To optimize the calix[4]arene structure for a phase-transfer catalyst,
we modified the upper rim with lipophilic tert-octyl groups and the l
ower rim with O(CH2CH2O)mMe (m=1, 2, and 3). Through two-phase solvent
extraction, H-1 NMR studies on the metal-binding site, and phase-tran
sfer catalysis we have reached conclusions that (i) lipophilic groups
introduced into the upper rim effectively enhance the catalytic activi
ty whereas (ii) to compose an effective ionophoric cavity on the lower
rim, OCH2CH2OMe (i.e., m=1) suffices and m=2 and m=3 rather decrease
the catalytic activity and cause emulsification. The optimized calix[4
]arene-based phase-transfer catalyst showed the catalytic activity com
parable with dicyclohexyl-18-crown-6.