Sonia Zoltowska, Stefano Mazzanti, Sara Stolfi, Jingsan Xu, Matej Huš, Ana Oberlintner, Matic Pavlin, Paolo Ghigna, Blaž Likozar, Piero Torelli, Luca Braglia, Davide Ravelli, Maurizio Fagnoni, Iker Agirrezabal-Telleria, Markus Antonietti, Paolo Giusto, Oleksandr Savateev
{"title":"非均相石墨氮化碳光催化与钴胺肟催化在上坡脱氢合成苯胺中的融合。","authors":"Sonia Zoltowska, Stefano Mazzanti, Sara Stolfi, Jingsan Xu, Matej Huš, Ana Oberlintner, Matic Pavlin, Paolo Ghigna, Blaž Likozar, Piero Torelli, Luca Braglia, Davide Ravelli, Maurizio Fagnoni, Iker Agirrezabal-Telleria, Markus Antonietti, Paolo Giusto, Oleksandr Savateev","doi":"10.1002/cssc.202402439","DOIUrl":null,"url":null,"abstract":"<p>Synthesis of substituted anilines upon nucleophilic addition of secondary amines to cyclohexanone derivatives followed by aromatization of the enamine by employing a combination of Ir-polypyridine complex as a photoredox catalyst and cobaloxime as H<sub>2</sub>-evolution catalyst is developed recently by Leonori et al. In this work, the homogeneous photoredox catalyst is replaced by a heterogeneous and metal-free mesoporous graphitic carbon nitride (mpg-CN). Substituted aromatic amine and H<sub>2</sub> are formed simultaneously. Combination of X-ray spectroscopies reveals charge transfer from cobaloxime to mpg-CN in the dark. Illumination of the catalytic system with visible light induces electron transfer from mpg-CN to cobaloxime and formation of persistent Co(II) species. The results of density functional theory modeling suggest that the studied reaction is strongly endothermic and endergonic. Thus, energy of photons is stored in the reaction products—H<sub>2</sub> and the aromatic amine.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":"18 12","pages":""},"PeriodicalIF":6.6000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cssc.202402439","citationCount":"0","resultStr":"{\"title\":\"Merging Heterogeneous Graphitic Carbon Nitride Photocatalysis with Cobaloxime Catalysis in Uphill Dehydrogenative Synthesis of Anilines\",\"authors\":\"Sonia Zoltowska, Stefano Mazzanti, Sara Stolfi, Jingsan Xu, Matej Huš, Ana Oberlintner, Matic Pavlin, Paolo Ghigna, Blaž Likozar, Piero Torelli, Luca Braglia, Davide Ravelli, Maurizio Fagnoni, Iker Agirrezabal-Telleria, Markus Antonietti, Paolo Giusto, Oleksandr Savateev\",\"doi\":\"10.1002/cssc.202402439\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Synthesis of substituted anilines upon nucleophilic addition of secondary amines to cyclohexanone derivatives followed by aromatization of the enamine by employing a combination of Ir-polypyridine complex as a photoredox catalyst and cobaloxime as H<sub>2</sub>-evolution catalyst is developed recently by Leonori et al. In this work, the homogeneous photoredox catalyst is replaced by a heterogeneous and metal-free mesoporous graphitic carbon nitride (mpg-CN). Substituted aromatic amine and H<sub>2</sub> are formed simultaneously. Combination of X-ray spectroscopies reveals charge transfer from cobaloxime to mpg-CN in the dark. Illumination of the catalytic system with visible light induces electron transfer from mpg-CN to cobaloxime and formation of persistent Co(II) species. The results of density functional theory modeling suggest that the studied reaction is strongly endothermic and endergonic. Thus, energy of photons is stored in the reaction products—H<sub>2</sub> and the aromatic amine.</p>\",\"PeriodicalId\":149,\"journal\":{\"name\":\"ChemSusChem\",\"volume\":\"18 12\",\"pages\":\"\"},\"PeriodicalIF\":6.6000,\"publicationDate\":\"2025-03-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cssc.202402439\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemSusChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cssc.202402439\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cssc.202402439","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Merging Heterogeneous Graphitic Carbon Nitride Photocatalysis with Cobaloxime Catalysis in Uphill Dehydrogenative Synthesis of Anilines
Synthesis of substituted anilines upon nucleophilic addition of secondary amines to cyclohexanone derivatives followed by aromatization of the enamine by employing a combination of Ir-polypyridine complex as a photoredox catalyst and cobaloxime as H2-evolution catalyst is developed recently by Leonori et al. In this work, the homogeneous photoredox catalyst is replaced by a heterogeneous and metal-free mesoporous graphitic carbon nitride (mpg-CN). Substituted aromatic amine and H2 are formed simultaneously. Combination of X-ray spectroscopies reveals charge transfer from cobaloxime to mpg-CN in the dark. Illumination of the catalytic system with visible light induces electron transfer from mpg-CN to cobaloxime and formation of persistent Co(II) species. The results of density functional theory modeling suggest that the studied reaction is strongly endothermic and endergonic. Thus, energy of photons is stored in the reaction products—H2 and the aromatic amine.
期刊介绍:
ChemSusChem
Impact Factor (2016): 7.226
Scope:
Interdisciplinary journal
Focuses on research at the interface of chemistry and sustainability
Features the best research on sustainability and energy
Areas Covered:
Chemistry
Materials Science
Chemical Engineering
Biotechnology