Search results for "Ferrous Compounds"

showing 7 items of 47 documents

Compensation of steric demand by cation–π interactions, cobaltocenium cations as guests in tetraurea calix[4]arene dimers

2003

The affinities of ferrocene (2) and the cobaltocenium cation (3+), which have roughly the same size and differ in their charge, towards the inner cavity of the dimeric capsule formed by tetraurea calix[4]arene (1) were studied in C2D4Cl2 solutions. While 3+, which occupies more than 75% of the internal volume of the dimer, is readily encapsulated this is not the case for 2. This is probably due to cation-pi interactions, which operate only between 3+ and the aromatic rings of the calix[4]arene dimer. We found that the affinity of the cobaltocenium cation is higher than that of the tropylium cation (4+) and is only 2-3 times less than that of the tetraethylammoniun cation (5+). From the vari…

Steric effectsMagnetic Resonance SpectroscopyMetallocenesTropylium cationStereochemistryDimerBiochemistryDiffusionchemistry.chemical_compoundPhenolsCationsCalixareneOrganometallic CompoundsUreaFerrous CompoundsPhysical and Theoretical ChemistryBenzeneOrganic ChemistryTetraethylammoniumHydrogen BondingAromaticityCobaltCrystallographychemistryFerroceneProton NMRCalixarenesDimerizationOrg. Biomol. Chem.
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Potential Application of Voltammetry of Microparticles for Dating Porcine Blood-based Binding Media used in Taiwanese Architectural Polychromies

2012

A method for dating Hemoglobine-containing archaeological samples using the voltammetry of microparticles is described. This is based on the record of the voltammetric response of such materials attached to paraffin-impregnated graphite electrodes in contact with aqueous acetate buffer. Signals attributable to the Fe(III)/Fe(II) iron couple and their catalytic enhancement in the presence of H(2)O(2) can be correlated, via first-order reaction kinetics, with the time of aging of the samples. The method has been applied to the study and dating of the polychromed architectural decoration of different parts of the architectural complex of the Longshan Temple in Lukang (18(th)  century, Taiwan).

Time FactorsAqueous solutionSwineChemistryOrganic ChemistryTaiwanAnalytical chemistryElectrochemical TechniquesHydrogen PeroxideGeneral ChemistryFerric CompoundsBiochemistryCatalysisGas Chromatography-Mass SpectrometryCatalysisHemoglobinsAnimalsGraphiteFerrous CompoundsElectrodesVoltammetryPorcine bloodGraphite electrodeNuclear chemistryChemistry - An Asian Journal
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Towards Iron(II) Complexes with Octahedral Geometry: Synthesis, Structure and Photophysical Properties

2020

The control of ligand-field splitting in iron (II) complexes is critical to slow down the metal-to-ligand charge transfer (MLCT)-excited states deactivation pathways. The gap between the metal-centered states is maximal when the coordination sphere of the complex approaches an ideal octahedral geometry. Two new iron(II) complexes (C1 and C2), prepared from pyridylNHC and pyridylquinoline type ligands, respectively, have a near-perfect octahedral coordination of the metal. The photophysics of the complexes have been further investigated by means of ultrafast spectroscopy and TD-DFT modeling. For C1, it is shown that&mdash

[CHIM.INOR] Chemical Sciences/Inorganic chemistryLigand field theoryCoordination sphereMaterials scienceIronPharmaceutical Scienceexcited states dynamics[CHIM.INOR]Chemical Sciences/Inorganic chemistryCrystallography X-RayLigands010402 general chemistry01 natural sciencesArticletime-resolved spectroscopyAnalytical Chemistrylcsh:QD241-441MetalX-Ray Diffractionlcsh:Organic chemistryDrug DiscoveryOctahedral molecular geometry[CHIM.CRIS]Chemical Sciences/Cristallographyiron (II) complexes[CHIM.COOR]Chemical Sciences/Coordination chemistryFerrous Compounds[CHIM.CRIS] Chemical Sciences/CristallographyPhysical and Theoretical Chemistryoctahedral geometrydensity functional theoryComputingMilieux_MISCELLANEOUSMolecular Structure010405 organic chemistryLigandOrganic Chemistry[CHIM.COOR] Chemical Sciences/Coordination chemistry0104 chemical sciences3. Good healthCrystallographyOctahedron[CHIM.OTHE] Chemical Sciences/OtherChemistry (miscellaneous)Excited statevisual_artvisual_art.visual_art_mediumThermodynamicsMolecular MedicineDensity functional theory[CHIM.OTHE]Chemical Sciences/Other
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The 2-oxoglutarate binding site of prolyl 4-hydroxylase. Identification of distinct subsites and evidence for 2-oxoglutarate decarboxylation in a lig…

1984

The structure and function of the 2-oxoglutarate binding site of prolyl 4-hydroxylase was studied by assaying the inhibitory potential of 24 selected aliphatic or aromatic compounds. All except one of them inhibited the enzyme competitively with respect to 2-oxoglutarate and noncompetitively with respect to Fe2+, the Ki values ranging from 0.8 microM to over 15 mM. The Ki values for the two most effective inhibitors, pyridine 2,5-dicarboxylate and 2,4-dicarboxylate, were about 0.8 microM and 2 microM, these compounds being the most potent inhibitors of prolyl 4-hydroxylase with respect to 2-oxoglutarate known so far. Only one of the compounds tested, 2-oxoadipinate, was able to support hydr…

chemistry.chemical_classificationCoordination sphereBinding SitesDecarboxylationStereochemistryIronProcollagen-Proline DioxygenaseChick EmbryoLigand (biochemistry)LigandsBiochemistryBinding CompetitiveDecarboxylationHydroxylationchemistry.chemical_compoundEnzymechemistryOxidoreductaseMoietyAnimalsKetoglutaric AcidsFerrous CompoundsBinding siteProtein BindingEuropean journal of biochemistry
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Expanding the 3d-4f heterometallic chemistry of the (py)2CO and pyCOpyCOpy ligands: structural, magnetic and Mössbauer spectroscopic studies of two F…

2011

Complex [Fe(II)Gd(III){pyCO(OEt)pyCOH(OEt)py}(3)](ClO(4))(2) (1) crystallizes in the Cc space group and contains one hexacoordinate ferrous ion and one enneacoordinate Gd(III) ion. Complex [Fe(2)(II)Gd(III){pyCO(OEt)py}(4)(NO(3))(H(2)O)][Gd(NO(3))(5)](0.5)(ClO(4)) (2) crystallizes in the C2/c space group and contains two hexacoordinate ferrous ions and one octacoordinate Gd(III) ion. Both complexes have been prepared by the metal-assisted ethanolysis of ligands di-2,6-(2-pyridylcarbonyl)pyridine (pyCOpyCOpy, dpcp) and di-2-pyridyl ketone ((py)(2)CO, dpk), which exhibit similar structures. Mössbauer spectroscopic studies of 2 revealed the presence of two quadrupole-split doublets of equal in…

chemistry.chemical_classificationModels MolecularKetoneChemistryStereochemistryPyridinesHexacoordinateGadoliniumCrystallography X-RayLigandsFerrousIonInorganic Chemistrychemistry.chemical_compoundCrystallographyMagneticsSpectroscopy MossbauerFerromagnetismPyridineMössbauer spectroscopyQuadrupoleFerrous CompoundsDalton transactions (Cambridge, England : 2003)
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A Mixed-Ligand Approach for Spin-Crossover Modulation in a Linear FeII Coordination Polymer

2014

In this work, we present a family of Fe(II) coordination polymers of general formula [Fe(btzx)(3-3x)(btix)(3x)](ClO4)2 with interesting spin-crossover properties. These coordination polymers have been synthesized using chemical mixtures of two different but closely related ligands, 1,4-bis(tetrazol-1-ylmethyl)benzene (btzx) and 1,4-bis(triazol-1-ylmethyl)benzene (btix), and the effect of a gradual substitution of the ligand in the spin transition temperature has been investigated. Several chemical mixtures have been structurally characterized by X-ray powder diffraction indicating a clear critical amount in the composition of the mixture after which mixed phases rather than a single phase c…

chemistry.chemical_classificationPolymersChemistryCoordination polymerLigandStereochemistrySpin transitionPolymerLigands3. Good healthInorganic ChemistryThermogravimetrychemistry.chemical_compoundCrystallographySpin crossoverThermogravimetryFerrous CompoundsPhysical and Theoretical ChemistryBenzenePowder DiffractionPowder diffractionInorganic Chemistry
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Cytotoxic effects of Jay Amin hydroxamic acid (JAHA), a ferrocene-based class I histone deacetylase inhibitor, on triple-negative MDA-MB231 breast ca…

2012

The histone deacetylase inhibitors (HDACis) are a class of chemically heterogeneous anticancer agents of which suberoylanilide hydroxamic acid (SAHA) is a prototypical member. SAHA derivatives may be obtained by three-dimensional manipulation of SAHA aryl cap, such as the incorporation of a ferrocene unit like that present in Jay Amin hydroxamic acid (JAHA) and homo-JAHA [ Spencer , et al. ( 2011 ) ACS Med. Chem. Lett. 2 , 358 - 362 ]. These metal-based SAHA analogues have been tested for their cytotoxic activity toward triple-negative MDA-MB231 breast cancer cells. The results obtained indicate that of the two compounds tested, only JAHA was prominently active on breast cancer cells with a…

medicine.drug_classCell SurvivalMetallocenesAntineoplastic AgentsApoptosisToxicologyHydroxamic AcidsStructure-Activity RelationshipIn vivoAnnexinmedicineTumor Cells CulturedCytotoxic T cellHumansFerrous CompoundsSettore BIO/06 - Anatomia Comparata E Citologiachemistry.chemical_classificationMembrane Potential MitochondrialReactive oxygen speciesDose-Response Relationship DrugMolecular StructureChemistryHistone deacetylase inhibitorCell CycleGeneral MedicineIn vitroHistone Deacetylase InhibitorsBiochemistryhistone deacetylase inhibitor breast cancer autophagy apoptosis mitochondria cell cycleApoptosisCancer researchHistone deacetylaseDrug Screening Assays AntitumorReactive Oxygen Species
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