Polymerization of lactides and lactones. IV. Ring-opening polymerization of epsilon-caprolactone by rare earth phenyl compounds

Citation
Xm. Deng et al., Polymerization of lactides and lactones. IV. Ring-opening polymerization of epsilon-caprolactone by rare earth phenyl compounds, J APPL POLY, 73(8), 1999, pp. 1401-1408
Citations number
28
Categorie Soggetti
Organic Chemistry/Polymer Science","Material Science & Engineering
Journal title
JOURNAL OF APPLIED POLYMER SCIENCE
ISSN journal
00218995 → ACNP
Volume
73
Issue
8
Year of publication
1999
Pages
1401 - 1408
Database
ISI
SICI code
0021-8995(19990822)73:8<1401:POLALI>2.0.ZU;2-W
Abstract
Ring-opening polymerization of epsilon-caprolactone (CL) has been initiated with rare earth phenyl compounds in both bulk and solution. These rare ear th phenyl initiators can give polycaprolactone (PCL) with high yield and hi gh molecular weight. The polymerization mechanism is through a coordination -deprotonation-insertion process, by which the monomer inserts on the Ln-O bond of rare earth enolate. The efficiency of rare earth phenyl compounds f or CL is high. The effects of reaction conditions, such as reaction time, r eaction temperature, and monomer/initiator molar ratio, on the polymerizati on are discussed. The polymer was characterized by FTIR, H-1-NMR. (C) 1999 John Wiley & Sons, Inc.