Ultrasensitive reversible chromophore reaction of BODIPY functions as high ratio double turn on probe

BODIPY dyes, though widely explored, have not been pursued as chromophore reaction based chemical probes. Here, the authors synthesize a meso-naked BODIPY core flanked with two electron-withdrawing groups, which undergoes a reversible change in conjugated structure in the presence of base and functi...

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Autores principales: Dehui Hu, Tao Zhang, Shayu Li, Tianjun Yu, Xiaohui Zhang, Rui Hu, Jiao Feng, Shuangqing Wang, Tongling Liang, Jianming Chen, Lyubov N. Sobenina, Boris A. Trofimov, Yi Li, Jinshi Ma, Guoqiang Yang
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Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/94a1cb8084f041c69ae0653901a9f2c0
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spelling oai:doaj.org-article:94a1cb8084f041c69ae0653901a9f2c02021-12-02T15:34:36ZUltrasensitive reversible chromophore reaction of BODIPY functions as high ratio double turn on probe10.1038/s41467-017-02270-02041-1723https://doaj.org/article/94a1cb8084f041c69ae0653901a9f2c02018-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-02270-0https://doaj.org/toc/2041-1723BODIPY dyes, though widely explored, have not been pursued as chromophore reaction based chemical probes. Here, the authors synthesize a meso-naked BODIPY core flanked with two electron-withdrawing groups, which undergoes a reversible change in conjugated structure in the presence of base and functions as a dual signal and ultrahigh turn-on ratio chemical probe.Dehui HuTao ZhangShayu LiTianjun YuXiaohui ZhangRui HuJiao FengShuangqing WangTongling LiangJianming ChenLyubov N. SobeninaBoris A. TrofimovYi LiJinshi MaGuoqiang YangNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Dehui Hu
Tao Zhang
Shayu Li
Tianjun Yu
Xiaohui Zhang
Rui Hu
Jiao Feng
Shuangqing Wang
Tongling Liang
Jianming Chen
Lyubov N. Sobenina
Boris A. Trofimov
Yi Li
Jinshi Ma
Guoqiang Yang
Ultrasensitive reversible chromophore reaction of BODIPY functions as high ratio double turn on probe
description BODIPY dyes, though widely explored, have not been pursued as chromophore reaction based chemical probes. Here, the authors synthesize a meso-naked BODIPY core flanked with two electron-withdrawing groups, which undergoes a reversible change in conjugated structure in the presence of base and functions as a dual signal and ultrahigh turn-on ratio chemical probe.
format article
author Dehui Hu
Tao Zhang
Shayu Li
Tianjun Yu
Xiaohui Zhang
Rui Hu
Jiao Feng
Shuangqing Wang
Tongling Liang
Jianming Chen
Lyubov N. Sobenina
Boris A. Trofimov
Yi Li
Jinshi Ma
Guoqiang Yang
author_facet Dehui Hu
Tao Zhang
Shayu Li
Tianjun Yu
Xiaohui Zhang
Rui Hu
Jiao Feng
Shuangqing Wang
Tongling Liang
Jianming Chen
Lyubov N. Sobenina
Boris A. Trofimov
Yi Li
Jinshi Ma
Guoqiang Yang
author_sort Dehui Hu
title Ultrasensitive reversible chromophore reaction of BODIPY functions as high ratio double turn on probe
title_short Ultrasensitive reversible chromophore reaction of BODIPY functions as high ratio double turn on probe
title_full Ultrasensitive reversible chromophore reaction of BODIPY functions as high ratio double turn on probe
title_fullStr Ultrasensitive reversible chromophore reaction of BODIPY functions as high ratio double turn on probe
title_full_unstemmed Ultrasensitive reversible chromophore reaction of BODIPY functions as high ratio double turn on probe
title_sort ultrasensitive reversible chromophore reaction of bodipy functions as high ratio double turn on probe
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/94a1cb8084f041c69ae0653901a9f2c0
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