| Literature DB >> 26223404 |
Sarah A Weicker1, Douglas W Stephan2.
Abstract
Silyl triflates of the form R4-n Si(OTf)n (n=1, 2; OTf=OSO3 CF3 ) are shown to activate carbon dioxide when paired with bulky alkyl-substituted Group 15 bases. Combinations of silyl triflates and 2,2,6,6-tetramethylpiperidine react with CO2 to afford silyl carbamates via a frustrated Lewis pair-type mechanism. With trialkylphosphines, the silyl triflates R3 Si(OTf) reversibly bind CO2 affording [R'3 P(CO2 )SiR3 ][OTf] whereas when Ph2 Si(OTf)2 is used one or two molecules of CO2 can be sequestered. The latter bis-CO2 product is favoured at low temperatures and by excess phosphine.Entities:
Keywords: carbon dioxide activation; frustrated Lewis pairs; phosphines; silicon; silyl triflates
Year: 2015 PMID: 26223404 DOI: 10.1002/chem.201501904
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236