Jalilehvand Farideh, Laffin Luke J
Department of Chemistry, University of Calgary, Calgary, Alberta, Canada.
Inorg Chem. 2008 Apr 21;47(8):3248-54. doi: 10.1021/ic7022538. Epub 2008 Mar 4.
Careful analysis of Pt L3-edge extended X-ray absorption fine structure (EXAFS) spectra shows that the hydrated platinum(II) ion in acidic (HClO 4) aqueous solution binds four water molecules with the Pt-O bond distance 2.01(2) A and one (or two) in the axial position at 2.39(2) A. The weak axial water coordination is in accordance with the unexpectedly small activation volume previously reported for water exchange in an interchange mechanism with associative character. The hydrated cis-diammineplatinum(II) complex has a similar coordination environment with two ammine and two aqua ligands strongly bound with Pt-O/N bond distances of 2.01(2) A and, in addition, one (or two) axial water molecule at 2.37(2) A. This result provides a new basis for theoretical computational studies aiming to connect the function of the anticancer drug cis-platin to its ligand exchange reactions, where usually four-coordinated square planar platinum(II) species are considered as the reactant and product. (195)Pt NMR spectroscopy has been used to characterize the Pt(II) complexes.
对铂L3边缘扩展X射线吸收精细结构(EXAFS)光谱的仔细分析表明,酸性(高氯酸)水溶液中的水合铂(II)离子与四个水分子结合,Pt-O键距为2.01(2) Å,轴向位置有一个(或两个)水分子,键距为2.39(2) Å。弱的轴向水配位与先前报道的在具有缔合特征的交换机制中水分子交换时意外小的活化体积一致。水合顺二氨合铂(II)配合物具有相似的配位环境,两个氨和两个水配体与Pt-O/N键距为2.01(2) Å紧密结合,此外,在2.37(2) Å处有一个(或两个)轴向水分子。这一结果为旨在将抗癌药物顺铂的功能与其配体交换反应联系起来的理论计算研究提供了新的基础,在这些研究中,通常将四配位平面正方形铂(II)物种视为反应物和产物。已使用(195)Pt核磁共振光谱对铂(II)配合物进行了表征。