Jianlin Yao, Yaxian Yuan, Renao Gu
Department of Chemistry, Suzhou University, 1 Shizi Street, Suzhou 215006, China.
Spectrochim Acta A Mol Biomol Spectrosc. 2006 Jul;64(4):1072-6. doi: 10.1016/j.saa.2005.09.017. Epub 2006 Feb 2.
The complexes of tropolone (HL) with different lanthanide metals of lanthanum (La), neodymium (Nd), samarium (Sm), ytterbium (Yb) have been prepared respectively in the non-aqueous solution by the direct electrochemical oxidation of sacrificial metal anodes, and characterized by normal Raman spectroscopy. By comparing the spectra of the ligands and their complexes, the stretching vibrational band of OH disappeared in complexes, and the frequencies shifts of some relevant bands were observed, particularly for the stretching vibration of CO. In the low frequency region, new metal ion sensitive bands at 400-700 cm(-1) were observed, which could be assigned to the stretching vibrational mode of the bonding of lanthanide with oxygen. The stretching vibration of lanthanide-oxygen of tropolonate complexes showed a metal ion sensitivity. All the obvious change in spectral feature of Raman spectra revealed that CO and OH were coordinated with the center metal ions through oxygen atoms. Based on Raman results, the structures of the above complexes were proposed.
通过牺牲金属阳极的直接电化学氧化,分别在非水溶液中制备了托酚酮(HL)与镧(La)、钕(Nd)、钐(Sm)、镱(Yb)等不同镧系金属的配合物,并采用常规拉曼光谱对其进行了表征。通过比较配体及其配合物的光谱,配合物中OH的伸缩振动带消失,观察到一些相关谱带的频率发生了位移,特别是CO的伸缩振动。在低频区域,观察到400 - 700 cm⁻¹处新的金属离子敏感谱带,该谱带可归属于镧系与氧键合的伸缩振动模式。托酚酮配合物中镧系 - 氧的伸缩振动表现出对金属离子的敏感性。拉曼光谱特征的所有明显变化表明,CO和OH通过氧原子与中心金属离子配位。基于拉曼结果,提出了上述配合物的结构。