Search results for "hate"

showing 10 items of 2099 documents

Tritopic phenanthroline and pyridine tail-tied aza-scorpiands

2010

The synthesis of two new tritopic double-scorpiand receptors in which two equivalent 5-(2-aminoethyl)-2,5,8-triaza[9]-(2,6)-pyridinophane moieties have been linked with 2,6-dimethylpyridine (L1) or 2,9-dimethylphenanthroline (L2) units is reported for the first time. Their acid-base behaviour and Zn(2+) coordination chemistry have been studied by pH-metric titrations, molecular dynamic calculations, NMR, UV-Vis and steady-state fluorescence techniques. L1 and L2 behave, respectively, as hexaprotic and heptaprotic bases in the experimental conditions used (298.1 +/- 0.1 K, 0.15 mol dm(-3) NaCl, pH range under study 2.0-11.0). These ligands are able to form mono-, bi- and trinuclear Zn(2+) co…

chemistry.chemical_classificationStereochemistryPhenanthrolineOrganic ChemistryPotentiometric titrationBiochemistryFluorescenceMedicinal chemistryPyrophosphateCoordination complexchemistry.chemical_compoundMolecular dynamicschemistryPyridineTitrationPhysical and Theoretical ChemistryOrganic & Biomolecular Chemistry
researchProduct

Synthesis and characterization of mono- and binuclear copper(II) complexes with 2,2′:6′,2″-terpyridine (terpy) and carboxylates: X-ray crystal struct…

1987

Abstract Perchlorate and hexafluorophosphate salts of monomeric [Cu(terpy)(OOCH)(OH2)]+ and dimeric [Cu(terpy)(OOCR)]22+ cations (terpy = 2,2′:6′,2″-terpyridine, R = CH3 or C2H5) have been synthesized and characterized by IR, electronic and ESR spectra, and analytical data. Spectroscopic results indicate a five-coordinate, close-to-square pyramidal geometry around the copper(II) ion. The half-field absorption in the ΔMs = 2 region of powdered X-band ESR spectra has been observed for the dimeric species. The crystal structure of [Cu(terpy)(OOCH)(OH2)](ClO4) has been determined by X-ray diffraction methods. The compound crystallizes in the space group P21/c with unit-cell dimensions: a = 7.34…

chemistry.chemical_classificationStereochemistrychemistry.chemical_elementCrystal structureCopperInorganic ChemistryPerchloratechemistry.chemical_compoundCrystallographychemistryHexafluorophosphateX-ray crystallographyMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryTerpyridineInorganic compoundPolyhedron
researchProduct

ChemInform Abstract: In situ DRIFT Spectroscopic Investigation on the Chemical Evolution of Zinc Phosphate Acid-Base Cement.

2010

Diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy has been used to follow the chemical evolution of zinc phosphate acid−base cement (ZPC), which has been prepared from unmodified, as well as from aluminum- and zinc-modified orthophosphoric acid. For the first time, amorphous dizinc cyclotetraphosphate octahydrate, Zn2P4O12·8H2O, although hydrolytically instable, has been observed as precursor phase prior to crystallization of α-hopeite, α-Zn3(PO4)2·4H2O, in both systems. Within minutes from onset of mixing the infrared spectrum of unmodified ZPC is dominated by the characteristic vibrations of α-hopeite, due to matrix crystallization. Setting of modified ZPC is strongly af…

chemistry.chemical_classificationSteric effectsDiffuse reflectance infrared fourier transformBase (chemistry)ChemistryInorganic chemistryZinc phosphateGeneral Medicinelaw.inventionAmorphous solidchemistry.chemical_compoundlawPhase (matter)CrystallizationSpectroscopyChemInform
researchProduct

Anion-π Interaction: An Influential Force in Solid State Molecular Microstructures

2013

The crystal structures of simple triphenyl(pentafluorobenzyl)phosphonium salts provide crucial data on the influence of anion size on the molecular structure of bis(pentafluorobenzyl)phosphonium cations containing two adjacent electron-deficient moieties. Whereas the bromide anions interact by anion-π interaction in a 1:1 mode with the pentafluorobenzene unit Z-configured, the bulkier anions iodide, tetrafluoroborate, and hexafluorophosphate result in a 1:2 tweezer-like anti-configuration in which one anion interacts simultaneously with two pentafluorobenzene units. When spatial separation of the two electron-deficient rings match the size of the anion, anion-π interactions induce a conform…

chemistry.chemical_classificationTetrafluoroborateOrganic ChemistryInorganic chemistryIodideCrystal structureCrystal engineeringchemistry.chemical_compoundCrystallographychemistryBromideHexafluorophosphateMoleculePhosphoniumPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
researchProduct

Gold(iii) tetraarylporphyrin amino acid derivatives: ligand or metal centred redox chemistry?

2015

EPR spectroscopy and DFT calculations show that the site of reduction of porphyrinato gold(iii) complexes depends on the counterions X, the meso substituents R and the solvent.

chemistry.chemical_classificationValence (chemistry)010405 organic chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesPorphyrin0104 chemical scienceschemistry.chemical_compoundElectron transferChemistrychemistryValence isomerHexafluorophosphateDensity functional theoryElectron configurationCounterionChemical science
researchProduct

Influence of anthropogenic activity on the lead isotope signature of Thau Lake sediments (southern France): origin and temporal evolution

2000

Lead concentrations and isotopic compositions were determined on both bulk sediments deposited in the Thau lake in southern France during the last 200 years, and leachates derived from a series of sequential leachings of the sediments, making it possible to identify the sources, natural (i.e. indigenous lithologic) or anthropogenic, and to quantify the different inputs of Pb. Two distinct inputs of Pb could be distinguished. One of these corresponds to the terrigenous material entering the basin, representative of the local natural Pb ‘background’. Its supply remained steady most of the time with 206Pb/207Pb ratios of 1.200±0.003, except at the time of heavy storms producing voluminous and …

chemistry.chemical_classificationWatershedLithologyTerrigenous sedimentGeochemistryMineralogyStormStructural basinPollutionSilicatechemistry.chemical_compoundchemistryGeochemistry and PetrologyEnvironmental ChemistryOrganic matterLeachateGeologyApplied Geochemistry
researchProduct

Yeast interaction on Chardonnay wine composition: Impact of strain and inoculation time.

2022

Abstract It is of great importance to understand the molecular characteristics and substantial chemical transformations due to yeast-yeast interaction. Non-targeted metabolomics was used to unravel must in fermentation composition, inoculated with non-Saccharomyces (NS) yeasts and Saccharomyces cerevisiae (S) for sequential fermentation. ultrahigh-resolution mass spectrometry was able to distinguish thousands of metabolites and provides deep insights into grape must composition allowing better understanding of the yeast-yeast interactome. The dominance of S, characterized by a metabolic richness not found with NS, is dependent on inoculation time and on the yeast species present. Co-inocula…

chemistry.chemical_classificationWineChardonnay Wine ; Inoculation Time ; Metabolomics ; Sequential Fermentation ; Yeast-yeast InteractionbiologyChemistrySaccharomyces cerevisiaeWineSaccharomyces cerevisiaeGeneral MedicinePentose phosphate pathwaybiology.organism_classificationInteractomeYeastAnalytical ChemistryMetabolomicsYeast DriedBiochemistryFermentationVitisFermentationAmino acid synthesisFood Science
researchProduct

Determination of albendazole and ivermectin residues in cattle and poultry-derived samples from India by micellar liquid chromatography

2021

We have developed a method, based on micellar liquid chromatography, to determine albendazole and ivermectin in dairy products and biological waste from bovine, as well as edible tissues from poultry. Anthelmitics were resolved in less than 10 min using a C18 column and a mobile phase of 0.15 mol/L sodium dodecyl sulfate – 6% 1-pentanol at buffered at pH 7 with a 0.01 M phosphate salt, running under isocratic mode at 1 mL/min. Detection was by absorbance at 292 nm. Method was successfully validated following official validation guidelines, in terms of: selectivity, sensitivity, calibration range (0.0125−0.5 mg/kg to 25−50 mg/kg), linearity (r2 > 9990), trueness (86.3–105.6%), precision (<12…

chemistry.chemical_classificationbiological wasteChromatographyanthelminticmicellar liquid chromatographydairy productsfood analysisalbendazoledrug residueSalt (chemistry)PhosphateAlbendazoleivermectinAbsorbancechemistry.chemical_compoundIvermectinchemistryMicellar liquid chromatographyfood compositionmedicineAnthelminticSodium dodecyl sulfateedible tissuesFood Sciencemedicine.drugJournal of Food Composition and Analysis
researchProduct

On the biochemical classification of yeast trehalases: Candida albicans contains two enzymes with mixed features of neutral and acid trehalase activi…

2009

Abstract Two enzymes endowed with trehalase activity are present in Candida albicans . The cytosolic trehalase (Ntc1p), displayed high activity in exponential phase regardless of the carbon source (glucose, trehalose or glycerol). Ntc1p activity was similar in neutral (pH 7.1) or acid (pH 4.5) conditions, strongly inhibited by ATP, weakly stimulated by divalent cations (Ca 2+ or Mn 2+ ) and unaffected in the presence of cyclic AMP. The Ntc1p activity decreased in stationary phase, except in glycerol-grown cultures, but the catalytic properties did not change. In turn, the cell wall-linked trehalase (Atc1p) showed elevated activity in resting cells or in cultures growing on trehalose or glyc…

chemistry.chemical_classificationbiologyBiophysicsTrehalase activityCell BiologyHydrogen-Ion Concentrationbiology.organism_classificationBiochemistryTrehaloseYeastDivalentFungal ProteinsIsoenzymesCytosolchemistry.chemical_compoundAdenosine TriphosphateEnzymechemistryBiochemistryCandida albicansCyclic AMPTrehalaseTrehalaseCandida albicansMolecular BiologyBiochemical and Biophysical Research Communications
researchProduct

Aggregation of sponge cells. Isolation and characterization of an inhibitor of aggregation receptor from the cell surface.

1979

From the cell membranes of the sponge Geodia cydonium a component was isolated and purified which inhibits the aggregation factor isolated from the same source; the component was termed anti-aggregation receptor. This molecule was characterized as a glycoprotein (54% neutral carbohydrate) and its molecular weight is in the range of 180,000 One biological site of the anti-aggregation receptor was determined to be D-galactose. Indirect evidence presented seems to indicate that this molecule is present in an active form in aggregation-deficient cells and absent in aggregation-susceptible cells.

chemistry.chemical_classificationbiologyCellCell MembraneGuanosine MonophosphateMembrane ProteinsCarbohydratebiology.organism_classificationBiochemistryPoriferaMolecular WeightSpongeKineticsMembranemedicine.anatomical_structurechemistryBiochemistrymedicineMoleculeAnimalsGeodiaGlycoproteinReceptorCell AggregationEuropean journal of biochemistry
researchProduct