Search results for "quantitative"

showing 10 items of 2409 documents

Allylammonium hydrogen oxalate hemihydrate

2014

In the title hydrated molecular salt, C3H8N+·C2HO4−·0.5H2O, the water O atom lies on a crystallographic twofold axis. The C=C—C—N torsion angle in the cation is 2.8 (3)° and the dihedral angle between the CO2and CO2H planes in the anion is 1.0 (4)°. In the crystal, the hydrogen oxalate ions are linked by O—H...O hydrogen bonds, generating [010] chains. The allylammonium cations bond to the chains through N—H...O and N—H...(O,O) hydrogen bonds. The water molecule accepts two N—H...O hydrogen bonds and makes two O—H...O hydrogen bonds. Together, the hydrogen bonds generate (100) sheets.

chemistry.chemical_classificationQuantitative Biology::Biomoleculescrystal structureCrystallographyHydrogenHydrogen bondchemistry.chemical_elementSalt (chemistry)General ChemistryCrystal structureDihedral angleCondensed Matter PhysicsOrganic PapersOxalateIonCrystalCrystallographychemistry.chemical_compoundchemistryQD901-999General Materials SciencePhysics::Atomic PhysicsPhysics::Chemical PhysicsActa Crystallographica Section E-Structure Reports Online
researchProduct

Temperature effects on counterion binding to spherical polyelectrolytes: the charge-discharge transition of lignosulfonate

1995

Abstract The effect of temperature on the effective charge numbers and diffusion coefficients of polyelectrolytes has not nobee dealth with in many studies. The present study concerns the temperature behavior of lignosulfonate. Lignosulfonate is a polydisperse polyelectrolyte whose molecules are compact spheres in aqueous solutions. One of its most remarkable properties is that is loses its charge in 0.1 M NaCl aqueous solution at about 40°C. In order to explain this charge-discharge transition, a theory for ion binding to spherical polyelectrolytes based on the relative population of two hydration states of the charged groups is presented. The water molecules adjacent to the charged groups…

chemistry.chemical_classificationQuantitative Biology::Biomoleculeseducation.field_of_studyGlobular proteinInorganic chemistryPopulationBiophysicsCharge numberElectrolyteIon-associationEffective nuclear chargePolyelectrolyteCondensed Matter::Soft Condensed MatterIon bindingchemistryChemical physicsElectrochemistryPhysical and Theoretical ChemistryeducationBioelectrochemistry and Bioenergetics
researchProduct

Biopartitioning micellar chromatography: An alternative high-throughput method for assessing the ecotoxicity of anilines and phenols

2007

An investigation of the use of the chromatographic retention (log k) as an in vitro approach for modelling the toxicity to Fathead Minnows of anilines and phenols is developed. A data set of 65 compounds with available experimental toxicity data was used. Log k data at three pH values were used for the compounds classification and two groups or 'MODEs' were identified. For one 'MODE' a quantitative retention-activity relationship (QRAR) model was calculated. Finally, it was used to estimate the toxicity to Fathead minnows of anilines and phenols for which experimental data are not available. These estimations were compared to those obtained from another toxicity (to Tetrahymena pyriformis) …

chemistry.chemical_classificationQuantitative structure–activity relationshipAniline CompoundsChromatographyToxicity dataTetrahymena pyriformisClinical BiochemistryCyprinidaeQuantitative Structure-Activity RelationshipAromatic amineExperimental dataCell BiologyGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundPhenolschemistryTetrahymena pyriformisToxicityAnimalsSpectrophotometry UltravioletPhenolsEcotoxicityChromatography Micellar Electrokinetic CapillaryJournal of Chromatography B
researchProduct

Conformational studies of bottle-brush polymers absorbed on a flat solid surface.

2010

The adsorption of a bottle-brush polymer end-grafted with one chain end of its backbone to a flat substrate surface is studied by Monte Carlo simulation of a coarse-grained model, that previously has been characterized in the bulk, assuming a dilute solution under good solvent conditions. Applying the bond fluctuation model on the simple cubic lattice, we vary the backbone chain length $N_b$ from $N_b=67$ to $N_b = 259$ effective monomeric units, the side chain length $N$ from N=6 to N=48, and the grafting density $\sigma=1$, i.e., parameters that correspond well to the experimentally accessible range. When the adsorption energy strength $\epsilon$ is varied, we find that the adsorption tra…

chemistry.chemical_classificationRange (particle radiation)Quantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodGeneral Physics and AstronomyBackbone chainThermodynamicsFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterGyrationCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerAdsorptionchemistrySide chainSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryThe Journal of chemical physics
researchProduct

Determination of tyrosine through a FIA-direct chemiluminescence procedure.

2003

A new FI-direct chemiluminescence method is proposed for the determination of tyrosine, based on the oxidation of the amino acid by K(3)Fe(CN)(6) in potassium hydroxide medium, at room temperature and enhanced by the presence of beta-cyclodextrin and formic acid. The dynamic range was linear over the range 1.0-10.0 mgl(-1). A large study of the influence of foreign compounds was performed, including amino acids; and, the method showed high selectivity. The reproducibility between days resulted in a rsd (in slope%) of 4.8 and the repeatability with a rsd (n=50, 10.0 mgl(-1)) of 3.1%, the LOD (s/n=3) was 50 mugl(-1) and sample throughput 98 h(-1).

chemistry.chemical_classificationReproducibilityPotassium hydroxideChromatographyChemistryFormic acidRepeatabilityAnalytical Chemistrylaw.inventionAmino acidchemistry.chemical_compoundlawTyrosineQuantitative analysis (chemistry)ChemiluminescenceTalanta
researchProduct

Monte Carlo methods for polymer chains in two - dimensional geometries (polymers at surfaces and interfaces)

1993

Coarse-grained models of polymers at interfaces can be defined such that their treatment by Monte Carlo simulation is most convenient and efficient for the problem at hand. This simulation strategy is briefly illustrated with three examples: (1) The orientational ordering of rigid rod-like polymers grafted to a surface, where “table methods” can be used, applying a fine discretization of the angles describing rod orientation. (2) Surface enrichment of one species in a polymer blend is treated by a semi-grand-canonical technique. (3) The number of configurations and structure of a star polymer attached with its center to a wall is studied by a “growth technique” generalizing simple sampling …

chemistry.chemical_classificationSurface (mathematics)Quantitative Biology::BiomoleculesMaterials sciencePolymers and PlasticsDiscretizationOrganic ChemistryMonte Carlo methodPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterchemistryComputational chemistrySimple (abstract algebra)Orientation (geometry)Materials ChemistryPolymer blendStatistical physicsMakromolekulare Chemie. Macromolecular Symposia
researchProduct

Chain linear dimensions in the surface-enriched layer of polymer mixtures

1992

We calculate the mean-square end-to-end distances and mean-square gyration radii using the bond fluctuation model for a binary polymer blend in the presence of a wall by Monte Carlo simulation. In the bulk, the size of the minority, low-concentration polymer species is compressed compared to the majority one. In the vicinity of the wall, where the minority polymer concentration is enriched due to attraction from the wall, the dimensions of the two types of polymers are approximately equal and are essentially the same as in an athermal polymer melt. Thus, the geometric constraint is more important to the structure of the polymers than the polymer-polymer and polymer-wall interactions.

chemistry.chemical_classificationSurface (mathematics)Quantitative Biology::BiomoleculesMonte Carlo methodMineralogyPolymer architecturePolymerGyrationCondensed Matter::Soft Condensed MatterchemistryChain (algebraic topology)Chemical physicsPolymer blendLayer (electronics)Die Makromolekulare Chemie, Theory and Simulations
researchProduct

Dynamics of macromolecules grafted in spherical brushes under good solvent conditions

2013

Spherical polymer brushes have a structure intermediate between star polymers and polymer brushes on flat substrates, and are important building blocks of polymer nanoparticles. Molecular dynamics simulations are presented for isolated spherical polymer brushes under good solvent conditions, varying the grafting density as well as the chain length, using a coarse-grained bead-spring model of flexible chains. We complement previous work on the static properties of the same model by analyzing the chain dynamics, studying the motions of monomers in relation to their position along the grafted chains, and extract suitable relaxation times. A qualitative discussion in terms of the Rouse model is…

chemistry.chemical_classificationWork (thermodynamics)Quantitative Biology::BiomoleculesPolymers and PlasticsPolymer scienceOrganic ChemistryRelaxation (NMR)NanoparticlePolymerInorganic ChemistryCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicsPlanarMonomerchemistryMaterials ChemistryMacromoleculeMacromolecules
researchProduct

Sorting of Enhanced Reference Raman Spectra of a Single Amino Acid Molecule

2014

In this contribution, we report the identification of the principal reference Raman spectra of a single cystein molecule. To that purpose, we design an active Surface Enhanced Raman Spectroscopy (SERS) template based on surfactant-less Chebyshev nanoparticles operating in a microfluidic platform. A principal component analysis is obtained from fluctuating spectra to sort the reference spectra of cystein. The assignment of Raman bands brings new insight into the conformation of an amino acid adsorbed onto gold nanoparticle.

chemistry.chemical_classification[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Quantitative Biology::BiomoleculesSortingNanoparticleActive surfaceQuantitative Biology::GenomicsSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidCrystallographysymbols.namesakeGeneral EnergyAdsorptionchemistrysymbolsMoleculePhysical and Theoretical ChemistryRaman spectroscopyComputingMilieux_MISCELLANEOUSThe Journal of Physical Chemistry C
researchProduct

Simultaneous Automated Determination of Catecholamines, Serotonin, and Their Metabolites in Brain Tissue by HPLC and Electrochemical Detection

1993

Abstract A robust procedure with minimal tissue sample pretreatment, based on reversed-phase, ion-pair high performance liquid chromatography (HPLC) combined with electrochemical detection has been developed for the automated and simultaneous determination of the biogenic amines norepinephrine (NE), epinephrine (E), dopamine (DA), 5-hydroxytryptamine (5-HT) and their metabolites 3-methoxy-4-hydroxyphenylethyleneglycol (MHPG), 3,4-dihydroxyacetic acid (DOPAC), homovanillic acid (HVA) and 5-hydroxyindolacetic acid (H I A A) in as little as 0.5 mg brain tissue. The chromatographic conditions remain stable for at least 8 weeks. In particular small amounts of samples which do not allow reexamina…

chemistry.chemical_classificationchemistry.chemical_compoundChromatographyColumn chromatographyChemistryMetaboliteBiogenic amineHomovanillic acidMolecular MedicineCentrifugationHigh-performance liquid chromatographyQuantitative analysis (chemistry)Homogenization (biology)Journal of Liquid Chromatography
researchProduct