Department of Chemistry, Faculty of Science, Banaras Hindu University, Varanasi, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2011 Dec;83(1):532-9. doi: 10.1016/j.saa.2011.08.079. Epub 2011 Sep 9.
A barbiturate derivative, 4-(2,4,6-trioxo-tetrahydro-pyrimidine-5-ylidenemethyl)-benzoic acid (L1) possessing functional complementarity to amides has been synthesized and characterized. Its binding separately with urea and acetamide was monitored using UV-vis, fluorescence and (1)H-NMR spectroscopic titrations. Experiments suggested stronger binding of L1 with urea as compared to acetamide. The solid adducts of L1 prepared separately with urea and acetamide were also characterized using IR, (1)H-NMR spectral and PXRD techniques. Theoretical studies on hydrogen bonded complexes of L1-urea and L1-acetamide in the gas phase, aqueous, and DMSO medium were carried out using density functional theory (DFT) at the B3LYP/6-31G** level. The theoretical calculations agreed to the experimental results.
一种巴比妥酸衍生物,4-(2,4,6-三氧代-四氢嘧啶-5-亚基甲基)-苯甲酸(L1),具有与酰胺互补的功能,已经被合成并进行了表征。使用紫外-可见光谱、荧光和(1)H-NMR 光谱滴定法分别监测其与尿素和乙酰胺的结合。实验表明,L1 与尿素的结合比与乙酰胺更强。L1 分别与尿素和乙酰胺制备的固体加合物也使用红外、(1)H-NMR 光谱和 PXRD 技术进行了表征。使用密度泛函理论(DFT)在 B3LYP/6-31G**水平上对 L1-尿素和 L1-乙酰胺在气相、水相和 DMSO 介质中的氢键复合物进行了理论研究。理论计算与实验结果一致。