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山东大学学报(工学版) ›› 2011, Vol. 41 ›› Issue (6): 103-108.

• 化学与化工 • 上一篇    下一篇

β-环糊精与白藜芦醇包合作用的理论研究

周美娟1,田春华1,王素娜1,陈效华2,刘继锋1,张翀1*   

  1. 1. 聊城大学化学化工学院, 山东 聊城 252059;   2. 重庆大学化学化工学院,  重庆 400030
  • 收稿日期:2011-05-30 出版日期:2011-12-16 发布日期:2011-05-30
  • 通讯作者: 张翀(1970-),男,山东济宁人,副教授,硕士生导师,博士,主要研究方向为环糊精的化学修饰.E-mail:zhangchong@lcu.edu.cn
  • 作者简介:周美娟(1985- ),女,山东高唐人,硕士研究生,主要研究方向为环糊精的化学修饰.E-mail:zmj1985110@163.com
  • 基金资助:

    国家自然科学基金资助项目(21003162;20108025);教育厅科研发展计划资助项目(J09LB15);山东省“泰山学者”建设工程专项经费资助项目

Theoretical study of the inclusion interaction of β-cyclodextrin with trans-Resveratrol

ZHOU Mei-juan1, TIAN Chun-hua1, WANG Su-na1, CHEN Xiao-hua2, LIU Ji-feng1, ZHANG Chong1*   

  1. 1. College of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252059, China;
    2. School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400030, China
  • Received:2011-05-30 Online:2011-12-16 Published:2011-05-30

摘要:

利用ONIOM (B3LYP/6-31G*:PM3)理论方法模拟了β-环糊精包合反式白藜芦醇 (trans-Resveratrol)的过程,首先分别以β-环糊精和反式白藜芦醇为单体,然后通过穿越和旋转两个包合过程探讨了反式白藜芦醇从β-环糊精大小口径穿越的稳定程度,反式白藜芦醇和β-环糊精形成包合物的驱动力,促进包合物稳定性的影响因素,以及在气态环境中β-环糊精与反式白藜芦醇形成包合物的驱动过程的类型。研究结果表明:β-环糊精可以包合反式白藜芦醇且反式白藜芦醇容易从β-环糊精的小口径进入形成稳定的包合物,电荷转移和偶极之间的相互作用是形成包合物的主要驱动力,氢键促进了包合物的稳定性,而且在298-15K和1atm的气态环境条件下,形成包合物的过程是焓驱动过程。

关键词: &beta, -环糊精, 反式白藜芦醇, 包合物

Abstract:

The inclusion process of β-cyclodextrin (β-CD) with trans-Resveratrol was studied by the ONIOM (B3LYP/6-31G*:PM3) method. The passing process and cycling process were simulated using β-cyclodextrin (β-CD) with trans-Resveratrol as monomers respectively. The two processes probed the stability of  trans-Resveratrol entering into the cavity of β-cyclodextrin from the narrow side (the primary hydroxyl group side) compared with its wide side (the secondary hydroxyl group side), the possible driving forces for the inclusion compounds, the factors influencing stability of the inclusion compounds and the driven type of forming inclusion compounds in the gas phase. The calculated data indicated that the transResveratrol could easily tend to enter into the cavity of β-cyclodextrin from the narrow side, the possible driving forces for the inclusion compounds were the charge transfer and dipoledipole interactions, hydrogen bonds played an important role in the stability of the inclusion compounds, and the formation of natural β-CD inclusion compounds was an enthalpy-driven process with temperature of 298-15 K and pressure of 1 atm in the gas phase.

Key words: β-cyclodextrin, transResveratrol, inclusion compound

中图分类号: 

  • O641.12+1
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