Mu Ge, Jiang Chenggang, Teets Thomas S
Department of Chemistry, University of Houston, Lamar Fleming Jr. Building, 3585 Cullen Blvd., Houston, 77204-5003, USA.
Chemistry. 2020 Sep 10;26(51):11877-11886. doi: 10.1002/chem.202002351. Epub 2020 Aug 13.
The utility of flexidentate pyridyl-substituted formazanate ligands for assembling dinuclear coordination complexes with iridium(III) and/or platinum(II) building blocks is demonstrated herein. The dinuclear complexes are prepared either via a stepwise strategy, adding one metal unit at a time, or via one-pot self-assembly. Eight of the new complexes, including both mononuclear precursors and dinuclear products, are structurally characterized by single-crystal X-ray diffraction and NMR spectroscopy, revealing several distinct binding modes of the formazanates. All complexes are characterized by UV/Vis absorption spectroscopy and cyclic voltammetry. The frontier orbitals are primarily localized on the formazanate ligand, and a characteristic, intense formazanate-centered π→π* absorption band is observed in the absorption spectra.
本文展示了柔性吡啶取代甲脒配体用于与铱(III)和/或铂(II)结构单元组装双核配位络合物的效用。双核络合物可通过逐步策略制备,即每次添加一个金属单元,也可通过一锅法自组装制备。其中八个新络合物,包括单核前体和双核产物,通过单晶X射线衍射和核磁共振光谱进行了结构表征,揭示了甲脒的几种不同结合模式。所有络合物都通过紫外/可见吸收光谱和循环伏安法进行了表征。前沿轨道主要定域在甲脒配体上,并且在吸收光谱中观察到一个以甲脒为中心的特征性强π→π*吸收带。