Journal of the American Chemical Society · 2013 · 182 citations · 55 references
Natural SciencesChemistryMaterials ScienceInorganic ChemistryMaterials ChemistryNanomaterialsCoordination ChemistryElectrode MaterialsMetal-ligand BondingPhotoelectrochemical MaterialsPhotoelectrochemistrySelf-assembly Of NanomaterialsBondingDirectional BondingElectroactive Supramolecular MaterialsElectrochemical OxidationHost-guest ComplexationHost-guest RelationsTetrahedral ComplexesTetrahedral Coordination
Self-assembly of octahedral Fe(II) ions and linear perylene bisimide (PBI) dyes with 2,2'-bipyridine groups covalently attached at the imide positions quantitatively yields an Fe4(PBI)6 tetrahedron by the directional bonding approach. With an edge length of 3.9 nm and estimated internal volume >950 Å(3), tetrahedron T is one of the largest M4L6 tetrahedra ever reported. Importantly, many of the desirable photo- and electroactive properties of the PBI ligands are transferred to the nanoscale metallosupramolecule. Tetrahedron T absorbs strongly across the visible spectrum out to 650 nm and exhibits a total of 7 highly reversible electrochemical oxidation and reduction waves spanning a 3.0 V range. This facile cycling of 34 electrons between +18 and -16 charged species is likely enabled due to the porous nature of the tetrahedron that allows the necessary counterions to freely flow in and out of the host. Host-guest encapsulation of C60 by T in acetonitrile was studied by (13)C NMR spectroscopy, UV-vis spectroscopy, and ESI-MS, confirming that the tetrahedron is a suitable host for large, functional guest molecules.
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Solubility of fullerene (C60) in a variety of solvents
Rodney S. Ruoff, Doris S. Tse, Ripudaman Malhotra et al. · The Journal of Physical Chemistry · 1993 · 1.1K citations