alpha-acetal-omega-bis(hydroxymethyl) heterodifunctional polystyrene: Synthesis, characterization, and investigation of intramolecular end-to-end ring closure

Citation
M. Schappacher et A. Deffieux, alpha-acetal-omega-bis(hydroxymethyl) heterodifunctional polystyrene: Synthesis, characterization, and investigation of intramolecular end-to-end ring closure, MACROMOLEC, 34(17), 2001, pp. 5827-5832
Citations number
21
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULES
ISSN journal
00249297 → ACNP
Volume
34
Issue
17
Year of publication
2001
Pages
5827 - 5832
Database
ISI
SICI code
0024-9297(20010814)34:17<5827:AHPS>2.0.ZU;2-#
Abstract
A route to macrocyclic polystyrene of controlled dimensions based on a new ring closure process has been investigated. It involved the direct coupling of an alpha -acetal,omega -bis(hydroxymethyl) heterodifunctional linear po lystyrene precursor previously prepared by living anionic polymerization. C yclization was achieved under high dilution, by intramolecular condensation of the polymer ends in the presence of a mild acid as catalyst. Macrocycli c polystyrenes were prepared directly in high yield (> 90%) without any nec essary fractionation step. The synthesis and structural characterization of both the linear alpha,omega -heterodifunctional precursors and the corresp onding cyclized polystyrenes, as well as a preliminary investigation of the ir stability and specific thermal properties, are reported.