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SQUARAINES CIS AND TRANS DERIVATIVES: PRACTICAL APPLICATION OF GROUP THEORY IN VIBRATIONAL SPECTROSCOPY

机译:Squaraines CIS和反式衍生物:群理论在振动光谱中的实际应用

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This work shows a practical application of the group theory to a relatively simple molecular system, as well its impact in the results obtained through vibrational spectroscopic techniques. Squaraines substituted by dicyanemethylene groups have been extensively studied, and after minor approaches in the sense to facilitate the point group determination, they were classified to the C2v (Cis) and D2h (Trans) groups. The Trans squaraine presents lower irreducible representations when compared to the Cis derivative; alterations in the arrangements of such systems promotes very interesting conjugation effects, since different reactivity from spectroscopic particularities. Especially to the Trans squaraine, there was a clear convergence between the data suggest by the calculations and those observed in their vibrational spectra, mainly that related to the inversion operation; strong bands visualized in a vibrational technique are not identified in other, mainly in region between 1800-1000 cm-1. The approach of local symmetry must to be adjust to better evaluation of the spectroscopic behavior of the Cis derivative, in this case, the theory suggests low symmetry, but in the spectra can be seen clearly a bigger symmetry. Then, the vibrational analysis by using different techniques was determinant to the discussion in a supramolecular level.
机译:该工作表明,该组理论对相对简单的分子系统的实际应用,同时它在通过振动光谱技术获得的结果中的影响。已广泛研究由二氰基甲基取代的鳞片,并且在意义上进行了次要方法以方便群体测定,它们被分类为C2V(CIS)和D2H(Trans)组。与顺式衍生物相比,跨鳞状呈较低的不可缩续的表示;这种系统的布置的改变促进了非常有趣的共轭效应,因为来自光谱特性的不同反应性。特别是对跨斯基塔克因,数据之间的透明会聚通过计算的数据和振动谱观察到的数据,主要是与反演操作相关的;以振动技术可视化的强带不鉴定为其他,主要在1800-1000cm-1之间。局部对称的方法必须调整以更好地评估顺式衍生物的光谱行为,在这种情况下,该理论表明对称性低,但在光谱中可以看出,可以看出更大的对称性。然后,使用不同技术的振动分析是在超分子水平中讨论的决定因素。

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