Cyclische diazastannylene : XIV. Das tetramere eines 1-oxa-2-sila-3-aza-4λ2-stannetidins mit S4-symmetrie |
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Authors: | M Veith M Grosser |
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Institution: | Institut für Anorganische Chemie der Technischen Universität Braunschweig, Pockelsstrasse 4, D-3300 Braunschweig B.R.D. |
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Abstract: | 1,3-Di-t-butyl-2,2-dimethyl-1,3,2,4λ2-diazasilastannetidine (II) reacts with 3,4,5-trimethoxybenzaldehyde to yield 3,4,5-trimethoxybenzaldehyde-t-butylimine (IV) and the title compound 2,2-dimethyl-3-t-butyl-1,2,3,4λ2-oxasilazastannetidine (III). III combines four different Main Group elements in one ring and is tetrameric in solvents as well as in the tetragonal crystalline state. An X-ray structure determination (R-value: 0.037) reveals the tetramer to have crystallographic S4-symmetry, and that the molecules of III interact via oxygen-tin bonds, which are perpendicular to the plane of the ring. The oxygen atoms thus adopt trigonal-planar coordination, while the tin atoms have grigonal-pyramidal environments. The tin atoms are substituted by three different ligands: one nitrogen and two chemically non-equivalent oxygen atoms (SnN: 209.5(9), SnO: 218.8(6), SnO′: 213.7(6) pm). Each tin atom thus represents a center of chirality, which due to symmetry must be divided into two R- and two S-enantiomers. As a consequence the whole tetrameric molecule belongs to the optically inactive “meso”-form. |
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