Abstract

Reaction of the tripodal ligand tris(2-benzimidazolylmethyl)amine (ntb) with hydrated lanthanide(III) perchlorates in methanol affords the complexes [Ln(ntb)2]3+ (Ln = Pr, Eu and Tb) in which the central Ln3+ ion is well encapsulated in a cubic coordination environment; in situ co-crystallization of the complexes in the presence of 4,4′-bipyridyl produces either a double salt containing the bipyridinium(1+) cation or adducts with two to three bipyridyl molecules, the latter adducts forming doubly interpenetrating two- or three-dimensional cationic networks.

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