Search results for "Moiety"

showing 10 items of 621 documents

Electrochemical Formation of 3,5-Diimido-1,2-dithiolanes by Dehydrogenative Coupling

2018

A synthetic approach to the cyclic disulfide moiety of 3,5-diimido-1,2-dithiolane derivatives starting with readily available precursors including the electrochemical coupling of dithioanilides is developed. The electrochemical key step provides sustainable synthetic access in high yields, using a very simple electrolysis setup.

Electrolysis010405 organic chemistryChemistryOrganic ChemistryDisulfide bond010402 general chemistryElectrochemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical scienceslaw.inventionCoupling (electronics)lawMoietyPhysical and Theoretical ChemistryOrganic Letters
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Simple and scalable electrochemical synthesis of 2,1-benzisoxazoles and quinoline N-oxides.

2019

Cathodic reduction of the nitro moiety and subsequent intramolecular cyclization affords different substituted 2,1-benzisoxazoles and quinoline N-oxides. This methodology allows the synthesis of two different types of heterocycles from common simple starting materials, using electrons as a sole reagent for this transformation. The electrolysis can be conducted in a very simple undivided electrolysis cell under constant current conditions. This permits working on a larger scale compared to other electrochemical methodologies and represents a significant advantage.

Electrolysis010405 organic chemistryElectrolytic cellQuinolineMetals and AlloysGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundchemistrylawReagentMaterials ChemistryCeramics and CompositesNitroConstant currentMoietyChemical communications (Cambridge, England)
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Flexible diphenylsulfone versus rigid dibenzothiophene-dioxide as acceptor moieties in donor-acceptor-donor TADF emitters for highly efficient OLEDs

2020

DG acknowledges funding from the ERDF PostDoc project No. 1.1.1.2/VIAA/1/16/177 . This research is/was funded by the European Regional Development Fund according to the supported activity ‘ Research Projects Implemented by World-class Researcher Groups ’ under Measure No. 01.2.2-LMT-K-718 . Ministry of Science and Technology (MOST), Taiwan , Grant No. MOST 106-2923-E-155-002-MY3 . This work was also supported by the Ministry of Education and Science of Ukraine (projects no. 0117U003908 and 0118U003862 ), and by the Olle Engkvist Byggmästare foundation (contract No. 189-0223 ). The quantum-chemical calculations were performed with computational resources provided by the High Performance Comp…

Electron mobilityPhotoluminescenceMaterials science02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesBiomaterialsMaterials ChemistryOLED:NATURAL SCIENCES:Physics [Research Subject Categories]MoleculeMoietySinglet stateDibenzothiophene dioxideElectrical and Electronic Engineeringdi-tert-butyldimethyldihydroacridineGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsDiphenylsulfoneAcceptor0104 chemical sciencesElectronic Optical and Magnetic MaterialsThermally activated delayed fluorescencQuantum efficiency0210 nano-technologyBipolar charge transportOrganic Electronics
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Towards the design of organocatalysts for nerve agents remediation: The case of the active hydrolysis of DCNP (a Tabun mimic) catalyzed by simple ami…

2015

We report herein a study of the hydrolysis of Tabun mimic DCNP in the presence of different amines, aminoalcohols and glycols as potential suitable organocatalysts for DCNP degradation. Experiments were performed in CD3CN in the presence of 5% D2O, which is a suitable solvent mixture to follow the DCNP hydrolysis. These studies allowed the definition of different DCNP depletion paths, resulting in the formation of diethylphosphoric acid, tetraethylpyrophosphate and phosphoramide species as final products. Without organocatalysts, DCNP hydrolysis occurred mainly via an autocatalysis path. Addition of tertiary amines in sub-stoichiometric amounts largely enhanced DCNP depletion whereas non-te…

Environmental EngineeringHealth Toxicology and MutagenesisOrganocatalystsCatalysisCatalysisNitrophenolsAutocatalysisGlycolschemistry.chemical_compoundHydrolysisQUIMICA ORGANICAEnvironmental ChemistryMoietyOrganic chemistryChemical Warfare AgentsAminesWaste Management and DisposalEnvironmental Restoration and RemediationTabunEthanolHydrolysisQUIMICA INORGANICAAmino AlcoholsPollutionOrganophosphatesSolventKineticsDiethylcyanophosphonatechemistryNerve agent simulantAmine gas treatingNerve AgentsJournal of Hazardous Materials
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A dft analysis of the participation of zwitterionic tacs in polar [3+2] cycloaddition reactions

2014

A set of seven non-substituted tri-atom-components (TACs) participating in [3+2] cycloaddition (32CA) reactions has been studied using the reactivity indices defined within the conceptual DFT at the B3LYP/6-31G(d) level of theory. This series of TACs shows a zwitterionic structure and low reactivity towards ethylene. The general characteristic of these TACs is their high nucleophilic and a low electrophilic behaviour. Activation energies computed at the MPWB1K/6-311G(d) level in dichloromethane point to that non-substituted TACs react quickly toward dicyanoethylene showing their ability to react towards electron-deficient ethylenes. However, when the TACs are electrophilically activated by …

EthyleneChemistryStereochemistryOrganic ChemistryRegioselectivityBiochemistryCycloadditionchemistry.chemical_compoundNucleophileComputational chemistryDrug DiscoveryElectrophileMoietyReactivity (chemistry)Lewis acids and bases
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Grafting of Hindered Phenol Groups onto Ethylene/α-Olefin Copolymer by Nitroxide Radical Coupling

2017

The covalent immobilization of hindered phenol groups, with potential antioxidant activity, onto an ethylene/α-olefin (EOC) copolymer was carried out by the nitroxide radical coupling (NRC) reaction performed in the melt with a peroxide and the 3,5-di-tert-butyl-4-hydroxybenzoyl-2,2,6,6-tetramethylpiperidine-1-oxyl radical (BHB-T). Functionalized EOC (EOC-g-(BHB-T)) was exposed to photo- and thermo-oxidation. By comparison with some model compounds bearing the (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) moiety or the hindered phenol unit, it was observed that the grafted BHB-T could effectively help the stabilization of the polymer matrix both under photo- and thermo-oxidation. In addit…

EthylenePolymers and Plastics02 engineering and technology010402 general chemistry01 natural sciencesPeroxideArticlelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrynitroxide radical couplingPolymer chemistryCopolymerMoietyantioxidant covalent immobilizationchemistry.chemical_classificationOlefin fiberhindered phenol moietyChemistry (all)General ChemistryPolymer021001 nanoscience & nanotechnologyGrafting0104 chemical scienceschemistryCovalent bondantioxidant covalent immobilization; nitroxide radical coupling; hindered phenol moiety; HAS-NOR antioxidant0210 nano-technologyHAS-NOR antioxidantPolymers
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“Functional Poly(ethylene glycol)”: PEG-Based Random Copolymers with 1,2-Diol Side Chains and Terminal Amino Functionality

2010

A series of poly(ethylene glycol-co-isopropylidene glyceryl glycidyl ether) (P(EO-co-IGG)) random copolymers with different fractions of 1,2-isopropylidene glyceryl glycidyl ether (IGG) units was synthesized. After acidic hydrolysis a new type of "functional PEGs", namely poly(ethylene glycol-co-glyceryl glycerol) (P(EO-co-GG)) was obtained. Using an initiator that releases a terminal amino moiety after deprotection, functional end groups with orthogonal reactivity to the in-chain groups were obtained. All polymers showed narrow molecular weight distributions (1.07-1.19), and control of the molecular weights was achieved in the range 5000-30 000 g/mol. Random incorporation of both comonomer…

EthylenePolymers and PlasticsPolyglycerolDiolHigh-Loading SupportPolymerizationInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerSide chainMoietychemistry.chemical_classificationReagentsTelechelic polymerOxide)Organic ChemistryPolymerSoluble PolymersRecoverable CatalystschemistryPolymerizationGlycidolBlock-CopolymersDerivativesMacromolecules
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Towards the fluorogenic detection of peroxide explosives through host-guest chemistry

2018

[EN] Two dansyl-modified beta-cyclodextrin derivatives (1 and 2) have been synthesized as host-guest sensory systems for the direct fluorescent detection of the peroxide explosives diacetone diperoxide (DADP) and triacetone triperoxide (TATP) in aqueous media. The sensing is based on the displacement of the dansyl moiety from the cavity of the cyclodextrin by the peroxide guest resulting in a decrease of the intensity of the fluorescence of the dye. Both systems showed similar fluorescent responses and were more sensitive towards TATP than DADP.

Explosive material1002macromolecular substances010402 general chemistryPhotochemistry01 natural sciencesPeroxide178chemistry.chemical_compoundpolycyclic compoundsMoietyhost–guest chemistryFluorescent sensorsHost–guest chemistrylcsh:Sciencechemistry.chemical_classificationCyclodextrinsMultidisciplinarycyclodextrinsCyclodextrinAqueous medium010405 organic chemistryperoxide explosivesFluorescence0104 chemical sciencesChemistrychemistryfluorescent sensorslcsh:QHost-guest chemistryPeroxide explosivesResearch Article
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Yeast Cell Wall Glycoproteins

1991

In higher cells, glycoproteins play a variety of functions as surface receptors, cell-cell mediators, carriers of enzyme activities, components of the extracellular matrix, etc. In most glycoproteins, the protein moiety will be the functional part whereas the carbohydrate moiety would contribute to the attainment of an adequate tertiary structure, modify the glycoprotein molecule making it more resistant to degradation, and facilitate its secretion.

Extracellular matrixchemistry.chemical_classificationCell wallBiochemistryChemistryMoietySecretionReceptorGlycoproteinProtein tertiary structureYeast
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Site-specific near-infrared fluorescent labelling of proteins on cysteine residues with meso -chloro-substituted heptamethine cyanine dyes

2018

International audience; Near-infrared (NIR) fluorescence imaging is a promising new medical imaging modality. Associated with a targeting molecule, NIR fluorophores can accumulate selectively in tissues of interest and become valuable tools for the diagnosis and therapy of various pathologies. To facilitate the design of targeted NIR imaging agents, it is important to identify simple and affordable fluorescent probes, allowing rapid labelling of biovectors such as proteins, ideally in a site-specific manner. Here, we demonstrate that heptamethine cyanine based fluorophores, such as IR-783, that contain a chloro-cyclohexyl moiety within their polymethine chain can react selectively, at neutr…

Fluorescence-lifetime imaging microscopyFluorophoreHalogenationProteins on cysteine residuesInfrared Rays010402 general chemistry01 natural sciencesBiochemistrychemistry.chemical_compoundMiceLabellingCell Line TumorMoietyAnimalsTissue Distribution[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyAmino Acid SequenceCysteinePhysical and Theoretical ChemistryCyanineheptamethine cyanine dyesPeptide sequenceFluorescent DyesStaining and Labeling010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryOptical ImagingProteinsCarbocyaninesFluorescenceCombinatorial chemistry0104 chemical sciences3. Good healthPeptidesCysteine
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