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Coordination polymerization of chlorophenyl glycidyl ethers

✍ Scribed by M. Bero; M. Danielewicz; J. Kasperczyk; E. Piechowiak; M. Rybczyk; A. Stolarzewicz; Z. Jedliński

Publisher
John Wiley and Sons
Year
1985
Tongue
English
Weight
376 KB
Volume
36
Category
Article
ISSN
0323-7648

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## Abstract As a complementary study of a previous work about the influence of the electronic effects of __p__‐substituted phenyl glycidyl ethers on the polymerization behaviour, a new series of monomers with electron‐withdrawing groups was prepared, i.e., highly reactive __p__‐functionalized poly(

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## Abstract A series of __p__‐substituted glycidyl phenyl ethersIUPAC nomenclature: 2,3‐epoxypropyl phenyl ether. with electron donor groups was prepared using a multistep synthetic method. These compounds were polymerized using four of the most common aluminium‐based coordinative initiators, (C~2

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Almtraet--The rate of polymerization of p-cresyl glycidyl ether induced by benzyldimethylamine is far more dependent on the catalyst concentration than on the temperature. The average degree of polymerization increases with conversion; its temperature dependence is more complex, and it is independen