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首页> 外文期刊>Chemical Physics: A Journal Devoted to Experimental and Theoretical Research Involving Problems of Both a Chemical and Physical Nature >Blue shifted F3CH center dot center dot center dot FCD3 and Cl3CH center dot center dot center dot FCD3 weakly H-bound complexes. Cryospectroscopic and ab initio study
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Blue shifted F3CH center dot center dot center dot FCD3 and Cl3CH center dot center dot center dot FCD3 weakly H-bound complexes. Cryospectroscopic and ab initio study

机译:蓝移的F3CH中心点中心点中心点FCD3和Cl3CH中心点中心点中心点FCD3弱H结合的络合物。低温光谱和从头算研究

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The FTIR spectra of F3CH/FCD3 and Cl3CH/FCD3 mixtures have been studied in liquefied Kr in the range of frequencies similar to 500-10000cm(-1). Spectroscopic evidence of a weak H-bonded complex formation in the solutions studied have been found. The blue frequency shift of the C-v1-H stretching vibration and of the majority of the combination and overtone bands, with the (v1) vibration being excited, were revealed for both F3CH/FCD3 and Cl3CH/FCD3 complexes characterized by the opposite change in the integrated intensity of the (v1) band. The effects observed are treated in the frame of features of the dipole moment function of molecules studied. In the case of both systems, ab initio MP2(Full)/6-31 +G(d,p) CP corrected calculations predict a linear structure and 2 non-linear stable structures with spectroscopic features being in qualitative agreement with experimental observations. Contributions of the components of the interaction energy in the frequency shift have been analysed by using the SAPT decomposition scheme. The NBO analysis performed suggests, that the competition between rehybridization/repolarization effect and hyperconjugation CT interaction might result in a transfer from the blue to red shift in the case of stronger H bonds. (c) 2005 Elsevier B.V. All rights reserved.
机译:F3CH / FCD3和Cl3CH / FCD3混合物的FTIR光谱已在液化Kr中研究,频率范围类似于500-10000cm(-1)。已发现所研究溶液中弱氢键结合物形成的光谱证据。对于F3CH / FCD3和Cl3CH / FCD3配合物,C-v1-H拉伸振动以及大多数组合和泛音带的蓝频移以及(v1)振动均被激发,表现出相反的变化(v1)波段的积分强度。在所研究分子的偶极矩函数的特征框架内处理观察到的效应。对于这两种系统,从头算起MP2(完全)/ 6-31 + G(d,p)CP校正的计算可以预测线性结构和2个非线性稳定结构,其光谱特征与实验观察在质量上一致。通过使用SAPT分解方案,分析了相互作用能量在频移中的贡献。进行的NBO分析表明,在更强的H键的情况下,复化/复极化效应与超共轭CT相互作用之间的竞争可能导致从蓝移到红移。 (c)2005 Elsevier B.V.保留所有权利。

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