Electrochemical C–H bond activation via cationic iridium hydride pincer complexes
Author:
Affiliation:
1. Department of Chemistry
2. University of North Carolina at Chapel Hill
3. Chapel Hill
4. USA
5. Oglethorpe University
6. High Point University
7. Rutgers, The State University of New Jersey
8. New Brunswick
Abstract
Electrochemical C–H activation proceeds at room temperature upon oxidation of a pincer-ligated iridium complex in the presence of base.
Funder
Division of Chemistry
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/SC/C9SC03076J
Reference28 articles.
1. Understanding and exploiting C–H bond activation
2. Evolution of C–H Bond Functionalization from Methane to Methodology
3. Dehydrogenation and Related Reactions Catalyzed by Iridium Pincer Complexes
4. Dihydrogen/Dihydride or Tetrahydride? An Experimental and Computational Investigation of Pincer Iridium Polyhydrides
5. Mechanism of Alkane Transfer-Dehydrogenation Catalyzed by a Pincer-Ligated Iridium Complex
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1. Oxidation-induced C–H bond activation in iridium pincer complexes;Dalton Transactions;2023
2. Cascade Nucleophilic Attack/Addition Cyclization Reactions to Synthesize Oxazolidin-2-imines via (Z)-2-Bromo-3-phenylprop-2-en-1-ols/3-phenylprop-2-yn-1-ols and Diphenyl Carbodiimides;The Journal of Organic Chemistry;2022-09-13
3. Catalytic Dehydrogenation of Alkanes by PCP–Pincer Iridium Complexes Using Proton and Electron Acceptors;ACS Catalysis;2021-02-22
4. Electrosynthetic Route to Cyclopentadienyl Rhenium Hydride Complexes Enabled by Electrochemical Investigations of their Redox-Induced Formation;Organometallics;2020-04-29
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