一种取代3,4-二氢嘧啶-2(1H)-酮性质的理论研究  

Theoretical study on the properties of a substituted 3,4-dihydropyrimidin-2(1H)-one

作　　者：马金广[1] 张纪明[1] 房玉真[1] 马万勇[1] 周建华[1] 

机构地区：[1]山东轻工业学院化学工程学院,山东济南250353

出　　处：《山东轻工业学院学报（自然科学版）》2007年第3期63-65,74,共4页Journal of Shandong Polytechnic University

基　　金：山东省自然科学基金资助项目(Y2006B42)

摘　　要：在6-31G*基组水平上,用B3LYP、HF和MP2三种方法对4-(4-氯苯基)-6-甲基-5-甲氧羰基-3,4-二氢嘧啶-2-酮进行了几何全优化,并对其电荷分布、前线分子轨道、成键情况以及自然键轨道(NBO)进行了分析。计算结果表明:B3LYP方法得到的分子构型与实验值最为接近,标题化合物中嘧啶环为船式构象。标题化合物的稳定性较差,可能具有很好的生物活性。嘧啶环中2个氮原子的孤对电子都与相邻键有强的相互作用。The structure of 4- （4- chlorophenyl） - 6 - methyl- 5 - methoxycaronyl - 3,4 - dihydropyrimidin -2（1H） - one was fully optimized at B3LYP/6 - 31G^＊, HF/6 - 31G^＊ and MP2/6 - 31G^＊ levels, and the charge distribution, frontier molecular orbital, bond formations and natural bond orbital （NBO） were also discussed. The calculated results show that the structure B3LYP method obtained is mostly approached to experiment, the pyridine ring in the title compound adopts boat conformation. The title compound may have good biological activities because of hard stability. The lone pair electrons of the two nitrogen atoms in the pyridine ring have strong interactions with neighboring bonds.

关 键 词：3 4-二氢嘧啶-2-酮 前线分子轨道 自然键轨道 理论研究 

分 类 号：O641[理学—物理化学]