4′-烷氧基-4-(ω-肉桂酰烷氧基)偶氮苯的合成及其光开关行为

ECSOC-25 Pub Date : 2021-11-14 DOI:10.3390/ecsoc-25-11685
Abdullah Al-Hemyari, Muna S. Bufaroosha, T. Thiemann
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引用次数: 0

摘要

为了寻找新的热致性和光开关材料,制备了一些4′-烷氧基-4- (ω -肉桂酰烷氧基)偶氮苯。合成过程包括4-硝基苯酚的O -烷基化,然后是硝基的还原(h2, Pd/C),苯胺的重氮化,随后与ω -羟基烷氧苯反应,然后是改性的appel型酯化(brccl3, pph3)。研究了这些物质的光化学行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of 4′-Alkoxy-4-(ω-cinnamoylalkoxy)azobenzenes and Their Photoswitchable Behavior
: In search of new thermotropic, photoswitchable materials, a number of 4′ -alkoxy-4- (ω -cinnamoylalkoxy)azobenzenes were prepared. The synthetic procedure included O -alkylation of 4-nitrophenol, followed by reduction of the nitro group (H 2 , Pd/C), diazotization of the aniline and subsequent reaction with ω -hydroxyalkoxybenzenes, followed by a modified Appel-type esterification (BrCCl 3 , PPh 3 ). The photochemical behavior of the substances was investigated.
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