Lowering the Barrier to C–H Activation at IrIII through Pincer Ligand Design
Author:
Affiliation:
1. Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States
Funder
Division of Chemistry
University of Pennsylvania
Center for Enabling New Technologies Through Catalysis
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.1c00080
Reference25 articles.
1. Selective Intermolecular Carbon-Hydrogen Bond Activation by Synthetic Metal Complexes in Homogeneous Solution
2. Large-Scale Selective Functionalization of Alkanes
3. Dehydrogenation and Related Reactions Catalyzed by Iridium Pincer Complexes
4. Dehydrogenation of Alkanes and Aliphatic Groups by Pincer-Ligated Metal Complexes
5. Reactions of iridium hydride pincer complexes with dioxygen: new dioxygen complexes and reversible O2 binding
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1. C–H Activation via Group 8–10 Pincer Complexes: A Mechanistic Approach;Inorganics;2024-08-15
2. SYNTHESIS, STRUCTURE, AND PROPERTIES OF THE NEW IRIDIUM(III) NITROSO COMPLEX: [Ir(NO)(AcOH)(AcO)2(NO2)2];Journal of Structural Chemistry;2023-02
3. Metal–Ligand–Anion Cooperation in C–H Bond Formation at Platinum(II);Journal of the American Chemical Society;2022-07-26
4. 3D vs. turbostratic: controlling metal–organic framework dimensionality via N-heterocyclic carbene chemistry;Chemical Science;2022
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