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首页> 外文期刊>The Journal of Chemical Physics >The (A)over-tilde (2)Sigma(+) state of Ar center dot NO
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The (A)over-tilde (2)Sigma(+) state of Ar center dot NO

机译:Ar中心点NO的(A)叠峰(2)Sigma(+)状态

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The (A) over tilde (2)Sigma (+) state of Ar . NO is studied using (1+1) resonance-enhanced multiphoton ionization (REMPI) spectroscopy. Higher quality spectra than obtained in other studies allow the identification of a number of previously unreported features. The spectrum is analyzed using two models: a rigid van der Waals complex in which NO is weakly bonded to Ar; and a complex in which the free internal rotation of NO is hindered by the anisotropy caused by the presence of the Ar atom. It is concluded that as the intermolecular stretch is excited, then the anisotropy decreases, and the angular motion of the complex becomes more and more like that of a free rotor. Near the origin, the complex has an average geometry approaching linear, whereas when the intermolecular stretch is excited, an average geometry closer to T-shaped occurs; however, when the anisotropy is small, the concept of geometry becomes ill-defined. (C) 2000 American Institute of Physics. [S0021-9606(00)00741-8]. [References: 38]
机译:Ar的(A)超过代字号(2)Sigma(+)。使用(1 + 1)共振增强多光子电离(REMPI)光谱研究了NO。比其他研究中获得的更高质量的光谱可以识别许多以前未报告的特征。使用两种模型分析光谱:刚性的范德华络合物,其中NO与Ar弱结合;以及由于Ar原子的存在而引起的各向异性,阻碍了NO的自由内部旋转的络合物。结论是,随着分子间拉伸的激发,各向异性减小,并且配合物的角运动越来越像自由转子的角运动。在原点附近,复合物的平均几何形状接近线性,而当分子间的拉伸被激发时,会出现更接近T形的平均几何形状。但是,当各向异性较小时,几何学的概念变得不明确。 (C)2000美国物理研究所。 [S0021-9606(00)00741-8]。 [参考:38]

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