首页> 外文学位 >High-Resolution Infrared Spectroscopy of van der Waals Clusters of Nitrous Oxide, Carbon Dioxide and OCS-R Complexes.
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High-Resolution Infrared Spectroscopy of van der Waals Clusters of Nitrous Oxide, Carbon Dioxide and OCS-R Complexes.

机译:一氧化二氮,二氧化碳和OCS-R络合物的范德华簇的高分辨率红外光谱。

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摘要

Weakly-bound van der Waals complexes containing OCS and various hydrocarbons, and clusters of N2O, and CO2 are studied by means of their rotationally-resolved infrared spectra. Clusters are generated in a pulsed supersonic jet expansion with two slit-shaped nozzles and probed with a tuneable diode laser.;Study of OCS-R complexes (R indicates certain hydrocarbons with chain or ring structures) commenced with the study of OCS-acetylene complex in the region of nu1 stretching fundamental of OCS (∼ 2060 cm --1). Two bands are observed and assigned to near-parallel and T-shaped isomers of OCS-acetylene. In addition to the normal species, the deuterated isotopic form is also studied.;Simple looking bands characteristic of a T-shaped structure are observed for complexes formed between OCS and ethylene, allene, propyne, dimethylacetylene, benzene, and cyclo-octatetraene. All the bands are observed to be red-shifted from the OCS monomer nu1 frequency.;Infrared bands in the CO2 nu3 region (∼ 2350 cm--1) are assigned to carbon dioxide clusters, (CO 2)N, with N = 6, 7, 9, 10, 11, 12, and 13. Assignments are aided by cluster calculations using two reliable CO2 intermolecular potential functions. These are the largest molecular clusters studied by infrared spectroscopy with rotational resolution. Two highly symmetric isomers with S6 and S4 symmetries are observed for (CO2)6. (CO2)13 is also symmetric with S6 symmetry, but all the remaining clusters are asymmetric tops. The bands have increasing blue-shifts with increasing cluster size, similar to predictions of resonant dipole-dipole model but considerably larger in magnitude.;N2O tetramer is studied in the region of N2O nu 1 fundamental (∼ 2220 cm--1). The previously observed oblate isomer of (N2O)4 is studied with considerably higher resolution. Isotopic substitution has confirmed a structure with D2d symmetry for this isomer. In addition to the oblate isomer, a new prolate isomer of (N2O)4 with S4 symmetry is observed.
机译:利用它们的旋转分辨红外光谱研究了弱结合的含有OCS和各种碳氢化合物的范德华络合物以及N2O和CO2的簇。团簇是在具有两个狭缝形喷嘴的脉冲超音速喷射膨胀中产生的,并用可调谐二极管激光器探测。; OCS-R配合物(R表示某些具有链或环结构的烃)的研究始于OCS-乙炔配合物的研究在nu1区域中,OCS的拉伸基数约为2060 cm -1。观察到两个带,并分配给OCS-乙炔的近平行和T形异构体。除正常物种外,还研究了氘化的同位素形式。在OCS与乙烯,丙二烯,丙炔,二甲基乙炔,苯和环辛酸酯之间形成的配合物中,观察到T型结构的简单特征带。观察到所有谱带都从OCS单体nu1频率发生了红移;; CO2 nu3区域(〜2350 cm--1)中的红外谱带分配给了二氧化碳簇(CO 2)N,其中N = 6 ,7、9、10、11、12和13。通过使用两个可靠的CO2分子间电势函数进行聚类计算,可以辅助分配。这些是具有旋转分辨率的红外光谱研究的最大分子簇。对于(CO2)6,观察到两个具有S6和S4对称性的高度对称异构体。 (CO2)13也具有S6对称性,但其余所有簇都是不对称的顶部。这些带的蓝移随着簇尺寸的增加而增加,类似于共振偶极-偶极子模型的预测,但幅度更大。;在N2O nu 1基本区域(〜2220 cm--1)研究了N2O四聚体。对先前观察到的(N2O)4的扁桃体异构体进行了研究,并获得了更高的分离度。同位素取代已证实该异构体具有D2d对称性。除扁桃体异构体外,还观察到具有S4对称性的(N2O)4的新的扁桃体异构体。

著录项

  • 作者

    Norooz Oliaee, Jalal.;

  • 作者单位

    University of Calgary (Canada).;

  • 授予单位 University of Calgary (Canada).;
  • 学科 Physics Condensed Matter.;Chemistry Physical.;Physics Optics.
  • 学位 Ph.D.
  • 年度 2013
  • 页码 206 p.
  • 总页数 206
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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