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Isomerization behavior of azobenzene chromophores attached to the side chain of organic polymer in organic-inorganic polymer hybrids

机译:有机-无机聚合物杂化物中偶氮苯发色团附着于有机聚合物侧链的异构化行为

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摘要

Isomerization behavior of azobenzene chromophores in organic-inorganic polymer hybrids was investigated. Polymer hybrids were prepared from azobenzene-modified poly(2-methyl-2-oxazoline) (POZO-A) and methyltrimethoxysilane (MeTMOS) or tetramethoxysilane (TMOS). Isomerization behavior in polymer hybrids was compared with that in DMSO solution or in films of POZO-A. Two kinds of model compounds were synthesized, and their isomerization behaviors were also examined. Photoinduced trans-to-cis isomerization took place in all samples. The cis isomer ratios in the photostationary state were found to be smaller in solid films than in solution. Especially, model compound having a triethoxysilyl group showed a markedly small cis isomer ratio. Thermal cis-to-trans isomerization was investigated kinetically. A distinct deviation from the first-order kinetics was observed in solid films.
机译:研究了偶氮苯发色团在有机-无机聚合物杂化物中的异构化行为。由偶氮苯改性的聚(2-甲基-2-恶唑啉)(POZO-A)和甲基三甲氧基硅烷(MeTMOS)或四甲氧基硅烷(TMOS)制备聚合物杂化物。将聚合物杂化物中的异构化行为与DMSO溶液或POZO-A薄膜中的异构化行为进行了比较。合成了两种模型化合物,并研究了它们的异构化行为。在所有样品中均发生了光诱导的反式-顺式异构化。发现在固态膜中光平稳状态下的顺式异构体比率比在溶液中小。特别地,具有三乙氧基甲硅烷基的模型化合物显示出显着小的顺式异构体比率。动力学研究了热的顺-反异构化。在固体膜中观察到与一级动力学明显不同。

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