Synthesis, crystal structure and photophysical study of luminescent three-coordinate cuprous bromide complexes based on pyrazole derivatives

被引:11
作者
Wu, Fengshou [1 ,2 ]
Tong, Hongbo [4 ]
Wang, Kai [1 ]
Zhang, Xiulan [1 ]
Zhang, Jie [3 ]
Wong, Wai-Kwok [2 ]
Zhu, Xunjin [2 ]
机构
[1] Wuhan Inst Technol, Key Lab Green Chem Proc, Minist Educ, Wuhan, Peoples R China
[2] Hong Kong Baptist Univ, Dept Chem, Hong Kong, Hong Kong, Peoples R China
[3] Taizhou Univ, Sch Pharmaceut & Chem Engn, Taizhou, Peoples R China
[4] Shanxi Univ, Inst Appl Chem, Taiyuan 030006, Peoples R China
基金
中国国家自然科学基金;
关键词
Cuprous bromide; luminescence; crystal structures; three coordinate; COPPER(I) HALIDE-COMPLEXES; LIGHT-EMITTING-DIODES; COORDINATION-COMPOUNDS; DELAYED FLUORESCENCE; EXCITED-STATES; LIGAND; EMISSION; SINGLET; IODIDE; CU(I);
D O I
10.1080/00958972.2016.1139102
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The 1 : 2 M-ratio reaction between cuprous bromide and pyrazole derivatives in toluene results in mononuclear Cu(I) complexes [CuBr(pyrazole)(2)]. The complexes have been characterized by H-1 NMR spectroscopy and elemental analysis. The molecular structure, established by single-crystal X-ray diffraction, features a trigonal planar geometry around copper, with monodentate pyrazole derivatives. All the Cu(I) complexes are luminescent in the solid state at ambient temperature. Intense blue or blue-green emission in the solid state is observed for these complexes, with the maxima ranging from 431 to 493 nm. The observed photoluminescence could be ascribed to the metal-to-ligand charge-transfer excited states, probably mixed with some halide-to-ligand character. The microsecond lifetime scale of the complexes implies that these transitions arise from the triplet excited states. [GRAPHICS] .
引用
收藏
页码:926 / 933
页数:8
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