Cargando…
Synthesis of a Dehydroabietyl Derivative Bearing a 2-(2′-Hydroxyphenyl)Benzimidazole Unit and Its Selective Cu(2+) Chemosensing
A dehydroabietyl derivative 2 bearing a 2-(2′-hydroxyphenyl)benzimidazole unit was synthesized and its sensing behaviors toward metal ions were investigated by UV-Vis and fluorescence spectroscopy methods. In THF solution, compound 2 exhibited excellent selectivity for Cu(II) over miscellaneous othe...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259128/ https://www.ncbi.nlm.nih.gov/pubmed/21189458 http://dx.doi.org/10.3390/molecules16010100 |
_version_ | 1783374615155834880 |
---|---|
author | Wang, Ying-Chun Liu, Lu-Zhi Pan, Ying-Ming Wang, Heng-Shan |
author_facet | Wang, Ying-Chun Liu, Lu-Zhi Pan, Ying-Ming Wang, Heng-Shan |
author_sort | Wang, Ying-Chun |
collection | PubMed |
description | A dehydroabietyl derivative 2 bearing a 2-(2′-hydroxyphenyl)benzimidazole unit was synthesized and its sensing behaviors toward metal ions were investigated by UV-Vis and fluorescence spectroscopy methods. In THF solution, compound 2 exhibited excellent selectivity for Cu(II) over miscellaneous other metal ions including Cr(II), Mn(II), Co(II), Ni(II), Zn(II), Cd(II), Al(III), Mg(II), Pb(II), Hg(II), Na(I), Li(I) and K(I) evidenced through the quenching of the fluorescence of the benzimidazole fragment. The reaction between 2 and Cu(2+) was found to be stoichiometric with the formation of a 1:1 complex. |
format | Online Article Text |
id | pubmed-6259128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62591282018-12-07 Synthesis of a Dehydroabietyl Derivative Bearing a 2-(2′-Hydroxyphenyl)Benzimidazole Unit and Its Selective Cu(2+) Chemosensing Wang, Ying-Chun Liu, Lu-Zhi Pan, Ying-Ming Wang, Heng-Shan Molecules Article A dehydroabietyl derivative 2 bearing a 2-(2′-hydroxyphenyl)benzimidazole unit was synthesized and its sensing behaviors toward metal ions were investigated by UV-Vis and fluorescence spectroscopy methods. In THF solution, compound 2 exhibited excellent selectivity for Cu(II) over miscellaneous other metal ions including Cr(II), Mn(II), Co(II), Ni(II), Zn(II), Cd(II), Al(III), Mg(II), Pb(II), Hg(II), Na(I), Li(I) and K(I) evidenced through the quenching of the fluorescence of the benzimidazole fragment. The reaction between 2 and Cu(2+) was found to be stoichiometric with the formation of a 1:1 complex. MDPI 2010-12-28 /pmc/articles/PMC6259128/ /pubmed/21189458 http://dx.doi.org/10.3390/molecules16010100 Text en © 2010 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Wang, Ying-Chun Liu, Lu-Zhi Pan, Ying-Ming Wang, Heng-Shan Synthesis of a Dehydroabietyl Derivative Bearing a 2-(2′-Hydroxyphenyl)Benzimidazole Unit and Its Selective Cu(2+) Chemosensing |
title | Synthesis of a Dehydroabietyl Derivative Bearing a 2-(2′-Hydroxyphenyl)Benzimidazole Unit and Its Selective Cu(2+) Chemosensing |
title_full | Synthesis of a Dehydroabietyl Derivative Bearing a 2-(2′-Hydroxyphenyl)Benzimidazole Unit and Its Selective Cu(2+) Chemosensing |
title_fullStr | Synthesis of a Dehydroabietyl Derivative Bearing a 2-(2′-Hydroxyphenyl)Benzimidazole Unit and Its Selective Cu(2+) Chemosensing |
title_full_unstemmed | Synthesis of a Dehydroabietyl Derivative Bearing a 2-(2′-Hydroxyphenyl)Benzimidazole Unit and Its Selective Cu(2+) Chemosensing |
title_short | Synthesis of a Dehydroabietyl Derivative Bearing a 2-(2′-Hydroxyphenyl)Benzimidazole Unit and Its Selective Cu(2+) Chemosensing |
title_sort | synthesis of a dehydroabietyl derivative bearing a 2-(2′-hydroxyphenyl)benzimidazole unit and its selective cu(2+) chemosensing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259128/ https://www.ncbi.nlm.nih.gov/pubmed/21189458 http://dx.doi.org/10.3390/molecules16010100 |
work_keys_str_mv | AT wangyingchun synthesisofadehydroabietylderivativebearinga22hydroxyphenylbenzimidazoleunitanditsselectivecu2chemosensing AT liuluzhi synthesisofadehydroabietylderivativebearinga22hydroxyphenylbenzimidazoleunitanditsselectivecu2chemosensing AT panyingming synthesisofadehydroabietylderivativebearinga22hydroxyphenylbenzimidazoleunitanditsselectivecu2chemosensing AT wanghengshan synthesisofadehydroabietylderivativebearinga22hydroxyphenylbenzimidazoleunitanditsselectivecu2chemosensing |