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首页> 外文期刊>Berichte der Bunsengesellschaft fur Physikalische Chemie >On FTIR Spectroscopy in Asynchronously Pulsed Supersonic Free Jet Expansions and on the Interpretation of Stretching Spectra of HF Clusters
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On FTIR Spectroscopy in Asynchronously Pulsed Supersonic Free Jet Expansions and on the Interpretation of Stretching Spectra of HF Clusters

机译:异步脉冲超音速自由射流膨胀中的FTIR光谱学和HF团簇的拉伸谱解释

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摘要

A novel experimental technique using an asynchronously pulsed nozzle in conjunction with an unmodified continuous scan high resolution interferometer (BOMEM DA002) is demonstrated for NH_3, N_2O, CH_4 and (HF)_n. Spectral artifacts associated with the pulsed mode of operation cancel rapidly during the ordinary averaging over several scans. The random averaging is analysed using synthetic interferograms. Combined with continuous jet FTIR spectroscopy, the new technique allows a wide range of expansion conditions to be realized. This has proven to be useful in the investigation of HF stretching spectra of HF clusters down to low temperatures. The tentative spectroscopic assignment of (HF)_n with (n = 4, 5, 6) resulting from this investigation and from harmonic ab initio predictions has recently been challenged by a size-selective secondary beam scattering OPO experiment. We propose an alternative interpretation of this scattering experiment which leads to agreement with our FTIR results and extensive ab initio predictions. The pentamer of HF is confirmed to be an important species in HF vapor. A key ingredient in the extended analysis is the assumption of combination bands of the type v_(HF) + v_(FF) along with the v_(HF) fundamentals. To back our assignment, n-dimensional varia-tional grid calculations for the HF stretching manifold in (HF)_n (n = 1-5) based on several thousand DZP MP2 ab initio points were carried out. The anharmonic HF stretching fundamental frequency shifts relative to monomeric HF are 19, 29 and 37% larger than the corresponding harmonic shifts for n = 3, 4, 5. Corrections for basis set superposition error and intermolecular zero point bond weakening effects approximately cancel with these anharmonicity contributions, thus explaining the good agreement between harmonic prediction and experiment. Transition dipole predictions for overtone absorptions in HF clusters at the SCF level show a loss of the large intensity enhancement found and predicted in the fundamental region.
机译:针对NH_3,N_2O,CH_4和(HF)_n,使用异步脉冲喷嘴结合未经修改的连续扫描高分辨率干涉仪(BOMEM DA002)的新颖实验技术得到了证明。与脉冲操作模式相关的频谱伪影在几次扫描的平均过程中会迅速消除。使用合成干涉图分析随机平均。结合连续射流FTIR光谱,这项新技术可实现各种扩展条件。事实证明,这对研究低温下的HF团簇的HF拉伸光谱很有用。这项研究和谐波从头算的预测所导致的(HF)_n的暂定光谱分配(n = 4、5、6)最近受到尺寸选择性二次光束散射OPO实验的挑战。我们提出了对该散射实验的另一种解释,从而与我们的FTIR结果和广泛的从头算预测相一致。 HF的五聚体被证实是HF蒸气中的重要物质。扩展分析中的关键要素是假设v_(HF)+ v_(FF)类型的组合频带以及v_(HF)基本面。为了支持我们的工作,我们基于数千个DZP MP2从头算点对(HF)_n(n = 1-5)中的HF拉伸歧管进行了n维变化网格计算。非谐HF拉伸相对于单体HF的基本频移比n = 3、4、5时相应的谐波频移大19%,29%和37%。基组叠加误差和分子间零点键弱化效应的校正被这些近似抵消了非谐性的贡献,从而解释了谐波预测与实验之间的良好一致性。在SCF级别的HF簇中,泛音吸收的跃迁偶极子预测表明,在基本区域中发现和预测的大强度增强没有了。

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