Supercritical fluid chromatography for separation of chiral planar metallocenes

Unsymmetrically disubstituted metallocene derivatives, characterized as the first sandwich structure, have found interest in asymmetrical synthesis and in medicinal chemistry as well. Besides, they present a particular case of chirality. Twenty original and six commercially available molecules presenting either i) a planar chirality or ii) an asymmetrical carbon containing group or iii) being symmetrically substituted were analyzed in supercritical fluid chromatography on eleven polysaccharide-based chiral stationary phases with carbon dioxide containing 30% of methanol or 2-propanol as a co-solvent mobile phase. A basic additive, either diethylamine, triethylamine or n-butylamine was also required at 1% to the co-solvent for elution. While some of the tested chiral stationary phases provided enantioseparation for the racemates, chlorinated cellulosic phases proved to be both highly retentive and highly enantioselective towards these particular species with the highest rate of success compared to their non-chlorinated counterparts. For instance, the resolution value was equal to 14.1 for one ferrocene derivative in one-hour analysis time on cellulose tris (3,5-dichlorophenylcarbamate) column with 30% 2propanol/1% n-butylamine while a single peak was observed under the same conditions on cellulose tris (3,5-dimethylphenylcarbamate) column. Experimental parameters were arbitrarily set at 150 bar outlet pressure, 40 & DEG;C temperature and 3 mL/min flow-rate. (C) 2022 Elsevier B.V. All rights reserved.

Automated summary

Unsymmetrically disubstituted metallocene derivatives with specific chirality were analyzed using polysaccharide-based chiral stationary phases in supercritical fluid chromatography. Chlorinated cellulosic phases demonstrated higher retention and enantioselectivity towards these derivatives compared to non-chlorinated counterparts, with successful enantioseparation of racemates achieved in some cases.