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分子团簇的理论与实验:OCS三聚体和四聚体的光谱

Theory vs. experiment for molecular clusters: Spectra of OCS trimers and tetramers.

作者信息

Evangelisti Luca, Perez Cristobal, Seifert Nathan A, Pate Brooks H, Dehghany M, Moazzen-Ahmadi N, McKellar A R W

机构信息

Department of Chemistry, University of Virginia, McCormick Road, Charlottesville, Virginia 22904, USA.

Department of Physics and Astronomy, University of Calgary, 2500 University Drive North West, Calgary, Alberta T2N 1N4, Canada.

出版信息

J Chem Phys. 2015 Mar 14;142(10):104309. doi: 10.1063/1.4914323.

Abstract

All singly substituted (13)C, (18)O, and (34)S isotopomers of the previously known OCS trimer are observed in natural abundance in a broad-band spectrum measured with a chirped-pulse Fourier transform microwave spectrometer. The complete substitution structure thus obtained critically tests (and confirms) the common assumption that monomers tend to retain their free structure in a weakly bound cluster. A new OCS trimer isomer is also observed, and its structure is determined to be barrel-shaped but with the monomers all approximately aligned, in contrast to the original trimer which is barrel-shaped with two monomers aligned and one anti-aligned. An OCS tetramer spectrum is assigned for the first time, and the tetramer structure resembles an original trimer with an OCS monomer added at the end with two sulfur atoms. Infrared spectra observed in the region of the OCS ν1 fundamental (≈2060 cm(-1)) are assigned to the same OCS tetramer, and another infrared band is tentatively assigned to a different tetramer isomer. The experimental results are compared and contrasted with theoretical predictions from the literature and from new cluster calculations which use an accurate OCS pair potential and assume pairwise additivity.

摘要

在用啁啾脉冲傅里叶变换微波光谱仪测量的宽带光谱中,观察到了先前已知的OCS三聚体的所有单取代(13)C、(18)O和(34)S同位素异构体,其丰度为自然丰度。由此获得的完整取代结构严格检验(并证实)了一个普遍假设,即单体在弱束缚簇中倾向于保持其自由结构。还观察到一种新的OCS三聚体异构体,其结构被确定为桶形,但单体大致全部排列整齐,这与原始三聚体不同,原始三聚体是桶形,有两个单体排列整齐,一个反排列。首次确定了OCS四聚体的光谱,其结构类似于在末端添加了一个带有两个硫原子的OCS单体的原始三聚体。在OCS ν1基频区域(≈2060 cm-1)观察到的红外光谱被指定为同一个OCS四聚体,另一个红外带暂定为不同的四聚体异构体。将实验结果与文献中的理论预测以及使用精确的OCS对势并假设成对加和性的新簇计算结果进行了比较和对比。

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