Insertion of phenyl isocyanate into mono- and diaminosilanes

ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES(2017)

Cited 16|Views31
No score
Abstract
The aminosilanes MenSi(NRR')(4-n) (n=2,3) with NRR'= ethylamino (NHEt), n-propylamino ((NHPr)-Pr-n), sec-butylamino n-octylamino (NI-InOct), n-dodecylamino (NH(n)Dodec), allylamino (NHA11), tert-butylamino (NH(t)Mu), diethylamino (NFt(2)), and anilino (NHPh) were synthesized and their reactions with phenyl isocyanate were studied. In all cases of these silanes Me,SiN RR' and Me2Si(NRR'), formal insertion of the -NCO group into their Si-N bonds was observed, i.e. formation of products with Si-N (rather than Si-O) bonds was found. In some cases, the products could be crystallized and their molecular structures have been elucidated with single-crystal X-ray diffraction analyses.
More
Translated text
Key words
amines,insertion,silanes,silicon-nitrogen bond,silylated urea
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined