Facile Synthesis of Asymmetric aza-Boron Dipyrromethene Analogues Bearing Quinoxaline Moiety

Facile Synthesis of Asymmetric aza-Boron Dipyrromethene Analogues Bearing Quinoxaline Moiety

An asymmetric aza-BODIPY analogue bearing quinoxaline moiety was synthesized via a titanium tetrachloride-mediated Schiff-base-forming reaction of 6,7-dimethyl-1,4-dihydroquinoxaline-2,3-dione and benzo[<i>d</i>]thiazol-2-amine. This novel aza-BODIPY analogue forms a complementary hydrog...

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Bibliographic Details
Main Authors: Ru Feng, Zuoxu Chen, Yue Wang, Jianming Pan, Soji Shimizu
Format: Article
Language:English
Published: MDPI AG 2023-12-01
Series:Molecules
Subjects:
aza-BODIPY
quinoxaline
hydrogen bonding
fluorescence
Online Access:https://www.mdpi.com/1420-3049/28/24/7940

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