1,2-Diaroyl Benzofurans: Synthesis and Photochromic Properties

IF 1.7 4区 化学 Q3 CHEMISTRY, ORGANIC Synlett Pub Date : 2024-08-15 DOI:10.1055/s-0043-1775039
Jianming Zhong, Shuangshuang Li, Zhaoxin Wang, Wang Zhou
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Abstract

A cascade reaction involving a base-promoted nucleophilic substitution reaction between diketones and α-bromoacetophenone derivatives and the subsequent selective condensation–cyclization was developed for the synthesis of 1,2-diaroyl benzofurans. 1,2-Diaroyl benzofurans with different functional groups and structures exhibit reversible photochromic behaviors in solution, solid state, and thin films with diverse colors, demonstrating a potential application in the field of optical functional materials.

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1,2-二芳基苯并呋喃:合成与光致变色特性
为了合成 1,2-二芳基苯并呋喃,研究人员开发了一种级联反应,包括二酮和α-溴苯乙酮衍生物之间的碱促进亲核取代反应以及随后的选择性缩合-环化反应。具有不同官能团和结构的 1,2-二芳基苯并呋喃在溶液、固态和薄膜中表现出可逆的光致变色行为,并呈现出不同的颜色,显示了其在光学功能材料领域的应用潜力。
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来源期刊
Synlett
Synlett 化学-有机化学
CiteScore
3.40
自引率
5.00%
发文量
369
审稿时长
1 months
期刊介绍: SYNLETT is an international journal reporting research results and current trends in chemical synthesis in short personalized reviews and preliminary communications. It covers all fields of scientific endeavor that involve organic synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines and offers the possibility to publish scientific primary data.
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