Abstract
The addition of carbon dioxide to (tBuPNP)CoH[tBuPNP = 2,6 - bis(di-tert-butylphosphinomethyl)pyridine] resulted in rapid insertion into the Co-H bond to form the corresponding K1- formate complex, which has been structurally characterized. Treatment of (tBuPNP)CoH with PhSiH3 resulted in oxidative addition to form trans-(tBuPNP)CoH2(SiH2Ph), which undergoes rapid exchange with excess free silane. With 0.5 mol % (tBuPNP)CoH, the catalytic hydrosilylation of CO2 with PhSiH3 to a mixture of oligomers containing silyl formate, bis(silyl)acetyl, and silyl ether subunits has been observed.
Original language | English (US) |
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Pages (from-to) | 9463-9465 |
Number of pages | 3 |
Journal | Inorganic Chemistry |
Volume | 53 |
Issue number | 18 |
DOIs | |
State | Published - Sep 15 2014 |
All Science Journal Classification (ASJC) codes
- Inorganic Chemistry
- Physical and Theoretical Chemistry