3d Metal Complexes in T-shaped Geometry as a Gateway to Metalloradical Reactivity
Author:
Affiliation:
1. Anorganisch-Chemisches Institut, Universität Heidelberg, 69120 Heidelberg, Germany
2. Department of Chemistry, University of Cincinnati, P.O. Box 210172, Cincinnati, Ohio 45221-0172, United States
Funder
Deutsche Forschungsgemeinschaft
Alexander von Humboldt-Stiftung
Universit?t Heidelberg
Publisher
American Chemical Society (ACS)
Subject
General Medicine,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.1c00737
Reference69 articles.
1. Stereoselective Hydrodehalogenation via a Radical-Based Mechanism Involving T-Shaped Chiral Nickel(I) Pincer Complexes
2. Catalytic C–F bond activation of geminal difluorocyclopropanes by nickel(i) complexes via a radical mechanism
3. Opening up the Valence Shell: A T‐Shaped Iron(I) Metalloradical and Its Potential for Atom Abstraction
4. Metalloradical Reactivity, Charge Transfer, and Atom Abstractions in a T-Shaped Iron(I) Complex
5. Catalysis without Precious Metals
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