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Ground- and excited-state reactivity of iron porphyrinogens
Authors:Bachmann Julien  Hodgkiss Justin M  Young Elizabeth R  Nocera Daniel G
Institution:Department of Chemistry, 6-335, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139-4307, USA.
Abstract:The iron(II) porphyrinogen dication, LDeltaDeltaFeII]2+, is a multielectron oxidant featuring the metal center in its reduced state and the ligand as the redox reservoir. Oxidations break the ligand's redox-active C-C bonds. Extremely short-lived excited states are consistent with extensive structural reorganization that accompanies charge-transfer excitation of the porphyrinogen.
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