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氯仿同位素物种的转动光谱:实验与从头算结构

Rotational Spectra of the Isotopic Species of Chloroform: Experimental and Ab Initio Structures.

作者信息

Colmont J, Priem D, Dréan P, Demaison J, Boggs JE

机构信息

UMR CNRS, Universitéde Lille I, Villeneuve d'Ascq Cedex, 59655, France

出版信息

J Mol Spectrosc. 1998 Sep;191(1):158-75. doi: 10.1006/jmsp.1998.7623.

Abstract

The millimeter-wave spectra of three different samples of chloroform (CHCl3, CDCl3, and 13CHCl3) have been measured between 145 and 470 GHz which corresponds to J values between 22 and 70. We report accurate rotational and centrifugal distortion constants for the ground vibrational states of 11 isotopic species. The experimental ro, rs, rIepsilon, rrhom, and rz structures have been determined using the determined rotational constants. The structure has also been calculated ab initio at the SCF, MP2, RQCISD, and B3LYP levels using triple zeta polarized basis sets. The experimental results are found in excellent agreement with the ab initio predictions. An approximate equilibrium structure has been obtained by combining the experimental results and the ab initio calculations: re(C-H) = 1.080 (2) Å, re(C-Cl) = 1.760 (2) Å, and anglee(HCCl) = 108.23 (2) degrees. Copyright 1998 Academic Press.

摘要

已测量了氯仿的三种不同样品(CHCl₃、CDCl₃和¹³CHCl₃)在145至470吉赫兹之间的毫米波光谱,这对应于J值在22至70之间。我们报告了11种同位素物种基振动态的精确转动常数和离心畸变常数。利用所确定的转动常数确定了实验性的r₀、rₛ、rIε、rρm和rz结构。还使用三重ζ极化基组在SCF、MP2、RQCISD和B3LYP水平上从头计算了结构。发现实验结果与从头计算预测结果非常吻合。通过结合实验结果和从头计算得到了一个近似平衡结构:rₑ(C - H)=1.080(2) Å,rₑ(C - Cl)=1.760(2) Å,以及∠(HCCl)=108.23(2)度。版权所有1998年学术出版社。

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