“…Mixed-valence complexes have been extensively investigated in the last decades for the fundamental study of electron transfer and electronic structure in general. − Mixed-valence compounds of iron, in particular, have attracted interest because of their presence in the active site of metalloproteins and their interesting properties like double exchange. , The coordination chemistry of complexes with Fe–F bonds is less well explored than that with other donor atoms, but complexes with Fe–F bonds have recently received increased attention in the field of magnetic materials − and catalysis . Three-dimensional (3D) network structures of mixed-valence iron fluorides have been explored − and are of relevance for cathode materials for rechargeable lithium batteries. − …”
The reaction of the new dinucleating ligand susan with Fe(BF)·6HO results in formation of the homovalent FeFe complex [(susan){Fe(μ-F)Fe}] and the mixed-valence FeFe complex [(susan){FeF(μ-F)FeF}] depending on the absence or presence of dioxygen, respectively. Complex [(susan){FeF(μ-F)FeF}] is the first molecular mixed-valence complex with a fluorido bridge. The short Fe-μ-F bond of 1.87 Å causes a large reorganization energy, resulting in a localized class II system with an intervalence charge-transfer band of high energy at 10000 cm.
“…Mixed-valence complexes have been extensively investigated in the last decades for the fundamental study of electron transfer and electronic structure in general. − Mixed-valence compounds of iron, in particular, have attracted interest because of their presence in the active site of metalloproteins and their interesting properties like double exchange. , The coordination chemistry of complexes with Fe–F bonds is less well explored than that with other donor atoms, but complexes with Fe–F bonds have recently received increased attention in the field of magnetic materials − and catalysis . Three-dimensional (3D) network structures of mixed-valence iron fluorides have been explored − and are of relevance for cathode materials for rechargeable lithium batteries. − …”
The reaction of the new dinucleating ligand susan with Fe(BF)·6HO results in formation of the homovalent FeFe complex [(susan){Fe(μ-F)Fe}] and the mixed-valence FeFe complex [(susan){FeF(μ-F)FeF}] depending on the absence or presence of dioxygen, respectively. Complex [(susan){FeF(μ-F)FeF}] is the first molecular mixed-valence complex with a fluorido bridge. The short Fe-μ-F bond of 1.87 Å causes a large reorganization energy, resulting in a localized class II system with an intervalence charge-transfer band of high energy at 10000 cm.
“…The Raman spectrum of Fe 2 F 5 is shown in Figure 5 of Supporting Information. X-ray diffraction, Mossbauer spectroscopy, and magnetic properties of Fe 2 F 5 suggest the formula [Fe 2+ ] [FeF 5 (H 2 O)] 2− . The bands at 493 and 410 cm −1 are assigned to the Fe−F stretching vibrations in the [FeF 5 (H 2 O)] 2− molecule (C 4v geometry) based on the Raman spectrum of FeF 6 3− .…”
Section: Resultsmentioning
confidence: 93%
“…Carbon can also be gasified, reducing iron oxides to zerovalent iron. During etching with hydrofluoric acid, the following reactions can occur ,, : Fe0+2H3O+→Fe2++2H2+2−OH;.25emFe2+≡false[Fefalse(H2Ofalse)6false]2+4Fe2++O2+4H+→4Fe3++2H2OFe2++2F−↔FeF2…”
Section: Discussionmentioning
confidence: 99%
“…However, since Fe 2 F 5 is a likely candidate formed during the etching, we synthesized this compound. Upon dissolution of Fe 2 F 5 , it is known that the cationic species is Fe 2+ and the anionic species is [FeF 5 (H 2 O)] 2- (13). The Fenton activity of Fe 2 F 5 observed in Figure 5 stems from the presence of Fe 2+ .…”
Section: Speciation Of Iron On Flammruss and Synthetic Carbonmentioning
The chemical and biological properties of iron-loaded manufactured carbon nanoparticles (Flammruss 101) were contrasted with those of an iron-loaded synthetic carbon particle. X-ray photoelectron spectroscopy was used to characterize the iron on the carbon particles. Production of hydroxyl free radicals via the Fenton reaction was monitored by electron paramagnetic resonance spectroscopy. The iron-loaded synthetic carbon particles produced a positive Fenton response, whereas the iron-loaded manufactured carbon particles did not. The source of the Fenton activity of the synthetic carbon particles is proposed to be a soluble iron compound that was formed during the synthesis of the particle. A likely candidate for the soluble iron species is Fe2F5, which was synthesized and its properties were examined. Higher toxicity of Fe2F5 toward murine macrophages compared with other simple iron salts was attributed to soluble iron that was stabilized by the fluoride ligand. The cytotoxicity of manufactured carbon particles toward murine macrophages decreased or remained unaltered upon impregnation with iron compounds.
7 H, O. ‐ Magnetische Messungen, Mößbauerspektren und diffuse Reflexionsspektren sprechen für die Formulierung des Heptahydrats als gemischtwertiges System der Klasse I (Robin, M.B., 1967).
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