon, C., Gisbertz, S., Savateev, A., Cruz, D., … Seeberger, P. H. (2019). Semi‐heterogeneous dual nickel/photocatalysis using carbon nitrides: Esterification of carboxylic acids with aryl halides. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201902785","ieee":"B. Pieber et al., “Semi‐heterogeneous dual nickel/photocatalysis using carbon nitrides: Esterification of carboxylic acids with aryl halides,” Angewandte Chemie International Edition, vol. 58, no. 28. Wiley, pp. 9575–9580, 2019.","ama":"Pieber B, Malik JA, Cavedon C, et al. Semi‐heterogeneous dual nickel/photocatalysis using carbon nitrides: Esterification of carboxylic acids with aryl halides. Angewandte Chemie International Edition. 2019;58(28):9575-9580. doi:10.1002/anie.201902785"},"publication":"Angewandte Chemie International Edition","date_published":"2019-07-08T00:00:00Z","scopus_import":"1","article_processing_charge":"No","day":"08","intvolume":" 58","status":"public","title":"Semi‐heterogeneous dual nickel/photocatalysis using carbon nitrides: Esterification of carboxylic acids with aryl halides","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"11957","oa_version":"None","type":"journal_article","issue":"28","abstract":[{"text":"Cross-coupling reactions mediated by dual nickel/photocatalysis are synthetically attractive but rely mainly on expensive, non-recyclable noble-metal complexes as photocatalysts. Heterogeneous semiconductors, which are commonly used for artificial photosynthesis and wastewater treatment, are a sustainable alternative. Graphitic carbon nitrides, a class of metal-free polymers that can be easily prepared from bulk chemicals, are heterogeneous semiconductors with high potential for photocatalytic organic transformations. Here, we demonstrate that graphitic carbon nitrides in combination with nickel catalysis can induce selective C−O cross-couplings of carboxylic acids with aryl halides, yielding the respective aryl esters in excellent yield and selectivity. The heterogeneous organic photocatalyst exhibits a broad substrate scope, is able to harvest green light, and can be recycled multiple times. In situ FTIR was used to track the reaction progress to study this transformation at different irradiation wavelengths and reaction scales.","lang":"eng"}]},{"tmp":{"name":"Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode","short":"CC BY-NC-ND (4.0)","image":"/images/cc_by_nc_nd.png"},"oa":1,"quality_controlled":"1","doi":"10.1002/anie.201901869","language":[{"iso":"eng"}],"month":"05","publication_identifier":{"issn":["1433-7851"]},"year":"2019","publication_status":"published","publisher":"Wiley","author":[{"full_name":"Petit, Yann K.","last_name":"Petit","first_name":"Yann K."},{"full_name":"Leypold, Christian","first_name":"Christian","last_name":"Leypold"},{"last_name":"Mahne","first_name":"Nika","full_name":"Mahne, Nika"},{"last_name":"Mourad","first_name":"Eléonore","full_name":"Mourad, Eléonore"},{"last_name":"Schafzahl","first_name":"Lukas","full_name":"Schafzahl, Lukas"},{"first_name":"Christian","last_name":"Slugovc","full_name":"Slugovc, Christian"},{"full_name":"Borisov, Sergey M.","last_name":"Borisov","first_name":"Sergey M."},{"full_name":"Freunberger, Stefan Alexander","last_name":"Freunberger","first_name":"Stefan Alexander","orcid":"0000-0003-2902-5319","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"}],"date_updated":"2021-01-12T08:12:42Z","date_created":"2020-01-15T07:19:27Z","volume":58,"file_date_updated":"2020-07-14T12:47:55Z","license":"https://creativecommons.org/licenses/by-nc-nd/4.0/","extern":"1","publication":"Angewandte Chemie International Edition","citation":{"short":"Y.K. Petit, C. Leypold, N. Mahne, E. Mourad, L. Schafzahl, C. Slugovc, S.M. Borisov, S.A. Freunberger, Angewandte Chemie International Edition 58 (2019) 6535–6539.","mla":"Petit, Yann K., et al. “DABCOnium: An Efficient and High-Voltage Stable Singlet Oxygen Quencher for Metal-O2 Cells.” Angewandte Chemie International Edition, vol. 58, no. 20, Wiley, 2019, pp. 6535–39, doi:10.1002/anie.201901869.","chicago":"Petit, Yann K., Christian Leypold, Nika Mahne, Eléonore Mourad, Lukas Schafzahl, Christian Slugovc, Sergey M. Borisov, and Stefan Alexander Freunberger. “DABCOnium: An Efficient and High-Voltage Stable Singlet Oxygen Quencher for Metal-O2 Cells.” Angewandte Chemie International Edition. Wiley, 2019. https://doi.org/10.1002/anie.201901869.","ama":"Petit YK, Leypold C, Mahne N, et al. DABCOnium: An efficient and high-voltage stable singlet oxygen quencher for metal-O2 cells. Angewandte Chemie International Edition. 2019;58(20):6535-6539. doi:10.1002/anie.201901869","ieee":"Y. K. Petit et al., “DABCOnium: An efficient and high-voltage stable singlet oxygen quencher for metal-O2 cells,” Angewandte Chemie International Edition, vol. 58, no. 20. Wiley, pp. 6535–6539, 2019.","apa":"Petit, Y. K., Leypold, C., Mahne, N., Mourad, E., Schafzahl, L., Slugovc, C., … Freunberger, S. A. (2019). DABCOnium: An efficient and high-voltage stable singlet oxygen quencher for metal-O2 cells. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201901869","ista":"Petit YK, Leypold C, Mahne N, Mourad E, Schafzahl L, Slugovc C, Borisov SM, Freunberger SA. 2019. DABCOnium: An efficient and high-voltage stable singlet oxygen quencher for metal-O2 cells. Angewandte Chemie International Edition. 58(20), 6535–6539."},"article_type":"original","page":"6535-6539","date_published":"2019-05-13T00:00:00Z","day":"13","has_accepted_license":"1","article_processing_charge":"No","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"7276","status":"public","title":"DABCOnium: An efficient and high-voltage stable singlet oxygen quencher for metal-O2 cells","ddc":["540"],"intvolume":" 58","oa_version":"Published Version","file":[{"file_size":952737,"content_type":"application/pdf","creator":"dernst","access_level":"open_access","file_name":"2019_AngewChemie_Petit.pdf","checksum":"9620b6a511a910d7abe1f26c42dc7f83","date_updated":"2020-07-14T12:47:55Z","date_created":"2020-01-22T16:16:54Z","relation":"main_file","file_id":"7356"}],"type":"journal_article","abstract":[{"text":"Singlet oxygen (1O2) causes a major fraction of the parasitic chemistry during the cycling of non‐aqueous alkali metal‐O2 batteries and also contributes to interfacial reactivity of transition‐metal oxide intercalation compounds. We introduce DABCOnium, the mono alkylated form of 1,4‐diazabicyclo[2.2.2]octane (DABCO), as an efficient 1O2 quencher with an unusually high oxidative stability of ca. 4.2 V vs. Li/Li+. Previous quenchers are strongly Lewis basic amines with too low oxidative stability. DABCOnium is an ionic liquid, non‐volatile, highly soluble in the electrolyte, stable against superoxide and peroxide, and compatible with lithium metal. The electrochemical stability covers the required range for metal–O2 batteries and greatly reduces 1O2 related parasitic chemistry as demonstrated for the Li–O2 cell.","lang":"eng"}],"issue":"20"},{"type":"journal_article","issue":"31","abstract":[{"text":"Solid reagents, leaching catalysts, and heterogeneous photocatalysts are commonly employed in batch processes but are ill-suited for continuous-flow chemistry. Heterogeneous catalysts for thermal reactions are typically used in packed-bed reactors, which cannot be penetrated by light and thus are not suitable for photocatalytic reactions involving solids. We demonstrate that serial micro-batch reactors (SMBRs) allow for the continuous utilization of solid materials together with liquids and gases in flow. This technology was utilized to develop selective and efficient fluorination reactions using a modified graphitic carbon nitride heterogeneous catalyst instead of costly homogeneous metal polypyridyl complexes. The merger of this inexpensive, recyclable catalyst and the SMBR approach enables sustainable and scalable photocatalysis.","lang":"eng"}],"intvolume":" 57","status":"public","title":"Continuous heterogeneous photocatalysis in serial micro-batch reactors","_id":"11958","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","oa_version":"None","scopus_import":"1","article_processing_charge":"No","day":"26","page":"9976-9979","article_type":"letter_note","citation":{"ama":"Pieber B, Shalom M, Antonietti M, Seeberger PH, Gilmore K. Continuous heterogeneous photocatalysis in serial micro-batch reactors. Angewandte Chemie International Edition. 2018;57(31):9976-9979. doi:10.1002/anie.201712568","ista":"Pieber B, Shalom M, Antonietti M, Seeberger PH, Gilmore K. 2018. Continuous heterogeneous photocatalysis in serial micro-batch reactors. Angewandte Chemie International Edition. 57(31), 9976–9979.","apa":"Pieber, B., Shalom, M., Antonietti, M., Seeberger, P. H., & Gilmore, K. (2018). Continuous heterogeneous photocatalysis in serial micro-batch reactors. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201712568","ieee":"B. Pieber, M. Shalom, M. Antonietti, P. H. Seeberger, and K. Gilmore, “Continuous heterogeneous photocatalysis in serial micro-batch reactors,” Angewandte Chemie International Edition, vol. 57, no. 31. Wiley, pp. 9976–9979, 2018.","mla":"Pieber, Bartholomäus, et al. “Continuous Heterogeneous Photocatalysis in Serial Micro-Batch Reactors.” Angewandte Chemie International Edition, vol. 57, no. 31, Wiley, 2018, pp. 9976–79, doi:10.1002/anie.201712568.","short":"B. Pieber, M. Shalom, M. Antonietti, P.H. Seeberger, K. Gilmore, Angewandte Chemie International Edition 57 (2018) 9976–9979.","chicago":"Pieber, Bartholomäus, Menny Shalom, Markus Antonietti, Peter H. Seeberger, and Kerry Gilmore. “Continuous Heterogeneous Photocatalysis in Serial Micro-Batch Reactors.” Angewandte Chemie International Edition. Wiley, 2018. https://doi.org/10.1002/anie.201712568."},"publication":"Angewandte Chemie International Edition","date_published":"2018-07-26T00:00:00Z","extern":"1","publisher":"Wiley","publication_status":"published","pmid":1,"year":"2018","volume":57,"date_created":"2022-08-24T10:57:25Z","date_updated":"2023-02-21T10:09:18Z","author":[{"full_name":"Pieber, Bartholomäus","first_name":"Bartholomäus","last_name":"Pieber","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X"},{"full_name":"Shalom, Menny","first_name":"Menny","last_name":"Shalom"},{"first_name":"Markus","last_name":"Antonietti","full_name":"Antonietti, Markus"},{"full_name":"Seeberger, Peter H.","first_name":"Peter H.","last_name":"Seeberger"},{"full_name":"Gilmore, Kerry","last_name":"Gilmore","first_name":"Kerry"}],"publication_identifier":{"eissn":[" 1521-3773"],"issn":["1433-7851"]},"month":"07","quality_controlled":"1","external_id":{"pmid":["29377383"]},"language":[{"iso":"eng"}],"doi":"10.1002/anie.201712568"},{"volume":57,"date_created":"2020-01-15T07:20:09Z","date_updated":"2021-01-12T08:12:42Z","author":[{"full_name":"Mahne, Nika","first_name":"Nika","last_name":"Mahne"},{"full_name":"Renfrew, Sara E.","first_name":"Sara E.","last_name":"Renfrew"},{"last_name":"McCloskey","first_name":"Bryan D.","full_name":"McCloskey, Bryan D."},{"full_name":"Freunberger, Stefan Alexander","last_name":"Freunberger","first_name":"Stefan Alexander","orcid":"0000-0003-2902-5319","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"}],"publisher":"Wiley","publication_status":"published","year":"2018","extern":"1","file_date_updated":"2020-07-14T12:47:55Z","language":[{"iso":"eng"}],"doi":"10.1002/anie.201802277","quality_controlled":"1","tmp":{"name":"Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode","short":"CC BY-NC-ND (4.0)","image":"/images/cc_by_nc_nd.png"},"oa":1,"publication_identifier":{"issn":["1433-7851"]},"month":"03","file":[{"file_size":657963,"content_type":"application/pdf","creator":"dernst","file_name":"2018_AngewChemie_Mahne.pdf","access_level":"open_access","date_updated":"2020-07-14T12:47:55Z","date_created":"2020-01-22T16:28:31Z","checksum":"45868d0adc2d13a506bb9a59eb4f409c","relation":"main_file","file_id":"7357"}],"oa_version":"Published Version","intvolume":" 57","title":"Electrochemical oxidation of Lithium Carbonate generates singlet oxygen","status":"public","ddc":["540"],"_id":"7277","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","issue":"19","abstract":[{"text":"Solid alkali metal carbonates are universal passivation layer components of intercalation battery materials and common side products in metal‐O2 batteries, and are believed to form and decompose reversibly in metal‐O2/CO2 cells. In these cathodes, Li2CO3 decomposes to CO2 when exposed to potentials above 3.8 V vs. Li/Li+. However, O2 evolution, as would be expected according to the decomposition reaction 2 Li2CO3→4 Li++4 e−+2 CO2+O2, is not detected. O atoms are thus unaccounted for, which was previously ascribed to unidentified parasitic reactions. Here, we show that highly reactive singlet oxygen (1O2) forms upon oxidizing Li2CO3 in an aprotic electrolyte and therefore does not evolve as O2. These results have substantial implications for the long‐term cyclability of batteries: they underpin the importance of avoiding 1O2 in metal‐O2 batteries, question the possibility of a reversible metal‐O2/CO2 battery based on a carbonate discharge product, and help explain the interfacial reactivity of transition‐metal cathodes with residual Li2CO3.","lang":"eng"}],"type":"journal_article","date_published":"2018-03-15T00:00:00Z","page":"5529-5533","article_type":"original","citation":{"mla":"Mahne, Nika, et al. “Electrochemical Oxidation of Lithium Carbonate Generates Singlet Oxygen.” Angewandte Chemie International Edition, vol. 57, no. 19, Wiley, 2018, pp. 5529–33, doi:10.1002/anie.201802277.","short":"N. Mahne, S.E. Renfrew, B.D. McCloskey, S.A. Freunberger, Angewandte Chemie International Edition 57 (2018) 5529–5533.","chicago":"Mahne, Nika, Sara E. Renfrew, Bryan D. McCloskey, and Stefan Alexander Freunberger. “Electrochemical Oxidation of Lithium Carbonate Generates Singlet Oxygen.” Angewandte Chemie International Edition. Wiley, 2018. https://doi.org/10.1002/anie.201802277.","ama":"Mahne N, Renfrew SE, McCloskey BD, Freunberger SA. Electrochemical oxidation of Lithium Carbonate generates singlet oxygen. Angewandte Chemie International Edition. 2018;57(19):5529-5533. doi:10.1002/anie.201802277","ista":"Mahne N, Renfrew SE, McCloskey BD, Freunberger SA. 2018. Electrochemical oxidation of Lithium Carbonate generates singlet oxygen. Angewandte Chemie International Edition. 57(19), 5529–5533.","ieee":"N. Mahne, S. E. Renfrew, B. D. McCloskey, and S. A. Freunberger, “Electrochemical oxidation of Lithium Carbonate generates singlet oxygen,” Angewandte Chemie International Edition, vol. 57, no. 19. Wiley, pp. 5529–5533, 2018.","apa":"Mahne, N., Renfrew, S. E., McCloskey, B. D., & Freunberger, S. A. (2018). Electrochemical oxidation of Lithium Carbonate generates singlet oxygen. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201802277"},"publication":"Angewandte Chemie International Edition","has_accepted_license":"1","article_processing_charge":"No","day":"15"},{"type":"journal_article","issue":"24","abstract":[{"lang":"eng","text":"Confining organic molecules to the surfaces of inorganic nanoparticles can induce intermolecular interactions between them, which can affect the composition of the mixed self-assembled monolayers obtained by co-adsorption from solution of two different molecules. Two thiolated ligands (a dialkylviologen and a zwitterionic sulfobetaine) that can interact with each other electrostatically were coadsorbed onto gold nanoparticles. The nanoparticles favor a narrow range of ratios of these two molecules that is largely independent of the molar ratio in solution. Changing the solution molar ratio of the two ligands by a factor of 5 000 affects the on-nanoparticle ratio of these ligands by only threefold. This behavior is reminiscent of the formation of insoluble inorganic salts (such as AgCl), which similarly compensate positive and negative charges upon crystallizing. Our results pave the way towards developing well-defined hybrid organic–inorganic nanostructures."}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"13377","intvolume":" 57","status":"public","title":"“Precipitation on nanoparticles”: Attractive intermolecular interactions stabilize specific ligand ratios on the surfaces of nanoparticles","oa_version":"Published Version","scopus_import":"1","keyword":["General Chemistry","Catalysis"],"article_processing_charge":"No","day":"11","citation":{"short":"Z. Chu, Y. Han, P. Král, R. Klajn, Angewandte Chemie International Edition 57 (2018) 7023–7027.","mla":"Chu, Zonglin, et al. “‘Precipitation on Nanoparticles’: Attractive Intermolecular Interactions Stabilize Specific Ligand Ratios on the Surfaces of Nanoparticles.” Angewandte Chemie International Edition, vol. 57, no. 24, Wiley, 2018, pp. 7023–27, doi:10.1002/anie.201800673.","chicago":"Chu, Zonglin, Yanxiao Han, Petr Král, and Rafal Klajn. “‘Precipitation on Nanoparticles’: Attractive Intermolecular Interactions Stabilize Specific Ligand Ratios on the Surfaces of Nanoparticles.” Angewandte Chemie International Edition. Wiley, 2018. https://doi.org/10.1002/anie.201800673.","ama":"Chu Z, Han Y, Král P, Klajn R. “Precipitation on nanoparticles”: Attractive intermolecular interactions stabilize specific ligand ratios on the surfaces of nanoparticles. Angewandte Chemie International Edition. 2018;57(24):7023-7027. doi:10.1002/anie.201800673","apa":"Chu, Z., Han, Y., Král, P., & Klajn, R. (2018). “Precipitation on nanoparticles”: Attractive intermolecular interactions stabilize specific ligand ratios on the surfaces of nanoparticles. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201800673","ieee":"Z. Chu, Y. Han, P. Král, and R. Klajn, “‘Precipitation on nanoparticles’: Attractive intermolecular interactions stabilize specific ligand ratios on the surfaces of nanoparticles,” Angewandte Chemie International Edition, vol. 57, no. 24. Wiley, pp. 7023–7027, 2018.","ista":"Chu Z, Han Y, Král P, Klajn R. 2018. “Precipitation on nanoparticles”: Attractive intermolecular interactions stabilize specific ligand ratios on the surfaces of nanoparticles. Angewandte Chemie International Edition. 57(24), 7023–7027."},"publication":"Angewandte Chemie International Edition","page":"7023-7027","article_type":"original","date_published":"2018-06-11T00:00:00Z","extern":"1","pmid":1,"year":"2018","publisher":"Wiley","publication_status":"published","author":[{"full_name":"Chu, Zonglin","first_name":"Zonglin","last_name":"Chu"},{"first_name":"Yanxiao","last_name":"Han","full_name":"Han, Yanxiao"},{"first_name":"Petr","last_name":"Král","full_name":"Král, Petr"},{"full_name":"Klajn, Rafal","last_name":"Klajn","first_name":"Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b"}],"volume":57,"date_updated":"2023-08-07T11:14:28Z","date_created":"2023-08-01T09:40:16Z","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"month":"06","oa":1,"external_id":{"pmid":["29673022"]},"main_file_link":[{"open_access":"1","url":"https://doi.org/10.1002/anie.201800673"}],"quality_controlled":"1","doi":"10.1002/anie.201800673","language":[{"iso":"eng"}]},{"month":"12","publication_identifier":{"issn":["1433-7851"]},"language":[{"iso":"eng"}],"doi":"10.1002/anie.201809847","quality_controlled":"1","isi":1,"oa":1,"external_id":{"isi":["000454575500020"]},"main_file_link":[{"url":"https://upcommons.upc.edu/bitstream/2117/130444/1/Zhang%20preprint.pdf","open_access":"1"}],"date_created":"2019-02-14T10:23:27Z","date_updated":"2023-09-19T14:28:31Z","volume":57,"author":[{"full_name":"Zhang, Yu","first_name":"Yu","last_name":"Zhang"},{"full_name":"Liu, Yu","first_name":"Yu","last_name":"Liu"},{"last_name":"Lim","first_name":"Khak Ho","full_name":"Lim, Khak Ho"},{"full_name":"Xing, Congcong","first_name":"Congcong","last_name":"Xing"},{"first_name":"Mengyao","last_name":"Li","full_name":"Li, Mengyao"},{"first_name":"Ting","last_name":"Zhang","full_name":"Zhang, Ting"},{"full_name":"Tang, Pengyi","first_name":"Pengyi","last_name":"Tang"},{"first_name":"Jordi","last_name":"Arbiol","full_name":"Arbiol, Jordi"},{"first_name":"Jordi","last_name":"Llorca","full_name":"Llorca, Jordi"},{"full_name":"Ng, Ka Ming","first_name":"Ka Ming","last_name":"Ng"},{"first_name":"Maria","last_name":"Ibáñez","id":"43C61214-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-5013-2843","full_name":"Ibáñez, Maria"},{"full_name":"Guardia, Pablo","last_name":"Guardia","first_name":"Pablo"},{"last_name":"Prato","first_name":"Mirko","full_name":"Prato, Mirko"},{"full_name":"Cadavid, Doris","first_name":"Doris","last_name":"Cadavid"},{"full_name":"Cabot, Andreu","last_name":"Cabot","first_name":"Andreu"}],"publication_status":"published","department":[{"_id":"MaIb"}],"publisher":"Wiley","year":"2018","day":"21","article_processing_charge":"No","scopus_import":"1","date_published":"2018-12-21T00:00:00Z","article_type":"original","page":"17063-17068","publication":"Angewandte Chemie International Edition","citation":{"short":"Y. Zhang, Y. Liu, K.H. Lim, C. Xing, M. Li, T. Zhang, P. Tang, J. Arbiol, J. Llorca, K.M. Ng, M. Ibáñez, P. Guardia, M. Prato, D. Cadavid, A. Cabot, Angewandte Chemie International Edition 57 (2018) 17063–17068.","mla":"Zhang, Yu, et al. “Tin Diselenide Molecular Precursor for Solution-Processable Thermoelectric Materials.” Angewandte Chemie International Edition, vol. 57, no. 52, Wiley, 2018, pp. 17063–68, doi:10.1002/anie.201809847.","chicago":"Zhang, Yu, Yu Liu, Khak Ho Lim, Congcong Xing, Mengyao Li, Ting Zhang, Pengyi Tang, et al. “Tin Diselenide Molecular Precursor for Solution-Processable Thermoelectric Materials.” Angewandte Chemie International Edition. Wiley, 2018. https://doi.org/10.1002/anie.201809847.","ama":"Zhang Y, Liu Y, Lim KH, et al. Tin diselenide molecular precursor for solution-processable thermoelectric materials. Angewandte Chemie International Edition. 2018;57(52):17063-17068. doi:10.1002/anie.201809847","ieee":"Y. Zhang et al., “Tin diselenide molecular precursor for solution-processable thermoelectric materials,” Angewandte Chemie International Edition, vol. 57, no. 52. Wiley, pp. 17063–17068, 2018.","apa":"Zhang, Y., Liu, Y., Lim, K. H., Xing, C., Li, M., Zhang, T., … Cabot, A. (2018). Tin diselenide molecular precursor for solution-processable thermoelectric materials. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201809847","ista":"Zhang Y, Liu Y, Lim KH, Xing C, Li M, Zhang T, Tang P, Arbiol J, Llorca J, Ng KM, Ibáñez M, Guardia P, Prato M, Cadavid D, Cabot A. 2018. Tin diselenide molecular precursor for solution-processable thermoelectric materials. Angewandte Chemie International Edition. 57(52), 17063–17068."},"abstract":[{"text":"In the present work, we detail a fast and simple solution-based method to synthesize hexagonal SnSe2 nanoplates (NPLs) and their use to produce crystallographically textured SnSe2 nanomaterials. We also demonstrate that the same strategy can be used to produce orthorhombic SnSe nanostructures and nanomaterials. NPLs are grown through a screw dislocation-driven mechanism. This mechanism typically results in pyramidal structures, but we demonstrate here that the growth from multiple dislocations results in flower-like structures. Crystallographically textured SnSe2 bulk nanomaterials obtained from the hot pressing of these SnSe2 structures display highly anisotropic charge and heat transport properties and thermoelectric (TE) figures of merit limited by relatively low electrical conductivities. To improve this parameter, SnSe2 NPLs are blended here with metal nanoparticles. The electrical conductivities of the blends are significantly improved with respect to bare SnSe2 NPLs, what translates into a three-fold increase of the TE Figure of merit, reaching unprecedented ZT values up to 0.65.","lang":"eng"}],"issue":"52","type":"journal_article","oa_version":"Submitted Version","title":"Tin diselenide molecular precursor for solution-processable thermoelectric materials","status":"public","intvolume":" 57","user_id":"c635000d-4b10-11ee-a964-aac5a93f6ac1","_id":"5982"},{"file_date_updated":"2020-07-14T12:47:55Z","extern":"1","year":"2017","publication_status":"published","publisher":"Wiley","author":[{"first_name":"Lukas","last_name":"Schafzahl","full_name":"Schafzahl, Lukas"},{"full_name":"Mahne, Nika","first_name":"Nika","last_name":"Mahne"},{"last_name":"Schafzahl","first_name":"Bettina","full_name":"Schafzahl, Bettina"},{"full_name":"Wilkening, Martin","last_name":"Wilkening","first_name":"Martin"},{"full_name":"Slugovc, Christian","first_name":"Christian","last_name":"Slugovc"},{"full_name":"Borisov, Sergey M.","last_name":"Borisov","first_name":"Sergey M."},{"full_name":"Freunberger, Stefan Alexander","first_name":"Stefan Alexander","last_name":"Freunberger","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","orcid":"0000-0003-2902-5319"}],"date_updated":"2021-01-12T08:12:47Z","date_created":"2020-01-15T12:15:05Z","volume":56,"month":"12","publication_identifier":{"issn":["1433-7851"]},"oa":1,"tmp":{"name":"Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc/4.0/legalcode","image":"/images/cc_by_nc.png","short":"CC BY-NC (4.0)"},"quality_controlled":"1","doi":"10.1002/anie.201709351","language":[{"iso":"eng"}],"type":"journal_article","abstract":[{"lang":"eng","text":"Aprotic sodium–O2 batteries require the reversible formation/dissolution of sodium superoxide (NaO2) on cycling. Poor cycle life has been associated with parasitic chemistry caused by the reactivity of electrolyte and electrode with NaO2, a strong nucleophile and base. Its reactivity can, however, not consistently explain the side reactions and irreversibility. Herein we show that singlet oxygen (1O2) forms at all stages of cycling and that it is a main driver for parasitic chemistry. It was detected in‐ and ex‐situ via a 1O2 trap that selectively and rapidly forms a stable adduct with 1O2. The 1O2 formation mechanism involves proton‐mediated superoxide disproportionation on discharge, rest, and charge below ca. 3.3 V, and direct electrochemical 1O2 evolution above ca. 3.3 V. Trace water, which is needed for high capacities also drives parasitic chemistry. Controlling the highly reactive singlet oxygen is thus crucial for achieving highly reversible cell operation."}],"issue":"49","_id":"7289","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","title":"Singlet oxygen during cycling of the aprotic sodium-O2 battery","ddc":["540"],"status":"public","intvolume":" 56","oa_version":"Published Version","file":[{"access_level":"open_access","file_name":"2017_AngChemieInternat_Schafzahl.pdf","creator":"dernst","content_type":"application/pdf","file_size":1013492,"file_id":"7362","relation":"main_file","checksum":"3c5b1e51954554dffb13c7d58f69836c","date_created":"2020-01-26T14:58:07Z","date_updated":"2020-07-14T12:47:55Z"}],"day":"04","has_accepted_license":"1","article_processing_charge":"No","publication":"Angewandte Chemie International Edition","citation":{"apa":"Schafzahl, L., Mahne, N., Schafzahl, B., Wilkening, M., Slugovc, C., Borisov, S. M., & Freunberger, S. A. (2017). Singlet oxygen during cycling of the aprotic sodium-O2 battery. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201709351","ieee":"L. Schafzahl et al., “Singlet oxygen during cycling of the aprotic sodium-O2 battery,” Angewandte Chemie International Edition, vol. 56, no. 49. Wiley, pp. 15728–15732, 2017.","ista":"Schafzahl L, Mahne N, Schafzahl B, Wilkening M, Slugovc C, Borisov SM, Freunberger SA. 2017. Singlet oxygen during cycling of the aprotic sodium-O2 battery. Angewandte Chemie International Edition. 56(49), 15728–15732.","ama":"Schafzahl L, Mahne N, Schafzahl B, et al. Singlet oxygen during cycling of the aprotic sodium-O2 battery. Angewandte Chemie International Edition. 2017;56(49):15728-15732. doi:10.1002/anie.201709351","chicago":"Schafzahl, Lukas, Nika Mahne, Bettina Schafzahl, Martin Wilkening, Christian Slugovc, Sergey M. Borisov, and Stefan Alexander Freunberger. “Singlet Oxygen during Cycling of the Aprotic Sodium-O2 Battery.” Angewandte Chemie International Edition. Wiley, 2017. https://doi.org/10.1002/anie.201709351.","short":"L. Schafzahl, N. Mahne, B. Schafzahl, M. Wilkening, C. Slugovc, S.M. Borisov, S.A. Freunberger, Angewandte Chemie International Edition 56 (2017) 15728–15732.","mla":"Schafzahl, Lukas, et al. “Singlet Oxygen during Cycling of the Aprotic Sodium-O2 Battery.” Angewandte Chemie International Edition, vol. 56, no. 49, Wiley, 2017, pp. 15728–32, doi:10.1002/anie.201709351."},"article_type":"original","page":"15728-15732","date_published":"2017-12-04T00:00:00Z"}]