Superior photochromic performance of naphthopyrans in a rigid host matrix using polymer conjugation: Fast, dark, and tunable

被引:61
作者
Malic, Nino [1 ,3 ,4 ]
Campbell, Jonathan A. [2 ,4 ]
Evans, Richard A. [1 ,3 ,4 ]
机构
[1] CSIRO Mol & Hlth Technol, Clayton, Vic 3169, Australia
[2] Univ New S Wales, Ctr Adv Macromol Design, Sydney, NSW 2052, Australia
[3] Univ New S Wales, Sch Chem Sci & Engn, Sydney, NSW 2052, Australia
[4] Cooperat Res Ctr Polymers, Melbourne, Vic 3168, Australia
关键词
D O I
10.1021/ma071792l
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The attachment of low T-g poly(n-butyl acrylate) polymers (M-n 4100 to 13 100) to naphthopyran photochromic dyes provided large tunable improvements in their photochromic performance in a rigid thermoset host polymer matrix. Both coloration and decoloration speeds were greatly increased, with the critical t(1/2) decoloration times reduced by 50-95% and t(3/4) decoloration times reduced by at least 63% through the use of these polymer conjugates. In addition, the optical density of the colored form of the dye-polymer conjugates rapidly reached a steady state absorption ca. 60-70% greater than the nonpolymer conjugated control dyes. The effect of the geometry of the polymer conjugates was examined, and it was found that mid-placement of the dye on the polymer provided secondary decoloration speed enhancement over end-placement. Thus, conjugation of low T-g poly(n-butyl acrylate) not only provides faster coloration and decoloration but also greatly increases optical density with near square-wave characteristics.
引用
收藏
页码:1206 / 1214
页数:9
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