Dalton Transactions · 2018 · 10 citations · 36 references
Natural SciencesChemistryMaterials ScienceCrystal StructureCoordination ChemistryCoordination PolymersMetal-ligand BondingSelf-assembled MaterialsSelf-assemblyTransition Metal ComplexesCoordination-driven Self-assemblyMetal-ligand Coordination PolymersMetal-organic Supramolecular AssembliesReversible AssemblyReversible Self-assemblySupramolecular Coordination Polymers
We report the design and synthesis of a Cu(ii) metallocycle (1) and use the possibility to expand the Cu(ii) coordination sphere to self-assemble mechanically interlocked species via interpenetration. Metallocycle 1 can be used as a platform to reversibly assemble a 1D + 1D → 1D coordination-driven polyrotaxane (3), where 1 acts as the hosting ring as well as the stopper, and 4,4'-bipyridine is the guest-axle. A coordinating solvent can substitute the 4,4'-bipyridine axle to disassemble the polyrotaxane (3 → 2) that is easily restored by further adding 4,4'-bipyridine (2 → 3). Other polyrotaxanes can be isolated by reacting 1 with pyridine (4) and phenylpyridine (5). Interconversion among the presented species is demonstrated and ensured by the open position of each copper center in platform 1.
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