101. Synthesis, characterization, and luminescent properties of three-coordinate copper(I) halide complexes containing a carbazolyl monodentate phosphine ligand
- Author
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Qian Li, Qiong Wei, Pei Xie, Li Liu, Xin-Xin Zhong, Fa-Bao Li, Nian-Yong Zhu, Wai-Yeung Wong, Wesley Ting-Kwok Chan, Hai-Mei Qin, and Njud S. Alharbi
- Subjects
Denticity ,Carbazole ,Ligand ,Supramolecular chemistry ,Halide ,chemistry.chemical_element ,02 engineering and technology ,Crystal structure ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Photochemistry ,01 natural sciences ,Copper ,0104 chemical sciences ,chemistry.chemical_compound ,Crystallography ,chemistry ,Materials Chemistry ,Physical and Theoretical Chemistry ,0210 nano-technology ,Phosphine - Abstract
A series of three-coordinate dinuclear copper halide complexes containing acarbazolyl monodentate phosphine ligand, [CuX(dppc)]2 (dppc =3,6-di-tert-butyl-9-[2-(diphenylphosphino)phenyl]carbazole, X = I (1), Br (2), and Cl (3)), were synthesized, and their molecular structures and photophysical properties were investigated. The structural analysis reveals that two copper(I) centers are bridged by two halogen ligands to form a dinuclear structure with a four-membered Cu2X2 ring. Crystal structures of 1-3 contain 1-D supramolecular arrays constructed by intermolecular C–H···π interactions. These complexes exhibit blue to green emission in the solid state at room temperature and have peak emission wavelengths at 492–495 nm with microsecond lifetimes and low emission quantum yields (< 0.01%). The emission of 1-3 mainly originates from MLCT, XLCT, and IL (intraligand) transitions. The three complexes displayed good thermal stability.
- Published
- 2018
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