Control over the integrative self-sorting of metallo-supramolecular assemblies opens up possibilities for introducing increased complexity and function into a single self-assembled architecture. Herein, the relationship between the geometry of three ligand components and morphology of three self-sorted heteroleptic [Pd2 L2 L'2 ]4+ cages is examined. Pd-mediated assembly of two bis-monodentate pyridyl ligands with native bite angles of 75° and 120° affords a cis-[Pd2 L2 L'2 ]4+ cage while the same reaction with two ligands with bite angles of 75° and 60° gives an unprecedented, self-penetrating structural motif; a trans-[Pd2 (anti-L)2 L'2 ]4+ heteroleptic cage with a "doubly bridged figure eight" topology. Each heteroleptic assembly can be formed by cage-to-cage conversion of the homoleptic precursors and morphological control of [Pd2 L2 L'2 ] cages is achieved by selective ligand displacement transformations in a system of three ligands and at least six possible cage products.
Keywords: cage compounds; morphological control; self-sorting; supramolecular chemistry; topology.
© 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.