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首页> 外文期刊>Journal of Materials Chemistry: An Interdisciplinary Journal dealing with Synthesis, Structures, Properties and Applications of Materials, Particulary Those Associated with Advanced Technology >A precursor strategy for the synthesis of low band-gap polymers: an efficient route to a series of near-infrared electrochromic polymers
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A precursor strategy for the synthesis of low band-gap polymers: an efficient route to a series of near-infrared electrochromic polymers

机译:低带隙聚合物合成的前体策略:一系列近红外电致变色聚合物的有效途径

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摘要

A precursor strategy for the synthesis and screening of a series of conjugated donor-acceptor polymers is demonstrated by successful preparation of low band-gap polymers (P2-P5) containing triphenylamine as an electron donor and several heterocycles as acceptors, such as [1,2,5]thiadiazolo [3,4-g]quinoxaline, [1,2,5]thiadiazolo[3,4-i]dibenzo[a,c]phenazine, benzo[1,2-c:4,5-c']bis([1,2,5] thiadiazole), and selenadiazole[3,4-f]benzo[c][l,2,5]thiadiazole, that are transformed from a single reactive polymer (PI). Polymers P2-P5 have the band gap of 1.71-1.29 eV and show the absorption and emission in the near infrared (NIR) spectral region. All the polymers are also NIR electrochromic. In particular, polymer P3 is electrochemically switchable between leaf-like green coloring and near-infrared absorbing states with an efficiency of 479 cm~2 C~(-1) at 1310 nm or 232 cm~2 C~(-1) at 1550 nm, making it potentially useful for electrically switchable day-to-night camouflage applications.
机译:通过成功制备含有三苯胺作为电子给体和几个杂环作为受体的低带隙聚合物(P2-P5),可以证明合成和筛选一系列共轭给体-受体聚合物的前体策略。 2,5]噻二唑[3,4-g]喹喔啉,[1,2,5]噻二唑[3,4-i]二苯并[a,c]吩嗪,苯并[1,2-c:4,5-c从单一反应性聚合物(PI)转化得到的']双([[1,2,5]噻二唑)和硒二唑[3,4-f]苯并[c] [1,2,5]噻二唑。聚合物P2-P5的带隙为1.71-1.29 eV,并在近红外(NIR)光谱区域显示吸收和发射。所有聚合物也是近红外电致变色的。尤其是,聚合物P3可在叶状绿色和近红外吸收状态之间进行电化学转换,在1310 nm处的效率为479 cm〜2 C〜(-1),在1550年时的效率为232 cm〜2 C〜(-1)纳米级,使其潜在地可用于日夜可电动切换的伪装应用。

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