4.8 Article

Extending supramolecular fullerene-porphyrin chemistry to pillared metal-organic frameworks

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.072602399

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  1. NIGMS NIH HHS [R01 GM023851, GM 23851] Funding Source: Medline

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Porphyrins and fullerenes are spontaneously attracted to each other. This supramolecular recognition element can be exploited to produce ordered arrays of interleaved porphyrins and fullerenes. C-60.H(2)TpyP.Pb(NO3)(2).1.5TCE (H(2)TpyP = tetra-4-pyridylporphyrin; TCE = 1,1,2,2-tetrachloroethane) crystallizes in the tetragonal P4/n space group and the structure has been solved to high resolution. The Pb2+ ions connect the pyridylporphyrins in infinite sheets with an interlayer spacing of 12.1 Angstrom. The fullerenes are intercalated between these layers, acting as pillars. The 6:6 ring juncture bonds of C-60 are centered over the porphyrins, bringing the layers into strict tetragonal register. This arranagement identifies the fullerene-porphyrin interaction as a structure-defining element. The same motif is seen in a related ribbon structure having C-70 intercalated into Hgl(2)-linked H(2)TpyTP. The supramolecular design principles involved in assembling these chromophores may have applications in materials science.

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