Investigation on cationic ring-opening polymerization of 1,5,7,11-tetraoxaspiro [5,5] undecane in the presence of low molecular weight tetraols
Author:
Publisher
Elsevier BV
Subject
Polymers and Plastics,Materials Chemistry,Organic Chemistry
Reference18 articles.
1. Synthesis of monomers that expand on polymerization. Synthesis and polymerization of 3,9-dimethylene-1,5,7,11-tetraoxaspiro[5.5]undecane
2. New aspect of cationic ring-opening polymerization of seven-membered spiroorthocarbonates: synthesis and polymerization of substituted 1,6,8,13-tetraoxaspiro[6.6]tridecanes
3. Properties’ improvement of epoxy resin using prepolymers prepared from diisocyanates and 3,9-dihydroxyethyl-3′,9′-dibenzyl-1,5,7,11-tetraoxaspiro(5,5)undecane
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1. Synthesis of the fluorene spiroorthocarbonate and the evaluation of its antishrinking activity in the cationic photopolymerization of an epoxy resin;Designed Monomers and Polymers;2012-12-03
2. Novel Tetraspiroorthocarbonates as Successful Anti-shrinking Agents for the Photopolymerization of Epoxy Monomers;Journal of Macromolecular Science, Part A;2012-03-23
3. Block Copolymers by Multi-Mode Polymerizations;Materials Science and Technology;2012-02-15
4. Novel diol spiro orthocarbonates derived from glycerol as anti-shrinkage additives for the cationic photopolymerization of epoxy monomers;Polymer International;2010-01-08
5. Synthesis of an oxetane-functionalized hemispiroorthocarbonate used as a low-shrinkage additive in the cationic ultraviolet curing of oxetane monomers;Journal of Applied Polymer Science;2009-05-05
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