Zheng Zhi-Xia, Lin Jin-Ming, Qu Feng
Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Beijing 100085, China.
J Chromatogr A. 2003 Jul 25;1007(1-2):189-96. doi: 10.1016/s0021-9673(03)00960-9.
Ligand-exchange micellar electrokinetic capillary chromatography was used for the chiral resolution of underivatized and dansyl amino acid enantiomers simultaneously. The separation was achieved by chiral copper(II)-L-valine complexes incorporated in micelles of sodium dodecyl sulfate (SDS). The enantioresolution was strongly affected by SDS and a concentration of 20 mM SDS was shown to be necessary for the separation. Other impacting factors were investigated including pH, the molar ratio of copper(II) to L-valine and the total concentration of complex. Using the proposed method, 11 different dansyl amino acids and two underivatized amino acids were separated successfully with a running electrolyte of 20 mM NH4OAc, 4 mM CuSO4, 8 mM L-valine and 20 mM SDS at pH 9.0 in less than 25 min. Experiments were also performed with other amino acid ligands in order to vary the stability and the sterical arrangement of the copper(II) complexes and the possible chiral recognition mechanism was also discussed briefly.
配体交换胶束电动毛细管色谱法用于同时拆分未衍生化的和丹磺酰化的氨基酸对映体。分离是通过将手性铜(II)-L-缬氨酸配合物掺入十二烷基硫酸钠(SDS)胶束中来实现的。对映体拆分受到SDS的强烈影响,结果表明20 mM SDS的浓度对于分离是必要的。还研究了其他影响因素,包括pH值、铜(II)与L-缬氨酸的摩尔比以及配合物的总浓度。使用所提出的方法,在pH 9.0的条件下,以20 mM NH4OAc、4 mM CuSO4、8 mM L-缬氨酸和20 mM SDS作为运行电解质,在不到25分钟的时间内成功分离了11种不同的丹磺酰化氨基酸和两种未衍生化氨基酸。还使用其他氨基酸配体进行了实验,以改变铜(II)配合物的稳定性和空间排列,并简要讨论了可能的手性识别机制。