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作 者:杨国生[1,2] 黄慕斌[1,2] 李高兰 杜爱琴[1,2] 戴庆 高如瑜[1,2] 陈茹玉 王琴荪[1,2]
机构地区:[1]山东大学化学学院 [2]南开大学元素有机化学研究所
出 处:《色谱》1998年第5期427-429,共3页Chinese Journal of Chromatography
基 金:国家自然科学基金;山东省青年自然科学基金
摘 要:利用Pirkle型手性固定相系统地研究了11种有机膦酸酯的手性分离情况。讨论了流动相中强组分异丙醇浓度和柱温对手性分离的影响。结果表明,手性分离系数随温度的升高和流动相中强组分浓度的增加而降低。讨论了有机膦酸酯不同取代基对手性分离的影响,指出手性分离中取代基位置的不同会直接影响手性分离结果,空间位阻过大同样会使手性分离系数降低。在选定的分离条件下,11种有机膦酸酯均可达到基线分离。根据手性分离结果给出了可能的手性分离机理。The enantiomers of eleven chiral organic phosphonates have been separated on Pirkle type chiral stationary phase ( N 3,5 dinitrobenzoyl L leucine aminopropyl silica gel) using mixture of isopropyl alcohol and hexane as mobile phase. The influences of the isopropyl alcohol content in mobile phase (2%, 5%, 10%,15%) and column temperature (20 40℃) on the retention and enantioselectivity have been investigated. The capacity factor k ′ and separation factor α of all solutes were decreased with increasing the isopropyl alcohol content and the column temperatures, but the dependence on temperature was not significant. The capacity factor k ′ and separation factor α were varied with the substituent in different positions. The separation of compounds No. 1 4 was the easiest and baseline separation occurs over the concentration of 5% 15% isopropyl alcohol in mobile phase. The baseline separation of compounds No. 5 9 was obtained when the concentration of isopropyl alcohol in mobile phase was 10% or lower. Only when the concentration of isopropyl alcohol in mobile phase was 2% or lower, the baseline separation of compounds No. 10 11 could be obtained. High stereo hinder substituent (R 2= i Pr, compounds No. 10 and 11) decreased the capacity factor k ′ and separation factor α . A possible chiral recognition mechanism is proposed. The enantioselectivity depends strongly upon the nature, position and size of substituents R 1 and R 2 of the organic phosphonate compounds.
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