Dinuclear iron carbonyl complex , which contains an elongated unsupported Fe-Fe bond, was synthesized by the reaction between Fe(CO) and phosphinyl radical . Thermal Fe-Fe bond homolysis led to the generation of a four-coordinate carbonyl-based iron-centered radical, , which is stabilized by π-donation. Complex exhibited high reactivity toward organic radicals to form diamagnetic five-coordinate Fe(ii) complexes.
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http://dx.doi.org/10.1039/c5sc02601f | DOI Listing |
Steroids
April 2024
Department of Chemistry, The University of the West Indies, Mona, Kingston 7, Jamaica. Electronic address:
Research published between 2001 and 2022 on the functionalization of remote positions of steroids, as well as the use of this technique in the generation of biologically active compounds has been reviewed. In the first section of the analysis established and novel methods for activation of sites deemed to be remote were reported. A series of manganese- (mainly), rhodium-, ruthenium- and osmium-centered porphyrins as catalysts in the presence of PIDA as oxidant have effected hydroxylation at C-1, -5, -6, -7, -11, -14, -15, -16, -17, -20, -24 and -25.
View Article and Find Full Text PDFiScience
January 2023
School of Environmental and Municipal Engineering, Xi'an University of Architecture and Technology, No. 13, Yanta Road, Xi'an, Shaanxi 710055, China.
The mechanism of spontaneous Fe/Fe redox cycling in iron-centered single-atom catalysts (I-SACs) is often overlooked. Consequently, pathways for continuous SO /HO⋅ generation during peroxymonosulfate (PMS) activation by I-SACs remain unclear. Herein, the evolution of the iron center and ligand in I-SACs was comprehensively investigated.
View Article and Find Full Text PDFInorg Chem
April 2020
Department of Chemistry and Pharmacy, Inorganic Chemistry, Friedrich-Alexander University Erlangen-Nürnberg, Egerlandstraße 1, 91058 Erlangen, Germany.
The synthesis and characterization of a series of homoleptic iron complexes [Fe(OCO)] supported by the tridentate bis-aryloxide benzimidazolin-2-ylidene pincer ligand OCO () is presented. While the reaction of 2 equiv of free ligand with a ferrous iron precursor leads to the isolation of the coordination polymer [Fe(OCOK)] (), treatment of with ferric iron salts allows for the synthesis and isolation of the mononuclear, octahedral bis-pincer compound K[Fe(OCO)] () and its crown-ether derivative [K(18c6)(THF)][Fe(OCO)] (). Electrochemical studies of suggested stable products upon further one- and two-electron oxidation.
View Article and Find Full Text PDFChem Sci
January 2016
Department of Chemistry , Graduate School of Science , Tohoku University, Aoba-ku , Sendai 980-8578 , Japan.
Dinuclear iron carbonyl complex , which contains an elongated unsupported Fe-Fe bond, was synthesized by the reaction between Fe(CO) and phosphinyl radical . Thermal Fe-Fe bond homolysis led to the generation of a four-coordinate carbonyl-based iron-centered radical, , which is stabilized by π-donation. Complex exhibited high reactivity toward organic radicals to form diamagnetic five-coordinate Fe(ii) complexes.
View Article and Find Full Text PDFInorg Chem
January 2013
Department of Chemistry, Princeton University, Princeton, New Jersey, 08544, United States.
Oxidation and reduction of the bis(imino)pyridine iron dinitrogen compound, ((iPr)PDI)FeN(2) ((iPr)PDI = 2,6-(2,6-(i)Pr(2)-C(6)H(3)-N═CMe)(2)C(5)H(3)N) has been examined to determine whether the redox events are metal or ligand based. Treatment of ((iPr)PDI)FeN(2) with [Cp(2)Fe][BAr(F)(4)] (BAr(F)(4) = B(3,5-(CF(3))(2)-C(6)H(3))(4)) in diethyl ether solution resulted in N(2) loss and isolation of [((iPr)PDI)Fe(OEt(2))][BAr(F)(4)]. The electronic structure of the compound was studied by SQUID magnetometry, X-ray diffraction, EPR and zero-field (57)Fe Mössbauer spectroscopy.
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