| Literature DB >> 24138018 |
Daniel J Meininger1, Jonathan D Caranto, Hadi D Arman, Zachary J Tonzetich.
Abstract
The chemistry of several iron(III) porphyrinates containing silanethiolate ligands is described. The complexes are prepared by protonolysis reactions of silanethiols with the iron(III) precursors, [Fe(OMe)(TPP)] and [Fe(OH)(H2O)(TMP)] (TPP = dianion of meso-tetraphenylporphine; TMP = dianion of meso-tetramesitylporphine). Each of the compounds has been fully characterized in solution and the solid state. The stability of the silanethiolate complexes versus other iron(III) porphyrinate complexes containing sulfur-based ligands allows for an examination of their reactivity with several biologically relevant small molecules including H2S, NO, and 1-methylimidazole. Electrochemically, the silanethiolate complexes display a quasi-reversible one-electron oxidation event at potentials higher than that observed for an analogous arenethiolate complex. The behavior of these complexes versus other sulfur-ligated iron(III) porphyrinates is discussed.Entities:
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Year: 2013 PMID: 24138018 PMCID: PMC3915880 DOI: 10.1021/ic401467k
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165