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首页> 外文期刊>Optics and Spectroscopy >FT-IR, FT-Raman Spectra and Quantum Mechanical Study of Piperidine-3-carboxylic Acid and Its Tautomers, Isomers
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FT-IR, FT-Raman Spectra and Quantum Mechanical Study of Piperidine-3-carboxylic Acid and Its Tautomers, Isomers

机译:哌啶-3-甲酸及其互变异构体,异构体的FT-IR,FT-拉曼光谱和量子力学研究

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摘要

The mid-IR, far-IR, and Raman spectra of piperidine-3-carboxylic acid were measured and interpreted with support of the MP2 and B3LYP/6-311++G(d, p) calculated harmonic vibrational spectra. 10 stable piperidine-3-carboxylic acid tautomers/isomers were found after B3LYP, calculations. The experimental absorption bands of carboxylate (COO~-) group show that the free piperidine-3-carboxylic acid molecule exists in zwitterionic form and the most stable tautomer (NAT-1) can be stabilized by an intramolecular N-H...O hydrogen bond. All vibrational frequencies of NAT-1 assigned in detail with the help of total energy distribution (TED). The experimental vibrational wave numbers were compared with the calculated data.
机译:在MP2和B3LYP / 6-311 ++ G(d,p)计算的谐波振动谱的支持下,测定并解释了哌啶-3-甲酸的中红外,远红外和拉曼光谱。经B3LYP计算,发现10个稳定的哌啶-3-羧酸互变异构体/异构体。羧酸根(COO〜-)的实验吸收带表明,游离哌啶-3-羧酸分子以两性离子形式存在,并且最稳定的互变异构体(NAT-1)可以通过分子内NH ... O氢键来稳定。借助总能量分布(TED)详细分配NAT-1的所有振动频率。将实验振动波数与计算数据进行比较。

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