Back to Search Start Over

A pyridyl-substituted cyclodisilazane [(Apy)2(μ-SiMe)2] (ApyH2 = 2-aminopyridine)

Authors :
Rui Li
Xin-E Duan
Wei Cao
Xue-Hong Wei
Source :
IUCrData, Vol 2, Iss 3, p x170400 (2017)
Publication Year :
2017
Publisher :
International Union of Crystallography, 2017.

Abstract

The title compound, C14H20N4Si2 or [(Apy)2(μ-SiMe)2], systematic name 2-[2,2,4,4-tetramethyl-3-(pyridin-2-yl)-1,3,2,4-diazadisiletidin-1-yl]pyridine, was obtained as a side product from the reaction of 2-amino-pyridine with LiBun followed by the addition of Me2NMe2SiCl in hexane. The compound was characterized by single-crystal X-ray diffraction analysis and NMR spectroscopy. The title compound lies about an inversion center at the centroid of the cyclodisilazane ring. The four-membered Si2N2 core is strictly planar with the two pyridyl rings placed centrosymmetrically on either side of the Si2N2 plane and are almost coplanar with the central four-membered ring.

Details

Language :
English
ISSN :
24143146
Volume :
2
Issue :
3
Database :
Directory of Open Access Journals
Journal :
IUCrData
Publication Type :
Academic Journal
Accession number :
edsdoj.28052b27b5934a39bb7ed1beb21f4db0
Document Type :
article
Full Text :
https://doi.org/10.1107/S241431461700400X