Wen Qing, Jäger Wolfgang
Department of Chemistry, University of Alberta, Edmonton, Alberta, Canada T6G 2G2.
J Phys Chem A. 2007 Mar 22;111(11):2093-7. doi: 10.1021/jp0663863. Epub 2007 Feb 23.
Rotational spectra of three isotopomers of the Xe-(H2O)2 van der Waals trimer were recorded using a pulsed-nozzle, Fourier transform microwave spectrometer. Nine [nine, four] a-type and twelve [eleven, seven] b-type transitions were measured for the 132Xe-(H2O)2 [129Xe-(H2O)2, 131Xe-(H2O)2] isotopomer. The determined rotational and centrifugal distortion constants were used to extract information about the structure and vibrational motions of the complex. The nuclear quadrupole hyperfine structures due to the 131Xe (nuclear spin quantum number I=3/2) nucleus were also detected. The large value of the off-diagonal nuclear quadrupole coupling constant chiab in particular provides detailed insight into the electronic environment of the xenon atom and the orientations of the water molecules within the complex. An effective structure that best reproduces the experimental 131Xe nuclear quadrupole coupling constants is rationalized by ab initio calculations. An overall goal of this line of work is to determine how the successive solvation of a xenon atom with water molecules affects the xenon electron distribution and its intermolecular interactions. The results may provide molecular level interpretations of 129Xe NMR data from, for example, imaging experiments.
使用脉冲喷嘴傅里叶变换微波光谱仪记录了Xe-(H₂O)₂范德华三聚体三种同位素异构体的转动光谱。对于¹³²Xe-(H₂O)₂[¹²⁹Xe-(H₂O)₂, ¹³¹Xe-(H₂O)₂]同位素异构体,测量了九条[九条, 四条]a型跃迁和十二条[十一条, 七条]b型跃迁。所确定的转动常数和离心畸变常数被用于提取有关该复合物结构和振动运动的信息。还检测到了由¹³¹Xe(核自旋量子数I = 3/2)原子核引起的核四极超精细结构。特别是非对角核四极耦合常数χab的较大值,提供了对氙原子的电子环境以及复合物中水分子取向的详细洞察。通过从头算计算对能最佳再现实验¹³¹Xe核四极耦合常数的有效结构进行了合理化分析。这一系列工作的总体目标是确定氙原子被水分子连续溶剂化如何影响氙的电子分布及其分子间相互作用。这些结果可能为例如成像实验中¹²⁹Xe NMR数据提供分子水平的解释。