Synlett 1995; 1995(9): 880-890
DOI: 10.1055/s-1995-5111
account
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Synthesis and Structure of Polysilacyclic Alkynes and Allenes

F. Hojo, W. Ando*
  • *Department of Chemistry, University of Tsukuba, Tsukuba, Ibaraki 305, Japan, Tel & Fax 81 298 53 4214; e-mail wando@sakura.cc.tsukuba.ac.jp
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
31. Dezember 2000 (online)

Six membered cyclic polysilaacetylenes were prepared by direct reaction of 1,4-dichlorotetrasilane with acetylene di-Grignard reagents. The reaction of cyclic polysilaacetylenes was studied. Similarly, several different types of cyclic polysilaallenes were prepared by direct reaction of dihalopolysilanes with either allene dianions and tetraanions. The longer bond lengths of Si-Si than that of C-C bond makes possible to synthesize highly strained unsaturated cyclic compounds, which had been unable to isolate. Herein, synthesis and structure of polysilacyclic alkynes, allenes, bisallenes, and betweenallene are discussed.