Search results for "Acceptor"

showing 10 items of 394 documents

Free-Standing Mono layer Two-Dimensional Supramolecular Organic Framework with Good Internal Order

2015

Utilizing dynamic self-assembly and self-sorting to obtain large-area, molecularly precise monolayered structures represents a promising approach toward two-dimensional supramolecular organic frameworks (2D SOF) or 2D supramolecular polymers. So far, related approaches suffer from small domain sizes, fragility and weak long-range internal order. Here we report on the self-assembly of a host-guest enhanced donor-acceptor interaction, consisting of a tris(methoxynaphthyl)-substituted truxene spacer, and a naphthalene diimide substituted with N-methyl viologenyl moieties as donor and acceptor monomers, respectively, in combination with cucurbit[8]uril as host monomer toward monolayers of an un…

chemistry.chemical_classification010405 organic chemistryChemistrySupramolecular chemistryNanotechnologyGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryAcceptorArticleCatalysis0104 chemical sciencesSupramolecular polymerschemistry.chemical_compoundCrystallographyColloid and Surface ChemistryMonomerTransmission electron microscopyMonolayerMoleculeSolubility
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Engineering faster transglycosidases and their acceptor specificity

2019

Transglycosidases are enzymes that have the potential to catalyze the synthesis of a wide range of high-value compounds starting from biomass-derived feedstocks. Improving their activity and broadening the substrate range are important goals to enable the widespread application of this family of biocatalysts. In this work, we engineered 20 mutants of the rice transglycosidase Os9BGlu31 and evaluated their catalysis in 462 reactions over 18 different substrates. This allowed us to identify mutants that expanded their substrate range and showed high activity, including W243L and W243N. We also developed double mutants that show very high activity on certain substrates and exceptional specific…

chemistry.chemical_classification010405 organic chemistryExternal validationSubstrate (chemistry)010402 general chemistry01 natural sciencesPollutionAcceptorCombinatorial chemistry0104 chemical sciencesCatalysisEnzymechemistryCheminformaticsEnvironmental ChemistryHigh activityGreen Chemistry
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Highly Functionalized Brønsted Acidic/Lewis Basic Hybrid Ferrocene Ligands: Synthesis and Coordination Chemistry

2019

International audience; A general challenging issue in the synthesis of hemilabile ferrocene ligands is the access to highly functionalized ferrocene starting materials. These can bear donor/acceptor atoms, additional functional and structuring spectator substituents, but the preparation of such species poses general synthetic difficulties. We report herein alternative synthetic routes to hybrid ferrocene donors such as tert-butylated phosphanylcarboxylic acids and their corresponding aldehydes. These hybrid ambiphilic species that combine Brønsted-acidic and Lewis-basic functional moieties in their structure were characterized by multinuclear NMR and single-crystal X-ray diffraction analys…

chemistry.chemical_classification010405 organic chemistryHydrogen bondSolid-state010402 general chemistry01 natural sciencesCombinatorial chemistryAcceptor0104 chemical sciencesCoordination complexInorganic Chemistrychemistry.chemical_compoundFerrocenechemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryBrønsted–Lowry acid–base theoryMutual influence
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Cruciform Electron Acceptors Based on Tetraindeno-Fused Spirofluorene

2017

Two cruciform tetraindenospirofluorene-based acceptors embedding carbonyl (Spiro-4O) and dicyanovinylene (Spiro-8CN) functionalities are synthesized in high yields. Single-crystal X-ray analysis reveals a one-dimensional π–π stacking arrangement for Spiro-4O, while Spiro-8CN adopts a unique two-dimensional isotropic π-interaction. Cyclic voltammetry suggests a high electron affinity of −3.76 eV for Spiro-8CN. Such a packing motif and low LUMO energy for Spiro-8CN are important for bulk electron transport.

chemistry.chemical_classification010405 organic chemistryStackingGeneral ChemistryElectron acceptor010402 general chemistryCondensed Matter Physics01 natural sciencesElectron transport chain0104 chemical sciencesCrystallographychemistryElectron affinity (data page)CruciformGeneral Materials ScienceCyclic voltammetryHOMO/LUMOCrystal Growth & Design
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Asymmetric addition of a nitrogen nucleophile to an enoate in the presence of a chiral phase-transfer catalyst: A novel approach toward enantiomerica…

2012

A proof of concept for the asymmetric organocatalytic aza-Michael addition reaction of nitrogen nucleophiles with simple and readily available alkyl enoates as acceptor molecules in the presence of a chiral phase-transfer catalyst has been demonstrated. The desired enantiomerically enriched beta-amino acid derivatives were obtained in up to 86% yield and with enantioselectivities of up to 37% ee. (C) 2012 Wiley Periodicals, Inc. Heteroatom Chem 23:202209, 2012; View this article online at . DOI 10.1002/hc.21004

chemistry.chemical_classificationAddition reactionchemistryNucleophileYield (chemistry)HeteroatomOrganic chemistryGeneral ChemistryAcceptorAlkylCatalysisAmino acidHeteroatom Chemistry
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Epoxidation of Olefins with a Silica-Supported Peracid

2012

Anhydrous [2-percarboxyethyl] functionalized silica (2a) is an advantageous oxidant for performing the epoxidation of olefins 1. Epoxides 3 do not undergo the ring-opening reactions catalyzed by the acidic silica surface, except for particularly activated cases such as styrene oxide. The hydrophilic and acidic character of the silica surface does not interfere with the directing effects exerted by allylic H-bond acceptor substituents. The alkenes 1 carrying hydroxyl groups react with silica-supported peracid 2a faster than unsubstituted alkenes, thus reversing the trend known for reactions with soluble peracids. These results are attributed to the H-bond interactions of substrate 1 with the…

chemistry.chemical_classificationAllylic rearrangementMolecular StructureChemistryCarboxylic acidOrganic ChemistrySubstrate (chemistry)AlkenesSilicon DioxideAcceptorCatalysisSilanolchemistry.chemical_compoundStyrene oxideAnhydrousEpoxy CompoundsOrganic chemistryThe Journal of Organic Chemistry
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Glass-forming non-symmetric bis-styryl-DWK-type dyes for infra-red radiation amplification systems

2019

Abstract A series of D-π-A type organic dyes with bulky triphenylmethyl moiety containing 2,6-bis-(4-substituted)styryl-4H-pyran-4-ylidene donor (D) fragments and different electron acceptors (A) were synthesized and investigated, mostly for potential applications in organic solid-state lasers as infra-red (IR) radiation amplification medium. Dye glass transition temperature is above 99 °C with thermal stability in the region from 173 °C to 326 °C which was slightly influenced by the electron acceptor fragment attached to the 4H-pyrane ring in 4-position. Introducing substituents in 4-position within one of the styryl-fragments with stronger electron withdrawing properties decreased ASE exc…

chemistry.chemical_classificationAmplified spontaneous emissionActive laser mediumDye laserMaterials sciencePhotoluminescenceOrganic Chemistry02 engineering and technologyElectron acceptor010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsInorganic ChemistrychemistryMoietyThermal stabilityElectrical and Electronic EngineeringPhysical and Theoretical Chemistry0210 nano-technologyGlass transitionSpectroscopyOptical Materials
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Fluorescence and amplified spontaneous emission of glass forming compounds containing styryl-4H-pyran-4-ylidene fragment

2012

Potential of glassy films of newly synthesised low molecular weight organic molecules for light amplification and lasing applications has been investigated by analysing fluorescence, transient differential absorption and amplified spontaneous emission properties. These non-symmetric and symmetric molecules contain styryl-4H-pyran-4-ylidene fragment with three different electron acceptor groups: dicyanomethylene, barbituric acid, indene-1,3-dione. Fluorescence quantum yields of the investigated compounds in solutions are between 0.32 and 0.54, while they drop down by an order of magnitude in thin solid films. Incorporation of bulky side groups reduced excitonic interactions enabling manifest…

chemistry.chemical_classificationAmplified spontaneous emissionBarbituric acidChemistryBiophysicsGeneral ChemistryElectron acceptorCondensed Matter PhysicsPhotochemistryBiochemistryFluorescenceAtomic and Molecular Physics and Opticschemistry.chemical_compoundPyranMoleculeLasing thresholdOrder of magnitudeJournal of Luminescence
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Glassy 2-(1-benzyl-2-styryl-6-methylpyridin-4(1H)-ylidene) fragment containing 1H-indene-1,3(2H)-dione and pyrimidine-2,4,6(1H,3H,5H)-trione derivati…

2020

A series of 2-(1-benzyl-2-(styryl)-6-methylpyridin-4(1H)-ylidene) fragment containing glassy organic compounds have been synthesized from relevant luminescent 4H-pyran-4-ylidene derivatives and investigated as potential solution processable emitters. Glass transition temperatures of synthesized 1H-pyridine compounds are above 100°C with thermal stabilities higher than 260°C. In the solutions of dichloromethane their absorption bands are in the range from 350 nm to 500 nm with photoluminescence from 500 nm to 650 nm. In a contrary to the 4H-pyran-4-ylidene derivatives, the incorporation of various electron acceptor fragments within the 1H-pyridine fragment containing molecules only slightly …

chemistry.chemical_classificationAmplified spontaneous emissionchemistry.chemical_compoundMaterials sciencePhotoluminescencechemistryMoleculeAbsorption (chemistry)IndeneElectron acceptorGlass transitionPhotochemistryLuminescenceFiber Lasers and Glass Photonics: Materials through Applications II
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The NreA Protein Functions as a Nitrate Receptor in the Staphylococcal Nitrate Regulation System

2013

Staphylococci are able to use nitrate as an alternative electron acceptor during anaerobic respiration. The regulation of energy metabolism is dependent on the presence of oxygen and nitrate. Under anaerobic conditions, staphylococci employ the nitrate regulatory element (Nre) for transcriptional activation of genes involved in reduction and transport of nitrate and nitrite. Of the three proteins that constitute the Nre system, NreB has been characterized as an oxygen sensor kinase and NreC has been characterized as its cognate response regulator. Here, we present structural and functional data that establish NreA as a new type of nitrate receptor. The structure of NreA with bound nitrate w…

chemistry.chemical_classificationAnaerobic respirationStaphylococcusIodideIsothermal titration calorimetryGene Expression Regulation BacterialElectron acceptorCrystallography X-RayResponse ElementsNitrate reductaseNitrate ReductaseProtein Structure SecondaryBacteria Anaerobicchemistry.chemical_compoundResponse regulatorNitratechemistryBiochemistryStructural BiologyMutationBinding siteMolecular BiologyJournal of Molecular Biology
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