Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for Cu+2

Garcia-Beltran, O; Mena N.; Friedrich L.C.; Netto-Ferreira J.C.; Vargas V.; Quina F.H.; Núñez M.T.; Cassels, B.K.

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.

Más información

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