Intramolecular energy transfer in actinide complexes of 6-methyl-2-(2-pyridyl)-benzimidazole (biz):: comparison between Cm3+ and Tb3+ systems

被引:5
作者
Assefa, Z
Yaita, T
Haire, RG
Tachimori, S
机构
[1] Oak Ridge Natl Lab, Div Chem Sci, Transuranium Chem Grp, Oak Ridge, TN 37831 USA
[2] Japan Atom Energy Res Inst, Dept Mat Sci, Tokai, Ibaraki 31911, Japan
关键词
sensitized emission; energy transfer; actinide spectroscopy; F-elements; photoluminescence;
D O I
10.1016/j.jssc.2004.09.017
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Coordination of the 6-methyl-2-(2-pyridyl)-benzimidazole ligand with actinide and lanthanide species can produce enhanced emission due to increased efficiency of intramolecular energy transfer to metal centers. A comparison between the curium and terbium systems indicates that the position of the ligand's triplet state is critical for the enhanced emission. The energy gap between the ligand's triplet state and the acceptor level in curium is about 1000 cm(-1), as compared to a similar to 600 cm(-1) gap in the terbium system. Due to the larger gap, the back transfer with curium is reduced and the radiative yield is significantly higher. The quantum yield for this "sensitized" emission increases to 6.2%, compared to the 0.26% value attained for the metal centered excitation prior to ligand addition. In the terbium case, the smaller donor/acceptor gap enhances back transfer and the energy transfer is less efficient than with the curium system. (c) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:505 / 510
页数:6
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