Search results for "cobalt."

showing 10 items of 969 documents

Differential study of substituted and unsubstituted cobalt phthalocyanines for gas sensor applications

2011

Abstract The conductivity of CoPc (cobalt phthalocyanine) and Co[(SO3Na)2,3Pc] was measured under a flow of two different gases (NH3 and O3), during exposure/recovery cycles. It appears that the relative responses are linearly related to the concentration, in the 20–200 ppb range for O3 and in the 20–200 ppm range for NH3. Observed during time, the sensing parameters allow a qualitative understanding of the kinetics. The comparative study of those products under both different gases gave interesting results for sensor applications. Whereas CoPc is sensitive to both gases, its sulfonated counterpart is only sensitive to NH3.

Range (particle radiation)OzoneKineticsInorganic chemistryMetals and AlloysCobalt phthalocyaninechemistry.chemical_elementConductivityCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundAmmoniachemistryMaterials ChemistryElectrical and Electronic EngineeringMolecular materialsInstrumentationCobaltSensors and Actuators B: Chemical
researchProduct

Evidence for H2S gas as an intermediate species in the reaction mechanism of trapping hydrogen by cobalt disulfide

2011

Cobalt sulfide prepared by aqueous precipitation using Na2S and a Co(II) salt is known to trap hydrogen at room temperature and low pressure. The importance of oxidation of the primary CoS precipitate with atmospheric oxygen with respect to its efficiency as a hydrogen absorber is demonstrated. This stage of oxidation produces a mixture of two solid phases: a partially crystallized cobalt hydroxide Co(OH)2 and an amorphous cobalt sulfide CoS2 with a Co(OH)2/CoS2 molar ratio of 1 as predicted by thermodynamics. This biphasic product is probably the basic cobalt sulfide CoSOH considered in older and even more recent work. This product traps molecular hydrogen with a H2/Co molar ratio of 0.5 w…

Reaction mechanismAqueous solutionHydrogenCobalt hydroxideRenewable Energy Sustainability and the EnvironmentChemistryHydrogen sulfideInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementCondensed Matter PhysicsCobalt sulfidechemistry.chemical_compoundFuel TechnologyCobaltStoichiometryInternational Journal of Hydrogen Energy
researchProduct

Über eine neue Methode zum Nachweis des als Primärprodukt der Autoxydation der Metalle Eisen, Nickel und Kobalt in Säure- und Salzlösungen gebildeten…

1971

H2O2 als Zwischenprodukt der Autoxydation (bzw. · OOH oder · OH) kann mit Hilfe der Phosphin-, Phosphinoxid- Methode bei Fe, Ni und Co wirksamer als mit Hilfe der Jodometrie erfast werden. In saurem Medium sind Tris-(m-aminophenyl)-phosphin (1), im alkalischen Bereich Tris-(p-carboxyphenyl)- phosphin (2) wirksame auch fur quantitative Bestimmungen geeignete Reagentien auf H2O2 · 1 und 2 reagieren bei hoheren Konzentrationen bis zu 20 ma1 schneller mit H2O2 als dieses mit der Eisengrenzflache. Ni und Co erzeugen mehr H2O2 als Fe. Bei Eisen entsteht im neutralen Medium mehr H2O2 als im sauren Bereich. Die unterschiedlichen Anfangsgeschwindigkeiten des Sauerstoffverbrauchs in sauerstoffhaltige…

Reaction mechanismAutoxidationMechanical EngineeringMetals and Alloyschemistry.chemical_elementSulfuric acidGeneral MedicineSurfaces Coatings and Filmschemistry.chemical_compoundNickelIodometrychemistryMechanics of MaterialsReagentMaterials ChemistryEnvironmental ChemistryHydrogen peroxideCobaltNuclear chemistryMaterials and Corrosion
researchProduct

Inhibition of VEGF expression through blockade of Hif1a and STAT3 signalling mediates the anti-angiogenic effect of melatonin in HepG2 liver cancer c…

2013

Background: Hepatocellular carcinoma (HCC) growth relies on angiogenesis via vascular endothelial growth factor (VEGF) release. Hypoxia within tumour environment leads to intracellular stabilisation of hypoxia inducible factor 1 alpha (Hif1α) and signal transducer and activator of transcription (STAT3). Melatonin induces apoptosis in HCC, and shows anti-angiogenic features in several tumours. In this study, we used human HepG2 liver cancer cells as an in vitro model to investigate the anti-angiogenic effects of melatonin. Methods: HepG2 cells were treated with melatonin under normoxic or CoCl2-induced hypoxia. Gene expression was analysed by RT–qPCR and western blot. Melatonin-induced anti-…

STAT3 Transcription FactorTranscriptional ActivationVascular Endothelial Growth Factor ACancer ResearchCarcinoma HepatocellularTranscription GeneticAngiogenesisAngiogenesis InhibitorsApoptosismelatoninP300-CBP Transcription FactorsHif1αBiologyMelatoninSTAT3chemistry.chemical_compoundHypoxia-Inducible Factor 1-AlphamedicineHuman Umbilical Vein Endothelial CellsHumansp300-CBP Transcription FactorsSTAT3Promoter Regions GeneticTube formationNeovascularization PathologicLiver NeoplasmsCobaltHep G2 Cellshepatocellular carcinomaHypoxia-Inducible Factor 1 alpha SubunitVEGFCell Hypoxiadigestive system diseasesCyclic S-OxidesVascular endothelial growth factorGene Expression Regulation NeoplasticVascular endothelial growth factor AOncologychemistryCancer researchbiology.proteinTranslational Therapeuticsmedicine.drugSignal Transduction
researchProduct

miR-20b modulates VEGF expression by targeting HIF-1 alpha and STAT3 in MCF-7 breast cancer cells.

2010

MicroRNAs (miRNAs) are small non-coding RNAs that regulate the expression of different genes, including genes involved in cancer progression. A functional link between hypoxia, a key feature of the tumor microenvironment, and miRNA expression has been documented. We investigated whether and how miR-20b can regulate the expression of vascular endothelial growth factor (VEGF) in MCF-7 breast cancer cells under normoxic and hypoxia-mimicking conditions (CoCl(2) exposure). Using immunoblotting, ELISA, and quantitative real-time PCR, we demonstrated that miR-20b decreased VEGF protein levels at 4 and 24 h following CoCl(2) treatment, and VEGF mRNA at 4 h of treatment. In addition, miR-20b reduce…

STAT3 Transcription FactorVascular Endothelial Growth Factor ATime FactorsPhysiologySettore MED/06 - Oncologia MedicaClinical BiochemistryDown-RegulationBreast NeoplasmsBiologyTransfectionchemistry.chemical_compoundmir20b VEGFCell Line TumormicroRNAHumansSTAT3Promoter Regions GeneticG alpha subunitRegulation of gene expressionTumor microenvironmentBinding SitesCell BiologyTransfectionCobaltHypoxia-Inducible Factor 1 alpha SubunitMolecular biologyCell HypoxiaVascular endothelial growth factorGene Expression Regulation NeoplasticMicroRNAsHIF1Achemistrybiology.proteinFemaleRNA InterferenceSignal TransductionJournal of cellular physiology
researchProduct

Synthesis and characterization of a novel dicyanamide-bridged Co(II) 1-D coordination polymer with a N 4 -donor Schiff base ligand

2017

The synthesis, structure and magnetic properties of a novel Co(II) 1D coordination polymer, [Co(L)(µ1,5-dca)(ClO4)2·MeOH]n (1) are described. Compound 1 contains two independent cationic Co(II) chains (CoA and CoB) which are parallel to the c direction and present short π-π and C-H⋯π interactions with two neighbouring chains along the b direction, giving rise to alternating layers of chains A and B in the bc plane. Variable-temperature magnetic susceptibility measurements shows a weak antiferromagnetic coupling among the adjacent cobalt(II) centres mediated through μ1,5-dca− bridge.

Schiff base010405 organic chemistryChemistryStereochemistryLigandCoordination polymerCationic polymerizationchemistry.chemical_element010402 general chemistry01 natural sciencesMagnetic susceptibilityAntiferromagnetic coupling0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundMaterials ChemistryPhysical and Theoretical ChemistryCobaltDicyanamideInorganica Chimica Acta
researchProduct

X-ray crystal structures of copper(II) and cobalt(II) complexes with Schiff base ligands. Reactivity towards dioxygen

2003

Copper(II) and cobalt(II) Schiff base complexes with derivatives of the pentadentate ligand bis(salicylideneimino-3-propyl)amine [H2salDPT] have been prepared. The X-ray crystal structures of the copper(II) complexes Cu[salDPT] and Cu[sal(n-propyltrimethylsilyl)DPT] were determined and revealed five-coordination at the metal centre in both cases. The 1 ∶ 1 dioxygen adduct of Co[sal(n-propyltrimethylsilyl)DPT] was also isolated and its X-ray molecular structure determined.

Schiff base010405 organic chemistryLigandInorganic chemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesCopper3. Good health0104 chemical sciencesAdductInorganic ChemistryMetalchemistry.chemical_compoundchemistryvisual_artPolymer chemistryvisual_art.visual_art_medium[CHIM.CRIS]Chemical Sciences/Cristallography[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Reactivity (chemistry)CobaltMOLECULAR-STRUCTURE
researchProduct

2-Amino-2-methyl-1,3-propanediol (ampdH2) as ligand backbone for the synthesis of cobalt complexes: Mononuclear Co(II), binuclear Co(II,III) and hexa…

2013

Abstract Three cobalt complexes have been synthesized using 2-amino-2-methyl-1,3-propanediol (ampdH2) and its Schiff base derivative ligands and structurally characterized. The three complexes 1, 2 and 3 are very different and consist of mononuclear Co(II), mixed-valence binuclear Co(II,III) and mixed-valence hexanuclear Co(II,III) complexes respectively. The properties of the coordinated donor atoms of the ligand play the predominant role in stabilizing the oxidation states of the cobalt centers. The presence of intermolecular hydrogen bonds in 1 via non-coordinating perchlorate ions lead to the formation of a 1D-Chain network while a sheet-like 2D network was observed in 3.

Schiff baseHydrogen bondLigandStereochemistryIntermolecular forcechemistry.chemical_elementInorganic ChemistryPerchloratechemistry.chemical_compoundchemistryPolymer chemistryX-ray crystallographyMaterials ChemistryPhysical and Theoretical ChemistryCobaltDerivative (chemistry)Polyhedron
researchProduct

Observation of novel oxygen⋯oxygen interaction in supramolecular assembly of cobalt(III) Schiff base complexes: a combined experimental and computati…

2015

Two mononuclear cobalt(III) Schiff base complexes with azide [Co(L)(N3)(L0 )] (1) and [Co(L)(N3)(L00)] (2) {where HL ¼ 1-((2-(diethylamino)ethylimino)methyl)naphthalene-2-ol, HL0 ¼ 2-hydroxy-1-naphthaldehyde and HL00 ¼ acetylacetone} have been synthesized and characterized by elemental analysis, IR and UV-Vis spectroscopy and single crystal X-ray diffraction studies. Both complexes show mononuclear structures with azide as terminal coligand. Structural features have been examined in detail that reveal the formation of interesting supramolecular networks generated through non-covalent forces including hydrogen bonding, C–H/H–C and C–H/p interactions. These interactions have been studied ener…

Schiff basekemianovel oxygenStereochemistryHydrogen bondGeneral Chemical EngineeringAcetylacetoneSupramolecular chemistrychemistry.chemical_elementGeneral ChemistrychemistrycobaltSupramolecular assemblychemistry.chemical_compoundCrystallographychemistryAzidekobolttiCobaltta116Natural bond orbitalRSC Advances: an international journal to further the chemical sciences
researchProduct

Controllo della sintesi e caratterizzazione di nanocompositi di oro e cobalto.

2012

Settore CHIM/03 - Chimica Generale E Inorganicananocompositioro e cobalto.controllo della sintesi
researchProduct