Structural and Magnetic Effects of meso-Substitution in Alkyl-Substituted Metalloporphyrinate π-Cation Radicals: Characterization of [Fe(TalkylP•)(Cl)]SbCl6 (alkyl = ethyl and n-propyl)
Author:
Affiliation:
1. The Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556
2. The Department of Physics, Knox College, Galesburg, Illinois 61401
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic101099z
Reference44 articles.
1. Dimerization of metalloporphyrin .pi.-cation radicals. Zinc complex [Zn(OEP.bul.)(OH2)]2(ClO4)2, a novel dimer
2. Dimerization of metalloporphyrin .pi. cation radicals. Characterization of two novel dimers: [Zn(OEP.cntdot.)(OH2)]2(ClO4)2 and [Ni(OEP)]2(ClO4)2
3. High-valent iron porphyrins: synthesis, x-ray structures, .pi.-cation radical formulation, and notable magnetic properties of chloro(meso-tetraphenylporphinato)iron(III) hexachloroantimonate and bis(perchlorato)(meso-tetraphenylporphinato)iron(III)
4. Spin coupling in metalloporphyrin .pi.-cation radicals
5. Metalloporphyrin .pi.-cation radicals: intrinsically ruffled or planar core conformations? Molecular structure mesitylporphinatocopper(II) hexachloroantimonate
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