1968
DOI: 10.1021/cr60252a001
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Photopolymerization of vinyl monomers

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Cited by 247 publications
(100 citation statements)
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References 172 publications
(223 reference statements)
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“…3,18 -20 Different dyes and reducing agents were used such as methylene blue, thionine, phenothiazine, sodium fluorescein, Dye-sensitized photopolymerization of vinyl monoriboflavin, etc., as dyes and triethanolamine, mers was the subject of extensive investigations ascorbic acid, para-substituted benzene sulfinate in 1950s and 1960s. 1 It was first reported by Bamions, etc., as reducing agents. Among these studford and Dewar 2 for styrene, by Oster and coies, the methylene blue sensitized photopolymerworkers for acrylamide and other vinyl monomers, 3,5 by Palit and co-workers for methyl methization of acrylamide in presence of a reducing acrylate, 6,7 and by other investigators.…”
Section: Introductionmentioning
confidence: 92%
“…3,18 -20 Different dyes and reducing agents were used such as methylene blue, thionine, phenothiazine, sodium fluorescein, Dye-sensitized photopolymerization of vinyl monoriboflavin, etc., as dyes and triethanolamine, mers was the subject of extensive investigations ascorbic acid, para-substituted benzene sulfinate in 1950s and 1960s. 1 It was first reported by Bamions, etc., as reducing agents. Among these studford and Dewar 2 for styrene, by Oster and coies, the methylene blue sensitized photopolymerworkers for acrylamide and other vinyl monomers, 3,5 by Palit and co-workers for methyl methization of acrylamide in presence of a reducing acrylate, 6,7 and by other investigators.…”
Section: Introductionmentioning
confidence: 92%
“…[14] In this procedure, these Rps are calculated from the decrease in the IR absorption monitored at 810 cml which assigned C-H perpendicular vibration of vinyl groups. [17][18][19][20][21] 3. Results…”
Section: Sensitivity Evaluationmentioning
confidence: 99%
“…The photopolymerization of a bichromophoric compound was examined quantitatively. In this system, the degree of conversion, p, is represented as: (1) where N 0 is the number ofbifunctional OC-10 molecules at the initial time, and N, that after irradiation time t. The total number of cyclobutane rings formed during irradiation time t, is N 0 -N. Since two terminal OBA groups are consumed for each intermolecular cycloaddition reaction, the total number of consumed OBA groups is represented as 2 (N 0 -N). In this bichromophoric compound, the number of terminal OBA groups is 2N 0 at the initial state.…”
Section: Stepwise Photopolymerizationmentioning
confidence: 99%