Martínez-Haya Bruno, Hurtado Paola, Hortal Ana R, Steill Jeffrey D, Oomens Jos, Merkling Patrick J
Departamento de Sistemas Físicos, Químicos y Naturales, Universidad Pablo de Olavide, 41013 Seville, Spain.
J Phys Chem A. 2009 Jul 9;113(27):7748-52. doi: 10.1021/jp902150v.
Infrared multiple photon dissociation action spectra of the binary and ternary gas-phase complexes formed by 15-crown-5 ether with potassium cations (15c5-K(+) and 15c5-K(+)-15c5) are reported. The spectra span the 800-1500 cm(-1) infrared range. Particularly significant differences are found in the position and structure of the CO-stretching band of the two types of complexes. The computational prediction at the DFT-B3LYP/6-31G* level of theory agrees well with the experimental observations, and provides a correlation between the spectral differences and the structural changes associated with the coordination of the ether oxygens with the alkali cation. The 15c5-K(+) complex adopts a pyramidal structure, with the cation lying above the center of mass of the ether ring at a distance similar to its ionic radius. The ternary 15c5-K(+)-15c5 complex features a less tight coordination of the cation and a relative rotation between the backbones of the two crown ethers, which minimizes the intermolecular repulsions between the oxygens.
报道了由15-冠-5醚与钾阳离子形成的二元和三元气相配合物(15c5-K⁺和15c5-K⁺-15c5)的红外多光子解离作用光谱。光谱覆盖800 - 1500 cm⁻¹红外范围。在两种配合物的CO伸缩带的位置和结构上发现了特别显著的差异。在DFT-B3LYP/6-31G*理论水平上的计算预测与实验观察结果吻合良好,并提供了光谱差异与醚氧与碱金属阳离子配位相关的结构变化之间的相关性。15c5-K⁺配合物采用金字塔结构,阳离子位于醚环质心上方,距离与其离子半径相近。三元15c5-K⁺-15c5配合物的特点是阳离子配位较松散,且两个冠醚主链之间存在相对旋转,这使氧之间的分子间排斥最小化。