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Borohydride B-H activation and dimerization by a doubly bonded, early-transition-metal organodimetallic complex. Ditantalladiborane syntheses as models for dehydrodimerization of methane to ethene

Journal Article · · Journal of the American Chemical Society; (USA)
DOI:https://doi.org/10.1021/ja00191a063· OSTI ID:5051114
There is considerable interest in hydrocarbon C-H activation from the theoretical and organometallic perspectives, particularly in discovering activation/functionalization pathways and bonding models for catalyst surface intermediates. The isoelectronic relationships between hydrocarbons and boranes have led to studies of metallaboranes as hydrocarbon-metal analogues, for example, distorted BH{sub 4}{sup {minus}} complexes are models for CH{sub 4} coordination in the transition state for C-H activation. Their discovery of vinylic C-H activation by the Ta{double bond}Ta complexes (C{sub 5}Me{sub 4}R){sub 2}Ta{sub 2}({mu}-X){sub 4} led them to examine reactivity toward B-H bonds. The reactions of BH{sub 4}{sup {minus}} with multiply bonded M-M compounds are unstudied, particularly for the early transition metals, hydroboration of M-C multiple bonds, but not M-M multiple bonds, has been reported. They wish to report new complexes with hexahydridodiborate (diborane(2-), unknown as a free species) ligands derived from BH{sub 4}{sup {minus}} B-H activation and dehydrodimerization by a M{double bond}M group.
DOE Contract Number:
FG22-85PC80513
OSTI ID:
5051114
Journal Information:
Journal of the American Chemical Society; (USA), Journal Name: Journal of the American Chemical Society; (USA) Vol. 111:9; ISSN 0002-7863; ISSN JACSA
Country of Publication:
United States
Language:
English