新型A-D-A型吩噻嗪衍生物的氧化荧光调制

IF 4.6 3区化学 Q2 CHEMISTRY, MULTIDISCIPLINARY

RSC Advances Pub Date : 2025-03-21 DOI:10.1039/D5RA01383F

Mengdi Lin, Shilong Zhang, Xuefeng Liang, Zhenhua Shan, Wenqian Yang and Haijiao Xie

引用次数: 0

摘要

通过自下而上的合成策略成功地合成了1,9-二甲基-2,8功能化吩噻嗪类药物。氧化后的光致发光量子产率高达52%，PLQY降低了6%，这为设计具有定制性能的基于ptz的推挽系统开辟了新的途径。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Modulation of fluorescence in novel A–D–A type phenothiazine derivatives via oxidation†

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Modulation of fluorescence in novel A–D–A type phenothiazine derivatives via oxidation†

1,9-Dimethyl-2,8-funtionalized phenothiazines were successfully developed through a bottom-up synthesis strategy. A high photoluminescence quantum yield of 52% was observed, upon oxidation, and a reduced PLQY of 6% was achieved which opens new avenues for designing PTZ-based push–pull systems with tailored properties.

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来源期刊

RSC Advances chemical sciences-

CiteScore

7.50

自引率

2.60%

发文量

3116

审稿时长

1.6 months

期刊介绍： An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.