The Journal of Organic Chemistry · 1997 · 105 citations · 39 references
Natural SciencesBiochemistryChemistryInorganic ChemistryOrganic ChemistrySpectroscopyCoordination ChemistryInorganic SynthesisLigand BindingMetal-ligand BondingTransition Metal ComplexesElectrochemical TransportElectrochemical WindowElectronic Structure EffectsElectronic Structure Of Metal ComplexesOxidationOxidation - Reduction PotentialPorphyrin ComplexesPorphyrin Redox Chemistry
We report a convenient and general synthesis of β-octafluoroporphyrins bearing meso -tetraaryl substituents, including the first synthesis and full characterization of a perfluorinated tetraarylporphyrin, perfluoro-5,10,15,20-tetraphenylporphyrin, 2 . The structural, spectroscopic, and electrochemical data indicate that β-octafluoro- meso -tetraarylporphyrins are a new class of planar, electron-deficient ligands. Particularly impressive is the 0.5 V window over which the formal oxidation potential can be tuned using only aryl substituents. The invariance of the ligand structure with increasingly positive formal oxidation potential is a key advance; electronic effects have been severed from the nonplanar conformations exhibited by all other highly electron-deficient porphyrins.
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van der Waals Volumes and Radii
A. Bondì · The Journal of Physical Chemistry · 1964 · 19.2K citations
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Activation of alkanes : the biomimetic approach
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Mechanism of Catalytic Oxygenation of Alkanes by Halogenated Iron Porphyrins
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