Ramić Elvir, Eichel Rüdiger-Albert, Dinse Klaus-Peter, Titz Alexander, Schmidt Boris
Eduard-Zintl-Institute and Clemens-Schöpf-Institute, Darmstadt University of Technology, D-64287 Darmstadt, Germany.
J Phys Chem B. 2006 Oct 19;110(41):20655-63. doi: 10.1021/jp061940u.
Multifrequency electron paramagnetic resonance (EPR) and electron nuclear double resonance (ENDOR) techniques were used to obtain structural information about the copper(II)-chelidamate complex. Well-resolved nitrogen ENDOR spectra could be recorded from solid solution samples by using selective excitation of spin packets. Evaluation of nuclear quadrupole and dipolar hyperfine interaction of the directly ligated nitrogen allowed for an identification of the bond direction to the copper ion within the eigen frame of the copper g-matrix. Invoking two-dimensional EPR techniques, additional hyperfine interaction with a "distant" nitrogen spin, identified as resulting from the solvent dimethylformamide (DMF), was observed. The experimental data are only consistent with formation of a stable pseudoplanar copper complex with single solvent ligation via its oxygen atom.
采用多频电子顺磁共振(EPR)和电子核双共振(ENDOR)技术来获取有关铜(II)-螯合氨基甲酸盐配合物的结构信息。通过对自旋包进行选择性激发,可以从固溶体样品中记录分辨率良好的氮ENDOR光谱。对直接配位的氮的核四极和偶极超精细相互作用进行评估,有助于在铜g矩阵的本征框架内确定与铜离子的键方向。运用二维EPR技术,观察到与一个“远距离”氮自旋的额外超精细相互作用,该氮自旋被确定为来自溶剂二甲基甲酰胺(DMF)。实验数据仅与通过其氧原子进行单溶剂配位形成稳定的假平面铜配合物相一致。