Trimethylsilyl Triflate as Initiator for the Cationic Polymerization of Heterocyclics and Alkenes. Model Reactions for the Cationic Grafting from Polysilanes

Abstract

Trimethylsilyl trifluoromethanesulfonate is one of the strongest silylating reagents. It reacts with a variety of nucleophiles including alcohols, amines, ethers, and esters. Reaction with cyclic ethers, iminoethers, and esters leads to silyl onium ions which initiate polymerization of strained heterocyclic monomers. The reactivity of the first silyl onium ions is lower than that of the subsequent alkyl onium ions. Therefore initiations rate constant (ki) is lower than propagation rate constant (kp). Reaction of poly(phenylmethylsilylene) with triflic acid leads to dearylation of polysilane and formation of very reactive silyl triflate groups along the chain of polysilane. These sites were used to initiate cationic polymerization of various monomers from polysilanes, and to prepare new graft copolymers based on polysilanes.

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Document Details

Document Type
Technical Report
Publication Date
Mar 23, 1989
Accession Number
ADA205774

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  • Jeffrey S. Hrkach
  • Krzysztof Matyjaszewski

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  • Carnegie Mellon University

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