首页> 外文期刊>Collection of Czechoslovak Chemical Communications >COMPARISON OF THE CONFORMATIONAL STABILITY FOR SEVERAL VINYLHALOMETHANES AND SILANES WITH EXPERIMENT USING MP2 PERTURBATION THEORY AND DFT
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COMPARISON OF THE CONFORMATIONAL STABILITY FOR SEVERAL VINYLHALOMETHANES AND SILANES WITH EXPERIMENT USING MP2 PERTURBATION THEORY AND DFT

机译:利用MP2扰动理论和DFT比较几种乙烯基卤代烷和硅烷的构象稳定性与实验。

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In recent literature it was reported that the valence triple zeta basis set augmented by polarization functions is not too reliable for vinyl monohalo-and dihalomethanes and-silanes,the halogen being fluorine and chlorine.The major conclusion was that a valence triple zeta basis is too small to be augmented by polarization functions in a balanced way,at least on vinylmonofluoromethane.Thus we decided to apply the 6-311++G** basis set to the complete series of methanes,silanes and germanes(the latter ones are just added for completeness because no experimental data are available for them and,moreover,we published them already previously)and to compare the results to experimental data available in the literature to see whether the failures of this basis set show up in the complete series of molecules.In the literature we found five such molecules and the information which of the conformers is the most stable.Indeed we found that predictions on the relative stability of conformers in those systems with this basis set and MP2 as well as DFT are with a 60:40 chance,three being correct predictions and two being incorrect ones out of the five.However,since the energy differences are rather small in these systems and due to the fact that-as a consequence of twofold degeneracy of the gauche conformer on the potential curve of the torsional vibration-the abundances of the conformers in equilibrium do not change too much,we decided to calculate also vibrational spectra for three examples and to compare them also to experiment.It is reported that besides the failures in total energy(we have chosen two examples where predictions of the nature of the stable conformer are correct,and one where it is not),the vibrational spectra are rather well reproduced,especially when experimental energies are used to calculate abundances in equilibrium in the case where the prediction of the stable conformer failed.
机译:在最近的文献中,据报道,极化功能增强的三价zeta基集对于乙烯基一卤代和二卤代甲烷和硅烷(卤素是氟和氯)不太可靠。主要结论是三价zeta基也是如此。很小,至少在乙烯基一氟甲烷上可以通过极化功能得到平衡的增强。因此,我们决定将6-311 ++ G **基集应用于甲烷,硅烷和锗烷的完整系列(刚刚添加了后者)为了完整起见,因为没有可用的实验数据,而且我们之前已经发表过),并将结果与​​文献中提供的实验数据进行比较,以查看这种基础结构的失效是否在完整的分子系列中显示出来。在文献中,我们发现了5个这样的分子,并且构象异构体中最稳定的信息也是如此。实际上,我们发现了关于构象异构体相对稳定性的预测具有此基础集和MP2以及DFT的系统有60:40的机会,其中三个是正确的预测,两个是不正确的预测。但是,由于这些系统中的能量差异很小,并且由于由于扭摆振动势能曲线上的gauche构象元发生两次简并的结果-构象元在平衡状态下的丰度变化不大,我们决定为三个示例计算振动谱并将其进行比较据报道,除了总能量的失败(我们选择了两个例子,其中关于稳定构象的性质的预测是正确的,还有一个例子没有,),振动光谱可以很好地重现,尤其是在实验时在稳定构象异构体的预测失败的情况下,使用能量来计算平衡时的丰度。

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