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hal.structure.identifierDepartment of Chemistry
dc.contributor.authorJANA, Tanmay K.
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorKUMAR, Dhurjati P.
hal.structure.identifierDepartment of Chemistry
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorPRADHAN, Rabindranath
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorDINDA, Subhajit
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorGHOSH, Pradip N.
hal.structure.identifierInstitut Lavoisier de Versailles [ILV]
dc.contributor.authorSIMMONET, Corine
hal.structure.identifierInstitut Lavoisier de Versailles [ILV]
dc.contributor.authorMARROT, Jérome
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorIMAZ, Inhar
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorWATTIAUX, Alain
hal.structure.identifierLaboratoire de chimie de coordination [LCC]
dc.contributor.authorSUTTER, Jean-Pascal
hal.structure.identifierInstitut Lavoisier de Versailles [ILV]
dc.contributor.authorSECHERESSE, Francis
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorBHATTACHARYYA, Ramgopal
dc.date.issued2009
dc.identifier.issn0020-1693
dc.description.abstractEnIron (II) and iron (III) complexes, [FeII(DEDTC)2(dppe)] · CH2Cl2 (1), [FeII(ETXANT)2(dppe)] (2) (DEDTC = diethyldithiocarbamate, ETXANT = ethyl xanthate, dppe = 1,2-bis (diphenylphosphino) ethane), and [FeIII(DEDTC)2(dppe)] [FeIIICl4] (3) have been synthesized and characterized. Since 3 contains two magnetic centers, an anion metathesis reaction has been conducted to replace the tetrahedral FeCl4− by a non-magnetic BPh4− ion producing [FeIII(DEDTC)2(dppe)]BPh4 (4) for the sake of unequivocal understanding of the magnetic behavior of the cation of 3. With the similar end in view, the well-known FeCl4− ion, the counter anion of 3, is trapped as PPh4[FeIIICl4] (5) and its magnetic property from 298 to 2 K has been studied. Besides the spectroscopic (IR, UV–Vis, NMR, EPR, Mass and XPS) characterization of the appropriate compounds, especially 2, others viz. 1, 3 and 4 have been structurally characterized by X-ray crystallography. While FeII complexes, 1 and 2, are diamagnetic, the FeIII systems, namely the cations of 3, and 4 behave as low-spin (S = 1/2) paramagnetic species from 298 to 50 K. Below 50 K 3 shows gradual increase of χMT up to 2 K suggesting ferromagnetic behavior while 4 exhibits gradual decrease of magnetic moment from 60 to 2 K, indicating the occurrence of weak antiferromagnetic interaction. These conclusions are supported by the Mössbauer studies of 3 and 4. The Mössbauer pattern of 1 exhibits a doublet site for diamagnetic (2–400 K) FeII. The compounds 1, 2 and 4 encompass interesting cyclic voltammetric responses involving FeII, FeIII and FeIV.
dc.language.isoen
dc.publisherElsevier
dc.subject.enIron complexes
dc.subject.enSulfur and phosphorous donors
dc.subject.enCrystal structure
dc.subject.enMössbauer spectra
dc.subject.enMagnetic studies
dc.subject.enCyclic voltammetry
dc.title.enSynthesis and structure of iron (III) and iron (II) complexes in S<sub>4</sub>P<sub>2</sub> environment created by diethyldithiocarbamate and 1,2-bis(diphenylphosphino)ethane chelation: Investigation of the electronic structure of the complexes by Mössbauer and magnetic studies
dc.typeArticle de revue
dc.identifier.doi10.1016/j.ica.2009.04.007
dc.subject.halChimie/Matériaux
bordeaux.journalInorganica Chimica Acta
bordeaux.page3583-3594
bordeaux.volume362
bordeaux.issue10
bordeaux.peerReviewedoui
hal.identifierhal-00528913
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00528913v1
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