2008
DOI: 10.1080/15421400802458548
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Effect of Polymethine Dyes with Various Electron-Donating Abilities of Terminal Groups on Thermopolymerization of Methylmethacrylate in Solutions

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Cited by 2 publications
(7 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%
“…This ability changes if the terminal heterocyclic groups deviate from the average electron-donating capacity in the direction of both increase and decrease [123]. In the case of the vinylogous series of indopolycarbocyanines (6)- (8) of one structural type it was established that they have different effects on the kinetics of the polymerization of MMA depending on the length of the polymethine chain, and dye (6) accelerates the reaction while dye (8) inhibits it.…”
Section: Methods Of Introduction Of Dyes Into the Polymer And Their Cmentioning
confidence: 98%
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