Zeng Yong-Pi, Gao Cheng-Wei, Hu Liang-Jiang, Chen Hao-Hua, Chen Guang-Ying, Li Gao-Nan, Niu Zhi-Gang
Acta Chim Slov. 2015;62(4):917-22. doi: 10.17344/acsi.2015.1744.
A new bis-cyclometalated iridium(III) complex [Ir(dmabt)(2)(bipy)][PF(6)] (3) (dmabt = 4-(benzo[d]thiazol-2-yl)-N,N-dimethylaniline, bipy = 2,2'-bipyridine) has been synthesized and fully characterized. The complex 3 has been determined by X-ray structure analyses which shows that the central iridium(III) ion assumes distorted octahedral geometry. The photoluminescence spectrum exhibits orange emission maximum at 612 nm with quantum yield of 17% at 298 K. The frontier molecular orbital diagrams and the spin-allowed singlet-singlet electronic transitions of 3 have been calculated with density functional theory (DFT) and time-dependent DFT (TD-DFT), and the UV-Vis spectra are discussed based on the theoretical calculations.
一种新型双环金属化铱(III)配合物[Ir(dmabt)(2)(bipy)][PF(6)](3)(dmabt = 4-(苯并[d]噻唑-2-基)-N,N-二甲基苯胺,bipy = 2,2'-联吡啶)已被合成并进行了全面表征。配合物3通过X射线结构分析确定,结果表明中心铱(III)离子呈扭曲的八面体几何构型。光致发光光谱在612 nm处呈现橙色发射最大值,在298 K时量子产率为17%。利用密度泛函理论(DFT)和含时密度泛函理论(TD-DFT)计算了3的前沿分子轨道图和自旋允许的单重态-单重态电子跃迁,并基于理论计算对紫外可见光谱进行了讨论。