Stereoregulation in cationic polymerization. III. High isospecificity withthe bulky phosphoric acid [(RO)(2)PO2H]/SnCI4 initiating systems: Design of counteranions via initiators

Citation
M. Ouchi et al., Stereoregulation in cationic polymerization. III. High isospecificity withthe bulky phosphoric acid [(RO)(2)PO2H]/SnCI4 initiating systems: Design of counteranions via initiators, J POL SC PC, 39(7), 2001, pp. 1067-1074
Citations number
26
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
ISSN journal
0887624X → ACNP
Volume
39
Issue
7
Year of publication
2001
Pages
1067 - 1074
Database
ISI
SICI code
0887-624X(20010401)39:7<1067:SICPIH>2.0.ZU;2-O
Abstract
In the cat;ionic polymerization of isobutyl vinyl ether (IBVE) with binary initiating systems consisting of a protonic acid as an initiator and a Lewi s acid as an activator/catalyst, phosphoric acid derivatives [(RO)(2)POOH] coupled with SnCl4 gave highly isotactic poly(IBVE)s, whereas those with a bulky substituent (R), [C4H9CH(C2H5)CH2O](2)POOH (7) and (n-C10H21)(2)POOH (8), led to the highest isotacticity [meso dyad (m) = 86%]. In contrast, is ospecificity was lower with IBVE-HCl and CF3COOH under the same conditions. From the effects of the polymerization temperature (-78 to 0 degreesC), it was concluded that the high isospecificity with 7 and 8 was due to an enth alpic factor. (C) 2001 John Wiley & Sons, Inc.