Search results for "Organo"

showing 10 items of 1460 documents

Enhancing extraction performance of organophosphorus flame retardants in water samples using titanium hierarchical porous silica materials as sorbent…

2021

Abstract A sorbent for the extraction of organophosphorus flame retardants has been proposed, based on UVM-7 (University of Valencia Materials) mesoporous silica doped with titanium. Designed cartridges have been applied to the extraction and preconcentration of flame retardants in water samples, followed by gas chromatography coupled to a mass spectrometry detector. Firstly, UVM-7 materials with different contents of titanium were synthesized and characterized by several techniques, thus confirming the proper mesoporous architecture. The potential of these materials was assessed in comparison with their morphological properties, resulting Ti50-UVM-7 the best solid phase. Several extraction…

Sorbent010402 general chemistry01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundOrganophosphorus CompoundsLimit of DetectionSolid phase extractionSolid Phase MicroextractionFlame RetardantsDetection limitTitaniumChromatographyChemistry010401 analytical chemistryOrganic ChemistryExtraction (chemistry)WaterGeneral MedicineMesoporous silicaSilicon DioxideOrganophosphates0104 chemical sciencesGas chromatographyAdsorptionMesoporous materialPorosityTriphenyl phosphateJournal of chromatography. A
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Programmed Formation of HCN Oligomers through Organosulfur Catalysis

2021

An efficient, inexpensive, and reliable synthesis of diaminomaleonitrile (DAMN, 1) is described starting from readily available acetone cyanohydrin as the source of hydrogen cyanide (HCN). Diaminomaleonitrile (DAMN) is known to be an important intermediate in heterocyclic and medicinal chemistry as well as being a possible precursor for the origin of life's hypothesis within prebiotic chemistry. The mechanism of its formation through organosulfur catalysis has been investigated by electrospray ionization mass spectrometry (ESI-MS) using two newly synthesized cationic "marker" molecules as a tool that allows for sensitive detection. As a result, the proposed mechanism of a thiocyanate-mediat…

Spectrometry Mass Electrospray IonizationChemistry PharmaceuticalElectrospray ionizationOrganic ChemistryCationic polymerizationCombinatorial chemistryCatalysisCatalysischemistry.chemical_compoundchemistryTetramerDiaminomaleonitrileMoleculeDisulfidesOrganosulfur compoundsAcetone cyanohydrinThe Journal of Organic Chemistry
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Synthesis, characterization, and crystal structure of [Cu(cinoxacinate)2] · 2H2O complex: A square-planar CuO4 chromophore. Antibacterial studies

1995

The structural and spectroscopic properties of a new copper (II) complex of cinoxacin (HCx) have been investigated. The complex [Cu(Cx)2].2H2O crystallizes in the monoclinic system, space group P2(1)/c. The cell dimensions are: a = 7.998(2), b = 7.622(1), c = 18.955(6) A, beta = 94.38(2) degree, V = 1154.6(6) A3, Z = 2. The structure was refined to R = 0.051. The crystal is composed of [Cu(Cx)2] units and uncoordinated water molecules. The Cu(II) ion, at a center of symmetry, is coordinated to two cinoxacinate (Cx) ligands related by the inversion center. Each cinoxacinate acts as bidentate ligand bonded to the cation through its carboxylate oxygen atom and through its exocyclic carbonyl ox…

Spectrophotometry InfraredStereochemistryCrystal structureMicrobial Sensitivity TestsCrystallography X-RayBiochemistryInorganic ChemistryCrystalchemistry.chemical_compoundEnterobacteriaceaeOrganometallic CompoundsMoleculeCarboxylateGroup 2 organometallic chemistryGram-Negative Aerobic BacteriaMolecular StructureChemistryLigandSpectrophotometry AtomicElectron Spin Resonance SpectroscopyChromophoreGram-Positive CocciSolubilityCinoxacinSpectrophotometry UltravioletCopperMonoclinic crystal system
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Syntheses, X-ray structures, and physicochemical properties of phenoxo-bridged dinuclear nickel(II) complexes: kinetics of transesterification of 2-h…

2009

Four dinuclear nickel(II) complexes [Ni(II)(2)(L(1))(O(2)CMe)(2)(H(2)O)(2)][PF(6)].MeOH.3H(2)O (1), [Ni(II)(2)(L(1))(O(2)CMe)(2)(NCS)] (2), [Ni(II)(2)(L(2))(O(2)CMe)(2)(MeOH)(H(2)O)][ClO(4)] (3), and [Ni(II)(2)(L(2))(O(2)CMe)(2)(MeOH)(H(2)O)][BPh(4)].3MeOH.H(2)O (4) have been synthesized [HL(1): 2,6-bis[N-methyl-N-(2-pyridylethyl)amino]-4-methylphenol; HL(2): 2,6-bis[3-(pyridin-2-yl)pyrazol-1-ylmethyl]-4-methylphenol]. Complexes 1, 3, and 4 are new while complex 2 was reported previously by Fenton and co-workers (the structure of 2 was presented but no physicochemical properties of this complex were reported; in this work such studies have been completed). X-ray crystallographic analyses of…

Spectrophotometry InfraredStereochemistryKineticschemistry.chemical_elementPyrazoleCrystallography X-RayMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMagneticsOrganophosphorus CompoundsBiomimeticsNickelOrganometallic CompoundsMoietyChelationPhysical and Theoretical ChemistryEsterificationHydrolysisX-rayTitrimetryEstersTransesterificationHydrogen-Ion ConcentrationOrganophosphatesNickelKineticschemistryPotentiometryEthylamineOxidation-ReductionInorganic chemistry
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Understanding the reactivity of transition metal complexes involving multiple spin states

2003

International audience; In coordination chemistry, many reactions involve several electronic states, in particular states of different spin. This phenomenon of ‘Multiple-State Reactivity’ has been recognized for some time, both for gas-phase reactions of ‘bare’ metal ions, and for transition metal complexes in solution. Until recently, however, much of the discussion of these systems has remained qualitative, because standard computational methods do not allow the location of the critical points for these processes, the Minimum Energy Crossing Points (MECPs) between states of different spin. Increased computational resources and new algorithms now enable MECPs to be located for large, reali…

Spin statesSpin acceleration010402 general chemistryPhotochemistry01 natural sciencesMetal L-edgeCoordination complexInorganic Chemistrychemistry.chemical_compoundTransition metalSpin crossoverMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryMinimum energy crossing pointOrganometallic chemistrychemistry.chemical_classification010405 organic chemistryMetal K-edgeSpin crossoverOxidative addition0104 chemical sciencesCoordination chemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryOrganometallic chemistryChemical physicsTwo-state reactivity
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Prenatal exposure to organochlorine compounds and lung function during childhood

2019

Introduction: Prenatal exposure to organochlorine compounds (OCs) can increase the risk of reported respiratory symptoms in children. It remains unclear whether these compounds can also impact on lung function. We assessed the association between prenatal exposure to OCs and lung function during childhood. Methods: We included 1308 mother-child pairs enrolled in a prospective cohort study. Prenatal concentrations of p,p′-dichlorodiphenyltrichloroethane [p,p′-DDT], p,p′-dichlorodiphenyldichloroethylene [p,p′-DDE], hexachlorobenzene [HCB], and seven polychlorinated biphenyls [PCBs] were measured in cord blood. Spirometry was performed in the offspring at ages 4 (n = 636) and 7 years (n = 1192…

Spirometry010504 meteorology & atmospheric sciencesOffspringPhysiology010501 environmental sciences01 natural sciencesFEV1/FVC ratioPregnancyStatistical significancePrenatal exposuremedicineHydrocarbons ChlorinatedHumansProspective StudiesRespiratory systemProspective cohort studyChildLungChildrenlcsh:Environmental sciences0105 earth and related environmental sciencesGeneral Environmental Science2. Zero hungerlcsh:GE1-350PregnancyDichlorodiphenyldichloroethylenemedicine.diagnostic_testbusiness.industryrespiratory systemOrganochlorine compoundsmedicine.diseaseFetal BloodLung function3. Good healthRespiratory Function Testsrespiratory tract diseasesQuartileChild PreschoolPrenatal Exposure Delayed EffectsFemalebusinessBirth cohort
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A Mesoporous 3D Hybrid Material with Dual Functionality for Hg2+Detection and Adsorption

2008

Dual-function hybrid material U1 was designed for simultaneous chromofluorogenic detection and removal of Hg(2+) in an aqueous environment. Mesoporous material UVM-7 (MCM41 type) with homogeneously distributed pores of about 2-3 nm in size, a large specific surface area exceeding 1000 m(2) g(-1), and nanoscale particles was used as an inorganic support. The mesoporous solid is decorated with thiol groups that were treated with squaraine dye III to give a 2,4-bis(4-dialkylaminophenyl)-3-hydroxy-4-alkylsulfanylcyclobut-2-enone (APC) derivative that is covalently anchored to the inorganic silica matrix. The solid was characterised by various techniques including X-ray diffraction, transmission…

Squaraine dyeAqueous solutionMolecular StructureSurface PropertiesChemistrySilica gelOrganic ChemistryInorganic chemistryMercuryGeneral ChemistrySilicon DioxideCatalysischemistry.chemical_compoundAdsorptionSpecific surface areaOrganosilicon CompoundsAdsorptionParticle SizeMesoporous materialHybrid materialPorosityFluorescent DyesFumed silicaChemistry - A European Journal
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Competitive Profiling of Ligandable Cysteines in Staphylococcus aureus with an Organogold Compound

2022

With the idea of exploiting metal-templated reactions to achieve selective modification of cysteines in proteins for antibacterial applications, an organometallic cyclometalated Au(III) compound was explored in a competitive chemoproteomic approach based on the isoDTB-ABPP (isotopically labelled desthiobiotin azide-activity-based protein profiling) technology in S. aureus cell extracts. In this way, more than 100 ligandable cysteines where identified, of which 10 were close to functional sites of proteins encoded by essential genes indicating potential for antibiotic development. Interestingly, more than 50% of the identified ligandable sites were not engaged by organic α-chloroacetamides i…

Staphylococcus aureusMaterials ChemistryMetals and AlloysCeramics and CompositesCysteineGeneral ChemistryOrganogold CompoundsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials
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tBuLi-Mediated One-Pot Direct Highly Selective Cross-Coupling of Two Distinct Aryl Bromides.

2015

A Pd-catalyzed direct cross-coupling of two distinct aryl bromides mediated by tBuLi is described. The use of [Pd-PEPPSI-IPr] or [Pd-PEPPSI-IPent] as catalyst allows for the efficient one-pot synthesis of unsymmetrical biaryls at room temperature. The key for this selective cross-coupling is the use of an ortho-substituted bromide that undergoes lithium-halogen exchange preferentially.

Stereochemistry22'-BIPYRIDINE COMPLEX2chemistry.chemical_elementORGANOLITHIUM COMPOUNDSCatalysisCatalysischemistry.chemical_compoundLOW-TEMPERATUREBromideOrganolithium compoundscross-couplingN-heterocyclic carbenesGRIGNARD-REAGENTSPD-PEPPSI-IPENT2'-BIPYRIDINE COMPLEXCARBON BOND FORMATIONArylOrganic ChemistryORGANIC-SYNTHESISGeneral ChemistryORTHO-SUBSTITUTED BIARYLSpalladiumHighly selectiveCombinatorial chemistryFUNCTIONALIZED ARYLCoupling (electronics)biarylschemistrylithiumOrganic synthesisUNSYMMETRICAL BIARYLSPalladiumChemistry (Weinheim an der Bergstrasse, Germany)
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Comparing the Antileishmanial Activity of Gold(I) and Gold(III) Compounds in L. amazonensis and L. braziliensis in Vitro

2020

Abstract Abstract: A series of mononuclear coordination or organometallic AuI/AuIII complexes (1–9) have been comparatively studied in vitro for their antileishmanial activity against promastigotes and amastigotes, the clinically relevant parasite form, of Leishmania amazonensis and Leishmania braziliensis. One of the cationic AuI bis‐N‐heterocyclic carbenes (3) has low EC50 values (ca. 4 μM) in promastigotes cells and no toxicity in host macrophages. Together with two other AuIII complexes (6 and 7), the compound is also extremely effective in intracellular amastigotes from L. amazonensis. Initial mechanistic studies include an evaluation of the gold complexes′ effect on L. amazonensis’ pl…

StereochemistryAntiprotozoal Agentsamastigotes01 natural sciencesBiochemistryMiceGold iiiParasitic Sensitivity TestsGold CompoundsDrug Discoverygold compoundsmedicineAnimalsGeneral Pharmacology Toxicology and PharmaceuticsAmastigoteleishmaniasisCells CulturedEC50LeishmaniaPharmacologyMice Inbred BALB CMolecular Structurebiology010405 organic chemistryChemistryCommunicationOrganic ChemistryLeishmaniasismedicine.diseasebiology.organism_classificationLeishmania braziliensisCommunicationsIn vitroddc:0104 chemical sciences010404 medicinal & biomolecular chemistryMolecular MedicinepromastigotesOrganogold CompoundsIntracellularChemMedChem
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