Investigations into oxidation induced ring opening of terarylenes containing π-extended thieno[<i>b</i>]thiophene units

Investigations into oxidation induced ring opening of terarylenes containing π-extended thieno[<i>b</i>]thiophene units
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含π-延伸噻吩并[<i>b</i>]噻吩单元的三萘嵌苯的氧化诱导开环研究

DOI:
10.1039/d2nj05726c
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发表时间:
2023
影响因子:
3.3
通讯作者:
Kawai Tsuyoshi
Kawai Tsuyoshi
中科院分区:
化学3区
文献类型:
--
作者:
Martin Colin J.;Goto Yora;Asato Ryosuke;Rapenne Gwenael;Kawai Tsuyoshi

文献摘要

相似文献

已经制备了四种具有延长的π-共轭噻吩并[b]噻吩单元的光致变色三萘嵌苯。根据噻吩并[b]噻吩单元的位置,排除光致变色环环化和环化回复行为。监测涉及热和级联环化回复的自发褪色反应,具体取决于分子结构。已经进行了电化学和计算研究,以阐明两种异构体中基态和阳离子态的相对稳定性。
Four photochromic terarylenes having extended π-conjugated thieno[b]thiophene units have been prepared. Photochromic ring-cyclization and cycloreversion behaviour are excluded depending on the position of thieno[b]thiophene units. A sponteneous fading reaction involving both thermal and cascade cycloreversion depending on molecular stucture is monitored. Electrochemical and computational studies have been conducted to elucidate the relative stability of their ground and cationic states in both isomers.