Search results for " Mossbauer"

showing 10 items of 30 documents

A PAS domain with an oxygen labile [4Fe-4S](2+) cluster in the oxygen sensor kinase NreB of Staphylococcus carnosus.

2008

The cytoplasmic histidine sensor kinase NreB of Staphylococcus carnosus responds to O(2) and controls together with the response regulator NreC the expression of genes of nitrate/nitrite respiration. nreBC homologous genes were found in Staphylococcus strains and Bacillus clausii, and a modified form was found in some Lactobacillus strains. NreB contains a sensory domain with similarity to heme B binding PAS domains. Anaerobically prepared NreB of S. carnosus exhibited a (diamagnetic) [4Fe-4S](2+) cluster when assessed by Mossbauer spectroscopy. Upon reaction with air, the cluster was degraded with a half-life of approximately 2.5 min. No significant amounts of Mossbauer or EPR detectable i…

Iron-Sulfur ProteinsbiologyHistidine KinaseChemistryLigandAirStaphylococcusHistidine kinasebiology.organism_classificationBiochemistrylaw.inventionOxygenHeme Bchemistry.chemical_compoundCrystallographyMagneticsSpectroscopy MossbauerPAS domainlawKinase activityElectron paramagnetic resonanceProtein KinasesHistidineStaphylococcus carnosusHalf-LifeBiochemistry
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Structural investigations on diorganotin and triorganotin(IV) phosphomycin derivatives.

2008

Abstract Four new diorganotin(IV), (R = Me, Bu), and triorganotin(IV), (R = Me, Ph), derivatives of the phosphomycin disodium salt antibiotic[(1R,2S)-1,2-epoxypropylphosphonate]Na2 have been synthesized and their solid state configuration studied by X-ray crystallography, FT-IR, Mossbauer, UV–Vis spectroscopies. The X-ray diffraction investigation, performed on the bis[trimethyltin(IV)]phosphomycin, showed that the coordination geometry at all the Sn atoms is trigonal bipyramidal. The structure of the complex forms an unusual polymeric zig-zag planar network. The FT-IR and the 119Sn Mossbauer studies supported the formation of trigonal bipyramidal (Tbp) molecular structures, both in the dio…

Lattice dynamicsPlanar networkChemistrySolid-statePOTENTIOMETRIC AND SPECTROPHOTOMETRIC TITRATIONSFT-IRInorganic ChemistryCrystallographyTrigonal bipyramidal molecular geometrySettore CHIM/03 - Chimica Generale E InorganicaORGANOTINMOSSBAUERMössbauer spectroscopyX-RAYMaterials ChemistryOrganotin FT-IR Mossbauer X-ray Potentiometric and spectrophotometric titrationsPhysical and Theoretical ChemistryCoordination geometry
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Hexanuclear iron(III) salicylaldoximato complexes presenting the [Fe6(mu3-O)2(mu2-OR)2]12+ core: syntheses, crystal structures, and spectroscopic and…

2006

The use of salicylaldehyde oxime (H2salox) in iron(III) carboxylate chemistry has yielded two new hexanuclear compounds [Fe6(mu3-O)2(O2CPh)10(salox)2(L)2].xMeCN.yH2O [L = MeCONH2, x = 6, y = 0 (1); L = H2O, x = 2, y = 3 (2)]. Compound 1 crystallizes in the triclinic space group P with (at 25 degrees C) a = 13.210(8) A, b = 13.87(1) A, c = 17.04(1) A, alpha = 105.79(2) degrees , beta = 96.72(2) degrees , gamma = 116.69(2) degrees , V = 2578.17(2) A(3), and Z = 1. Compound 2 crystallizes in the monoclinic space group C2/c with (at 25 degrees C) a = 21.81(1) A, b = 17.93(1) A, c = 27.72(1) A, beta = 111.70(2) degrees , V = 10070(10) A(3), and Z = 4. Complexes 1 and 2 contain the [Fe6(mu3-O)2(m…

Magnetic Resonance SpectroscopyMolecular StructureChemistryLigandStereochemistryCrystal structureTriclinic crystal systemOximeChemistry InorganicCrystallography X-RayInorganic ChemistryCrystallographychemistry.chemical_compoundMagneticsSpectroscopy MossbauerSalicylaldehydeCarboxylatePhysical and Theoretical ChemistryAcetonitrileIron CompoundsMonoclinic crystal systemInorganic chemistry
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The interaction of Fe(III), adriamycin and daunomycin with nucleotides and DNA and their effects on cell growth of fibroblasts (NIH-3T3)

1996

The interactions of the iron complexes of the anthracycline antitumour drugs daunomycin (DN) and adriamycin (ADM) with the mononucleotide AMP, herring sperm DNA, plasmic pBR322 and immortalized 3T3 fibroblasts were studied. By means of Mössbauer spectroscopy it was demonstrated that DNA is a powerful ferric iron chelator as compared with AMP, which is not able to compete with DN or acetohydroxamic acid for ferric iron. The difference between AMP and DNA is postulated to be based on the chelate effect. The Mössbauer spectra of the ternary Fe-anthracycline-DNA systems differ from Fe-anthracycline binary complexes, indicating rearrangement reactions. Dialysis experiments clearly disclose the f…

MaleBase pairStereochemistryIronIntercalation (chemistry)General Biochemistry Genetics and Molecular BiologyBiomaterialsMiceSpectroscopy Mossbauerchemistry.chemical_compoundmedicineAnimalsNucleotideCytotoxicitychemistry.chemical_classificationChemistryCell growthAcetohydroxamic acidDaunorubicinFishesMetals and AlloysBiological Transport3T3 CellsDNASpermatozoaAdenosine MonophosphateDoxorubicinFerricGeneral Agricultural and Biological SciencesCell DivisionDNAPlasmidsmedicine.drugBiometals
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Organometallic complexes with biological molecules. XVIII. Alkyltin(IV) cephalexinate complexes: synthesis, solid state and solution phase investigat…

2004

Abstract Dialkyltin(IV) and trialkyltin(IV) complexes of the deacetoxycephalo-sporin-antibiotic cephalexin [7-( d -2-amino-2-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid] (Hceph) have been synthesized and investigated both in solid and solution phase. Analytical and thermogravimetric data supported the general formula Alk 2 SnOHceph · H 2 O and Alk 3 Snceph · H 2 O (Alk=Me, n -Bu), while structural information has been gained by FT-IR, 119 Sn Mossbauer and 1 H, 13 C, 119 Sn NMR data. In particular, IR results suggested polymeric structures both for Alk 2 SnOHceph · H 2 O and Alk 3 Snceph · H 2 O. Moreover, cephalexin appears to behave as monoanionic tridentate ligand coordinating th…

MaleThermogravimetric analysisDenticitySpectrophotometry InfraredStereochemistryMolecular Conformationchemistry.chemical_elementorganotin(IV)proton nuclear magnetic resonanceBiochemistryMedicinal chemistryChromosomesMossbauerInorganic ChemistrySpectroscopy Mossbauerchemistry.chemical_compoundantibiotic; cephalexin; organotin(IV); Mossbauer; cytotoxicitySpermatocytescomplex formationantibioticMössbauer spectroscopyOrganotin CompoundsAnimaliaAnimalsMoietyBrachidontes pharaoniCarboxylateNuclear Magnetic Resonance BiomolecularCephalexinMolecular StructureChemistryarticlesolid stateNuclear magnetic resonance spectroscopycarbon nuclear magnetic resonanceBivalviaAnti-Bacterial AgentsspermatocyteSettore CHIM/03 - Chimica Generale E InorganicaMolluscaThermogravimetryMössbauercytotoxicitycefalexinorganometallic compoundChromosome breakagedrug synthesiTinMutagensJournal of Inorganic Biochemistry
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Jarosite and hematite at Meridiani Planum from Opportunity's Mossbauer Spectrometer.

2004

Mössbauer spectra measured by the Opportunity rover revealed four mineralogical components in Meridiani Planum at Eagle crater: jarosite- and hematite-rich outcrop, hematite-rich soil, olivine-bearing basaltic soil, and a pyroxene-bearing basaltic rock (Bounce rock). Spherules, interpreted to be concretions, are hematite-rich and dispersed throughout the outcrop. Hematitic soils both within and outside Eagle crater are dominated by spherules and their fragments. Olivine-bearing basaltic soil is present throughout the region. Bounce rock is probably an impact erratic. Because jarosite is a hydroxide sulfate mineral, its presence at Meridiani Planum is mineralogical evidence for aqueous proc…

Meridiani PlanumGeologic SedimentsExtraterrestrial EnvironmentOutcropMineralogyMagnesium CompoundsMarsengineering.materialFerric CompoundsSpectroscopy MossbauerImpact craterConcretionJarositeComposition of MarsSpacecraftMineralsMultidisciplinaryMineralSulfatesSilicatesWaterHematitevisual_artvisual_art.visual_art_mediumengineeringGeologyIron CompoundsScience (New York, N.Y.)
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Synthesis, characterization, crystal structures and in vitro antistaphylococcal activity of organotin(IV) derivatives with 5,7-disubstituted-1,2,4-tr…

2011

Abstract New organotin(IV) complexes of 5,7-ditertbutyl-1,2,4-triazolo[1,5-a]pyrimidine ( dbtp ) and 5,7-diphenyl-1,2,4-triazolo[1,5-a]pyrimidine ( dptp ) with 1:1 and/or 1:2 stoichiometry were synthesized and investigated by X-ray diffraction, FT-IR and 119 Sn Mossbauer in the solid state and by 1 H and 13 C NMR spectroscopy, in solution. Moreover, the crystal and molecular structures of Et 2 SnCl 2 (dbtp) 2 and Ph 2 SnCl 2 (EtOH) 2 (dptp) 2 are reported. The complexes contain hexacoordinated tin atoms: in Et 2 SnCl 2 (dbtp) 2 two 5,7-ditertbutyl-1,2,4-triazolo[1,5-a]pyrimidine molecules coordinate classically the tin atom through N(3) atom and the coordination around the tin atom shows a …

Methicillin-Resistant Staphylococcus aureusTRIAZOLOPYRIMIDINE ORGANOTIN(IV)Staphylococcus aureusMagnetic Resonance SpectroscopyPyrimidineStereochemistrychemistry.chemical_elementOrganotin(IV)Crystal structureBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundSpectroscopy MossbauerX-Ray DiffractionMössbauer spectroscopySpectroscopy Fourier Transform InfraredEscherichia coliOrganotin CompoundsMoleculeANTIMICROBIAL ACTIVITYTriazolopyrimidine; Organotin(IV); X-ray-structure; 119Sn Mössbauer; Antimicrobial activityCarbon-13 NMRTriazolesAnti-Bacterial AgentsTrigonal bipyramidal molecular geometryPyrimidineschemistryOctahedronSettore CHIM/03 - Chimica Generale E InorganicaPseudomonas aeruginosaTriazolopyrimidine119SN MÖSSBAUERTinX-RAY-STRUCTUREJournal of inorganic biochemistry
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Characterization of diorganotin(IV) complexes with captopril. The first crystallographically authenticated metal complex of this anti-hypertensive ag…

2003

Abstract Diorganotin(IV) complexes R 2 Sn(cap) (capH 2 = N -[( S )-3-mercapto-2-methylpropionyl]- l -proline; R=Me, Et, n -Bu and t -Bu) were prepared and characterised. The FTIR and Raman spectra demonstrated that the organotin(IV) moieties interact with the {S} atom of the ligand, while the other coordination sites are the carboxylate and the amide –CO groups. Mossbauer Δ data showed that the diorganotin(IV) compounds adopt slightly distorted trigonal-bipyramidal (tbp) geometry. A single-crystal X-ray study was performed on the compound Me 2 Sn(cap): the Sn atom is five-coordinated in a distorted tbp environment, with two {O} atoms in the axial positions and the {S} and two {C} atoms in t…

Models MolecularCaptoprilMagnetic Resonance SpectroscopyCrystallography X-RaySpectrum Analysis RamanBiochemistryInorganic ChemistryMetalSpectroscopy Mossbauerchemistry.chemical_compoundsymbols.namesakeAmideSpectroscopy Fourier Transform InfraredMössbauer spectroscopyAtomOrganotin CompoundsCarboxylateFourier transform infrared spectroscopyAntihypertensive AgentsLigandCrystallographychemistryvisual_artsymbolsvisual_art.visual_art_mediumRaman spectroscopyJournal of Inorganic Biochemistry
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Spin crossover of ferric complexes with catecholate derivatives. Single-crystal X-ray structure, magnetic and Mössbauer investigations.

2005

Complexes of general formula [(TPA)Fe(R-Cat)]X·nS were synthesised with different catecholate derivatives and anions (TPA = tris(2-pyridylmethyl)amine, R-Cat2− = 4,5-(NO2)2-Cat2− denoted DNC2−; 3,4,5,6-Cl4-Cat2− denoted TCC2−; 3-OMe-Cat2−; 4-Me-Cat2− and X = BPh4−; NO3−; PF6−; ClO4−; S = solvent molecule). Their magnetic behaviours in the solid state show a general feature along the series, viz., the occurrence of a thermally-induced spin crossover process. The transition curves are continuous with transition temperatures ranging from ca. 84 to 257 K. The crystal structures of [(TPA)Fe(DNC)]X (X = PF6−; BPh4−) and [(TPA)Fe(TCC)]X·nS (X = PF6−; NO3− and n = 1, S = H2O; ClO4− and n = 1, S = H…

Models MolecularChemistryStereochemistryCatecholsTemperatureSpace groupWaterCrystal structureElectronCrystallography X-RayLigandsFerric CompoundsInorganic ChemistryCrystallographyMagneticsSpectroscopy MossbauerSpin crossoverMössbauer spectroscopymedicineFerricSpin (physics)Single crystalmedicine.drugDalton transactions (Cambridge, England : 2003)
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Structural and magnetic investigations of the mixed-valence Fe(II,III) two-dimensional layer complex, [Fe2(II) Fe2(III)(HCOO)10(C6H7N)6]n.

2004

The structure of the complex, [Fe2(II)Fe2(III)(HCOO)10(C6H7N6)n, (1) exhibits a neutral two-dimensional layer network of alternating iron(II) and iron(III) ions, bridged equatorially by formate groups. All iron atoms are octahedrally coordinated, with iron(III) coordinating axially to one gamma-picoline and one formate group, while the iron(II) centers interact axially with two gamma-picoline groups, above and below the layer plane. The complex crystallizes in the triclinic space group P1 at all studied temperatures [at 120 K, the cell dimensions are: a = 10.228(1), b = 12.071(1), c = 12.072(1) A, alpha = 89.801(2), beta = 71.149(2), gamma = 73.371(2) degrees]. An intralayer antiferromagnet…

Models MolecularValence (chemistry)ChemistryStereochemistryExchange interactionTemperatureCrystal structureTriclinic crystal systemCrystallography X-RayMagnetic susceptibilityFerric CompoundsAtomic and Molecular Physics and OpticsCrystallographyMagneticsSpectroscopy MossbauerMössbauer spectroscopyOrganometallic CompoundsAntiferromagnetismMoleculeFerrous CompoundsPhysical and Theoretical ChemistryChemphyschem : a European journal of chemical physics and physical chemistry
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