Search results for "SSB"

showing 10 items of 537 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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Mossbauer spectroscopic studies on the molecular dynamics of organotin(IV) polymers

1981

Abstract Linear organotin(IV) polymers with tin appended to the polymer chain or inserted into the polymer backbone have been characterized by Mossbauer spectroscopy. The lattice dynamics of three representative examples of these classes, as well as of a cross-linked organotin(IV) polymer, have been investigated by temperature-dependent Mossbauer spectroscopy. It has been shown that parameters associated with polymers having low interchain interactions practically correspond to those of molecular, non-coupled, solids.

Lattice dynamicschemistry.chemical_classificationOrganic ChemistryInorganic chemistrychemistry.chemical_elementPolymerBiochemistryInorganic ChemistryMolecular dynamicschemistryMössbauer spectroscopyMaterials ChemistryPhysical chemistryPhysical and Theoretical ChemistryTinJournal of Organometallic Chemistry
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Nonheme Fe(IV) Oxo Complexes of Two New Pentadentate Ligands and Their Hydrogen-Atom and Oxygen-Atom Transfer Reactions.

2015

Two new pentadentate {N5} donor ligands based on the N4Py (N4Py = N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine) framework have been synthesized, viz. [N-(1-methyl-2-benzimidazolyl)methyl-N-(2-pyridyl)methyl-N-(bis-2-pyridyl methyl)amine] (L1) and [N-bis(1-methyl-2-benzimidazolyl)methyl-N-(bis-2-pyridylmethyl)amine] (L2), where one or two pyridyl arms of N4Py have been replaced by corresponding (N-methyl)benzimidazolyl-containing arms. The complexes [FeII(CH3CN)(L)]2+ (L = L1 (1); L2 (2)) were synthesized, and reaction of these ferrous complexes with iodosylbenzene led to the formation of the ferryl complexes [FeIV(O)(L)]2+ (L = L1 (3); L2 (4)), which were characterized by UV–vis spe…

Ligand field theoryModels MolecularStereochemistryPyridinesIronMolecular ConformationSulfidesIron compoundsLigandsMedicinal chemistryRedoxReaccions químiquesInorganic Chemistrychemistry.chemical_compoundChemical reactionsMössbauer spectroscopyElectrochemistryOrganometallic Compoundspentadentate ligandsPhysical and Theoretical ChemistrySpectroscopyta116LigandChemistryMethylamineFerro -- CompostosHydrogen atomOxygeniron complexesAmine gas treatingOxidation-ReductionHydrogenInorganic chemistry
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Advances in Mössbauer Emission Spectroscopy

1990

After effects following nuclear transformation have been extensively studied in a large variety of matrices by Mossbauer Emission Spectroscopy (MES). The branching ratios of transient atomic charge states and energetically unstable states of the environment, excitations of electronic ligand field states and populations out of equilibrium within the electronic ground state manifold have been studied. Recent developments and also new insights and understandings of different aspects of the aftereffects of radioactive decay of57Co in semiconductors and molecular crystals are reviewed. A detailed picture of the decay process within the electronic states of the nucleogenic Fe3+ species could be o…

Ligand field theoryNuclear and High Energy PhysicsAuger electron spectroscopyPhononChemistryCondensed Matter PhysicsAtomic and Molecular Physics and OpticsNucleogenicMössbauer spectroscopyEmission spectrumPhysical and Theoretical ChemistryAtomic physicsGround stateRadioactive decayHyperfine Interactions
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Spin crossover in hexakis(1-(2-chloroethyl)-tetrazole)iron(II) complexes; synthesis and magnetic properties

2002

Abstract The spin-crossover complexes [Fe(teec)6](X)2 (with teec=1-(2-chloroethyl)-tetrazole and X=BF4, ClO4, PF6) possess two iron(II) sites each having a different spin-crossover behaviour. The magnetic behaviour of the complexes obtained by slow crystallisation differs strongly from those obtained by precipitation. This difference results in either a spin crossover of 50% (X=ClO4, crystalline), two gradual steps (X=BF4, PF6), or two steps, of which one is gradual and the other having a thermal hysteresis (X=ClO4 precipitated). Both 57Fe Mossbauer spectroscopy and magnetic susceptibility measurements have been recorded as a function of T. The crystal structure of [Fe(teec)6](BF4)2 has bee…

Ligand field theorySpin transitionCrystal structureMagnetic susceptibilitylaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySpin crossoverlawMössbauer spectroscopyMaterials ChemistryTetrazolePhysical and Theoretical ChemistryCrystallizationInorganica Chimica Acta
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Studies on adducts of organotin(IV) halides with bis(acetylacetone)ethylenediimine

1971

The solid state configuration of 1/1 adducts, formed by mono-, di- and tri-organotin(IV) halides with the potentially tetradentate ligand bis(acetylacetone)ethylenediimine, has been investigated. The infrared spectra suggest that the neutral ligand coordinates SnIV through N (or O) atoms of the H-bonded acetylacetoneimine moieties. The skeletal vibrations associated to Sn-C and Sn-Cl bonds are consistent with square planar configurations of the organotin(IV) halide moieties, where SnCl3 and C3Sn groups would be T-shaped, and Alk2SnCl2 would have trans-dialkyl, trans-dichloro arrangements. The latter configuration is supported by the magnitude of the quadrupole splittings. Measurements of th…

LigandAcetylacetoneOrganic ChemistryInorganic chemistrychemistry.chemical_elementInfrared spectroscopyHalideBiochemistryAdductInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOctahedronMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinJournal of Organometallic Chemistry
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Re-visiting of 5-[(E)-2-(aryl)-1-diazenyl]-quinolin-8-ol with tweaking of Sn–Ph groups: Synthesis, spectroscopic characterization and X-ray crystallo…

2008

Abstract Reactions of sodium 5-[(E)-2-(aryl)-1-diazenyl]quinolin-8-olates (LH, where the aryl group is an R-substituted phenyl ring such that for L1H: R = H; L2H: R = 2′-CH3; L3H: R = 3′-CH3; L4H: R = 4′-CH3; L5H: R = 4′-OCH3 and L6H: R = 4′-OC2H5) with Ph3SnCl in a 1:1 molar ratio yielded complexes of composition Ph3SnL. The complexes have been characterized by 1H, 13C, 119Sn NMR, IR and 119mSn Mossbauer spectroscopic techniques in combination with elemental analyses. The crystal structures of Ph3SnL1 · 0.5C6H6 (1), Ph3SnL2 (2), Ph3SnL5 · C6H6 (5) and Ph3SnL6 · 0.5C6H6 (6) were determined. The results of the X-ray studies indicated that the benzene solvated compounds 1, 5 and 6 are distort…

LigandArylOrganic ChemistryCrystal structureRing (chemistry)BiochemistryInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySquare pyramidX-ray crystallographyMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryBenzeneJournal of Organometallic Chemistry
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Synthesis, characterization and crystal structures of polymeric and dimeric triphenyltin(IV) complexes of 4-[((E)-1-{2-hydroxy-5-[(E)-2-(2-carboxyphe…

2005

Abstract The triphenyltin(IV) complexes of 4-[((E)-1-{2-hydroxy-5-[(E)-2-(2-carboxyphenyl)-1-diazenyl]phenyl}methylidene)amino]aryls (aryls = 4-CH3, 4-Br, 4-Cl, 4-OCH3) have been synthesized and characterized by 1H-, 13C-, 119Sn-NMR, ESI mass spectrometry, IR and 119mSn Mossbauer spectroscopic techniques in combination with elemental analysis. The crystal structures of a representative carboxylate ligand (aryl = 4-CH3) and three Sn complexes, viz., polymeric (Ph3Sn[O2CC6H4{N N(C6H3-4-OH(C(H) NC6H4X-4))}-o])n (X = Me (1) and Br (2)) and dimeric (Ph3Sn[O2CC6H4{N N(C6H3-4-OH(C(H) NC6H4X-4))}-o])2 (X = OMe (4)) complexes are reported. The coordination environment in each complex is trigonal bip…

LigandChemistryStereochemistryElectrospray ionizationOrganic ChemistryESI mass spectrometryCrystal structureBiochemistryMedicinal chemistryInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundMössbauer spectroscopyMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Light-induced decarboxylation in a photo-responsive iron-containing complex based on polyoxometalate and oxalato ligands.

2016

A new iron-oxalato polyoxometalate exhibits a remarkable photocoloration effect in the solid state based entirely on an intramolecular process.

LigandDecarboxylation02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesOxalate0104 chemical scienceschemistry.chemical_compoundElectron transferChemistrychemistryIntramolecular forceMössbauer spectroscopyPolyoxometalate0210 nano-technologyDerivative (chemistry)Chemical science
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