Search results for "Organometallic Compound"

showing 10 items of 245 documents

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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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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Fluorescence emission and enhanced photochemical stability of Zn(II)-5-triethyl ammonium methyl salicylidene ortho-phenylendiiminate interacting with…

2010

Abstract The photophysical and photochemical properties of the cationic Zn II complex of 5-triethyl ammonium methyl salicylidene ortho-phenylendiimine (ZnL 2+ ) interacting with native DNA were investigated by steady state and time-resolved fluorescence spectroscopies. Experimental results indicate that, in the presence of DNA, ZnL 2+ is efficiently protected from a photochemical process, which occurs when it is in the free state dispersed in aqueous solution. The analysis of the absorption and emission spectra of ZnL 2+ , both stored in the dark and after exposure to tungsten lamp light for 24 h, corroborated by quantum chemical calculations, allowed us to point out that ZnL 2+ undergoes a…

Intercalation (chemistry)Context (language use)PhotochemistryBiochemistryFluorescence spectroscopyFluorescenceInorganic ChemistrySchiff baseIntercalationOrganometallic CompoundsMoleculeFluorescence spectroscopyPhotooxidationSettore CHIM/02 - Chimica FisicaAqueous solutionChemistrySpectrum AnalysisDNAPhotochemical ProcessesFluorescenceIntercalating AgentsSolventZincSettore CHIM/03 - Chimica Generale E InorganicaSolventsSteady state (chemistry)Oxidation-ReductionJournal of inorganic biochemistry
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Fluorescent organometallic rhodium(I) and ruthenium(II) metallodrugs with 4-ethylthio-1,8-naphthalimide ligands: Antiproliferative effects, cellular …

2018

Fluorescent 4-ethylthio-1,8-naphthalimides containing rhodium(I) N-heterocyclic carbene (NHC) and ruthenium (II) NHC fragments were synthesised and evaluated for their antiproliferative effects, cellular uptake and DNA-binding activity. Both types of organometallics triggered ligand dependent efficient cytotoxic effects against tumor cells with the rhodium(I) NHC derivatives causing stronger effects than the ruthenium (II) NHC analogues. Antiproliferative effects could also be observed against several pathogenic Gram-positive bacterial strains, whereas the growth of Gram-negative bacteria was not substantially affected. Cellular uptake was confirmed by atomic absorption spectroscopy as well…

Intercalation (chemistry)Fluorescent DyeLigands01 natural sciencesAntineoplastic Agentchemistry.chemical_compoundNeoplasmsDrug DiscoveryMoietyCell DeathBacterial InfectionsGeneral MedicineIntercalating AgentsNaphthalimideAnti-Bacterial AgentsRutheniumNaphthalimidesSettore CHIM/03 - Chimica Generale E InorganicaHumanStereochemistrychemistry.chemical_elementAntineoplastic AgentsLigandCarbene010402 general chemistryG-quadruplexBacterial InfectionRutheniumRhodiumCell Line TumorAnti-Bacterial AgentOrganometallic CompoundsG-QuadruplexeHumansRhodiumBioorganometallicFluorescent DyesGroup 2 organometallic chemistryCell ProliferationPharmacologyOrganometallic CompoundBacteria010405 organic chemistryLigandOrganic ChemistryIntercalating Agent0104 chemical sciencesG-QuadruplexeschemistryNeoplasmDrug Screening Assays AntitumorCarbene
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Luminescent Ionic Transition-Metal Complexes for Light-Emitting Electrochemical Cells

2012

Higher efficiency in the end-use of energy requires substantial progress in lighting concepts. All the technologies under development are based on solid-state electroluminescent materials and belong to the general area of solid-state lighting (SSL). The two main technologies being developed in SSL are light-emitting diodes (LEDs) and organic light-emitting diodes (OLEDs), but in recent years, light-emitting electrochemical cells (LECs) have emerged as an alternative option. The luminescent materials in LECs are either luminescent polymers together with ionic salts or ionic species, such as ionic transition-metal complexes (iTMCs). Cyclometalated complexes of Ir(III) are by far the most util…

IonsMaterials scienceLuminescenceLightMolecular StructureIonic bondingNanotechnologycopper(I) complexes; electroluminescence; iridium(III) complexes; light-emitting electrochemical cells; ruthenium(II) complexesGeneral ChemistryElectrochemical TechniquesElectroluminescenceCatalysisElectrochemical celllaw.inventionTransition metallawOLEDOrganometallic CompoundsTransition ElementsLuminescenceLight-emitting diodeDiode
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Reversible Colorimetric Probes for Mercury Sensing

2005

The selectivity and sensitivity of two colorimetric sensors based on the ruthenium complexes N719 [bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) bis(tetrabutylammonium) bis(thiocyanate)] and N749 [(2,2':6',2' '-terpyridine-4,4',4' '-tricarboxylate)ruthenium(II) tris(tetrabutylammonium) tris(isothiocyanate)] are described. It was found that mercury ions coordinate reversibly to the sulfur atom of the dyes' NCS groups. This interaction induces a color change in the dyes at submicromolar concentrations of mercury. Furthermore, the color change of these dyes is selective for mercury(II) when compared with other ions such as lead(II), cadmium(II), zinc(II), or iron(II). The detection limit…

IronInorganic chemistrychemistry.chemical_elementBiosensing TechniquesBiochemistrySensitivity and SpecificityCatalysischemistry.chemical_compoundColloid and Surface ChemistryIsothiocyanatesOrganometallic CompoundsColoring AgentsIonsTitaniumAqueous solutionThiocyanateMolecular StructureChemistryGeneral ChemistryMercuryChemical sensorTransition metal ionsMercury (element)RutheniumZincLeadRuthenium CompoundsColorimetrySpectrophotometry UltravioletSelectivityThiocyanatesCadmium
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