2006
DOI: 10.1016/j.radphyschem.2006.01.013
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1-(Bromoacetyl)pyrene, a novel photoinitiator for the copolymerization of styrene and methylmethacrylate

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Cited by 34 publications
(15 citation statements)
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“…Considering the requirement for photoinitiators to strongly absorb in the visible range, a wide range of structures have been examined over the years, as exemplified with chromones, [26][27][28] benzophenones, [29][30][31][32][33][34] pyrenes, [35][36][37][38][39][40] diketopyrrolopyrroles, [41][42][43] coumarins, [44][45][46][47][48][49][50], iron complexes, [51][52][53][54][55][56][57] 2,3-diphenylquinoxaline derivatives, [58] naphthalimides, [59][60][61][62][63][64][65][66][67][68][69][70][71] squaraines, [72][73]…”
Section: Figure 1 the Characteristic Features Of Photopolymerizationmentioning
confidence: 99%
“…Considering the requirement for photoinitiators to strongly absorb in the visible range, a wide range of structures have been examined over the years, as exemplified with chromones, [26][27][28] benzophenones, [29][30][31][32][33][34] pyrenes, [35][36][37][38][39][40] diketopyrrolopyrroles, [41][42][43] coumarins, [44][45][46][47][48][49][50], iron complexes, [51][52][53][54][55][56][57] 2,3-diphenylquinoxaline derivatives, [58] naphthalimides, [59][60][61][62][63][64][65][66][67][68][69][70][71] squaraines, [72][73]…”
Section: Figure 1 the Characteristic Features Of Photopolymerizationmentioning
confidence: 99%
“…This specificity is notably used advantageously with photopolymerizable glues and dental adhesives. Considering that visible light photopolymerization can be activated between 400 and 800 nm, numerous dyes absorbing in the visible range have been proposed, as exemplified with acridine-1,8-diones [36][37][38], carbazoles [39][40][41][42][43][44], pyrenes [45][46][47][48][49][50], iridium complexes, [51][52][53][54][55][56][57][58][59], copper complexes [60][61][62][63][64][65][66][67][68][69][70], squaraines [71][72][73], camphorquinones [74,75], perylenes [76][77][78], iodonium salts [79][80][81], benzophenones [82]...…”
Section: Introductionmentioning
confidence: 99%
“…[129] Access to azapolyacenes is also possible with pyrene, by oxidation of the adjacent aromatic rings, enabling to prepare pyrene-diones or pyrene-tetraones. [130] Historically, 1-(bromoacetyl)pyrene (Pyr_2) which is a derivative of pyrene (Pyr_1) has been extensively studied by Daswal and coworkers as a UV-photoinitiator for the copolymerization of styrene with n-butyl acrylate, [131] methyl methacrylate [132] or acrylonitrile in solution (See Figure 4). [133] In these different studies, modification of the substitution pattern of pyrene was determined as strongly influencing the reactivity of the pyrene.…”
Section: Introductionmentioning
confidence: 99%