Fe(II) and Fe(III) Mononuclear Complexes with a Pentadentate Ligand Built on the 1,3-Diaminopropane Unit. Structures and Spectroscopic and Electrochemical Properties. Reaction with H2O2
Two new iron complexes, [L5 3FeIICl]PF6 (1·PF6) and [(L5 3H+)FeIIICl3]PF6 (2·PF6), were synthesized (L5 3 = N-methyl-N,N‘,N‘-tris(2-pyridylmethyl)propane-1,3-diamine), and their molecular structures were determined by X-ray crystallography. Their behavior in solution was studied by UV−vis spectrosco...
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Veröffentlicht in: | Inorganic chemistry 2003-04, Vol.42 (7), p.2470-2477 |
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creator | Balland, Véronique Banse, Frédéric Anxolabéhère-Mallart, Elodie Ghiladi, Morten Mattioli, Tony A Philouze, Christian Blondin, Geneviève Girerd, Jean-Jacques |
description | Two new iron complexes, [L5 3FeIICl]PF6 (1·PF6) and [(L5 3H+)FeIIICl3]PF6 (2·PF6), were synthesized (L5 3 = N-methyl-N,N‘,N‘-tris(2-pyridylmethyl)propane-1,3-diamine), and their molecular structures were determined by X-ray crystallography. Their behavior in solution was studied by UV−vis spectroscopy and electrochemistry. Upon addition of a base to an acetonitrile solution of 2, the new unsymmetrical dinuclear complex [L5 3FeIIIOFeIIICl3]+ was detected. Treating 1 with hydrogen peroxide has allowed us to detect the low spin [L5 3FeIIIOOH]2+. Its spectroscopic properties (UV−vis, EPR and resonance Raman) are similar to those reported for related FeOOH complexes obtained with amine/pyridine ligands. Using stopped-flow absorption spectroscopy, the formation and degradation of [L5 3FeIIIOOH]2+ has been monitored, and a mechanism is proposed to reproduce the kinetic data. |
doi_str_mv | 10.1021/ic025905n |
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Structures and Spectroscopic and Electrochemical Properties. Reaction with H2O2</title><source>ACS Publications</source><creator>Balland, Véronique ; Banse, Frédéric ; Anxolabéhère-Mallart, Elodie ; Ghiladi, Morten ; Mattioli, Tony A ; Philouze, Christian ; Blondin, Geneviève ; Girerd, Jean-Jacques</creator><creatorcontrib>Balland, Véronique ; Banse, Frédéric ; Anxolabéhère-Mallart, Elodie ; Ghiladi, Morten ; Mattioli, Tony A ; Philouze, Christian ; Blondin, Geneviève ; Girerd, Jean-Jacques</creatorcontrib><description>Two new iron complexes, [L5 3FeIICl]PF6 (1·PF6) and [(L5 3H+)FeIIICl3]PF6 (2·PF6), were synthesized (L5 3 = N-methyl-N,N‘,N‘-tris(2-pyridylmethyl)propane-1,3-diamine), and their molecular structures were determined by X-ray crystallography. Their behavior in solution was studied by UV−vis spectroscopy and electrochemistry. Upon addition of a base to an acetonitrile solution of 2, the new unsymmetrical dinuclear complex [L5 3FeIIIOFeIIICl3]+ was detected. Treating 1 with hydrogen peroxide has allowed us to detect the low spin [L5 3FeIIIOOH]2+. Its spectroscopic properties (UV−vis, EPR and resonance Raman) are similar to those reported for related FeOOH complexes obtained with amine/pyridine ligands. 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Its spectroscopic properties (UV−vis, EPR and resonance Raman) are similar to those reported for related FeOOH complexes obtained with amine/pyridine ligands. Using stopped-flow absorption spectroscopy, the formation and degradation of [L5 3FeIIIOOH]2+ has been monitored, and a mechanism is proposed to reproduce the kinetic data.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>12665386</pmid><doi>10.1021/ic025905n</doi><tpages>8</tpages></addata></record> |
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title | Fe(II) and Fe(III) Mononuclear Complexes with a Pentadentate Ligand Built on the 1,3-Diaminopropane Unit. Structures and Spectroscopic and Electrochemical Properties. Reaction with H2O2 |
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