Abstract
Abstract Calix[6]arene bearing three carboxylate groups arranged in C3 symmetry formed a 1 : 1 complex with UO22+ and showed much more excellent selectivity factors for UO22+ in solvent extraction than calix[6]arene bearing six carboxylate groups. This establishes that the essence of “super-uranophiles” is related to the molecular design of C3 symmetry.
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