Search results for "Chlorides"

showing 10 items of 86 documents

Analytical and mineralogical studies of ore and impurities from a chromite mineral using X-ray analysis, electrochemical and microscopy techniques

2007

A wide analytical study of South African chromite ore, material with high interest in ceramic industry, has been carried out. With this purpose, an accurate chemical identification and mineralogical characterization of the mineral and the gangue have been performed using X-ray fluorescence (XRF), voltammetry, X-ray diffraction (XRD), light microscopy (LM), and scanning electron microscopy (SEM/EDX). The elemental composition of the sample (ore and gangue) has been obtained by XRF. The voltammetric analysis has allowed to demonstrate that iron in the sample was as Fe(II). The main compound of the chromite ore was a spinel (magnesiochromite ferroan), identified by XRD from the sample, which c…

MicroscopyMineralsMineralClinical Laboratory TechniquesSpinelMetallurgyAnalytical chemistryOxidesengineering.materialChemistry Techniques AnalyticalSilicateAnalytical ChemistrySouth Africachemistry.chemical_compoundChloridesX-Ray DiffractionchemistryImpurityElectrochemistryengineeringGangueChromiteChloriteLabradoriteTalanta
researchProduct

A synthetic molecular pentafoil knot

2011

Knots are being discovered with increasing frequency in both biological and synthetic macromolecules and have been fundamental topological targets for chemical synthesis for the past two decades. Here, we report on the synthesis of the most complex non-DNA molecular knot prepared to date: the self-assembly of five bis-aldehyde and five bis-amine building blocks about five metal cations and one chloride anion to form a 160-atom-loop molecular pentafoil knot (five crossing points). The structure and topology of the knot is established by NMR spectroscopy, mass spectrometry and X-ray crystallography, revealing a symmetrical closed-loop double helicate with the chloride anion held at the centre…

Models MolecularMagnetic Resonance SpectroscopyMacromolecular SubstancesPyridinesStereochemistryIronGeneral Chemical EngineeringCatenaneContext (language use)Crystallography X-RayLigandsChloridesMolecular knotAminesta116Topology (chemistry)Trefoil knotAldehydesMolecular StructurePolymer scienceHydrogen bondChemistryDNAGeneral ChemistryMechanically interlocked molecular architecturesIminesKnot (mathematics)Nature Chemistry
researchProduct

Synthesis of highly functionalized 9,10-phenanthrenequinones by oxidative coupling using MoCl5.

2012

The strong oxidative power of molybdenum pentachloride gives rise to an efficient oxidative C-C bond formation of benzil derivatives to the corresponding 9,10-phenanthrenequinones. A highly complementary method to previous approaches was developed. The required derivatives are accessible in a modular fashion and in excellent yields. By this approach the orchid-derived natural product cypripediquinone A was synthesized for the first time.

Models MolecularMolybdenumNatural productMolecular StructureOxidative CouplingOrganic ChemistryBond formationMolybdenum pentachloridePhenanthrenesPhotochemistryBiochemistryCombinatorial chemistrychemistry.chemical_compoundchemistryChloridesMoleculeOxidative coupling of methaneBenzilPhysical and Theoretical ChemistryOrganic letters
researchProduct

Novel Domino Oxidative Coupling: C−C Bond Formation Sequence to Highly Functionalized Dibenzo[a,c]cycloheptenes

2011

A domino sequence involving various MoCl(5)-mediated oxidations followed by trapping and supposed [3,3]-sigmatropic rearrangement provides a fast access to the full carbon skeleton of metasequirin-B. A variety of different moieties R(1) and R(2) are tolerated.

MolybdenumMolecular StructureOxidative CouplingChemistryStereochemistryOrganic ChemistryCarbon skeletonSequence (biology)DibenzocycloheptenesBond formationBiochemistryCatalysisLignansDominoChloridesCyclizationBenzene DerivativesOxidative coupling of methanePhysical and Theoretical ChemistryOxidation-ReductionOrganic Letters
researchProduct

Oxidative cyclization reaction of 2-aryl-substituted cinnamates to form phenanthrene carboxylates by using MoCl5.

2014

The oxidative cyclization reaction of 2-aryl cinnamates and derivatives thereof can be easily performed with MoCl5 as the oxidant. This powerful reagent allows oxidative coupling reactions for which other reagents fail. The best results are obtained when the 2-phenyl substituent of the cinnamate is equipped with two methoxy groups. Even iodo moieties in the bay region of phenanthrene are tolerated under the reaction conditions. If naphthalene moieties are involved, a rearrangement of the skeleton occurs, providing an elegant route to highly functionalized angular arenes. The cyclization is demonstrated for 15 example substrates with isolated yields of up to 99 % for the phenanthrene derivat…

MolybdenumOxidative cyclizationArylOrganic ChemistrySubstituentCarboxylic AcidsGeneral ChemistryPhenanthrenePhenanthrenesMedicinal chemistryCatalysischemistry.chemical_compoundchemistryChloridesCinnamatesCyclizationReagentCinnamatesOrganic chemistryOxidative coupling of methaneOxidation-ReductionNaphthaleneChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

The Recognition of Viologen Derivatives in Water by N-Alkyl Ammonium Resorcinarene Chlorides

2017

Three water-soluble N-alkyl ammonium resorcinarene chlorides decorated with terminal hydroxyl groups at the lower rims were synthesized and characterized. The receptors were decorated at the upper rim with either terminal hydroxyl, rigid cyclohexyl, or flexible benzyl groups. The binding affinities of these receptors toward three viologen derivatives, two of which possess an acetylmethyl group attached to one of the pyridine nitrogens, in water were investigated via 1H NMR spectroscopy, fluorescence spectroscopy, and isothermal titration calorimetry (ITC). ITC quantification of the binding process gave association constants of up to 103 M-1. Analyses reveal a spontaneous binding process whi…

N-alkyl ammonium resorcinarene chloridesviologen derivatives
researchProduct

Self-templated synthesis of novel carbon nanoarchitectures for efficient electrocatalysis

2016

AbstractThe cost-efficient large-scale production of novel carbon nanostructure with high performance is still a challenge, restricting their applications in catalysis. Herein, we present a low-cost one-pot and one-step approach for the synthesis of both N-doped graphene (NG) and N-doped carbon nanotubes (NCNTs) from self-templated organic nanoplates. By varying the FeCl3 concentration in the precursor, we can control the formation of graphene or CNTs. To the best of our knowledge, this is the first example for the controllable synthesis of graphene or CNTs by varying the precursors’ compositions. This provides a simple and cost-effective route for the large-scale production of both NG and …

NanostructureMaterials sciencechemistry.chemical_elementNanotechnology02 engineering and technologyCarbon nanotube010402 general chemistryElectrochemistryElectrocatalystFerric Compounds01 natural sciencesArticleCatalysislaw.inventionCatalysisChlorideslawElectrochemistryGraphiteMultidisciplinaryNanotubes CarbonGraphene021001 nanoscience & nanotechnology0104 chemical scienceschemistryGraphite0210 nano-technologyCarbonScientific Reports
researchProduct

Mechanism of Reaction of Melatonin with Human Myeloperoxidase

2001

Recently, it was suggested that melatonin (N-acetyl-5-methoxytryptamine) is oxidized by activated neutrophils in a reaction most probably involving myeloperoxidase (Biochem. Biophys. Res. Commun. (2000) 279, 657-662). Myeloperoxidase (MPO) is the most abundant protein of neutrophils and is involved in killing invading pathogens. To clarify if melatonin is a substrate of MPO, we investigated the oxidation of melatonin by its redox intermediates compounds I and II using transient-state spectral and kinetic measurements at 25 degrees C. Spectral and kinetic analysis revealed that both compound I and compound II oxidize melatonin via one-electron processes. The second-order rate constant measur…

NeutrophilsStereochemistryBiophysicsElectron donorIn Vitro TechniquesBiochemistryRedoxMedicinal chemistrySubstrate SpecificityElectron TransportSuperoxide dismutaseMelatoninchemistry.chemical_compoundReaction rate constantChloridesmedicineHumansMolecular BiologySodium cyanideMelatoninPeroxidasebiologyCyclohexanonesChemistryCell BiologyHydrogen-Ion ConcentrationKineticsSpectrophotometryMyeloperoxidasebiology.proteinFerricOxidation-Reductionmedicine.drugBiochemical and Biophysical Research Communications
researchProduct

Effect of pulp and paper mill effluent (BKME) on physiological parameters of roach (Rutilus rutilus) infected by the digenean Rhipidocotyle fennica.

2002

Physiological parameters were measured after experimental infection of roach (Rutilus rutilus L.) with Rhipidocotyle fennica Gibson, Valtonen et Taskinen, 1992 (Digenea) cercariae. The fish were caught from two lakes: a eutrophic bleached kraft mill effluent (BKME)-contaminated lake and an oligotrophic unpolluted lake. The intensity of infection was followed up to 10 days post infection (p.i.) and physiological parameters indicating non-specific stress responses and the condition of fish were examined simultaneously. The mean abundance, the number of parasites per fish, of R. fennica was significantly higher in the fish from the contaminated water during the first two days p.i., probably re…

PaperVeterinary medicineCyprinidaeIndustrial WasteTransferases (Other Substituted Phosphate Groups)Trematode InfectionsBiologyengineering.materialDigeneaHost-Parasite InteractionsFish DiseasesFish physiologyChloridesparasitic diseasesAnimalsEffluentAlkyl and Aryl Transferasesbusiness.industryEcologyPulp (paper)Paper millbiology.organism_classificationAlkaline PhosphataseRhipidocotyle fennicaHematocritengineeringParasitologyCalciumTrematodaRutilusEutrophicationbusinessWater Pollutants ChemicalFolia parasitologica
researchProduct

Effect of depolarizing GABAA-mediated membrane responses on excitability of Cajal-Retzius cells in the immature rat neocortex

2011

In immature neurons activation of ionotropic GABA receptors induces depolarizing membrane responses due to a high intracellular Cl− concentration ([Cl−]i). However, it is difficult to draw conclusions about the functional consequences of subthreshold GABAergic depolarizations, since GABAergic membrane shunting and additional effects on voltage-dependent ion channels or action potential threshold must be considered. To systematically investigate factors that determine the GABAergic effect on neuronal excitability we performed whole cell patch-clamp recordings from Cajal-Retzius cells in immature rat neocortex, using [Cl−]i between 10 and 50 mM. The effect of focal GABA application was quant…

Patch-Clamp TechniquesPhysiologyModels NeurologicalAction PotentialsDifferential ThresholdNeocortexMembrane PotentialsGABA AntagonistsChloridesInterneuronsmedicineAnimalsPatch clampGABAergic NeuronsRats WistarReceptorgamma-Aminobutyric AcidNeocortexGABAA receptorChemistryGeneral NeuroscienceReceptors GABA-ARatsPyridazinesRheobasemedicine.anatomical_structureAnimals NewbornIon Channel GatingNeuroscienceShunting inhibitionIntracellularIonotropic effectJournal of Neurophysiology
researchProduct