Rapid reversible borane to boryl hydride exchange by metal shuttling on the carborane cluster surface
Author:
Affiliation:
1. Department of Chemistry and Biochemistry
2. University of South Carolina
3. Columbia
4. USA
5. Leibniz Institute for Solid State and Materials Research
6. 01069 Dresden
7. Germany
Abstract
The ruthenium carboranyl pincer complex featuring fluxional ”cage-walking“ of the metal center is an efficient catalyst for cyclooctane transfer dehydrogenation.
Funder
American Chemical Society Petroleum Research Fund
Division of Chemistry
H2020 Excellent Science
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/SC/C7SC01846K
Reference79 articles.
1. Metallaboratranes Derived from a Triphosphanyl–Borane: IntrinsicC3 Symmetry Supported by a Z-Type Ligand
2. Analogies between Metallaboratranes, Triboronates, and Boron Pincer Ligand Complexes
3. Reversible H2 Addition across a Nickel–Borane Unit as a Promising Strategy for Catalysis
4. Functional group migrations between boron and metal centres within transition metal–borane and –boryl complexes and cleavage of H–H, E–H and E–E′ bonds
5. Syntheses of PBP Pincer Iridium Complexes: A Supporting Boryl Ligand
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