Hydrogen oxidation catalysis by a nickel diphosphine complex with pendant tert-butyl amines

Jenny Y. Yang; Shentan Chen; William G. Dougherty; W. Scott Kassel; R. Morris Bullock; Daniel L. Dubois; Simone Raugei; Roger Rousseau; Michel Dupuis; M. Rakowski Dubois

doi:10.1039/c0cc03246h

Hydrogen oxidation catalysis by a nickel diphosphine complex with pendant tert-butyl amines

Jenny Y. Yang, Shentan Chen, William G. Dougherty, W. Scott Kassel, R. Morris Bullock, Daniel L. Dubois, Simone Raugei, Roger Rousseau, Michel Dupuis, M. Rakowski Dubois

Pacific Northwest National Laboratory

Research output: Contribution to journal › Article › peer-review

89 Citations (Scopus)

Abstract

A bis-diphosphine nickel complex with tert-butyl functionalized pendant amines [Ni(P^Cy₂N^t-Bu₂) ₂]²⁺ has been synthesized. It is a highly active electrocatalyst for the oxidation of hydrogen in the presence of base. The turnover rate of 50 s^-1 under 1.0 atm H₂ at a potential of -0.77 V vs. the ferrocene couple is 5 times faster than the rate reported heretofore for any other synthetic molecular H₂ oxidation catalyst.

Original language	English
Pages (from-to)	8618-8620
Number of pages	3
Journal	Chemical Communications
Volume	46
Issue number	45
DOIs	https://doi.org/10.1039/c0cc03246h
Publication status	Published - Dec 7 2010

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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Hydrogen oxidation catalysis by a nickel diphosphine complex with pendant tert-butyl amines. / Yang, Jenny Y.; Chen, Shentan; Dougherty, William G.; Kassel, W. Scott; Bullock, R. Morris ; Dubois, Daniel L.; Raugei, Simone ; Rousseau, Roger ; Dupuis, Michel; Dubois, M. Rakowski.

In: Chemical Communications, Vol. 46, No. 45, 07.12.2010, p. 8618-8620.

Research output: Contribution to journal › Article › peer-review

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abstract = "A bis-diphosphine nickel complex with tert-butyl functionalized pendant amines [Ni(PCy2Nt-Bu2) 2]2+ has been synthesized. It is a highly active electrocatalyst for the oxidation of hydrogen in the presence of base. The turnover rate of 50 s-1 under 1.0 atm H2 at a potential of -0.77 V vs. the ferrocene couple is 5 times faster than the rate reported heretofore for any other synthetic molecular H2 oxidation catalyst.",

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AU - Dubois, Daniel L.

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