Abstract
Herein we report the competitive crystallization of urea-functionalized hydrogen-bonded helical frameworks as a new approach to separating anions from aqueous mixtures. N,N′-Bis( m-pyridylurea) ( 1) containing orthogonal pyridine and urea hydrogen-bonding functionalities forms upon monoprotonation with 1 equiv of HX acids (X = Cl −, Br −, I −, NO 3 −, and ClO 4 −) an isomorphous series of crystalline hydrogen-bonded helices assembled by pyridinium···pyridine hydrogen bonds, with the urea functional groups binding the anions through chelate hydrogen bonding. The helices are further connected in the crystals by CH···X − and pyridinium···X − interactions, as well as π-stacking interactions. Competitive crystallization experiments and lattice energy calculations of the 1·HX crystals showed the solvation-based Hofmeister bias that typically dominates anion separation selectivities from water was attenuated, but not completely overturned. The observed selectivity is apparently a result of the relatively soft and unspecific hydrogen-bonding environment around the anions in the crystals, combined with the high flexibility of the helices, which expand or contract as necessary to accommodate each anion.
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