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β-Cyclodextrin is first immobilized on the gel supports of polyacrylamide and agarose. The resulting stationary phase containing β-cyclodextrin chemically bonded on polyacrylamide shows novel selectivity in the liquid chromatographic separation of disubstituted benzene isomers. Thep-isomers are retained more strongly compared with the o-or m-isomers.
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Tanaka et al. (1981) studied this question.
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