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Carbosilanes pp 99-217 | Cite as

Reactions of Carbosilanes

  • Gerhard Fritz
  • Eberhard Matern

Abstract

There are some principal objectives in the study of the reactivity of carbosilanes: First, to what extent are the generally known reactions of Si-functional groups (Chapt. I.2) transferable to the silicon atoms of a carbosilane skeleton? Second, under what circumstances do changes such as Si—C cleavage and rearrangement occur in the molecular skeleton? These objectives overlap partly with those presented in Chapt. II.4 but require separate study. Of particular interest was an investigation into the effects of skeletal substituents on the behavior of the silicon and carbon atoms. Further, what about the stability of the molecular skeleton in compounds containing CH2 or CCl2 groups, respectively? What is the effect of SiCl, SiF and SiH groups? What are the reactions of the CCl2 and CH2 groups? Here the compounds (Cl3Si)2CH2, (Cl2Si—CH2)3, tetrasilaadamantane and their derivatives served as models for such investigations.

Keywords

Mole Equivalent Ring Cleavage Molecular Skeleton Phosphorus Ylide Ether Cleavage 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin, Heidelberg 1986

Authors and Affiliations

  • Gerhard Fritz
    • 1
  • Eberhard Matern
    • 1
  1. 1.Institute of Inorganic ChemistryUniversity of KarlsruheKarlsruhe 1Federal Republic of Germany

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