https://www.selleckchem.com/products/blu-451.html
The NHC-coordinated trisilacyclopropylidene (A) is shown to behave as the basic component of an FLP used in combination with the Lewis acid B(C6F4H)3 (i.e. B(2,3,5,6-C6F4H)3). This FLP cleaves dihydrogen highly selectively at room temperature giving rise to the ionic compound [(NHC)SiH(Mes2SiSiMes2)][HB(C6F4H)3] 1 in 90% isolated yield. Further reaction of the FLP with Ph2NH and acetone yielded compounds [(NHC)SiH(Mes2SiSiMes2)][Ph2NB(C6F4H)3] 2 and [(NHC)SiH(Mes2SiSiMes2)][MeC(CH2)OB(C6F4H)3] 3 in 75% and 80% yield, respectively. React
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