Preparations of Triphenylmethyl Salts and Their Use in the Cationic Polymerization of α-Methylstyrene. Counteranion and Polymer Structure

Toyoki Kunitake, Shun'ichi Tsugawa

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Triphenylmethyl salts which contain metal chlorides or bromides as the anion were prepared systematically, and employed as initiator for the cationic polymerization of α-methylstyrene. The isotactic unit content of the polymer was found to correlate with the anion size in a relatively simple way except for pentacoordinate anions. This was explicable by considering the steric effect of the counteranion and the coulombic interaction of the growing ion pair. Pentacoordinated counteranions gave rise to greater amounts of the isotactic unit than expected from their sizes, and, in the case of Ph3SnCl4Br, the polymer steric structure was dependent on the initiator concentration. These results were attributed to the peculiar structural characteristics of these anions.

Original languageEnglish
Pages (from-to)709-713
Number of pages5
JournalMacromolecules
Volume8
Issue number6
DOIs
Publication statusPublished - Nov 1 1975

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Cationic polymerization
Anions
Polymers
Negative ions
Salts
Bromides
Chlorides
Metals
Ions
vinyltoluene

All Science Journal Classification (ASJC) codes

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

Cite this

Preparations of Triphenylmethyl Salts and Their Use in the Cationic Polymerization of α-Methylstyrene. Counteranion and Polymer Structure. / Kunitake, Toyoki; Tsugawa, Shun'ichi.

In: Macromolecules, Vol. 8, No. 6, 01.11.1975, p. 709-713.

Research output: Contribution to journalArticle

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