Search results for "Sulfoxide"

showing 10 items of 313 documents

Induction of micronuclei in V79 Chinese hamster cells by tetrachlorohydroquinone, a metabolite of pentachlorophenol

1992

Tetrachlorohydroquinone, a metabolite of the fungicide pentachlorophenol, induced significant dose-related increases in micronuclei in V79 Chinese hamster cells without exogenous metabolic activation. The lowest observed effective dose was 10 microM, where the relative survival was about 62%. At the highest dose tested, 20 microM, the relative survival was about 8% and the frequency of cells with micronuclei was about 6 times the solvent control frequency. The induction of micronuclei by tetrachlorohydroquinone was significantly inhibited by the hydroxyl radical scavenger dimethyl sulfoxide at 5% (v/v).

PentachlorophenolMetaboliteHamsterToxicologycomplex mixturesChinese hamsterchemistry.chemical_compoundCricetulusCricetinaeGeneticsAnimalsDimethyl SulfoxideCells CulturedMicronuclei Chromosome-DefectiveCarcinogenMicronucleus TestsbiologyDimethyl sulfoxidebiology.organism_classificationMolecular biologyEffective dose (pharmacology)HydroquinonesPentachlorophenolchemistryBiochemistryMicronucleus testDNA DamageMutation Research/Genetic Toxicology
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Determination of Aldicarb, Aldicarb Sulfoxide, and Aldicarb Sulfone in Oranges by Simple Gas–Liquid Chromatography with Nitrogen–Phosphorus Detection

1994

Abstract A reversed-phase liquid chromatographic method, using an acetonitrile–water gradient mobile phase, and a gas-liquid chromatographic method with nitrogen–phosphorus and flame photometric detection were compared for simultaneous and separate determinations of trace quantities of aldicarb and its metabolites aldicarb sulfone and aldicarb sulfoxide. One hundred gram samples of fortified oranges were extracted with water–acetone, water-acetonitrile, or water–methanol, and the extracts were partitioned with methylene chloride. Partitioning with other organic solvents such as chloroform, ethyl acetate, or methyl isobutyl ketone was also investigated. When performed under optimal condition…

PharmacologyChromatographyAldicarbChemistryAldicarb sulfoxideAldicarb sulfoneNitrogen phosphorusAnalytical ChemistryReaction productchemistry.chemical_compoundEnvironmental ChemistryGas chromatographyAgronomy and Crop ScienceFood ScienceJournal of AOAC INTERNATIONAL
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Bis-Sulfone- and Bis-Sulfoxide-Spirobifluorenes: Polar Acceptor Hosts with Tunable Solubilities for Blue-Phosphorescent Light-Emitting Devices

2016

Bis-sulfone- and bis-sulfoxide-spirobifluorenes are a promising class of high-triplet-energy electron-acceptor hosts for blue phosphorescent light-emitting devices. The molecular design and synthetic route are simple and facilitate tailoring of the solubilities of the host materials without lowering the high-energy triplet state. The syntheses and characterization (including single-crystal structures) of four electron-accepting hosts are reported; the trend in their reduction potentials is consistent with the electron-withdrawing nature of the sulfone or sulfoxide substituents. Emission maxima of 421–432 nm overlap with the MLCT absorption of the sky-blue emitter bis(4,6-difluorophenyl-pyri…

Phosphine oxidechemistry.chemical_classificationOrganic ChemistrySulfoxide02 engineering and technologyElectron acceptor010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesAcceptor0104 chemical sciencesSulfonechemistry.chemical_compoundchemistryOLEDPhysical and Theoretical ChemistryTriplet state0210 nano-technologyPhosphorescenceEuropean Journal of Organic Chemistry
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Phosphororganische Verbindungen, 85. Kinetische Untersuchungen der Umsetzung organischer Phosphorverbindungen mit Nucleophilen und Supernucleophilen

1977

Bei der alkalischen Spaltung von quartaren Phosphoniumsalzen und tertiaren Phosphinoxiden zeigt HOO⊖ keinen α-Effekt. Die Spaltung der P–C-Bindung wird auch nicht durch Gruppen erleichtert, welche uber die Ausbildung von H-Brucken den Angriff von HOO⊖ am Phosphoniumzentrum fordern. — In Ubereinstimmung mit den Ergebnissen anderer Autoren wird bei der Hydrolyse der Phosphin-, Phosphon- und Phosphorsaureester 1, 2 und 3 in Gegenwart von H2O2 ein α-Effekt beobachtet, der sich in einer Hydrolysebeschleunigung um einen Faktor von ca. 100 ausdruckt. Die Hydrolysegeschwindigkeit nimmt sowohl mit HO⊖ als auch mit HOO⊖ entsprechend folgender Reihenfolge ab: Diphenylphosphinsaure-(p-nitrophenyl)ester…

Phosphine oxidechemistry.chemical_compoundHydrolysisNucleophileChemistryOrganic ChemistryPolymer chemistryPhosphonium saltSulfoxidePhosphoniumPhysical and Theoretical ChemistryPeroxidePhosphineJustus Liebigs Annalen der Chemie
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Evaluation of Charge‐Regulated Supramolecular Copolymerization to Tune the Time Scale for Oxidative Disassembly of β‐Sheet Comonomers

2019

A multistimuli-responsive supramolecular copolymerization is reported. The copolymerization is driven by hydrogen bond encoded β-sheet-based charge co-assembly into 1D nanorods in water, using glutamic acid or lysine residues in either of the peptide comonomers. The incorporation of methionine as hydrophobic amino acid supports β-sheet formation, but oxidation of the thioether side-chain to a sulfoxide functional group destabilizes the β-sheet ordered domains and induces disassembly of the supramolecular polymers. Using H2 O2 as reactive oxygen species, the time scale and kinetics of the oxidative disassembly are probed. Compared to the charge neutral homopolymers, it is found that the oxid…

Polymers and PlasticsMacromolecular SubstancesPolymersSupramolecular chemistryBeta sheet02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundThioetherAmphiphilePolymer chemistryMaterials ChemistryCopolymerAmino Acidschemistry.chemical_classificationNanotubesHydrogen bondOrganic ChemistryHydrogen BondingSulfoxideHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesSupramolecular polymerschemistryProtein Conformation beta-StrandPeptidesReactive Oxygen Species0210 nano-technologyOxidation-ReductionMacromolecular Rapid Communications
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Enhancing Sensitivity of Microflow-Based Bottom-Up Proteomics through Postcolumn Solvent Addition.

2019

The introduction of more sensitive mass spectrometers allows researchers to adapt front-end liquid chromatography (LC) to individual needs for the analysis of complex proteomes. Where absolute sensitivity is not paramount, it is advantageous to switch from a highly sensitive nanoflow-LC setup, the de facto standard platform in mass-spectrometry (MS)-based discovery proteomics, to a more robust, high-throughput-compatible microflow or conventional-flow setup. To enhance the microflow-LC-MS electrospray process of complex proteomic samples, we tested the effects of different solvents, including 2-propanol, methanol, and acetonitrile, pure or as mixture with dimethyl sulfoxide, which were adde…

ProteomicsElectrospraySpectrometry Mass Electrospray IonizationChromatographyChemistryDimethyl sulfoxideElectrospray ionization010401 analytical chemistry010402 general chemistryMass spectrometry01 natural sciences0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundSolventsHumansNanotechnologyDimethyl SulfoxideBottom-up proteomicsMethanolAcetonitrilePeptidesChromatography High Pressure LiquidHeLa CellsAnalytical chemistry
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Solid state polymerization causing transition to a ferromagnetic state. Crystal structures and magnetic properties of [Cu2(dpp)(H2O)(dmso)Cl4]·dmso a…

2001

The preparation, crystal structures and variable-temperature magnetic susceptibility data for [Cu2(dpp)(H2O)(dmso)Cl4]·dmso (1a) and [Cu2(dpp)Cl4]n (2) (dpp = 2,3-bis(2-pyridyl)pyrazine, dmso = dimethyl sulfoxide) are reported. 1a consists of dinuclear dpp-bridged molecules with chlorine, water and dmso serving as terminal ligands. The two copper atoms are crystallographically independent, with distorted square pyramidal and trigonal bipyramidal coordination geometries, respectively. In a first approximation 2 may be described as a chain compound with out-of-plane mono-μ-chloro bridges (Cu–Cl–Cu–Cl). Only one of the crystallographically independent copper atoms participates in this chain fo…

PyrazineStereochemistrychemistry.chemical_elementSulfoxideGeneral ChemistryCrystal structureCopperMagnetic susceptibilitySquare pyramidal molecular geometryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographychemistryIsostructuralJournal of the Chemical Society, Dalton Transactions
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Organomercury(II) derivatives of 2-thiouracil. An infrared and proton magnetic resonance study of structures

1983

Abstract The novel complexes RHg(s2UraH−1) (R = Me, Ph) where s2UraH−1 is the monoanion of 2-thiouracil, have been synthesized. Comparison of the infrared spectra of the solid complexes and of 1H nuclear magnetic resonance spectra of the complexes in dimethyl-d6 sulfoxide with spectra of s2 Ura and Na[s2UraH−1] allows the recognition of the existence of isomers in the solid, with bonding to exocyclic sulfur and to pyrimidine nitrogens. In solution, a simpler pattern is observed, with 2J(1H199Hg) indicating bonding to sulfur only.

PyrimidineInfraredAnalytical chemistryInfrared spectroscopychemistry.chemical_elementSulfoxideSulfurSpectral lineThiouracilInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryOrganomercuryPhysical and Theoretical ChemistryInorganica Chimica Acta
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The contribution of hydrogen peroxide to the radiosensitizing effect of gold nanoparticles

2019

Abstract Plasmid DNA in aerated aqueous solution is used as a probe to determine whose of the reactive oxygen species (ROS) generated after absorption of ultra-soft X-rays (USX) take part in biomolecule damage in the presence and in absence of Gold Nano-Particles (GNP) and specific scavengers. Citrate-coated GNPs with core sizes of 6, 10 and 25 nm are synthetized and characterized, especially in terms of plasmon band shift, ζ-potential and hydrodynamic radii (respectively 9, 21 and 30 nm). We confirm the radiosensitizing effect of GNP and show that the SSB number per plasmid increases when, for a same mass of gold element, the core size of the gold nanoparticles decreases. Hydroxyl radicals…

Radiation-Sensitizing AgentsFormatesRadicalMetal Nanoparticles02 engineering and technologyPhotochemistry01 natural sciencesCitric AcidMetalchemistry.chemical_compoundColloid and Surface ChemistryPyruvic Acid0103 physical sciences[CHIM]Chemical SciencesMoleculeDimethyl SulfoxideDNA Breaks Single-StrandedParticle SizeTromethaminePhysical and Theoretical ChemistryHydrogen peroxideComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationReactive oxygen speciesQuenching (fluorescence)Aqueous solution010304 chemical physicsHydroxyl RadicalX-RaysFree Radical ScavengersHydrogen PeroxideSurfaces and InterfacesGeneral Medicine021001 nanoscience & nanotechnologySolutionschemistryColloidal goldvisual_artvisual_art.visual_art_mediumGold0210 nano-technologyPlasmidsBiotechnologyColloids and Surfaces B: Biointerfaces
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CCDC 689575: Experimental Crystal Structure Determination

2009

Related Article: J.L.G.Ruano, J.Aleman, S.Catalan, V.Marcos, S.Monteagudo, A.Parra, C.del Pozo, S.Fustero|2008|Angew.Chem.,Int.Ed.|47|7941|doi:10.1002/anie.200802885

Space GroupCrystallography(+)-N-((SS2S3S)-1-Chloro-11-difluoro-3-(2-(p-tolylsulfoxide)phenyl)butan-2-yl)-4-methoxybenzenamineCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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