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首页> 外文期刊>Dyes and Pigments >Toward multi-addressable molecular systems: Efficient synthesis and photochromic performance of unsymmetrical bisthienylethenes
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Toward multi-addressable molecular systems: Efficient synthesis and photochromic performance of unsymmetrical bisthienylethenes

机译:迈向多址分子系统:不对称双联噻吩基乙烯的高效合成和光致变色性能

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摘要

Various synthetic routes have been compared to access to unsymmetrical 1,2-bisthienylper-fluorocyclopentenes having one electro-withdrawing formyl group. The strategy based on key mono-susbtituted cyclopentenes appears to be the most reliable and versatile synthetic approach. Applying this controlled sequential synthesis to appropriate thiophenic building blocks leads to the preparation of π-conjugated extended push—pull system where photochromic performance were characterised.
机译:已经比较了各种合成途径来获得具有一个吸电甲酰基的不对称的1,2-双噻吩基全氟环戊烯。基于关键的单取代环戊烯的策略似乎是最可靠,用途最广泛的合成方法。将这种受控的顺序合成方法应用于适当的噻吩结构单元,可以制备特征在于光致变色性能的π共轭扩展推挽系统。

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