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dc.contributor.authorMatzapetakis, M.en
dc.contributor.authorKarligiano, N.en
dc.contributor.authorBino, A.en
dc.contributor.authorDakanali, M.en
dc.contributor.authorRaptopoulou, C. P.en
dc.contributor.authorTangoulis, V.en
dc.contributor.authorTerzis, A.en
dc.contributor.authorGiapintzakis, Johnen
dc.contributor.authorSalifoglou, A.en
dc.creatorMatzapetakis, M.en
dc.creatorKarligiano, N.en
dc.creatorBino, A.en
dc.creatorDakanali, M.en
dc.creatorRaptopoulou, C. P.en
dc.creatorTangoulis, V.en
dc.creatorTerzis, A.en
dc.creatorGiapintzakis, Johnen
dc.creatorSalifoglou, A.en
dc.date.accessioned2019-05-06T12:24:09Z
dc.date.available2019-05-06T12:24:09Z
dc.date.issued2000
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/48627
dc.description.abstractThe first two mononuclear manganese citrate complexes, (NH4)4[Mn(II)(C6H5O7)2] (1) and (NH4)5[Mn(III)(C6H4O7)2]·2H2O (2) were synthesized in aqueous solutions near physiological pH values. They were isolated in their pure crystalline forms and characterized by elemental analyses and spectroscopic techniques, including UV/visible, electron paramagnetic resonance, Fourier transformed infrared, and magnetic susceptibility measurements. Compound 1 crystallizes in the monoclinic space group P21/c, with a = 8.777(1) Å, b = 13.656(3) Å, c = 9.162(2) Å, β = 113.62(2)°, V = 1006.2(6) Å3, and Z = 2. Compound 2 crystallizes in the triclinic space group P1, with a = 9.606(3) Å, b = 9.914(3) Å, c = 7.247(3) Å, α = 91.05(1)°, β = 105.60(1)°, γ = 119.16(1)°, V = 571.3(3) Å3, and Z = 1. The X-ray crystal structures of 1 and 2 revealed that, in both cases, the manganese ion is six-coordinate and is bound by two citrate ligands in a distorted octahedral fashion. In the case of complex 1, the citrate ion binds to Mn2+ as a triply deprotonated ligand, retaining the central carbon hydroxyl hydrogen, whereas, in the case of compound 2, the citrate ligand coordinates to Mn3+ as a fully deprotonated entity. Compound 2 contains water molecules of crystallization in the unit cell which, through extensive hydrogen-bonding interactions, bestow considerable stability upon the Mn3+-citrate assembly. There are significant contributions to the stabilities of the assembled lattices in 1 and 2 arising from the ammonium counterions neutralizing the high anionic charges of the complexes. The EPR spectra attest to the presence of paramagnetic Mn2+ and Mn3+ species in the solid state. Corroborative evidence is obtained from the magnetic susceptibility measurements in the range 5-300 K. Complexes 1 and 2 present clear cases of mononuclear manganese citrate species relevant to manganese speciation in biological media and potentially related to the beneficial as well as toxic effects of manganese on humans.en
dc.language.isoengen
dc.sourceInorganic chemistryen
dc.subjectarticleen
dc.subjectunclassified drugen
dc.subjectchemical analysisen
dc.subjectsynthesisen
dc.subjectmagnetismen
dc.subjectcrystal structureen
dc.subjectcrystallizationen
dc.subjectmanganese derivativeen
dc.subjectstructure analysisen
dc.subjectsodium chlorideen
dc.subjectX ray crystallographyen
dc.subjectmolecular stabilityen
dc.subjectaqueous solutionen
dc.subjectcomplex formationen
dc.subjectFourier analysisen
dc.subjectcitric aciden
dc.subjectliganden
dc.subjectpHen
dc.subjectsolubilityen
dc.subjectwateren
dc.subjectammoniaen
dc.subjectchemical bindingen
dc.subjecthydrogen bonden
dc.subjectmanganeseen
dc.subjectmanganese citrateen
dc.subjectsoliden
dc.titleManganese citrate chemistry: Syntheses, spectroscopic studies, and structural characterizations of novel mononuclear, water-soluble manganese citrate complexesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1021/ic9912631
dc.description.volume39
dc.description.startingpage4044
dc.description.endingpage4051
dc.author.facultyΠολυτεχνική Σχολή / Faculty of Engineering
dc.author.departmentΤμήμα Μηχανικών Μηχανολογίας και Κατασκευαστικής / Department of Mechanical and Manufacturing Engineering
dc.type.uhtypeArticleen
dc.contributor.orcidGiapintzakis, John [0000-0002-7277-2662]
dc.description.totalnumpages4044-4051
dc.gnosis.orcid0000-0002-7277-2662


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