2008
DOI: 10.1080/15421400801918195
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Influence of Cationic Symmetric Polymethine Dyes on Radical Polymerization of Methylmethacrylate in Solution

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Cited by 2 publications
(3 citation statements)
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“…The authors suggest that this is due to the high fluorescent ability of the dyes since nonluminescent azo and anthraquinone dyes conversely retard such reactions [206][207][208]. However, the most recent investigations do not support this suggestion [121][122][123]. It was shown that the carbocyanine dye based on benz[c,d]indole, which has extremely weak fluorescence ability [209], substantially accelerates the radical polymerization of MMA [123].…”
Section: Structurally Dyed Polymersmentioning
confidence: 93%
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“…The authors suggest that this is due to the high fluorescent ability of the dyes since nonluminescent azo and anthraquinone dyes conversely retard such reactions [206][207][208]. However, the most recent investigations do not support this suggestion [121][122][123]. It was shown that the carbocyanine dye based on benz[c,d]indole, which has extremely weak fluorescence ability [209], substantially accelerates the radical polymerization of MMA [123].…”
Section: Structurally Dyed Polymersmentioning
confidence: 93%
“…It was found that the series of cationic polymethine dyes is capable of initiating the radical thermopolymerization of MMA extremely effectively in the mass [120] and in solution [121][122][123] without an initiator. This ability changes if the terminal heterocyclic groups deviate from the average electron-donating capacity in the direction of both increase and decrease [123].…”
Section: Methods Of Introduction Of Dyes Into the Polymer And Their Cmentioning
confidence: 99%
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