Skogsberg U, Allenmark S
Department of Chemistry, Göteborg University, Sweden.
J Chromatogr A. 2001 Jul 6;921(2):161-7. doi: 10.1016/s0021-9673(01)00858-5.
The equilibrium constants K+ and K- for formation of the diastereomeric complexes of the two enantiomers of O,O'-dibenzoyltartaric acid (DBTA) with the chiral selector N,N'-diallyltartardiamide bis-(4-tert.-butylbenzoate) (TBB) have been determined by 1H-NMR. The experiments were performed at different temperatures in CDCl3 or in cyclohexane-d12/2-propanol-d8 mixtures. The equilibrium constants from the 1H-NMR results have been compared with the retention factors (k') obtained from the chromatographic resolution of rac. DBTA on a Kromasil CHI-TBB column with the same solvents as mobile phases. A satisfactory correlation between the 1H-NMR data and the chromatographic data was found.
通过1H-NMR测定了O,O'-二苯甲酰酒石酸(DBTA)的两种对映体与手性选择剂N,N'-二烯丙基酒石二酰胺双(4-叔丁基苯甲酸酯)(TBB)形成非对映体复合物的平衡常数K+和K-。实验在CDCl3中或在环己烷-d12/2-丙醇-d8混合物中于不同温度下进行。将1H-NMR结果得到的平衡常数与在Kromasil CHI-TBB柱上以相同溶剂作为流动相进行外消旋DBTA色谱拆分得到的保留因子(k')进行了比较。发现1H-NMR数据与色谱数据之间存在令人满意的相关性。