A novel chiral bonded stationary phase(CBSP) for ligand exchange chromatography was prepared by bonding ( S ) 1,2,3,4 tetrahydro 3 isoquinoline carboxylic acid prepared from L Phe to YWG 80 silica gel via 3 glycidyloxypropyltrimethoxysilane as a coupling agent. Chromatographic resolutions of some DL amino acids were achieved on the CBSP by using an aqueous solution of 2 mmol/L N(C 2H 5) 3, 2 mmol/L HAc and 0 2 mmol/L Cu(Ac) 2 as the mobile phase with a flow rate 1 0 mL/min, column temperature 50 ℃ and detection at 254 nm. The enantioselectivity α of the DL amino acids on the CBSP was found to be between 1 11 and 1 51. The elution order of D isomer before L isomer on the CBSP was observed for all the DL amino acids resolved except DL Val. For DL Pro, DL Val and DL Leu the elution order through the CBSP was different from that through the chiral ligand exchange phases prepared from L Pro or L hydroxyl proline with a five\|membered ring structure. [WT5HZ]
