Oligosilanes with attached silatranyl units were obtained by reactions of potassium oligosilanides with a silatranyl triflate. Interaction between Si and N atoms was observed in the Si-29 NMR spectra (upfield-shifted SiO3 resonances) and in the solid-state structures (Si-N distances between 2.29 and 2.16 angstrom). The Si-N interaction can be "switched off" either by protonation of the nitrogen lone pair or by potassium silanide formation caused by trimethylsilyl group cleavage in the presence of potassium tert-butoxide.
A method for the synthesis of 1-chlorosilatrane by the reaction of organyltrichlorosilanes RSiCl(3) (R = Vin, Ph) and tetrachlorosilane with triethanolamine or its hydrochloride was developed. This simple and economical method allows obtaining 1-chlorosilatrane in 60% yield.
A new method for the preparation of 1-(chloromethyl)- and 1-(dichloromethyl)silatranes
作者:N. F. Lazareva、I. M. Lazarev
DOI:10.1007/s11172-018-2285-2
日期:2018.9
A preparative method for the synthesis of 1-(chloromethyl)- and 1-(dichloromethyl)silatranes was developed based on the reactions of 1-chlorosilatrane with the binary P(NMe2)3–СHX3 system (X3 = HBrCl, Cl3).
Oligosilanes with attached silatranyl units were obtained by reactions of potassium oligosilanides with a silatranyl triflate. Interaction between Si and N atoms was observed in the Si-29 NMR spectra (upfield-shifted SiO3 resonances) and in the solid-state structures (Si-N distances between 2.29 and 2.16 angstrom). The Si-N interaction can be "switched off" either by protonation of the nitrogen lone pair or by potassium silanide formation caused by trimethylsilyl group cleavage in the presence of potassium tert-butoxide.
A new route to 1-chlorosilatrane
作者:M. G. Voronkov、G. A. Kuznetsova、V. P. Baryshok
DOI:10.1134/s1070363210100075
日期:2010.10
A method for the synthesis of 1-chlorosilatrane by the reaction of organyltrichlorosilanes RSiCl(3) (R = Vin, Ph) and tetrachlorosilane with triethanolamine or its hydrochloride was developed. This simple and economical method allows obtaining 1-chlorosilatrane in 60% yield.