Abstract

The chromatographic behavior of uroporphyrin I, uroporphyrin III, coproporphyrin I, coproporphyrin III, and protoporphyrin IX has been examined using silica gel 60F 254 , polyamide 11F 254 , and cellulose F TLC plates as stationary phases. Homologous series of n -alcohols, acetonitrile, and tetrahydrofuran were used as mobile phases. Chromatographic retention data and a possible retention mechanism are discussed. The electrostatic interactions operating in these chromatographic systems were analyzed by studying relationship between log (1/ R F ) values and the molecular polarizabilities of the solvents.

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