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α-(联苯)-取代 2,2'-联吡啶基推-拉型荧光染料的合成及光物理性质

Synthesis and Photophysical Properties of α-(-Biphenyl)-Substituted 2,2'-Bipyridine-Based Push-Pull Fluorophores.

机构信息

Chemical Engineering Institute, Ural Federal University, 19 Mira St., Yekaterinburg 620002, Russia.

I. Ya. Postovsky Institute of Organic Synthesis of RAS, Ural Division, 22/20 S. Kovalevskoy/Akademicheskaya St., Yekaterinburg 62099, Russia.

出版信息

Molecules. 2022 Oct 13;27(20):6879. doi: 10.3390/molecules27206879.

DOI:10.3390/molecules27206879
PMID:36296472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9608819/
Abstract

A series of new α-(-biphenyl)-substituted 2,2'-bipyridines were obtained through the combination of the ipso-nucleophilic aromatic substitution of the C5-cyano group, aza-Diels-Alder and Suzuki cross-coupling reactions, starting from 5-cyano-1,2,4-triazines. For the obtained compounds, photophysical and fluorosolvatochromic properties were studied. Fluorophores and demonstrated unexpected AIEE activity, while and showed promising nitroexplosive detection abilities.

摘要

一系列新型的α-(-联苯)-取代 2,2'-联吡啶是通过 C5-氰基的原位亲核芳香取代、氮杂 Diels-Alder 反应和 Suzuki 交叉偶联反应,从 5-氰基-1,2,4-三嗪出发得到的。对所得到的化合物进行了光物理和氟溶剂化变色性质的研究。荧光团 和 表现出意外的 AIEE 活性,而 和 表现出有前途的硝基爆炸物检测能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/cd57437c451d/molecules-27-06879-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/baf4d7f20411/molecules-27-06879-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/1076ea8c3abf/molecules-27-06879-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/b0a9ea8c4bf2/molecules-27-06879-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/9131590546f5/molecules-27-06879-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/e50cbe37093d/molecules-27-06879-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/758cec775e6f/molecules-27-06879-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/d7c472f1862d/molecules-27-06879-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/457d2e610c82/molecules-27-06879-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/d252100354e7/molecules-27-06879-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/cd57437c451d/molecules-27-06879-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/baf4d7f20411/molecules-27-06879-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/1076ea8c3abf/molecules-27-06879-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/b0a9ea8c4bf2/molecules-27-06879-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/9131590546f5/molecules-27-06879-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/e50cbe37093d/molecules-27-06879-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/758cec775e6f/molecules-27-06879-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/d7c472f1862d/molecules-27-06879-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/457d2e610c82/molecules-27-06879-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/d252100354e7/molecules-27-06879-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25db/9608819/cd57437c451d/molecules-27-06879-g009.jpg

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