Metal-centred versus ligand-centred luminescence quenching of a macrocyclic copper(II) complex

被引:24
作者
Bernhardt, PV [1 ]
Flanagan, BM [1 ]
Riley, MJ [1 ]
机构
[1] Univ Queensland, Dept Chem, Brisbane, Qld 4072, Australia
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1999年 / 20期
关键词
D O I
10.1039/a902881a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The new macrocyclic ligand trans-6-(9-anthracenylmethylamino)-6,13-dimethyl-1,4,8,11-tetraazacyclotetradecan-13-amine has been synthesized and characterised as its copper(II) complex and the crystal structure of this complex has been determined. Fluorescence of the anthracenyl group of the macrocycle is quenched in its free base form and when complexed with Cu(II). Fluorescence returns when Lewis acids such as H(+) and Zn(II) are added to solutions of the ligand, indicating that photoinduced electron transfer from the amine lone pairs is responsible for fluorescence quenching in the free base form. By contrast, fluorescence of the complex is quenched by intramolecular electronic energy transfer.
引用
收藏
页码:3579 / 3584
页数:6
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