Journal
ORGANOMETALLICS
Volume 34, Issue 21, Pages 5203-5206Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.5b00824
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Funding
- NSF under CCI Center for Enabling New Technologies through Catalysis (CENTC) [CHE-1205189]
- NSF CENTC REU program
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1205189] Funding Source: National Science Foundation
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A single homogeneous nickel(II) complex, supported by the tris(3,5-dimethylpyrazoly)borate ligand and 2-hydroxyquinoline ancillary ligand, is shown to catalyze both acceptorless dehydrogenation of alcohols and hydrogenation of carbonyl compounds under mild conditions. Products from the catalytic reactions were isolated with good yields. A mechanistic investigation highlights the critical role of the 2-hydroxyquinoline ligand in the catalysis and argues against a stepwise dehydrogenation pathway.
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