Abstract
Selectivity of the reported dimethyl-substituted ( R,R)- 1, the diisobutyl-substituted ( R,R)- 2 acridino-18-crown-6 ethers and the newly synthesized acridino-crown ether ( S,S)- 3 containing the methyl groups one carbon–carbon bond further away from the acridine unit was studied towards the enantiomers of the hydrogen perchlorate salts of α-phenylethylamine, α-(1-naphthyl)ethylamine, phenylglycine methyl ester and phenylalanine methyl ester using fluorescence.
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