Photoinduced recoordination of metal cations in complexes with chromogenic crown ethers

被引:19
|
作者
Rusalov, M. V. [1 ]
Uzhinov, B. M. [1 ]
Alfimov, M. V. [2 ]
Gromov, S. P. [2 ]
机构
[1] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119991, Russia
[2] Russian Acad Sci, Photochem Ctr, Moscow 119421, Russia
关键词
RESPONSIVE FLUORESCENT COMPOUNDS; INTRAMOLECULAR CHARGE-TRANSFER; PHOTOPHYSICAL PROPERTIES; ALPHA; OMEGA-ALKANEDIYLDIAMMONIUM IONS; SPECTROSCOPIC PROPERTIES; CYCLIC POLYETHERS; EXCITED-STATE; MONOAZA-CROWN; INFRARED NIR; BINDING;
D O I
10.1070/RC2010v079n12ABEH004170
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A fast photochemical process, namely, photoinduced recoordination of a metal cation in the cavity of a chromogenic crown compound is considered. The photoinduced recoordination of cations is an efficient intramolecular adiabatic relaxation process resulting in the decrease in the excited-state energies of metal complexes, which in some cases may precede the complete release of the cation to the solution. The principles of molecular design of optical sensors based on crown ethers and the photo induced recoordination and cation photoejection mechanisms are discussed. The attention is focused on the effect of photoinduced recoordination on the spectral luminescence properties of the complexes of crown-containing dyes, on the effect of complexation on the intramolecular charge transfer and cation recoordination in nonexcited complexes and on theoretical methods for investigation of these processes. The bibliography includes 74 references.
引用
收藏
页码:1099 / 1121
页数:23
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