Search results for "Metallic"

showing 10 items of 813 documents

Selective opening of nanoscopic capped mesoporous inorganic materials with nerve agent simulants; an application to design chromo-fluorogenic probes.

2011

A hybrid nanoscopic capped mesoporous material, that is selectively opened in the presence of nerve agent simulants, has been prepared and used as a probe for the chromo-fluorogenic detection of these chemicals. © 2011 The Royal Society of Chemistry.

INGENIERIA DE LA CONSTRUCCIONMaterials scienceSilicon dioxideSomanNanotechnologyCatalysisArticleMolecular hybridizationchemistry.chemical_compoundQUIMICA ORGANICAMCM-41QUIMICA ANALITICAMaterials ChemistrymedicineOrganometallic CompoundsNanotechnologyChemical Warfare AgentsNanoscopic scaleTabunGroup 2 organometallic chemistryNerve agentFluorescent DyesSelective openingChemical warfare agentQUIMICA INORGANICAMetals and AlloysHydrogen BondingGeneral ChemistrySilicon DioxideSarinMcm 41Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesDrug determinationInorganic materialsColorimetryMesoporous materialControlled studyPorositymedicine.drugChemical communications (Cambridge, England)
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Metal complexes of anxiolitic drugs. X-Ray crystal structure and electronic properties of aquobromazepam(oxalato O1 O2) copper(II)

1987

The crystal structure of the title compound has been determined from single-crystal x-ray diffraction data. The copper(II) ion is surrounded by two nitrogen atoms of the bromazepam** molecule [N(imine) and N(pyridine)], and two oxygen atoms of the oxalate ion in a square planar arrangement. One molecule of water is linked to the copper(II) ion in the axial position. The complex has been also characterized by electronic, e.s.r. and i.r. spectra.

ImineMetals and Alloyschemistry.chemical_elementCrystal structureComputer Science::Computational GeometryCopperOxalateIonInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPyridineMaterials ChemistryMoleculeOrganometallic chemistryTransition Metal Chemistry
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Production of specific antibodies and development of a non-isotopic immunoassay for carbamazepine by the carbonyl metallo-immunoassay (CMIA) method.

1995

Abstract As part of our ongoing work to extend the range of applications of the non-isotopic carbonyl metalloimmunoassay (CMIA), previously developed in our laboratory, we describe here the first CMIA study of carbamazepine. The CMIA method uses a metal carbonyl complex as a non-isotopic tracer, and in this case we chose to employ the dicobalt hexacarbonyl moiety (Co2(CO)6) attached to an alkyne. Two organometallic tracers, 3 and 7 , were synthesized, differentiated by the nature and length of the spacer arm of the Co2(CO)6 moiety. Two different coupling methods were subsequently used to synthesize the immunogens 1 and 2, the first one used a carbodiimide, while the second, employed dimethy…

ImmunologyAlkyneCross ReactionsBinding Competitivechemistry.chemical_compoundDimethyl AdipimidateAntibody SpecificityDibenzazepinesSpectroscopy Fourier Transform InfraredmedicineOrganometallic CompoundsImmunology and AllergyMoietyAnimalsCarbodiimidechemistry.chemical_classificationAntiserumImmunoassayChromatographymedicine.diagnostic_testCobaltTiterCarbamazepinechemistryDimethyl AdipimidateDicyclohexylcarbodiimideImmunoassayAnticonvulsantsImmunizationRabbitsQuantitative analysis (chemistry)HaptensJournal of immunological methods
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Novel mixed-valence Cu compounds formed by Cu(II) dimers with double oximato bridges: in situ formation of anionic layer [Cu2(SCN)3]n(n-).

2013

Two new N3O donor ketoxime Schiff bases (HL(1) and HL(2)) have been synthesized by condensing N,N-dimethylethylenediamine with diacetylmonoxime and benzilmonoxime, respectively in a 1:1 ratio. Reaction of Cu(ClO4)2·6H2O with HL(1) resulted in a discrete oximato-bridged dinuclear Cu(II) complex [Cu2(L(1))2(H2O)2](ClO4)2 (1). The same reaction in presence of NaSCN affords the complex {[Cu(II)2(L(1))2][Cu(I)4(μ(1,3)-SCN)4(μ(1,1,3)-SCN)2]}n (2), where partial Cu(II)→Cu(I) reduction is observed. In 2, arrays of [Cu(II)2(L(1))2](2+) cationic units are inserted in between 2D {[Cu(I)4(SCN)6](2-)}n layers and connected via μ(1,1,3)-SCN(-) links, thus forming a 3D network. On the other hand, reaction…

In situAnionsModels MolecularStereochemistryAnionchemistry.chemical_elementInfrared spectroscopy010402 general chemistryCrystallography X-RayAnions; Copper; Crystallography X-Ray; Dimerization; Models Molecular; Molecular Structure; Organometallic Compounds; Oximes; Thiocyanates01 natural sciencesInorganic ChemistryOximeModelsOximes[CHIM.CRIS]Chemical Sciences/CristallographyOrganometallic CompoundsMolecule[CHIM]Chemical SciencesGroup 2 organometallic chemistryOrganometallic CompoundCrystallographyValence (chemistry)Molecular Structure010405 organic chemistryCationic polymerizationMolecular[CHIM.MATE]Chemical Sciences/Material chemistryCopper0104 chemical sciencesCrystallographychemistryX-RaySingle crystalDimerizationCopperThiocyanatesDalton transactions (Cambridge, England : 2003)
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A mixed-valence Cu(I)–Cu(II) and metal–metal bond containing coordination polymer obtained from an in situ oxidation reaction route

2006

Abstract A new mixed-valence copper coordination polymer with copper–copper metal bonds in a two-dimensional network was generated from an in situ oxidation reaction route under hydrothermal conditions. The synthesis of this coordination polymer demonstrated that the novel compounds that may not be accessible using the known methods could be synthesized via an oxidation reaction route. The reaction conditions are mild enough to keep the building blocks intact during the oxidation and self-assembly process under hydrothermal conditions.

In situValence (chemistry)Coordination polymerInorganic chemistrychemistry.chemical_elementCopperRedoxHydrothermal circulationInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryMetal metalPhysical and Theoretical ChemistryMetallic bondingInorganica Chimica Acta
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Enantioselective zinc/BINOL-catalysed alkynylation of aldimines generated in situ from α-amido sulfones.

2012

Chiral nonracemic N-Cbz-protected propargylic amines have been prepared by the addition of terminal alkynes to imines generated in situ from α-amido sulfones in the presence of diethylzinc and BINOL-type ligands as catalysts. The reactions give good yields and high enantioselectivities (ee values up to 95 %) for a good number of aromatic and heteroaromatic α-amido sulfones and alkynes.

In situchemistry.chemical_classificationAldimineNucleophilic additionOrganic ChemistryEnantioselective synthesischemistry.chemical_elementStereoisomerismStereoisomerismGeneral ChemistryZincNaphtholsDiethylzincLigandsCatalysisCatalysischemistry.chemical_compoundZincchemistryAlkynesOrganometallic CompoundsOrganic chemistrySulfonesAminesChemistry (Weinheim an der Bergstrasse, Germany)
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Elaboration of ammonia gas sensors based on electrodeposited polypyrrole - cobalt phthalocyanine hybrid films

2013

The electrochemical incorporation of a sulfonated cobalt phthalocyanine (sCoPc) in conducting polypyrrole (PPy) was done, in the presence or absence of LiClO4, in order to use the resulting hybrid material for the sensing of ammonia. After electrochemical deposition, the morphological features and structural properties of polypyrrole/phthalocyanine hybrid films were investigated and compared to those of polypyrrole films. A gas sensor consisting in platinum microelectrodes arrays was fabricated using silicon microtechnologies, and the polypyrrole and polypyrrole/phthalocyanine films were electrochemically deposited on the platinum microelectrodes arrays of this gas sensor. When exposed to a…

IndolesSiliconPolymersInorganic chemistrychemistry.chemical_element02 engineering and technology010402 general chemistryElectrochemistryPolypyrroleSensitivity and Specificity01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundAmmoniaOrganometallic CompoundsPyrrolesComputingMilieux_MISCELLANEOUSPlatinumchemistry.chemical_classificationAir PollutantsPerchloratesElectric ConductivityReproducibility of ResultsPolymer021001 nanoscience & nanotechnologyElectroplating0104 chemical sciencesMicroelectrodechemistryLithium CompoundsPhthalocyanine0210 nano-technologyPlatinumHybrid materialMicroelectrodes
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Double stimuli-responsive polysaccharide block copolymers as green macrosurfactants for near-infrared photodynamic therapy

2019

The NIR absorbing photosensitizer phthalocyanine zinc (PC(Zn)) was stabilized in aqueous media as water-dispersible nanoparticles with a reduction- and pH-responsive full polysaccharide block copolymer. A cellular uptake and also photo switchable intracellular activity of the cargo upon irradiation at wavelengths in the near infrared region were shown. The block copolymer was synthesized by applying a copper-free click strategy based on a thiol exchange reaction, creating an amphiphilic double-stimuli-responsive mixed disulfide. The dual-sensitive polysaccharide micelles represent a non-toxic and biodegradable green macrosurfactant for the delivery of phthalocyanine zinc. By encapsulation i…

Indolesmedicine.medical_treatmentBiological Availabilitychemistry.chemical_elementNanoparticlePhotodynamic therapy02 engineering and technologyZincIsoindoles010402 general chemistryPhotochemistry01 natural sciencesMicelleSurface-Active Agentschemistry.chemical_compoundPolysaccharidesAmphiphileOrganometallic CompoundsmedicineCopolymerHumansPhotosensitizerMicellesPhotosensitizing AgentsChemistryDextransGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesPhotochemotherapyZinc CompoundsPhthalocyanineNanoparticles0210 nano-technologyHeLa CellsSoft Matter
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Sequential injection analysis (SIA)-chemiluminescence determination of indomethacin using tris[(2,2'-bipyridyl)]ruthenium(III) as reagent and its app…

2006

Abstract Automated sequential injection (SIA) method for chemiluminescence (CL) determination of nonsteroidal anti-inflammatory drug indomethacin ( I ) was devised. The CL radiation was emitted in the reaction of I (dissolved in aqueous 50% v/v ethanol) with intermediate reagent tris(2,2′-bipyridyl)ruthenium(III) (Ru(bipy) 3 3+ ) in the presence of acetate. The Ru(bipy) 3 3+ was generated on-line in the SIA system by the oxidation of 0.5 mM tris(2,2′-bipyridyl)ruthenium(II) (Ru(bipy) 3 2+ ) with Ce(IV) ammonium sulphate in diluted sulphuric acid. The optimum sequence, concentrations, and aspirated volumes of reactant zones were: 15 mM Ce(IV) in 50 mM sulphuric acid 41 μL, 0.5 mM Ru(bipy) 3 …

IndomethacinAnalytical chemistrychemistry.chemical_elementBiochemistryDosage formAnalytical Chemistrylaw.inventionlawSpectrophotometrymedicineOrganometallic CompoundsEnvironmental ChemistrySpectroscopyChemiluminescenceDetection limitDosage FormsAqueous solutionmedicine.diagnostic_testMolecular StructureReproducibility of ResultsRutheniumStandard curvechemistryReagentCalibrationFlow Injection AnalysisLuminescent MeasurementsSolventsNuclear chemistryAnalytica chimica acta
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Complexes of organometallic compounds. XLVI. Synthesis of adducts formed by organotin(IV) trichlorides with 1,2-bis(diphenylphosphino)ethane, and the…

1977

Abstract Adducts between RSnCl 3 (R = Me, Bu n , Oct n , Ph) and 1,2-bisz(diphenylphosphino)ethane, DPE, have 1:1 composition. In Mossbauer spectroscopic experiences at variable absorber temperature the area under the resonant peaks, A, has been measured for RSnCl 3 ·DPE, R = Me, Ph; slopes plots of in A vs. T suggest strong coupling between Mossbauer atoms, which has been interpreted in terms of solid state polymeric structures, due to DPE acting as a bridging bis-monodentate ligand. Infrared data indicate the covalency of SnCl bonds. Three possible structural isomers of octahedral type are then proposed, one having trans -P 2 and two cis -P 2 atoms. A choice between these structures has …

InfraredInorganic chemistryInfrared spectroscopyAdductInorganic Chemistrychemistry.chemical_compoundCrystallography12-Bis(diphenylphosphino)ethaneOctahedronchemistryMössbauer spectroscopyMaterials ChemistryStructural isomerPhysical and Theoretical ChemistryGroup 2 organometallic chemistryInorganica Chimica Acta
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