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Articles by Patrick Enders
Front Cover: Cation Radical Newman‐Kwart Rearrangement Enabled by Heterogeneous Photocatalysis under Mild Conditions (ChemCatChem 23/2023)
Dr. Dirk Michalik Leibniz Institute for Catalysis, Albert-Einstein-Str. 29a, 18059 Rostock, Germany Institute of Chemistry, Rostock University, Albert-Einstein-Str. 3a, 18059 Rostock, Germany Search for more papers by this author
Quantitative prediction of excited-state decay rates for radical anion photocatalysts
Quantitative prediction of excited-state decay rates for radical anion photocatalysts† Leandro D. Mena, ab José L. Borioni, ab Sofia Caby, ab Patrick Enders, cd Miguel A. Argüello Cordero, e Franziska Fennel, e Robert Francke, cd Stefan Lochbrunner e and Javier I. Bardagi *ab Abstract We present a computational approach for predicting key properties of organic radical anions, including excited-state lifetimes and redox potentials.
Cation Radical Newman‐Kwart Rearrangement Enabled by Heterogeneous Photocatalysis under Mild Conditions
Abstract A photochemical rearrangement of O-aryl thiocarbamates to the corresponding S-aryl compounds that is triggered by heterogeneous electron transfer between the substrate and photo-excited titanium dioxide is presented. The rearrangement is the key-reaction in the three-step conversion of phenols into the corresponding thiophenols.
How to Harness Electrochemical Mediators for Photocatalysis – A Systematic Approach Using the Phenanthro[9,10‐d]imidazole Framework as a Test Case
Abstract The mediator portfolio of electrosynthesis holds untapped potential for photocatalytic applications. A systematic approach toward harnessing electrochemical mediators for photocatalysis is presented using the phenanthroimidazole framework, a known electrocatalytic system, as a test case. As a result, a much broader platform becomes accessible that allows both oxidative and reductive transformations by choosing the type of energy input (light or electricity).
Amino acid-based H2S donors: N-thiocarboxyanhydrides that release H2S with innocuous byproducts
Amino acid-based H2S donors: N-thiocarboxyanhydrides that release H2S with innocuous byproducts† Kuljeet Kaur, ab Patrick Enders, ac Yumeng Zhu, a Abigail F. Bratton, a Chadwick R. Powell,a Khosrow Kashfi d and John B.
Electrochemical Instability of Highly Fluorinated Tetraphenyl Borates and the Syntheses of their Respective Biphenyls
S. Beil, S. Moehle, P. Enders and S. R. Waldvogel, Chem. Commun., 2018, Accepted Manuscript , DOI: 10.1039/C8CC02996B If you are not the author of this article and you wish to reproduce material from it in a third party non-RSC publication you must formally request permission using RightsLink. Go to our Instructions for using RightsLink page for details.
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