Issue 15, 1990

Hypervalent silicon via intramolecular co-ordination in a four-membered ring system: synthesis and structure of SiCl2X[2-C(SiMe3)2C5H4N](X = H or Me); X-ray structures of the former complex and of SiCl2Me(2-CPh2C5H4N)

Abstract

Reaction of SiCl3X (X = H or Me) with LiR [R = 2-C(SiMe3)2C5H4N] yields the novel hpervalent five-co-ordinate compounds SiRCl2X which show strong Intramolecular Si–N interactions in the four-membered chelate ring [Si–N 2.066(9)Å for X = H (X-ray)] which persists in solution; the related compounds, SiR′Cl2X (X = H or Me for R′= 2-CPh2C5H4N) have four-co-ordinate silicon (deduced from the 29Si NMR spectra and, for X = Me, an X-ray structure).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1006-1008

Hypervalent silicon via intramolecular co-ordination in a four-membered ring system: synthesis and structure of SiCl2X[2-C(SiMe3)2C5H4N](X = H or Me); X-ray structures of the former complex and of SiCl2Me(2-CPh2C5H4N)

T. van den Ancker, B. S. Jolly, M. F. Lappert, C. L. Raston, B. W. Skelton and A. H. White, J. Chem. Soc., Chem. Commun., 1990, 1006 DOI: 10.1039/C39900001006

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