Abstract
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 [Pd2L2L′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-[Pd2L2L′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)2L′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 [Pd2L2L′2] cages is achieved by selective ligand displacement transformations in a system of three ligands and at least six possible cage products.
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Bloch, W. M., Holstein, J. J., Hiller, W., & Clever, G. H. (2017). Morphological Control of Heteroleptic cis- and trans-Pd2L2L′2 Cages. Angewandte Chemie - International Edition, 56(28), 8285–8289. https://doi.org/10.1002/anie.201702573
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