Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane
Author(s) -
Feng Wang,
Oriol Planas,
Josep Cornellà
Publication year - 2019
Publication title -
journal of the american chemical society
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.9b00594
Subject(s) - ammonia borane , chemistry , catalysis , transfer hydrogenation , borane , reactivity (psychology) , transition metal , frustrated lewis pair , ammonia , hydrogen , catalytic cycle , photochemistry , combinatorial chemistry , organic chemistry , ruthenium , hydrogen production , lewis acids and bases , medicine , alternative medicine , pathology
A catalytic transfer-hydrogenation utilizing a well-defined Bi(I) complex as catalyst and ammonia-borane as transfer agent has been developed. This transformation represents a unique example of low-valent pnictogen catalysis cycling between oxidation states I and III, and proved useful for the hydrogenation of azoarenes and the partial reduction of nitroarenes. Interestingly, the bismuthinidene catalyst performs well in the presence of low-valent transition-metal sensitive functional groups and presents orthogonal reactivity compared to analogous phosphorus-based catalysis. Mechanistic investigations suggest the intermediacy of an elusive bismuthine species, which is proposed to be responsible for the hydrogenation and the formation of hydrogen.
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