Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor

A novel fluorescence sensor (BIP) bearing NH and OH subunits displayed a highly selective and sensitive recognition property for fluoride over other anions. Fluoride-driven ESPT, poorly used in anion recognition and sensing, was suggested to be responsible for the fluorescence enhancement with a blu...

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Detalles Bibliográficos
Autores principales: Liu, Kai, Zhao, Xiaojun, Liu, Qingxiang, Huo, Jianzhong, Zhu, Bolin, Diao, Shihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419554/
https://www.ncbi.nlm.nih.gov/pubmed/25977729
http://dx.doi.org/10.3762/bjoc.11.61
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author Liu, Kai
Zhao, Xiaojun
Liu, Qingxiang
Huo, Jianzhong
Zhu, Bolin
Diao, Shihua
author_facet Liu, Kai
Zhao, Xiaojun
Liu, Qingxiang
Huo, Jianzhong
Zhu, Bolin
Diao, Shihua
author_sort Liu, Kai
collection PubMed
description A novel fluorescence sensor (BIP) bearing NH and OH subunits displayed a highly selective and sensitive recognition property for fluoride over other anions. Fluoride-driven ESPT, poorly used in anion recognition and sensing, was suggested to be responsible for the fluorescence enhancement with a blue shift of 35 nm in the emission spectrum.
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spelling pubmed-44195542015-05-14 Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor Liu, Kai Zhao, Xiaojun Liu, Qingxiang Huo, Jianzhong Zhu, Bolin Diao, Shihua Beilstein J Org Chem Letter A novel fluorescence sensor (BIP) bearing NH and OH subunits displayed a highly selective and sensitive recognition property for fluoride over other anions. Fluoride-driven ESPT, poorly used in anion recognition and sensing, was suggested to be responsible for the fluorescence enhancement with a blue shift of 35 nm in the emission spectrum. Beilstein-Institut 2015-04-24 /pmc/articles/PMC4419554/ /pubmed/25977729 http://dx.doi.org/10.3762/bjoc.11.61 Text en Copyright © 2015, Liu et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Liu, Kai
Zhao, Xiaojun
Liu, Qingxiang
Huo, Jianzhong
Zhu, Bolin
Diao, Shihua
Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor
title Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor
title_full Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor
title_fullStr Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor
title_full_unstemmed Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor
title_short Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor
title_sort fluoride-driven ‘turn on’ espt in the binding with a novel benzimidazole-based sensor
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419554/
https://www.ncbi.nlm.nih.gov/pubmed/25977729
http://dx.doi.org/10.3762/bjoc.11.61
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AT huojianzhong fluoridedriventurnonesptinthebindingwithanovelbenzimidazolebasedsensor
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