化学
电子顺磁共振
吡啶
钳子运动
二聚体
单体
铜
配体(生物化学)
扩展X射线吸收精细结构
质子化
无水的
药物化学
羟甲基
高分子化学
光化学
无机化学
吸收光谱法
有机化学
物理
核磁共振
量子力学
催化作用
离子
生物化学
聚合物
受体
作者
Axel Klein,K. Butsch,Sait Elmas,Christian Biewer,Dominikus Heift,S. Nitsche,Irene Schlipf,H. Bertagnolli
出处
期刊:Polyhedron
[Elsevier]
日期:2012-01-01
卷期号:31 (1): 649-656
被引量:16
标识
DOI:10.1016/j.poly.2011.10.023
摘要
The oxido-pincer ligand pydotH2 (2,6-bis(1-hydroxy-1-o-tolyl-ethyl-η2O,O′)pyridine) forms two different CuII containing complexes when prepared from anhydrous CuCl2. A combination of EPR spectroscopy and EXAFS allowed to structurally characterise the light-green dimer of the formula [(pydotH2)CuCl(μ-Cl)2ClCu(pydotH2)] and the penta-coordinate olive-green monomer [(pydotH2)CuCl2]. The molecular entities imply that the ligand remains protonated upon coordination. When dissolved in DMF both compounds form monomeric species [(pydotH2)CuCl2(DMF)] which could be characterised in detail by EPR, UV–Vis/NIR spectroscopy and electrochemical measurements. The assignments were supported by comparison with CuII complexes of the related ligands 2,6-bis(hydroxymethyl)pyridine (pydimH2) and 2,6-bis(1-hydroxy-1-methyl)pyridine (pydipH2).
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