Search results for "Conjugation"

showing 10 items of 121 documents

Star-Shaped Conjugated Systems

2010

The present review deals with the preparation and the properties of star-shaped conjugated compounds. Three, four or six conjugated arms are attached to cross-conjugated cores, which consist of single atoms (B, C+, N), benzene or azine rings or polycyclic ring systems, as for example triphenylene or tristriazolotriazine. Many of these shape-persistent [n]star compounds tend to π-stacking and self-organization, and exhibit interesting properties in materials science: Linear and non-linear optics, electrical conductivity, electroluminescence, formation of liquid crystalline phases, etc.

Materials scienceoptoelectronics[n]starsTriphenyleneReviewStar (graph theory)ElectroluminescenceConjugated systemRing (chemistry)lcsh:Technologychemistry.chemical_compoundElectrical resistivity and conductivityCC couplingOrganic chemistryGeneral Materials ScienceBenzenelcsh:Microscopylcsh:QC120-168.85lcsh:QH201-278.5lcsh:TAzineCrystallographychemistrylcsh:TA1-2040lcsh:Descriptive and experimental mechanicslcsh:Electrical engineering. Electronics. Nuclear engineeringlcsh:Engineering (General). Civil engineering (General)lcsh:TK1-9971conjugationMaterials
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Synthesis of site-heterologous haptens for high-affinity anti-pyraclostrobin antibody generation.

2011

The design and synthesis of functional chemical derivatives of small organic molecules is usually a key step for the intricate production of a variety of bioconjugates. In this respect, the derivatization site at which the spacer arm is introduced in immunizing conjugates constitutes a highly critical parameter for the generation of high-affinity and selective antibodies. However, due to the usual complexity of the required synthetic procedures, the appropriate comparison of alternative tethering positions has often been neglected. In the present study, meticulous strategies were followed to prepare synthetic derivatives of pyraclostrobin with the same linkers located at diverse rationally-…

Models MolecularMolecular modelStereochemistryHeterologousBiochemistryAntibodieschemistry.chemical_compoundAntibody generationMoleculePhysical and Theoretical ChemistryImmunoassaysDerivatizationBioconjugationMolecular StructureOrganic ChemistryStrobilurinsCombinatorial chemistryAffinitieschemistryComputer assisted molecular modelingPyrazolesCarbamatesHaptenHaptensConjugateOrganicbiomolecular chemistry
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A quantum-chemical study of the structure, vibrations and SiH bond properties of disilylamine, NH(SiH3)2.

2002

Quantum-chemical calculations at HF, MP2 and B3LYP levels with 6-31G* and 6-311G** basis sets are reported for disilylamine, NH(SiH3)2. The equilibrium structure is found to vary with both level and basis set, all but one of the structures exhibiting a small lack of planarity of the HNSi2 system. The barrier to inversion, however, is found to be very low, at most 38 cm(-1). Vibration frequencies and intensities are calculated. The frequencies are scaled, where possible, either using updated infrared data or with the aid of factors transferred from N(CH3)(SiH3)2. Unobserved frequencies due to the v(s)NSi2, deltaNSi2 and delta(perpendicular)NH modes are predicted near 610, 210 and 360 cm(-1),…

Models MolecularSiliconSpectrophotometry InfraredChemistrySilicon CompoundsBiophysicsInfrared spectroscopyHydrogen atomHyperconjugationSpectrum Analysis RamanPotential energyAtomic and Molecular Physics and OpticsBiophysical PhenomenaAnalytical Chemistrysymbols.namesakesymbolsQuantum TheoryAtomic physicsInstrumentationMulliken population analysisSpectroscopyBasis setRaman scatteringNatural bond orbitalSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Polymeric and bio-hybrid nanovectors for drug delivery and imaging devices.

2014

Nanotechnology applied to the Medicine is providing new tools to the current therapeutic and diagnostic approaches to fight cancer and other diseases. However, many of the proposed nanodevices show some deficits related to both their inherent properties and performance, and the synthetic strategies proposed for their production. In the present work, a new promising approach based on e-beam radiation-induced radical crosslinking of a water soluble, biocompatible synthetic polymer has been developed. In particular, the possibility of generating Poly-N-(Vinyl- Pyrrolidone)(PVP)-based nanocarriers, i.e. nanogels with a base PVP structure, tailored physico-chemical properties (particles size dis…

Nanogele-beam irradiationBio-imagingbio-conjugationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieDrug-delivery
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Structure and biological evaluation of amino-functionalized PVP nanogels for fast cellular internalization

2013

Abstract Aminopropyl methacrylamide chloride-graft-poly(N-vinyl pyrrolidone) nanogels (NGs) were designed to exploit the favorable properties of poly(N-vinyl pyrrolidone) (PVP), such as its high affinity to water and complexation ability of ions, molecules and macromolecules, with the availability of primary amino groups for bioconjugation reactions. A thorough structural characterization of the nanoscalar networks was performed via 1 H NMR and solid state 13 C NMR spectroscopies, while solid state NMR relaxation time measurements completed the NGs description in terms of polymer network density. Information on the hydrodynamic size and surface charge densities were sought via dynamic light…

Nanogels Poly(N-vinyl pyrrolidone) Microemulsion polymerization Proton spin–lattice relaxation time Cellular internalizationPolymers and PlasticsGeneral Chemical EngineeringNanogelsBiochemistrychemistry.chemical_compoundproton spin- lattice relaxation timeDynamic light scatteringmicroemulsion polymerizationPolymer chemistryMaterials ChemistryEnvironmental ChemistryMethacrylamideBovine serum albuminBioconjugationbiologyChemistryGeneral ChemistryCarbon-13 NMRCombinatorial chemistrypoly(N-vinyl pyrrolidone)biology.proteinProton NMRcellular internalizationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieNanocarriersMacromolecule
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Biomolecular conjugation inside synthetic polymer nanopores via glycoprotein-lectin interactions

2011

We demonstrate the supramolecular bioconjugation of concanavalin A (Con A) protein with glycoenzyme horseradish peroxidase (HRP) inside single nanopores, fabricated in heavy ion tracked polymer membranes. Firstly, the HRP-enzyme was covalently immobilized on the inner wall of the pores using carbodiimide coupling chemistry. The immobilized HRP-enzyme molecules bear sugar (mannose) groups available for the binding of Con A protein. Secondly, the bioconjugation of Con A on the pore wall was achieved through its biospecific interactions with the mannose residues of the HRP enzyme. The immobilization of biomolecules inside the nanopore leads to the reduction of the available area for ionic tran…

NanometresSynthetic membraneTransport equationNanoporesInformation processingRectification propertiesCylinders (shapes)Materials TestingConcanavalin AGeneral Materials ScienceFunctional polymersConical nanoporeschemistry.chemical_classificationChemistryBlocking effectElectric rectifiersComputer simulationEnzymesData processingNanoporeEnzyme moleculesFunctional polymersMolecular imprintingPorosityBio-molecularInner wallsMolecular imprintingSupramolecular chemistryNanotechnologyHorseradish peroxidaseIonic transportsNanocapsulesBio-conjugationMoleculeParticle SizeAqueous solutionsGlycoproteinsBiomoleculesBioconjugationBiomoleculeNanostructuresModel simulationChemical engineeringModels ChemicalPolymer membraneConductance stateFISICA APLICADABiospecific interactionSynthetic polymersSugarsSupramolecular chemistryPore wallCarbodiimide-coupling chemistry
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Silicatein conjugation inside nanoconfined geometries through immobilized NTA–Ni(ii) chelates

2013

The chemical modification and bioconjugation processes inside confined geometries by His-tagged silicatein promote sensitive changes in the polarity and surface charge density that mainly contribute to the ionic current rectification properties of the single conical nanopores.

Nitrilotriacetic AcidPhysics::Biological PhysicsBioconjugationMolecular StructureChemistryMetals and AlloysChemical modificationIonic bondingCharge densityGeneral ChemistryCathepsinsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNanoporeChemical engineeringNickelOrganometallic CompoundsMaterials ChemistryCeramics and CompositesNanoparticlesOrganic chemistryChelationChelating AgentsChemical Communications
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Measurement of CP asymmetries in the decays B0 → K*0 μ+μ- and B+ → K+ μ+μ-

2014

The direct CP asymmetries of the decays B 0 → K *0 μ + μ − and B + → K + μ + μ − are measured using pp collision data corresponding to an integrated luminosity of 3.0 fb−1 collected with the LHCb detector. The respective control modes B 0 → J/ψK *0 and B + → J/ψK + are used to account for detection and production asymmetries. The measurements are made in several intervals of μ + μ − invariant mass squared, with the ϕ(1020) and charmonium resonance regions excluded. Under the hypothesis of zero CP asymmetry in the control modes, the average values of the asymmetries are ACP(B0→K∗0μ+μ−)=−0.035±0.024±0.003,ACP(B+→K+μ+μ−)=0.012±0.017±0.001, where the first uncertainties are statistical and the …

Nuclear and High Energy PhysicsParticle physicsB physicmedia_common.quotation_subject14.40.NdFlavour Changing Neutral CurrentsLHCb - Abteilung HofmannHadrons01 natural sciencesAsymmetryB physicsNOPhysics Particles & FieldsLuminosityStandard Model0103 physical sciencesLeptonic semileptonic and radiative decays of bottom mesonInvariant mass010306 general physicsLarge Hadron Collider (France and Switzerland)QCmedia_commonPhysicsFlavour Changing Neutral CurrentScience & TechnologyHadron-Hadron Scattering010308 nuclear & particles physicsPhysicsHigh Energy Physics::PhenomenologyGran Col·lisionador d'HadronsParticle physicsResonanceCharge conjugation parity time reversal and other discrete symmetrieLHCbCP violationRare decay13.20.HePhysical SciencesBottom mesons (|B|>0)11.30.ErFísica nuclearB physics; CP violation; Flavour Changing Neutral Currents; Hadron-Hadron Scattering; Rare decayProduction (computer science)High Energy Physics::ExperimentLHCFísica de partículesExperiments
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Backward frequency doubling of near infrared picosecond pulses.

2014

We report on backward second-harmonic generation using ps laser pulses in congruent lithium niobate with 3.2 µm periodic poling. Three resonant peaks were measured between 1530 and 1730 nm, corresponding to 16th, 17th and 18th quasi-phase-matching orders in the backward configuration, with a conversion efficiency of 4.75 x 10(-5%)/W for the 16th order. We could also discriminate the contributions from inverted domains randomized in duty-cycle.

Optical amplifierMaterials sciencebusiness.industryLithium niobateEnergy conversion efficiencyNonlinear OpticSecond-harmonic generationSettore ING-INF/02 - Campi ElettromagneticiLaserHarmonic generation and mixingSettore ING-INF/01 - ElettronicaAtomic and Molecular Physics and Opticslaw.inventionchemistry.chemical_compoundOpticschemistryPeriodic polinglawParametric ProcessePicosecondPicosecond phenomenabusinessPhase conjugationOptics express
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Observation of Time-Reversal Violation in the B0 Meson System

2012

Although CP violation in the B meson system has been well established by the B factories, there has been no direct observation of time reversal violation. The decays of entangled neutral B mesons into definite flavor states ($B^0$ or $\bar{B}^0$), and $J/\psi K_S^0$ or $c\bar{c} K_S^0$ final states (referred to as $B_+$ or $B_-$), allow comparisons between the probabilities of four pairs of T-conjugated transitions, for example, $\bar{B}^0 \rightarrow B_-$ and $B_- \rightarrow \bar{B}^0$, as a function of the time difference between the two B decays. Using 468 million $B\bar{B}$ pairs produced in $\Upsilon(4S)$ decays collected by the BABAR detector at SLAC, we measure T-violating parameter…

Particle physicsMesonElectron–positron annihilationFOS: Physical sciencesGeneral Physics and AstronomyQuantum entanglementBottom mesons01 natural sciencesMeasure (mathematics)High Energy Physics - ExperimentNuclear physicsHigh Energy Physics - Experiment (hep-ex)Physics and Astronomy (all)Decays of bottom mesonDecays of bottom mesons; Charge conjugation parity time reversal and other discrete symmetries; Bottom mesons0103 physical sciences[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex]B mesonCharge conjugation parity time reversal and other discrete symmetries010306 general physicsPhysics010308 nuclear & particles physicsSettore FIS/01 - Fisica SperimentaleHigh Energy Physics::PhenomenologyParticle physicsTime evolutionFísicaCharge conjugation parity time reversal and other discrete symmetrieSupersymmetryDecays of bottom mesonsHepBaBarPACS: 13.25.Hw 11.30.Er 14.40.NdCP violationHigh Energy Physics::ExperimentFísica de partículesExperiments
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