Photophysical Properties of {[Au(CN)2]-}2 Dimers Trapped in a Supramolecular Electron-Acceptor Organic Framework

被引:13
作者
Abouelwafa, Ahmed S. [1 ,2 ,3 ]
Anson, Christopher E. [1 ]
Hauser, Andreas [3 ]
Patterson, Howard H. [4 ]
Baril-Robert, Francois [4 ]
Li, Xiaobo [4 ]
Powell, Annie K. [1 ,2 ]
机构
[1] Karlsruhe Inst Technol, Inst Anorgan Chem, D-76128 Karlsruhe, Germany
[2] Karlsruhe Inst Technol, Inst Nanotechnol, D-76021 Karlsruhe, Germany
[3] Univ Geneva, Dept Chim Phys, CH-1211 Geneva, Switzerland
[4] Univ Maine, Dept Chem, Orono, ME 04469 USA
基金
瑞士国家科学基金会; 美国国家科学基金会;
关键词
CHARGE-TRANSFER COMPLEXES; TUNABLE ENERGY-TRANSFER; METHYL VIOLOGEN; INTRAZEOLITE PHOTOCHEMISTRY; COORDINATION POLYMERS; PHYSICAL-PROPERTIES; GOLD(I) COMPLEXES; CRYSTAL-STRUCTURE; METAL; ION;
D O I
10.1021/ic201109u
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Dicyanoaurate reacts with the organic acceptor molecule, 1,1'-bis(2,4-dinitrophenyl)-4,4'-bipyridinium, DNP, to form a supramolecular complex with the general formula {[Au(CN)(2)](2)DNP}center dot 4H(2)O. The complex was characterized by X-ray crystallography, and its photophysical properties were investigated in the solid-state. Although the initial (DNP)Cl-2 compound does not show photoluminescence behavior and the dicyanoaurate shows photoluminescence only in the UV range, the resulting supramolecular complex displays two simultaneous, essentially independent, photoluminescence bands in the visible range originating from individual contributions of the DNP unit and the dicyanoaurate dimers. This unusual simultaneous photoluminescence behavior displayed by both the dicyanoaurate donor units and the redox-active 4,4'-bipyridinium acceptor have lifetimes of 0.5 mu s and several hundred mu s, respectively.
引用
收藏
页码:1294 / 1301
页数:8
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