Vivancos Ángela, Bautista Delia, González-Herrero Pablo
Departamento de Química Inorgánica, Facultad de Química, Universidad de Murcia, Apdo. 4021, 30071, Murcia, Spain.
SAI, Universidad de Murcia, Apdo. 4021, 30071, Murcia, Spain.
Chemistry. 2019 Apr 23;25(23):6014-6025. doi: 10.1002/chem.201900489. Epub 2019 Mar 29.
The synthesis, structure, and photophysical properties of luminescent Pt complexes that combine cyclometalated 1,2,3-triazolylidene and bi- or terdentate 2,6-diarylpyridine ligands are reported. The targeted complexes represent the first examples of Pt species with a cyclometalated mesoionic aryl-NHC ligand. They exhibit moderate or weak emissions in fluid solution at 298 K arising from LC states, which become very intense in poly(methyl methacrylate) (PMMA) matrices at 298 K. DFT and TD-DFT calculations confirm that the chromophoric ligand is the cyclometalated 2,6-diarylpyridine and show that the aryl-NHC ligand exerts a beneficial effect on the emission efficiencies of these derivatives by increasing the energy of deactivating LMCT excited states with respect to comparable Pt complexes with cyclometalated 2-arylpyridine ligands.
报道了结合环金属化1,2,3 - 三唑亚基和双齿或三齿2,6 - 二芳基吡啶配体的发光铂配合物的合成、结构和光物理性质。目标配合物代表了具有环金属化中离子芳基 - NHC配体的铂物种的首个实例。它们在298 K的流体溶液中由于LC态而表现出中等或较弱的发射,而在298 K的聚甲基丙烯酸甲酯(PMMA)基质中发射变得非常强烈。DFT和TD - DFT计算证实发色配体是环金属化的2,6 - 二芳基吡啶,并表明芳基 - NHC配体通过相对于具有环金属化2 - 芳基吡啶配体的可比铂配合物增加失活LMCT激发态的能量,对这些衍生物的发射效率产生有益影响。