Double-chain alkyl amphiphiles with oligo-l-glutamic acid-head group were prepared. These compounds were dispersed in water at pH 8 to 9 to form bilayer aggregates, in which helical and hollow structures were contained. New CD bands were observed in the solution.

L-Glutamate derivatives 1 and 2 having two N-dodecylamide groups formed highly-oriented aggregates in benzene, which underwent phase transition and phase separation behaviours analogous to those of lipid membranes.

Fig. 2 Concentration dependence of first-order rate constant (k 1 ) for MC-SP thermal isomerization of lipids 1-3 in benzene. 20 °C. Dotted lines indicate the c.a.c. values determined by this method. The error limits of k 1 values are within ±10%.∑

An L-glutamate derivative having one carboxylic and two dodecylamide groups form highly-oriented aggregates in benzene, which interact with a cationic achiral dye to produce extremely strong exciton coupling around the absorption band of the dye.

Resorcinol-type calix[4]arenes bearing four alkyl side chains ([4]Ar-Rn) have been applied as a liquid surfactant-membrane in the concentration process of Cs+. [4]Ar-Rn formed a highly stable water-in-oil (w/o) emulsion for a mixture of toluene and HCl solution, and the w/o emulsion became a w/o/w emulsion by stirring it in a Cs+ solution. The Cs+ in the outer aqueous solution was transported through the liquid surfactant-membrane of w/o/w emulsion into the inner HCl solution. [4]Ar-R6 was the most effective emulsifier capable carrying Cs+ in the [4]Ar-Rn bearing alkyl chains of various lengths. The final amount of the transported Cs+ was 9 times as much as the molar of [4]Ar-R6 in 100 min at the initially 10 times molar Cs+ in the outer solution (turnover number: 9). Moreover, the Cs+ was transported selectively from a mixture of alkali metal ions (Cs+, Na+, and K+) by using 2 × 10−4 mol of [4]Ar-R6.