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Tautomeric transformations of piroxicam in solution: a combined experimental and theoretical study

机译:吡罗昔康在溶液中的互变异构转化:结合实验和理论研究

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摘要

Piroxicam tautomerism was studied in solution by using UV-Vis spectroscopy, NMR measurements and advanced chemometrics. It has been found that in ethanol and DMSO the enol-amide tautomer is present mainly as a sandwich type dimer. The addition of water leads to distortion of the aggregate and to gradual shift of the equilibrium towards the zwitterionic tautomer. Quantitative data for the aggregation and the tautomeric equilibria are presented. Quantum chemical calculations (M06-2X/TZVP) have been used to explain stability of the tautomers as a function of the solvent and concentration.
机译:通过使用紫外-可见光谱,NMR测量和先进的化学计量学对溶液中的吡罗昔康互变异构进行了研究。已经发现在乙醇和DMSO中,烯醇酰胺互变异构体主要以夹心型二聚体存在。加水导致聚集体变形并导致平衡逐渐向两性离子互变异构体转移。给出了聚集和互变异构平衡的定量数据。量子化学计算(M06-2X / TZVP)已用于解释互变异构体的稳定性与溶剂和浓度的关系。

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