Journal
ORGANOMETALLICS
Volume 37, Issue 6, Pages 906-914Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.7b00889
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Funding
- JSPS KAKENHI [JP15K21707, JP15H05796]
- Nanotechnology Platform of the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan
- Grants-in-Aid for Scientific Research [15K21707] Funding Source: KAKEN
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Half-sandwich Cp*Rh-III complexes (Cp* = eta(5)-1,2,3,4,5-pentamethylcydopentadienyl) supported by 2,2'-bipyridine or 4,4'-di-tert-butyl-2,2'-bipyridine catalyze dehydrogenation of dimethylamine borane (Me2NH center dot BH3) to produce H-2 and dimethylamino borane dimer (Me2N-BH2)(2) with turnovers of 2200. The Ir-III analogues, on the other hand, display dramatically poorer catalytic activity. Mechanistic inferences drawn from stoichiometric reactions and DFT calculations suggest noninnocent involvement of the Cp* moiety as a proton shuttle.
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