Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for Cu+2
Abstract
The novel coumarin-based 'turn-on' fluorescent probe (E)-3-(2,5- dimethoxybenzylideneamino)-7-hydroxy-2H-chromen-2-one (MGM) was designed, synthesized, and characterized. This compound shows high selectivity for Cu +2, combined with a large fluorescence enhancement upon binding to Cu 2+. Benesi-Hildebrand and Job plots demonstrate that the stoichiometry of the Cu 2+ complex formed is 2:1. Preliminary studies employing epifluorescence microscopy demonstrated that Cu +2 could be imaged in human neuroblastoma SH-SY5Y cells treated with MGM. © 2012 Elsevier Ltd. All rights reserved.
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Título según WOS: | Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for Cu+2 |
Título según SCOPUS: | Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for Cu +2 |
Título de la Revista: | TETRAHEDRON LETTERS |
Volumen: | 53 |
Número: | 39 |
Editorial: | PERGAMON-ELSEVIER SCIENCE LTD |
Fecha de publicación: | 2012 |
Página de inicio: | 5280 |
Página final: | 5283 |
Idioma: | English |
URL: | http://www.scopus.com/inward/record.url?eid=2-s2.0-84865513224&partnerID=40&md5=d2f5fa66feee8931aeb1139347661fbc |
DOI: |
10.1016/j.tetlet.2012.07.082 |
Notas: | ISI, SCOPUS |