Mono- and bis-N-functionalised cyclen with benzimidazolylmethyl pendant arms: Sensitive and selective fluorescent probes for zinc and copper ions

被引:8
作者
El Majzoub, Abir [1 ]
CadiouA, Cyril [1 ]
Dechamps-Olivier, Isabelle [1 ]
Chuburu, Francoise [1 ]
Aplincourt, Michel [1 ]
Tinant, Bernard [2 ]
机构
[1] Univ Reims, Grp Chim Coordinat, ICMR, CNRS,UMR 6229, F-51687 Reims 2, France
[2] Dept Chim, Unite CSTR, B-1348 Louvain, Belgium
关键词
Macrocyclic ligands; Fluorescent probes; UV-Vis and fluorimetric titrations; Zn2+; Cu2+; EFFECTIVE CORE POTENTIALS; MOLECULAR CALCULATIONS; METAL-COMPLEXES; COORDINATION-COMPOUNDS; ELECTRONIC-PROPERTIES; MACROCYCLIC LIGANDS; MAIN-GROUP; SENSORS; STABILITY; STEREOCHEMISTRY;
D O I
10.1016/j.ica.2008.06.007
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The Zn2+ and Cu2+ complexes of L-1 and L-2 ligands (L-1: 1-(benzimidazol-2-ylmethyl)-1,4,7,10-tetraazacyclododecane, L-2: 1,7-bis(benzimidazol-2-ylmethyl)-1,4,7,10-tetraazacyclododecane) were synthesised and characterised by means of NMR, EPR, and UV-Vis spectroscopies, X-ray determination and molecular modelisation (HF-DFT(B3LYP)/LANL2DZ). These studies showed that the 1: 1 complexes were formed in which the benzimidazole arm(s) are coordinated to the metal ion. On addition of successive amounts of Zn2+ in CH3CN, the. fluorescence emission of L-1 increased linearly by a factor of 50 and the one of L-2 by a factor of 5 while on addition of successive amounts of Cu2+ in CH3CN, the. fluorescence emission of L-2 decreased linearly to 80% of its initial value. (C) 2008 Elsevier B. V. All rights reserved.
引用
收藏
页码:1169 / 1178
页数:10
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