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Discrimination of Glycine Enantiomers by the Biologically Important Phosphocompounds:A Theoretical Prediction

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【作者】 杨刚刘成卜祖元刚付玉杰周丽君

【Author】 YANG Ganga,b LIU Cheng-Bub ZU Yuan-Ganga FU Yu-Jiea ZHOU Li-Juna a(Key Laboratory of Forest Plant Ecology,Ministry of Education,Northeast Forestry University,Harbin 150040,China) b(Institute of Theoretical Chemistry,Shandong University,Jinan 250100,China)

【机构】 Key Laboratory of Forest Plant Ecology, Ministry of Education, Northeast Forestry University,Harbin 150040, ChinaInstitute of Theoretical Chemistry, Shandong University,Jinan 250100, China

【摘要】 With the aid of high-level B3LYP and MP2 calculations,three new neutral structures of glycine(iin,ivn and vn,see Fig.2) were obtained and validated by frequency calculations.The structural and energetic analyses showed that iin,ivn and vn are enantiomers to the previous IIn,IVn and Vn(J.Am.Chem.Soc.1992,114,9568.),respectively.Owing to the presence of these novel conformers,a redistribution of the populations of glycine conformers is resulted in and causes the remarkable decrease of the most stabilized Ip(from 48% to 38%).It indicated that the simple glycine molecule can show chirality under certain conditions.The interacting modes of glycine enantiomeric pairs(e.g.,ivn and IVn) with PG showed large differences(Fig.4);in addition,their interaction energies corrected with basis set superposition errors(BSSE) were calculated to be-66.81 and-46.99 kJ mol-1,respectively.Accordingly,the glycine enantiomers can be potentially applied to the chiral recognition in biological and pharmaceutical areas.

【Abstract】 With the aid of high-level B3LYP and MP2 calculations,three new neutral structures of glycine(iin,ivn and vn,see Fig.2) were obtained and validated by frequency calculations.The structural and energetic analyses showed that iin,ivn and vn are enantiomers to the previous IIn,IVn and Vn(J.Am.Chem.Soc.1992,114,9568.),respectively.Owing to the presence of these novel conformers,a redistribution of the populations of glycine conformers is resulted in and causes the remarkable decrease of the most stabilized Ip(from 48% to 38%).It indicated that the simple glycine molecule can show chirality under certain conditions.The interacting modes of glycine enantiomeric pairs(e.g.,ivn and IVn) with PG showed large differences(Fig.4);in addition,their interaction energies corrected with basis set superposition errors(BSSE) were calculated to be–66.81 and–46.99 kJ mol-1,respectively.Accordingly,the glycine enantiomers can be potentially applied to the chiral recognition in biological and pharmaceutical areas.

【基金】 supported by the Major State Basic Research Development Programs (No. 2004CB719902);the National Natural Science Foundation of China (No. 20633060);the Talented Funds of Northeast Forestry University (No. 220-602042)
  • 【文献出处】 结构化学 ,Chinese Journal of Structural Chemistry , 编辑部邮箱 ,2009年05期
  • 【分类号】O621.2
  • 【下载频次】38
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