Search results for "cyanides"

showing 10 items of 30 documents

Determination of cyanide by a flow injection analysis-atomic absorption spectrometric method

1999

A new flow injection analysis (FIA) procedure is proposed for the indirect atomic absorption spectrometric determination of cyanide. The FIA manifold is based on the insertion of the sample into a distilled water carrier, then the sample flows through a solid-phase reactor filled with silver iodide entrapped in polymeric resin beads. The calibration graph is linear over the range 0.2-6.0 mg l-1 of cyanide (correlation coefficient 0.9974), the detection limit is 0.1 mg l-1, the sample throughput is 193 h-1 and the RSD is 0.8%. The method is simple, quick and more selective than other published FIA procedures. The reproducibility obtained by using different solid-phase reactors and solutions …

Flow injection analysisDetection limitCyanidesChromatographymedicine.diagnostic_testChemistryCalibration curveSpectrophotometry AtomicCyanideSilver iodideAnalytical chemistryBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundDistilled waterlawSpectrophotometryFlow Injection AnalysisElectrochemistrymedicineEnvironmental ChemistryAtomic absorption spectroscopySpectroscopyThe Analyst
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Cyanide binding and heme cavity conformational transitions in **Drosophila melanogaster** hexacoordinate hemoglobin

2006

The reason for the presence of hemoglobin-like molecules in insects, such as Drosophila melanogaster, that live in fully aerobic environments has yet to be determined. Heme endogenous hexacoordination (where HisE7 and HisF8 axial ligands to the heme Fe atom are both provided by the protein) is a recently discovered mechanism proposed to modulate O-2 affinity in hemoglobins from different species. Previous results have shown that D. melanogaster hemoglobin 1 (product of the glob1 gene) displays heme endogenous hexacoordination in both the ferrous and ferric states. Here we present kinetic data characterizing the exogenous cyanide ligand binding process, and the three-dimensional structure (a…

HemeproteinStereochemistryProtein ConformationCyanideMolecular Sequence DataNeuroglobinNerve Tissue ProteinsHemeCrystallography X-RayLigandsBiochemistrychemistry.chemical_compoundHemoglobinsMiceSequence Analysis ProteinMelanogasterAnimalsDrosophila ProteinsHumansCRYSTAL-STRUCTUREHistidineHemeBinding SitesCyanidesbiologyCytoglobinCytoglobinHexacoordinatebiology.organism_classificationGlobinsFERRIC APLYSIAKineticsDrosophila melanogasterchemistryHUMAN NEUROGLOBINAPLYSIA-LIMACINA MYOGLOBINX-RAYHemoglobinDrosophila melanogaster
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Action of metyrapone on the redox state of free nicotinamide-adenine dinucleotide and on oxygen consumption of perfused rat livers and isolated mitoc…

1971

Metyrapone [2-methyl-1,2-bis-(3-pyridyl)-1-propanone] in a concentration of 5 mM increased the lactate/pyruvate ratio and theΒ-hydroxybutyrate/ acetoacetate ratio in the perfusion fluid of the isolated rat liver by a factor of 6 indicating a considerable shift in the ratio of free [NAD]/[NADH] in both the cytoplasmic and the mitochondrial compartment. Oxygen uptake of the isolated liver was decreased to about one half. The onset of the inhibitory effect on the respiration of the isolated organ was immediate. The inhibition lasted for at least 1 h.

Malemedicine.medical_specialtychemistry.chemical_elementHydroxybutyratesMitochondria LiverNicotinamide adenine dinucleotideIn Vitro TechniquesOxygenRedoxAcetoacetatesElectron Transportchemistry.chemical_compoundHydroxybutyrate DehydrogenaseOxygen ConsumptionInternal medicineRespirationmedicineAnimalsPyruvatesPharmacologyMetyraponeChemistryGeneral MedicineCompartment (chemistry)MetyraponeNADRatsPerfusionKineticsEndocrinologyBiochemistryLiverCytoplasmSpectrophotometryDepression ChemicalLactatesNAD+ kinasemedicine.drugFerrocyanidesPolarographyNaunyn-Schmiedebergs Archiv fur Pharmakologie
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Magnetic and magneto-optical properties of nickel hexacyanoferrate/chromate thin films

2017

One of the most important challenges of modern science and technology is the quest for novel and tuneable materials, the properties of which can be widely controlled by chemical modifications or external stimuli. Simultaneously, an interest in the development of magnetic thin films also gains significant attention. In the current paper we bring together both these challenges and present a study of a new type of low-dimensional nickel hexacyanoferrate/chromate system. Thin films were obtained by the "layer by layer" deposition technique, where the ratio of Fe/Cr was controlled by the dipping sequence. The scope of this work is a comprehensive analysis of structural, spectroscopic and magneti…

Materials scienceCyanidesChromate conversion coatingGeneral Chemical EngineeringLayer by layerchemistry.chemical_elementNanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesNickelchemistryMagnetic propertiesDeposition (phase transition)Elements químicsThin film0210 nano-technologyMaterial propertiesScience technology and societyChemical compositionChemical modification
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Magneto-Optical Properties of Electrodeposited Thin Films of the Molecule-Based Magnet Cr5.5(CN)12·11.5H2O

2011

Prof. E. Coronado , M. Makarewicz , J. P. Prieto-Ruiz , Dr. H. Prima-Garcia , Dr. F. M. Romero Instituto de Ciencia Molecular (ICMol) Universitat de Valencia C/Catedratico Jose Beltran, 2, 46980-Paterna, Spain E-mail: eugenio.coronado@uv.es; helena.prima@uv.es; fmrm@uv.es

Materials scienceCyanidesMechanical EngineeringNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyMicroscopy Atomic Force01 natural sciencesElectroplating0104 chemical sciencesMagneto opticalMagneticsMechanics of MaterialsMagnetChromium CompoundsMoleculeGeneral Materials ScienceThin filmParticle Size0210 nano-technologyMolecule-based magnetsFerrocyanidesAdvanced Materials
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The Unique Versatility of the Double Metal Cyanide (DMC) Catalyst: Introducing Siloxane Segments to Polypropylene Oxide by Ring-Opening Copolymerizat…

2020

The combination of hydrophobic polydimethylsiloxane (PDMS) blocks with hydrophilic polyether segments plays a key role for silicone surfactants. Capitalizing on the double metal cyanide (DMC) catalyst, the direct (i.e., statistical) copolymerization of cyclic siloxanes and epoxides is shown to be feasible. The solvent-free one-pot copolymerization of hexamethylcyclotrisiloxane and propylene oxide results in the formation of gradient propylene oxide (PPO)-PDMS copolymers. Copolymers with up to 46% siloxane content with low dispersities (Ð < 1.2) are obtained in the molecular weight range of 2100-2900 g mol-1 . The polymerization kinetics are investigated by pressure monitoring and in situ 1 …

Materials sciencePolymers and PlasticsSiloxanesOxide02 engineering and technology010402 general chemistryPolypropylenes01 natural sciencesRing-opening polymerizationPolymerizationContact anglechemistry.chemical_compoundSiliconeMaterials ChemistryCopolymerPropylene oxideCyanidesPolydimethylsiloxaneOrganic ChemistryOxides021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringSiloxane0210 nano-technologyMacromolecular rapid communications
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Guest Effect on Nanopatterned Spin-Crossover Thin Films

2011

International audience; Nanopatterned thin films of the metal–organic framework {Fe(bpac)[Pt(CN)4]} (bpac=bis(4‐pyridyl)acetylene) are elaborated by the combination of a sequential assembly process and a lithographic method. Raman microspectroscopy is used to probe the temperature dependence of the spin state of the iron(II) ions in the films (40–90 nm in thickness), and reveals an incomplete but cooperative spin transition comparable to that of the bulk material. Adsorption/desorption of pyridine guest molecules is found to have a substantial influence on the spin‐crossover properties of the thin layers. This interplay between host–guest and spin‐crossover properties in thin films and nano…

Materials scienceSpin statesSpin transitionNanotechnology02 engineering and technologyMicroscopy Atomic ForceSpectrum Analysis Raman010402 general chemistry01 natural sciencesBiomaterialssymbols.namesakeSpin crossoverMetals HeavyDesorptionTransition TemperatureGeneral Materials ScienceThin film[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsCyanidesThin layersTransition temperatureGeneral Chemistry021001 nanoscience & nanotechnologyNanostructures0104 chemical sciencessymbolsPhysical chemistrySpin Labels0210 nano-technologyRaman spectroscopyBiotechnology
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Synthesis and antibacterial activity of iron-hexacyanocobaltate nanoparticles.

2018

This paper deals with the synthesis and characterization of iron-hexacyanocobaltate (FeHCC) and its antibacterial properties. The nanoparticles were prepared by a facile co-precipitation technique. Crystal structure, particle morphology, and elemental composition were determined using X-ray Powder Diffraction, X-ray fluorescence spectroscopy, Transmission Electron Microscopy (TEM), and Infrared Spectroscopy (IR). The antibacterial activity of the FeHCC nanoparticles was tested against Escherichia coli and Staphylococcus aureus as models for Gram-negative and Gram-positive bacteria, respectively, by bacterial counting method and microscopic visualization (TEM, FEG-SEM, and fluorescence micro…

Metal-hexacyanoferrateStaphylococcus aureusIronColony Count MicrobialInfrared spectroscopyNanoparticleMetal Nanoparticles02 engineering and technologyMicrobial Sensitivity TestsBacterial growth010402 general chemistrymedicine.disease_cause01 natural sciencesBiochemistryFluorescence spectroscopyInorganic ChemistryMicroscopy Electron TransmissionmedicineFluorescence microscopeEscherichia coliEscherichia coliCyanidesChemistryIron-hexacyanocobaltateCobalt021001 nanoscience & nanotechnology0104 chemical sciencesAnti-Bacterial AgentsSpectrometry FluorescenceStaphylococcus aureuMicroscopy Electron ScanningAntibacterial activity0210 nano-technologyAntibacterial activityReactive Oxygen SpeciesNuclear chemistryMacromoleculeJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
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Reaction between Indazole and Pd-Bound Isocyanides-A Theoretical Mechanistic Study

2018

The mechanism of the addition of indazole (Ind)&mdash

Models Molecular3003Activation of small moleculesIndazolesisocyanideIsocyanidePharmaceutical ScienceDFT calculationProtonation010402 general chemistryDFT calculationsactivation of small molecule01 natural sciencesMedicinal chemistryArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundDeprotonationNucleophilelcsh:Organic chemistryTheoreticalModelsDrug DiscoveryNitrilesPhysical and Theoretical ChemistryMechanical PhenomenaIndazoleNucleophilic additionCyanidesMolecular Structure010405 organic chemistrynitrileDrug Discovery3003 Pharmaceutical ScienceOrganic ChemistryRegioselectivityMolecularIsocyanidesModels TheoreticalTautomer0104 chemical sciencesnucleophilic additionchemistryChemistry (miscellaneous)Settore CHIM/03 - Chimica Generale E InorganicaMolecular Medicinereaction mechanismActivation of small molecules; DFT calculations; Isocyanides; Nitriles; Nucleophilic addition; Reaction mechanism; Cyanides; Indazoles; Models Molecular; Molecular Structure; Palladium; Mechanical Phenomena; Models Theoretical; Analytical Chemistry; Chemistry (miscellaneous); Molecular Medicine; 3003; Drug Discovery3003 Pharmaceutical Science; Physical and Theoretical Chemistry; Organic ChemistryPalladium
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A Germanium Isocyanide Complex Featuring (n -> π*) Back-Bonding and Its Conversion to a Hydride/Cyanide Product via C–H Bond Activation under Mild Co…

2012

Reaction of the diarylgermylene Ge(Ar(Me(6)))(2) [Ar(Me(6)) = C(6)H(3)-2,6-(C(6)H(2)-2,4,6-(CH(3))(3))(2)] with tert-butyl isocyanide gave the Lewis adduct species (Ar(Me(6)))(2)GeCNBu(t), in which the isocyanide ligand displays a decreased C-N stretching frequency consistent with an n → π* back-bonding interaction. Density functional theory confirmed that the HOMO is a Ge-C bonding combination between the lone pair of electrons on the germanium atom and the C-N π* orbital of the isocyanide ligand. The complex undergoes facile C-H bond activation to produce a new diarylgermanium hydride/cyanide species and isobutene via heterolytic cleavage of the N-Bu(t) bond.

Models MolecularC h bondCyanidesLigandHydrideGermaniumIsocyanideCyanidechemistry.chemical_elementGermaniumHydrogen BondingGeneral ChemistryPhotochemistryCrystallography X-RayBiochemistryMedicinal chemistryCatalysisAdductchemistry.chemical_compoundColloid and Surface ChemistrychemistryOrganometallic Compoundsta116Pi backbondingHydrogenJournal of the American Chemical Society
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