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含有环金属化1,2,3 - 三唑亚基以及双齿或三齿2,6 - 二芳基吡啶配体的发光铂(IV)配合物

Luminescent Platinum(IV) Complexes Bearing Cyclometalated 1,2,3-Triazolylidene and Bi- or Terdentate 2,6-Diarylpyridine Ligands.

作者信息

Vivancos Ángela, Bautista Delia, González-Herrero Pablo

机构信息

Departamento de Química Inorgánica, Facultad de Química, Universidad de Murcia, Apdo. 4021, 30071, Murcia, Spain.

SAI, Universidad de Murcia, Apdo. 4021, 30071, Murcia, Spain.

出版信息

Chemistry. 2019 Apr 23;25(23):6014-6025. doi: 10.1002/chem.201900489. Epub 2019 Mar 29.

DOI:10.1002/chem.201900489
PMID:30807669
Abstract

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.

摘要

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。

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