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Effect of sparteine on the photopolymerization of methyl and ethyl methacrylates with bis(cyclopentadienyl)titanium dichloride in a water–methanol mixture
Author(s) -
Sato Tsuneyuki,
Shibata Hirofumi,
Seno Makiko
Publication year - 2001
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/1097-4628(20010502)80:5<815::aid-app1159>3.0.co;2-b
Subject(s) - photopolymer , methyl methacrylate , chemistry , tetrahydrofuran , polymer chemistry , reagent , methacrylate , titanium , polymerization , chelation , solvent , polymer , organic chemistry
The photopolymerization of methyl methacrylate (MMA) with bis(cyclopentadienyl)titanium dichloride (Cp 2 TiCl 2 ) in a H 2 O‐MeOH [1 : 1 (v/v)] mixture was examined at 40°C in the presence of 2,2′‐bipyridyl (Bipy), 1,10‐phenanthlorine (Phen) or sparteine (Spr) as the chelating reagent. The presence of these chelating reagents retarded the photopolymerization. Poly(MMA)s formed in the presence of them were found to contain a considerable fraction of the benzene‐insoluble part, in contrast to the ones in the absence of them. Spr was the most effective for formation of the insoluble part. The benzene‐insoluble poly(MMA) was insoluble in usual organic solvents including acetone, tetrahydrofuran, ethyl acetate, and dimethyl sulfoxide, suggesting crosslinking. However, poly(MMA) reproduced by hydrolysis of the insoluble part followed by methylation was soluble in usual organic solvents, indicating no crosslinking between polymer main chains. The insoluble part was thermally more stable than the soluble part. Polymerization of ethyl methacrylate in the presence of Spr gave similar results. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 815–822, 2001