Electron Transfer to Benzenes by Photoactivated Neutral Organic Electron Donor Molecules
2012; Wiley; Volume: 124; Issue: 15 Linguagem: Inglês
10.1002/ange.201200084
ISSN1521-3757
AutoresElise Cahard, Franziska Schoenebeck, Jean Garnier, Sylvain P. Y. Cutulic, Shengze Zhou, John A. Murphy,
Tópico(s)Radical Photochemical Reactions
ResumoAngewandte ChemieVolume 124, Issue 15 p. 3733-3736 Zuschrift Electron Transfer to Benzenes by Photoactivated Neutral Organic Electron Donor Molecules† Elise Cahard, Elise Cahard Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorProf. Dr. Franziska Schoenebeck, Corresponding Author Prof. Dr. Franziska Schoenebeck [email protected] ETH Zürich Laboratory for Organic Chemistry, Wolfgang Pauli Straße 10, 8093 Zürich (Switzerland) Franziska Schoenebeck, ETH Zürich Laboratory for Organic Chemistry, Wolfgang Pauli Straße 10, 8093 Zürich (Switzerland) John A. Murphy, Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorJean Garnier, Jean Garnier Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorSylvain P. Y. Cutulic, Sylvain P. Y. Cutulic Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorDr. Shengze Zhou, Dr. Shengze Zhou Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorProf. Dr. John A. Murphy, Corresponding Author Prof. Dr. John A. Murphy [email protected] Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK) Franziska Schoenebeck, ETH Zürich Laboratory for Organic Chemistry, Wolfgang Pauli Straße 10, 8093 Zürich (Switzerland) John A. Murphy, Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this author Elise Cahard, Elise Cahard Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorProf. Dr. Franziska Schoenebeck, Corresponding Author Prof. Dr. Franziska Schoenebeck [email protected] ETH Zürich Laboratory for Organic Chemistry, Wolfgang Pauli Straße 10, 8093 Zürich (Switzerland) Franziska Schoenebeck, ETH Zürich Laboratory for Organic Chemistry, Wolfgang Pauli Straße 10, 8093 Zürich (Switzerland) John A. Murphy, Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorJean Garnier, Jean Garnier Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorSylvain P. Y. Cutulic, Sylvain P. Y. Cutulic Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorDr. Shengze Zhou, Dr. Shengze Zhou Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this authorProf. Dr. John A. Murphy, Corresponding Author Prof. Dr. John A. Murphy [email protected] Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK) Franziska Schoenebeck, ETH Zürich Laboratory for Organic Chemistry, Wolfgang Pauli Straße 10, 8093 Zürich (Switzerland) John A. Murphy, Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL (UK)Search for more papers by this author First published: 02 March 2012 https://doi.org/10.1002/ange.201200084Citations: 31 † We thank the EPSRC and the ETH for funding and the EPSRC National Mass Spectrometry Service, Swansea, for spectra, and we thank Markus Reiher (ETH) for helpful discussions. Read the full textAboutPDF ToolsRequest permissionAdd to favorites ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Graphical Abstract Leistungsstarke Reduktionen: Einfache organische Elektronendonoren, die einzig aus den Elementen Kohlenstoff, Wasserstoff und Stickstoff bestehen, reduzieren nach Anregung mit Licht Benzolringe, die sich im Grundzustand befinden, zu Radikalanionen (DMF=Dimethylformamid). Supporting Information Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Filename Description ange_201200084_sm_miscellaneous_information.pdf800.9 KB miscellaneous_information Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article. References 1J. Mortensen, J. Heinze, Angew. 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