Published March 28, 2004 | Version public
Journal Article

Synthesis and reactivity of nickel complexes supported by the tris(phosphino) borate ligand [PhB(Ch_2PPh_2)_3]^-

Abstract

The chemistry of nickel complexes supported by phosphine donor ligands has gained recent interest due to the ability of these species to catalyze a variety of chemical transformations. A series of divalent, monovalent, and zerovalent nickel complexes supported by the strongly electron-releasing, monoanionic tris(phosphino) borate ligand, [PhBP_3]=[PhB(CH_2PPh 2)_3]^-, have been synthesized to explore their coordination chemistry and reactivity. The characterization of these complexes will be presented, with comparisons drawn to isostructural nickel complexes supported by neutral phosphine ligands.

Additional Information

© 2004 American Chemical Society.

Additional details

Identifiers

Eprint ID
47521
Resolver ID
CaltechAUTHORS:20140728-100808567

Dates

Created
2014-07-28
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Updated
2019-11-26
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