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Journal of Polymer Science

Abstract

Anionic polymerizations of butyl cyanoacrylate were initiated in tetrahydrofuran (plus a few experiments in 1,2-dimethoxyethane) by the salts tetrabutylammonium hydroxide, bromide, acetate and three substituted acetates. The hydroxide gives near-ideal

‘living polymerization’ kinetics, with kp close to 106l·mol−1. s−1 at 20°C. The kinetics of the reactions initiated by the acetates and bromide are analysed by the slow-initiation-no-termination theory, using values of the initiation rate constants evaluated in Part 1. The kp values derived are in the same range as those from the OH-initiated reactions and those of the zwitterionic polymerizations initiated with covalent bases, i.e., tertiary phosphines and amines. A ca. 4-fold variation of kp with concentration of active species is given a speculative analysis in terms of dissociation from paired to free ions, yielding tentative estimates for kmath image ≈ 105 and kmath image ≈ 107l·mol−1·s−1 in THF at 20°C. Molecular weights were all high Mn ≈ 106, with Mw/Mn ≈ 2.

 

 

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