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Synthesis of Bisimidazole Derivatives for Selective Sensing of Fluoride Ion

Rapid and efficient analysis of fluoride ion is crucial to providing key information for fluoride ion hazard assessment and pollution management. In this study, we synthesized one symmetrical structure called 1,4-bis(4,5-diphenyl-1H-imidazol-2-yl)benzene (1a) and two asymmetrical structures, namely...

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Detalles Bibliográficos
Autores principales: Zhang, Liang, Liu, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151418/
https://www.ncbi.nlm.nih.gov/pubmed/28891996
http://dx.doi.org/10.3390/molecules22091519
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author Zhang, Liang
Liu, Fang
author_facet Zhang, Liang
Liu, Fang
author_sort Zhang, Liang
collection PubMed
description Rapid and efficient analysis of fluoride ion is crucial to providing key information for fluoride ion hazard assessment and pollution management. In this study, we synthesized one symmetrical structure called 1,4-bis(4,5-diphenyl-1H-imidazol-2-yl)benzene (1a) and two asymmetrical structures, namely 2-(4-(4,5-diphenyl-1H-imidazol-2-yl)phenyl)-1H-phenanthro(9,10-d)imidazole (1b) and 2-(4-(4,5-diphenyl-1H-imidazol-2-yl)phenyl)-1H-imidazo(4,5-f)(1,10)phenanthroline (1c), which served as an efficient anion sensor for fluoride ion over a wide range of other anions (Cl(−), Br(−), I(−), NO(3)(−), ClO(4)(−), HSO(4)(−), BF(4)(−), and PF(6)(−)) owing to imidazole group in the main backbone. The absorption intensity of compound 1a at λ(max) 358 nm slightly decreased; however, a new band at λ(max) 414 nm appeared upon the addition of fluoride ion, while no evident change occurred upon the addition of eight other anions. The photoluminescence intensity of compound 1a at λ(max) 426 nm was nearly quenched and fluorescence emission spectra were broadened when fluoride ion was added into dimethyl sulfoxide (DMSO) solution of compound 1a. Compared with the optical behaviors of the DMSO solution of compound 1a in the presence of Bu(4)N(+)F(−), compounds 1b and 1c exhibited considerable sensitivity to fluoride ion due to the increase in coplanarity. Furthermore, compared with the fluorescence emission behaviors of the DMSO solutions of compounds 1a and 1b in the presence of Bu(4)N(+)F(−), compound 1c exhibited the most significant sensitivity to fluoride ion due to the charge transfer enhancement. Consequently, the detection limits of compounds 1a–1c increased from 5.47 × 10(−6) M to 4.21 × 10(−6) M to 9.12 × 10(−7) M. Furthermore, the largest red shift (75 nm) of the DMSO solution compound 1c in the presence of fluoride ion can be observed. Our results suggest that the increase in coplanarity and the introduction of electron-withdrawing groups to the imidazole backbone can improve the performance in detecting fluoride ion.
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spelling pubmed-61514182018-11-13 Synthesis of Bisimidazole Derivatives for Selective Sensing of Fluoride Ion Zhang, Liang Liu, Fang Molecules Communication Rapid and efficient analysis of fluoride ion is crucial to providing key information for fluoride ion hazard assessment and pollution management. In this study, we synthesized one symmetrical structure called 1,4-bis(4,5-diphenyl-1H-imidazol-2-yl)benzene (1a) and two asymmetrical structures, namely 2-(4-(4,5-diphenyl-1H-imidazol-2-yl)phenyl)-1H-phenanthro(9,10-d)imidazole (1b) and 2-(4-(4,5-diphenyl-1H-imidazol-2-yl)phenyl)-1H-imidazo(4,5-f)(1,10)phenanthroline (1c), which served as an efficient anion sensor for fluoride ion over a wide range of other anions (Cl(−), Br(−), I(−), NO(3)(−), ClO(4)(−), HSO(4)(−), BF(4)(−), and PF(6)(−)) owing to imidazole group in the main backbone. The absorption intensity of compound 1a at λ(max) 358 nm slightly decreased; however, a new band at λ(max) 414 nm appeared upon the addition of fluoride ion, while no evident change occurred upon the addition of eight other anions. The photoluminescence intensity of compound 1a at λ(max) 426 nm was nearly quenched and fluorescence emission spectra were broadened when fluoride ion was added into dimethyl sulfoxide (DMSO) solution of compound 1a. Compared with the optical behaviors of the DMSO solution of compound 1a in the presence of Bu(4)N(+)F(−), compounds 1b and 1c exhibited considerable sensitivity to fluoride ion due to the increase in coplanarity. Furthermore, compared with the fluorescence emission behaviors of the DMSO solutions of compounds 1a and 1b in the presence of Bu(4)N(+)F(−), compound 1c exhibited the most significant sensitivity to fluoride ion due to the charge transfer enhancement. Consequently, the detection limits of compounds 1a–1c increased from 5.47 × 10(−6) M to 4.21 × 10(−6) M to 9.12 × 10(−7) M. Furthermore, the largest red shift (75 nm) of the DMSO solution compound 1c in the presence of fluoride ion can be observed. Our results suggest that the increase in coplanarity and the introduction of electron-withdrawing groups to the imidazole backbone can improve the performance in detecting fluoride ion. MDPI 2017-09-11 /pmc/articles/PMC6151418/ /pubmed/28891996 http://dx.doi.org/10.3390/molecules22091519 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Zhang, Liang
Liu, Fang
Synthesis of Bisimidazole Derivatives for Selective Sensing of Fluoride Ion
title Synthesis of Bisimidazole Derivatives for Selective Sensing of Fluoride Ion
title_full Synthesis of Bisimidazole Derivatives for Selective Sensing of Fluoride Ion
title_fullStr Synthesis of Bisimidazole Derivatives for Selective Sensing of Fluoride Ion
title_full_unstemmed Synthesis of Bisimidazole Derivatives for Selective Sensing of Fluoride Ion
title_short Synthesis of Bisimidazole Derivatives for Selective Sensing of Fluoride Ion
title_sort synthesis of bisimidazole derivatives for selective sensing of fluoride ion
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151418/
https://www.ncbi.nlm.nih.gov/pubmed/28891996
http://dx.doi.org/10.3390/molecules22091519
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