Emission properties of Sm complexes substituted with asymmetric β-diketonato ligands in solution

被引:12
|
作者
Harada, Takashi [1 ]
Tokuda, Keisuke [1 ]
Nishiyama, Katsura [1 ]
机构
[1] Shimane Univ, Fac Educ, Matsue, Shimane 6908504, Japan
关键词
Sm complex; Rare-earth material; beta-Diketonato; Pybox; Additive color tuning; Molecular symmetry; EU(III) COMPLEX; LUMINESCENCE; INTENSITIES; EUROPIUM; SPECTRA; POLYMER; MODEL;
D O I
10.1016/j.molliq.2014.05.028
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Trivalent samarium (Sm) complexes show four emission bands due to the 4f-4f transition in the visible 550-750 nm region, where the 645 nm transition has the dominant intensity. In this paper we have synthesized the three Sm complexes with varying pybox and beta-diketonato ligands, to investigate the relative intensity among the emission bands. We have shown that the beta-diketonato ligands with asymmetric molecular structures enhance the relative intensity of the 645 nm transition by approximately 20% compared to that with symmetric ligands. By virtue of such a property, Sm complexes can be used as possible candidates for deep red emitting materials. As a strategy on the molecular design, it has also been confirmed that the introduction of heavy atoms such as fluorine to the beta-diketonato moiety should be of essential to obtain a high emission quantum yield. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 80
页数:4
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