Gas Chromatographic Enantiomer Separation of Atropisomeric PCBs Using Modified Cyclodextrins as Chiral Phases

Columns containing different types of cyclodextrin derivatives have been evaluated for chiral gas chromatographic separation of atropisomeric PCBs, <i>o,p´</i>-DDT and <i>o,p´</i>-DDD. Separation was attempted on columns containing mixed chiral selectors, and the performance of two closely related selectors was also examined. The cyclodextrins were: permethylated- β -CD (PM- β -CD), heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-β-CD (2,3-M-6-TBDMS- β -CD), heptakis(2,3-di-O-methyl-6-<i>O-tert</i>-hexyldimethylsilyl)- β -CD (2,3-M-6-THDMS- β -CD), and heptakis(2,3-di-O-ethyl-6-<i>O-tert</i>-hexyldimethylsilyl)- β -cyclodextrin (2,3-E-6-THDMS- β -CD). The cyclodextrins were dissolved in OV-1701 or in a dimethylsiloxane/silarylene copolymer containing 5% phenyl in the backbone. The application of mixed chiral selectors led to improved separations, however; at most eleven PCB congeners were separated on a single column. Chiral resolution of <i>o,p´</i>-DDD was achieved. The use of a dimethylsiloxane/silarylene copolymer as a matrix for the cyclodextrins is a promising approach. With such a matrix, blocking of the CD cavities by silicone substituent groups can be avoided, and a reasonable CD solubility can be provided. The selectivity of heptakis(2,3-di-O-ethyl-6-O-<i>tert</i>-hexyldimethylsilyl)- β -CD and heptakis(2,3-di-O-methyl-6-<i>O-tert</i>-hexyldimethylsilyl)- β -CD was quite different, the former selector could separate four congeners, while the latter separated ten congeners.