Search results for "COMB"

showing 10 items of 7115 documents

Acetylcholine-responsive cargo release using acetylcholinesterase-capped nanomaterials

2019

[EN] Mesoporous silica nanoparticles capped with acetylcholinesterase, through boronic ester linkages, selectively release an entrapped cargo in the presence of acetylcholine.

inorganic chemicalsNanoparticlemacromolecular substances010402 general chemistry01 natural sciencesCatalysisNanomaterialschemistry.chemical_compoundQUIMICA ORGANICAQUIMICA ANALITICAMaterials ChemistrymedicineBIOQUIMICA Y BIOLOGIA MOLECULAR010405 organic chemistryQUIMICA INORGANICAtechnology industry and agricultureMetals and AlloysGeneral ChemistryMesoporous silicaCombinatorial chemistryAcetylcholinesterase0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsstomatognathic diseaseschemistryCeramics and CompositesAcetylcholinemedicine.drug
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The study of time-resolved absorption and luminescence in PbWO4 crystals

2000

Abstract The transient absorption and luminescence under pulsed electron beam excitation were studied for undoped and La3+ doped PbWO4 crystals. The absorption band at ∼1.0 eV is suggested to be due to self-trapped electrons and the absorption band at 3.5 eV may be due to self-trapped holes. The formation of luminescence centers via electron–hole recombination is affected by La3+ in doped crystals. The large fraction of electrons and holes undergoes thermostimulated recombination within geminate pairs and the spatial separation of geminate pairs components is important in recombination process. The intrinsic (blue) luminescence arises in this recombination. The mechanism of La3+ influence o…

inorganic chemicalsNuclear and High Energy PhysicsAbsorption bandChemistryUltrafast laser spectroscopyDopingElectronAtomic physicsAbsorption (electromagnetic radiation)LuminescenceInstrumentationRecombinationExcitationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Truncated recombinant light harvesting complex II proteins are substrates for a protein kinase associated with photosystem II core complexes

1998

AbstractPrevious studies directed towards understanding phosphorylation of the chlorophyll a/b binding proteins comprising light harvesting complex II (LHC II) have concentrated on a single phosphorylation site located close to the N-terminus of the mature proteins. Here we show that a series of recombinant pea Lhcb1 proteins, each missing an N-terminal segment including this site, are nevertheless phosphorylated by a protein kinase associated with a photosystem II core complex preparation. An Lhcb1 protein missing the first 58 amino acid residues is not, however, phosphorylated. The results demonstrate that the LHC II proteins are phosphorylated at one or more sites, the implications of wh…

inorganic chemicalsPhotosystem IIMacromolecular SubstancesMolecular Sequence DataPhotosynthetic Reaction Center Complex ProteinsLight-Harvesting Protein ComplexesBiophysicsmacromolecular substancesBiologyBiochemistryDNA-binding proteinProtein kinaseThylakoid membraneSubstrate Specificitylaw.inventionStructural BiologylawGeneticsProtein phosphorylationAmino Acid SequencePhosphorylationProtein kinase AMolecular BiologyPlant ProteinsKinasePeasPeaPhotosystem II Protein Complexfood and beveragesCell BiologySpinachPeptide FragmentsRecombinant Proteinsenzymes and coenzymes (carbohydrates)BiochemistryThylakoidRecombinant DNALight harvesting proteinPhosphorylationbacteriaCarrier ProteinsProtein KinasesFEBS Letters
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Cisplatin plus weekly vinorelbine versus cisplatin plus vinorelbine on days 1 and 8 in advanced non-small cell lung cancer: a prospective randomized …

2008

Summary Purpose A phase III randomized trial was carried out to compare two schedules of the vinorelbine (VNR)–cisplatin (CDDP) regimen in patients with locally advanced unresectable poor prognosis stage IIIB or metastatic stage IV non-small cell lung cancer. The primary endpoints were overall survival (OS) and analysis of toxicity, while secondary endpoints included response rates, time-to-progression (TTP) and quality of life (QoL). Patients and methods Eligible patients were randomized to receive: (a) VNR 25 mg/m 2 on day 1, 8 and 15 plus CDDP 100 mg/m 2 on day 1 every 4 weeks or (b) VNR 30 mg/m 2 on day 1 and 8 plus CDDP 80 mg/m 2 on day 1 every 3 weeks. All patients were chemotherapy-n…

inorganic chemicalsPulmonary and Respiratory MedicineAdultMaleCancer Researchmedicine.medical_specialtyRandomizationLung NeoplasmsVinorelbineVinblastineGastroenterologyStatistics Nonparametriclaw.inventionRandomized controlled triallawInternal medicineCarcinoma Non-Small-Cell LungAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansProspective StudiesLung cancerProspective cohort studyneoplasmsAgedNeoplasm StagingChi-Square Distributionbusiness.industryVinorelbineMiddle Agedmedicine.diseaseVinblastineSurgeryRegimenLogistic ModelsTreatment OutcomeOncologyItalyDisease ProgressionQuality of LifeFemaleCisplatinbusinessFebrile neutropeniamedicine.drugLung cancer (Amsterdam, Netherlands)
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Nanolayered Cobalt-Molybdenum Sulfides as Highly Chemo- and Regioselective Catalysts for the Hydrogenation of Quinoline Derivatives

2018

[EN] Herein, a general protocol for the preparation of a broad range of valuable N-heterocyclic products by hydrogenation of quinolines and related N-heteroarenes is described. Interestingly, the catalytic hydrogenation of the N-heteroarene ring is chemoselectively performed when other facile reducible functional groups, including alkenes, ketones, cyanides, carboxylic acids, esters, and amides, are present. The key to successful catalysis relies on the use of a nanolayered cobalt-molybdenum sulfide catalyst hydrothermally synthesized from earth-abundant metal precursors. This heterogeneous system displays a tunable composition of phases that allows for catalyst regeneration. Its catalytic …

inorganic chemicalsSulfidechemistry.chemical_element010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysisCatalysisMetalchemistry.chemical_compoundQUIMICA ORGANICAChemo-/regioselective hydrogenationN-heterocycleschemistry.chemical_classificationHeterogeneous catalysis010405 organic chemistryQuinolineRegioselectivityGeneral ChemistryCombinatorial chemistry0104 chemical sciencesCo-Mo-S catalystschemistryMolybdenumvisual_artvisual_art.visual_art_mediumQuinolinesCobalt
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Promoting the activity and selectivity of high surface area Ni–Ce–O mixed oxides by gold deposition for VOC catalytic combustion

2011

Gold supported on nickel cerium oxide catalysts (Ni–Ce–O) have been studied for the total oxidation of propane, as a model for hydrocarbon volatile organic compound emission control. High surface area Ni–Ce–O catalysts were synthesized using a very simple evaporation method, where cerium and nickel salts were evaporated in the presence of a mixture of methanol and oxalic acid. Gold catalysts were prepared following a deposition–precipitation method. A very efficient catalyst for the oxidation of propane, in terms of both activity and selectivity, was obtained. This high activity has been related to the high surface area of the catalyst (and therefore to the presence of more active sites ava…

inorganic chemicalschemistry.chemical_classificationCerium oxideorganic chemicalsGeneral Chemical EngineeringInorganic chemistryOxalic acidchemistry.chemical_elementCatalytic combustionGeneral ChemistryIndustrial and Manufacturing EngineeringCatalysisCeriumchemistry.chemical_compoundNickelHydrocarbonCatalytic oxidationchemistryEnvironmental Chemistryheterocyclic compoundsChemical Engineering Journal
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Organic matter and wettability characteristics of wildfire ash from Mediterranean conifer forests

2015

Abstract Thermogravimetric analysis (TGA) and water repellency (wettability) determination of ash samples collected following wildfires at four different Mediterranean conifer forest sites in eastern Spain were conducted to provide insights into variations in key chemical and physical characteristics of ash. TGA allowed the evaluation of organic matter (OM) and inorganic carbonate (IC) characteristics and their role in ash wettability. Thermogravimetric profiles were recorded for 40 ash samples (ten from each site). The persistence of water repellency of all ash samples was assessed by the Water Drop Penetration Time (WDPT) test. OM contents decreased, whilst OM stability indices and IC con…

inorganic chemicalschemistry.chemical_classificationMediterranean climateHydrologyThermogravimetric analysisPhysicsCarbon sinkCombustionchemistry.chemical_compoundchemistryWater repellentEnvironmental chemistryEnvironmental scienceCarbonateOrganic matterWettingBiologyEarth-Surface Processes
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Novel oxybispyridylboronic acids: synthesis and study of their reactivity in Suzuki-type cross-coupling reactions

2007

Abstract This paper sets forth the synthesis of novel oxybispyridylboronic acids, which are prepared from the corresponding halo-oxybispyridines via halogen–metal exchange using n-butyllithium and treatment with triisopropylborate. A range of efficient cross-coupling reactions of these novel boronic acids with selected aryl halides is described. This strategy produces novel pyridylethers of interest in cholinergic medicinal chemistry.

inorganic chemicalschemistry.chemical_compoundchemistryArylOrganic ChemistryDrug DiscoveryOrganic chemistryHalideReactivity (chemistry)General MedicineBiochemistryCombinatorial chemistryCoupling reactionTetrahedron
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Bifunctional Acid-Base Catalysis

2011

Acid-base catalysis with bifunctional catalysts is a very prominent catalytic strategy in both small-molecule organocatalysts as well as enzyme catalysis. In both worlds, small-molecule catalysts and enzymatic catalysis, a variety of different general acids or hydrogen bond donors are used. In this chapter, important parallels between small molecule catalysts and enzymes are discussed, and a comparison is also made to the emerging field of frustrated Lewis pair catalysis.

inorganic chemicalschemistry.chemical_compoundchemistryHydrogen bondTetrahedral carbonyl addition compoundOxyanion holeBifunctionalCombinatorial chemistryFrustrated Lewis pairBifunctional catalystCatalysisEnzyme catalysis
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Soluble/MOF-Supported Palladium Single Atoms Catalyze the Ligand-, Additive-, and Solvent-Free Aerobic Oxidation of Benzyl Alcohols to Benzoic Acids.

2021

Metal single-atom catalysts (SACs) promise great rewards in terms of metal atom efficiency. However, the requirement of particular conditions and supports for their synthesis, together with the need of solvents and additives for catalytic implementation, often precludes their use under industrially viable conditions. Here, we show that palladium single atoms are spontaneously formed after dissolving tiny amounts of palladium salts in neat benzyl alcohols, to catalyze their direct aerobic oxidation to benzoic acids without ligands, additives, or solvents. With this result in hand, the gram-scale preparation and stabilization of Pd SACs within the functional channels of a novel methyl-cystein…

inorganic chemicalschemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysisMetalColloid and Surface ChemistryAtom economyMetal·lúrgiaDissolutionSolvent freeChemistryLigandQuímicaGeneral ChemistryCombinatorial chemistry0104 chemical sciencesSoluble/MOFOrganic reactionAlcoholsvisual_artvisual_art.visual_art_mediumPalladiumJournal of the American Chemical Society
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