Search results for "coupling [Higgs particle]"

showing 10 items of 443 documents

Absorptive effects inK+Λphotoproduction on nucleons and nuclei

1989

Incorporating final state correlation effects, we have reinvestigated the ..gamma.. /sup 1/H..-->..K/sup +/..lambda.. elementary process. Our model not only resolves the persisting trouble of the small KN..lambda.. coupling constant, but also yields agreement with cross section data at higher energies. Using our amplitudes, we calculate angular distributions for the reaction /sup 16/O(..gamma..,K/sup +/)/sub ..lambda..//sup 16/N . While the forward cross section increases with increasing energy, the total cross section is almost constant from E/sub ..gamma../ = 1.2 GeV through 2 GeV, suggesting that rather low photon energies hold promise for exploration of hypernuclear excitations.

Nuclear physicsPhysicsNuclear reactionCoupling constantNuclear and High Energy PhysicsAngular momentumMesonBranching fractionHadronElementary particleAtomic physicsNucleonPhysical Review C
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Probing the quenching of gA by single and double beta decays

2013

Abstract Ground-state-to-ground-state two-neutrino double beta ( 2 ν β β ) decays and single beta (EC and β − ) decays are studied for the A = 100 (100Mo 100Tc 100Ru), A = 116 (116Cd 116In 116Sn) and A = 128 (128Te 128I 128Xe) nuclear systems by using the proton–neutron quasiparticle random-phase approximation exploiting realistic effective interactions in very large single-particle bases. The aim of this exercise is to see if both the single-beta and double-beta decay observables related to the ground states of the initial, intermediate and final nuclei participant in the decays can be described simultaneously by changing the value of the axial-vector coupling constant g A . In spite of th…

Nuclear physicsPhysicsQuenchingCoupling constantNuclear and High Energy PhysicsQuasiparticleObservableBeta (velocity)Atomic physicsPhysics Letters B
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In vitro blood brain barrier exposure to mycotoxins and carotenoids pumpkin extract alters mitochondrial gene expression and oxidative stress.

2021

Abstract Food and feed are daily exposed to mycotoxin contamination which effects may be counteracted by antioxidants like carotenoids. Some mycotoxins as well as carotenoids penetrate the blood brain barrier (BBB) inducing alterations related to redox balance in the mitochondria. Therefore, the in vitro BBB model ECV304 was subcultured for 7 days and exposed to beauvericine, enniatins, ochratoxin A, zearalenone (100 nM each), individually and combined, and pumpkin extract (500 nM). Reactive oxygen species were measured by fluorescence using the dichlorofluorescein diacetate probe at 0 h, 2 h and 4 h. Intracellular ROS generation reported was condition dependent. RNA extraction was performe…

Ochratoxin ADown-RegulationGene ExpressionMitochondrionToxicologymedicine.disease_causeCell LineElectron Transport Complex IV03 medical and health scienceschemistry.chemical_compound0404 agricultural biotechnologyCucurbitaDichlorofluoresceinDepsipeptidesGene expressionmedicineHumansOxidoreductases Acting on Sulfur Group DonorsUncoupling Protein 2MycotoxinCarotenoid030304 developmental biologychemistry.chemical_classification0303 health sciencesReactive oxygen speciesChemistryPlant Extractsfood and beverages04 agricultural and veterinary sciencesGeneral MedicineMycotoxins040401 food scienceCarotenoidsMitochondriaUp-RegulationOxidative StressGenes MitochondrialBiochemistryBlood-Brain BarrierCarrier ProteinsReactive Oxygen SpeciesOxidative stressFood ScienceFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association
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Energy-Linked Reactions Catalyzed by the Purified ATPase Complex (F0F1) from Rhodospirillum rubrum Chromatophores

1980

1. The isolation of the F0F1-ATPase complex from Rhodospirillum rubrum chromatophores by the use of taurodeoxycholate is described. 2. The enzyme preparation contains about 12 polypeptides; five are subunits of the F1 moiety. 3. The ATPase activity of the purified enzyme is dependent on the addition of phospholipids. 4. Km-vales for Mg2+-ATP and Ca2+-ATP are similar to the values obtained for the membrane-bound enzyme. 5. The F0F1-ATPase complex is more than 70% inhibited by oligomycin and N,N′-dicyclohexyl-carbodiimide. 6. The F0F1-ATPase complex was integrated into liposomes. The reconstituted proteoliposomes catalyzed energy transduction as shown by ATP-dependent quenching of acridine dy…

OligomycinMacromolecular SubstancesBiologyRhodospirillum rubrumBiochemistryFluorescenceMembrane Lipidschemistry.chemical_compoundAdenosine TriphosphateMoietyAdenosine Triphosphataseschemistry.chemical_classificationLiposomeQuenching (fluorescence)Cell-Free SystemUncoupling AgentsATPase complexRhodospirillum rubrumMembrane ProteinsBacterial Chromatophoresbiology.organism_classificationFluorescenceMolecular WeightEnzymeSolubilitychemistryBiochemistryLiposomesEuropean Journal of Biochemistry
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Synthesis of rigid ethynyl-bridged polytopic picolinate ligands for MOF applications

2015

Abstract Segmented homopolytopic ligands that consist of a rigid central arylene platform, ethynylene spacers, and terminal chelating picolinate subunits have been synthesized in good yields in a two-step procedure involving a Sonogashira-type cross coupling reaction between the ester methyl 5-bromopyridine-2-carboxylate and several arylacetylenes, followed by hydrolysis of the resulting methyl picolinates. A similar strategy has been employed for the preparation of heteroditopic ligands containing picolinate and a second non-chelating pyridine or benzoate unit. The compounds are potential candidates for organic linkers in metal–organic frameworks (MOFs).

Organic ChemistryAryleneSonogashira couplingBiochemistryCombinatorial chemistryCoupling reactionchemistry.chemical_compoundHydrolysischemistryDrug DiscoveryPyridineOrganic chemistryMetal-organic frameworkChelationTetrahedron Letters
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Oxidative (Cross-)Coupling Reactions Mediated by C-H Activation of Thiophene Derivatives by Using Molybdenum(V) Reagents

2014

Oxidative coupling by using molybdenum pentachloride provides fast and modular access to sophisticated thienoacenes in excellent yields. The coupling process can be accomplished with thiophene and benzothiophene derivatives and provides various complex skeletons such as spirocyclic compounds. In this approach, the first cross-coupling reactions with the use of MoCl5 were established and important motifs for semiconducting materials were synthesized.

Organic ChemistryBenzothiophenechemistry.chemical_elementOxidative phosphorylationCombinatorial chemistryCoupling reactionCoupling (electronics)chemistry.chemical_compoundchemistryMolybdenumReagentThiopheneOrganic chemistryOxidative coupling of methanePhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Highly selective electrosynthesis of biphenols on graphite electrodes in fluorinated media.

2011

The direct and selective phenol coupling reaction that provides biphenols still represents a challenge in organic synthesis. The recently developed electrosynthesis on boron-doped diamond anodes with fluorinated additives was developed further to allow the application to less-expensive electrodes and fluorinated media. This advanced protocol allows the highly selective anodic phenol coupling reaction on graphite with a broad scope.

Organic ChemistryInorganic chemistryDiamondGeneral Chemistryengineering.materialElectrosynthesisElectrochemistryCombinatorial chemistryCatalysisCoupling reactionchemistry.chemical_compoundchemistryElectrodeengineeringPhenolOrganic synthesisGraphiteChemistry (Weinheim an der Bergstrasse, Germany)
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Synthesis of New 8-Arylisoquinoline Derivatives by Application of Palladium-Catalyzed Suzuki Cross-Coupling Reactions.

2005

Abstract New 8-(het)aryltetrahydroisoquinolines ( 10–14 ), 8-aryltetrahydroisoquinolin-4-ols ( 15 , 16 ), and 8-phenylisoquinolin-4-ol ( 17 ), flexible analogues of aporphine, were synthesized in good yields using palladium-catalyzed Suzuki cross-coupling reactions from 8-bromotetrahydroisoquinolin-4-one ( 6 ) as a common intermediate. We also describe the synthesis of this novel intermediate through an easy and efficient method, which involved intramolecular Friedel–Crafts cyclization.

Organic Chemistrychemistry.chemical_elementGeneral MedicineBiochemistryCombinatorial chemistryCoupling reactionCatalysischemistry.chemical_compoundchemistryIntramolecular forceDrug DiscoveryOrganic chemistryAporphinePalladiumChemInform
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Polycondensed nitrogen heterocycles. Part17. Isoxazolo[4,3-d]pyrazolo[3,4-f][1,2,3]triazepine. A new ring system

1987

The title compounds were prepared by nitration of compounds 2, reduction of the dinitro derivatives 4 and diazotization of the diamino derivatives 6 followed by an intramolecular coupling reaction. Compound 4a showed good activity against Salmonella cholerasuis and Clostridium perfringens bacteria.

Organic Chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyClostridium perfringensmedicine.disease_causeRing (chemistry)NitrogenCoupling reactionSalmonella cholerasuischemistry.chemical_compoundchemistryIntramolecular forceNitrationmedicineOrganic chemistryJournal of Heterocyclic Chemistry
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Palladium nanoparticles immobilized on halloysite nanotubes covered by a multilayer network for catalytic applications

2018

The synthesis of pure fine chemicals for industrial purposes is one of the most attractive challenges of chemical research. The use of catalytic pathways mediated by palladium nanoparticles (PdNPs) for C-C bond formation is a useful way to obtain these kinds of compounds. To achieve this objective, the PdNPs can be efficiently loaded on a functionalized natural nanostructured support such as halloysite nanotubes (HNTs). Hybrid materials based on thiol functionalized halloysite nanotubes and highly cross-linked imidazolium salts were successfully developed and used for the stabilization of PdNPs. The HNT/Pd hybrids were thoroughly characterized from a physico-chemical point of view and teste…

Palladium nanoparticles immobilized on halloysite nanotubes02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteCatalysisCoupling reactionCatalysisSuzuki reactionMaterials ChemistrySettore CHIM/02 - Chimica FisicaChemistryPalladium nanoparticlesSettore CHIM/06 - Chimica OrganicaGeneral ChemistryPalladium nanoparticles halloysite nanotubes catalyst021001 nanoscience & nanotechnology0104 chemical sciencesTurnover numberChemical engineeringMicrowave irradiationengineering0210 nano-technologyHybrid materialHalloysite nanotubes cross-coupling reactionsNew Journal of Chemistry
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