Kinetic treatment of slow initiation in living carbocationic polymerization and investigation of benzyl halides as initiators for the polymerization of isobutylene

Daniela Held, Béla Iván, Axel H.E. Müller

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

In contrast to earlier conclusions it is demonstrated that kinetic analysis of incremental monomer addition (IMA) experiments for living carbocationic polymerizations with slow initiation leads only to the ratio of apparent rate constants of initiation and propagation. The apparent rate constants depend on the true (bimolecular) rate constants and on the positions of the equilibria between dormant and active states of initiator and polymer chain ends, respectively. The same considerations are true for other living processes involving dormant species, e.g., group transfer polymerization or controlled radical polymerization. Slow initiation of living carbocationic polymerization of isobutylene (IB) was found with benzyl halide initiators, such as 4-methylbenzyl bromide, 4-methylbenzyl chloride, and 2,4,6-trimethylbenzyl chloride (TMBC), in conjunction with TiCl4 as co-initiator in the presence of N,N-dimethylacetamide in 40:60 v/v CH2Cl2/hexane solvent mixture at -78 °C. The obtained ratio of apparent rate constant of initiation and propagation is compared to other initiators. TMBC led to a new asymmetric telechelic polyisobutylene (PIB) with tertiary chlorine and 2,4,6-trimethylbenzyl end groups, which can be further derivatized.

Original languageEnglish
Pages (from-to)7199-7202
Number of pages4
JournalMacromolecules
Volume31
Issue number21
DOIs
Publication statusPublished - Oct 20 1998

ASJC Scopus subject areas

  • Organic Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry
  • Materials Chemistry

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