化学
结晶学
配体(生物化学)
发光
八面体分子几何学
晶体结构
方形金字塔分子几何
二面角
分子间力
配位几何学
单晶
猝灭(荧光)
质子化
氢键
离子
荧光
分子
物理
光电子学
有机化学
量子力学
生物化学
受体
作者
Zhe‐Peng Deng,Lulu Gao,Jianghai Chen,Wenqing Hu,Yue-Hui Jia,Yi-Gang Sun,Yin–Xia Sun,Yong‐Min Liang
标识
DOI:10.1016/j.ica.2024.122315
摘要
The innovative ligand H2L, featuring a benzimidazole structure substituted with 8-hydroxyquinoline and equipped with N,O donor sites, underwent successful synthesis and meticulous characterization. Notably, this ligand was exclusively synthesized through catalysis under protonated conditions, accompanied by an in-depth exploration of the catalytic mechanism. Employing single-crystal X-ray diffraction, we acquired and authenticated four distinct asymmetric double-decker sandwich mononuclear transition metal complexes: [Cu(HL)2]·2H2O, [Co(HL)2]·CH3OH, [Ni(HL)2] and [Zn(HL)2]·CH2Cl2. Among these, complex 1 revealed an intriguing five-coordinate Cu(II) center adopting a distorted square pyramidal geometry, whereas the central metal ions in complexes 2–4 exhibited a six-coordinate configuration, characterized by a distorted octahedral geometry. Noteworthy is the observation that the dihedral angles within the crystal structures of complexes 2–4 approached approximately 90° to a significant extent. To delve deeper into the electronic properties and transitions, meticulous DFT and TD-DFT calculations were performed on both the ligand H2L and complexes 1–4. Furthermore, a comprehensive investigation into the luminescence properties of both H2L and its complexes was conducted, revealing a pronounced luminescence quenching effect in the complexes compared to the ligand. Through thorough analysis utilizing Hirshfeld surface examination and IRI analysis, various weak intermolecular interactions within the system were elucidated.
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