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Polymerization photoinitiated by carbonyl compounds. XI. Styrene polymerization photoinitiated by cyclododecanones
Authors:M Biondic  S Giacopello  R Erra Bassells  M V Encinas  E A Lissi
Abstract:To establish their potential as source of biradicals to initiate free-radical polymerization, 2-methyl- and 2,2,12-trimethylcyclododecanones were photolyzed in the presence of styrene. The initiation efficiency of both ketones is low—0.03. The molecular weight of the obtained polymer is ca. 25% higher than that obtained employing photoinitiators that produce monoradicals. This difference is explained in terms of a mixed polymerization mechanism comprising mono- and biradicals. © 1996 John Wiley & Sons, Inc.
Keywords:photoinitiation  cyclododecanones  photopolymerization
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