首页> 外文期刊>Structural Chemistry >IR spectra of nitrobenzene and nitrobenzene-N-15 in the gas phase, ab initio analysis of vibrational spectra and reliable force fields of nitrobenzene and 1,3,5-trinitrobenzene. Investigation of equilibrium geometry and internal rotation in these simplest aromatic nitro compounds with one and three rotors by means of electron diffraction, spectroscopic, and quantum chemistry data
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IR spectra of nitrobenzene and nitrobenzene-N-15 in the gas phase, ab initio analysis of vibrational spectra and reliable force fields of nitrobenzene and 1,3,5-trinitrobenzene. Investigation of equilibrium geometry and internal rotation in these simplest aromatic nitro compounds with one and three rotors by means of electron diffraction, spectroscopic, and quantum chemistry data

机译:气相中硝基苯和硝基苯-N-15的红外光谱,从头算分析硝基苯和1,3,5-三硝基苯的振动光谱以及可靠的力场。通过电子衍射,光谱和量子化学数据研究这些最简单的带有一个和三个转子的芳香族硝基化合物的平衡几何构型和内部旋转

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The IR spectra of gaseous nitrobenzene (NB) and its N-15 isotopomer have been obtained in the frequency range of 3500-250 cm(-1), and the far-IR spectra of their solutions and the NB neat liquid sample have been recorded in the range of 600-30 cm(-1). A detailed description of the spectra of NB and 1,3,5-trinitrobenzene (sym-TNB) and their isotopomers has been accomplished using the force fields calculated at the MP2(full)/aug-cc-pVTZ and MP2(full)/cc-pVTZ levels. Transferability of the refined scale factors for the calculated force constants obtained by the Pulay technique has been used to provide evidence for validity of both interpreting the NB and sym-TNB spectra and refining the calculated force fields. The direct and inverse spectral problems have been solved by variational technique to determine torsional energy levels and refine the potential function by optimizing the V (k) coefficients in its Fourier series expansion. The height of the MP2(full) barrier to internal rotation has been reduced from 5.5 to 4.5 kcal/mol due to extension of the used basis set from 6-31(d,p) to aug-cc-pVTZ. The method of joint dynamic structural analysis of the GED, MW, and vibrational spectroscopy, and ab initio data in terms of the PES parameters have been applied to investigation of equilibrium geometry and internal rotation in the nonrigid NB and sym-TNB molecules having one and three coupled internal rotors, respectively. The experimental r (e)-parameter values of both molecules (C (2v) and D (3h) point group symmetries) are in agreement with those obtained by ab initio calculations. This paper is dedicated to Professor Magdolna Hargittai on the occasion of her 70th birthday.
机译:气态硝基苯(NB)及其N-15异构体的红外光谱已在3500-250 cm(-1)的频率范围内获得,并记录了其溶液和NB纯液体样品的远红外光谱在600-30 cm(-1)范围内。 NB和1,3,5-三硝基苯(sym-TNB)及其同位异构体的光谱的详细描述已使用在MP2(full)/ aug-cc-pVTZ和MP2(full)/ cc-pVTZ级别。通过Pulay技术获得的计算得出的力常数的精化比例因子的可传递性已被用来为解释NB和sym-TNB谱以及精炼计算出的力场的有效性提供证据。通过变分技术解决了直接和反频谱问题,确定了扭转能级并通过优化傅立叶级数展开中的V(k)系数来优化势函数。由于使用的基准范围从6-31(d,p)扩展到aug-cc-pVTZ,MP2(完全)内部旋转屏障的高度已从5.5 kcal / mol从5.5 kcal / mol降低了。 GED,MW和振动光谱的联合动态结构分析方法以及从PES参数开始的从头算数据已应用于研究非刚性NB和sym-TNB分子中具有一个和一个三个耦合的内部转子。两种分子(C(2v)和D(3h)点群对称性)的实验r(e)参数值与从头算得到的结果一致。本文专门献给Magdolna Hargittai教授70岁生日之际。

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