Search results for "solution"

showing 10 items of 5638 documents

Cytochemical techniques for zinc and heavy metals localization in nerve cells

2002

Zinc is one of the most abundant oligoelements in the living cell. It appears tightly bound to metallothioneins, loosely bound to some metalloproteins and nucleic acids, or even as free ion. Small amounts of zinc ions (in the nanomolar range) regulate a plentitude of enzymatic proteins, receptors, and transcription factors; thus, cells need accurate homeostasis of zinc ions. Some neurons have developed mechanisms to accumulate zinc in specific membrane compartments ("vesicular zinc") which can be revealed using histochemical techniques. This article is a short report on the different direct-indirect experimental approaches for zinc and heavy metal detection in neurons. Substances giving a b…

chemistry.chemical_classificationHistologyChemistryPrecipitation (chemistry)Metal ions in aqueous solutionchemistry.chemical_elementSalt (chemistry)ZincMetalMedical Laboratory TechnologyMembraneBiochemistryvisual_artNucleic acidMetalloproteinvisual_art.visual_art_mediumAnatomyInstrumentationMicroscopy Research and Technique
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Dimethoxy aromatic compounds. IV.—determination of stereochemistry of 2,3,6,7-tetraalkoxy-9,10-dihalomethyl-9,10-dihydroanthracenes by13C NMR chemica…

1987

The analysis of the 13C NMR spectra of several 2,3,6,7-tetraalkoxy-9,10-dihalomethyl-9,10-dihydroanthracenes showed a strong dependence of the chemical shift values on the orientation of the halomethyl groups. On this basis it was possible to determine both the configuration (cis or trans) and conformation of the isomers, even if only one isomer was available.

chemistry.chemical_classificationHydrocarbonChemistryStereochemistryChemical shiftChemical solutionGeneral Materials ScienceGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRMagnetic Resonance in Chemistry
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Complex Formation of DNA with Oppositely Charged Polyelectrolytes of Different Chain Topology:  Cylindrical Brushes and Dendrimers

2007

The complex formation between DNA (pUC19-supercoiled DNA, 2686 base pairs) and some polycations of different chain topologies in aqueous solution was studied by light scattering, gel electrophoresis, and AFM. The investigated polycations comprised cylindrical brush polymers with quaternized poly(vinylpyridine) and polyethylene imine side chains as well as a fifth generation dendrimer thus covering a broad molar mass regime of 3 × 104 g mol-1 < Mw < 1 × 107 g mol-1 and very different chemical charges/molecule, Z+, of 127 < Z+ < 5500. Irrespective of the polycation, the complexes formed in dilute solution exhibited a similar size in terms of the mean square radius of gyration, 〈Rg2〉, i.e., 30…

chemistry.chemical_classificationHydrodynamic radiusMolar massAqueous solutionPolymers and PlasticsOrganic ChemistryPolymerPolyelectrolyteInorganic ChemistryCrystallographychemistryDendrimerPolymer chemistryMaterials ChemistrySide chainRadius of gyrationMacromolecules
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17O NMR study of isomeric monochloro- and monohydroxy-benzaldehydes and chlorinated salicylaldehydes

1991

The 17O NMR chemical shifts of isomeric monochloro- and monohydroxy-benzaldehydes and chlorinated salicylaldehydes were measured at 40°C for 0.25 M CDCI3 solutions. The 17O NMR chemical shift of the carbonyl oxygen of the compounds studied varies from 506 to 573 ppm measured from external D2O. The observed variation is probably mainly due to the intramolecular hydrogen bonding between the adjacent carbonyl and hydroxyl groups. The 17O NMR chemical shift range of the hydroxyl oxygen is from 80 to 98 ppm.

chemistry.chemical_classificationHydrogen bondChemical shiftchemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyAldehydeMedicinal chemistryOxygenchemistryIntramolecular forceOrganic chemistryChemical solutionGeneral Materials ScienceMagnetic Resonance in Chemistry
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Size Exclusion Chromatography of Proteins on Improved Bonded Silica Columns

1985

Publisher Summary This chapter discusses the size exclusion chromatography (SEC) of proteins on improved bonded silica columns. Over the past few years, the use of high performance liquid chromatography (HPLC) has been extended to protein chemistry as a powerful separation and isolation technique. A spectrum of variants providing high resolution potential—ion exchange, reversed phase, hydrophobic interaction, affinity, and size exclusion—is available. Of these, SEC is the simplest with respect to method development and equipment design: proteins are separated according to their size in a short and predictable time span under isocratic conditions. The SEC columns are packed with micro-partic…

chemistry.chemical_classificationHydrophobic effectChromatographychemistryResolution (mass spectrometry)Phase (matter)Size-exclusion chromatographyHigh resolutionPolymerProtein chemistryHigh-performance liquid chromatography
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Stopped-Flow and DFT Studies of Proton Transfer and Isomerization of 5-Amino-3-imino-1,2,6,7-tetracyano-3H-pyrrolizine and Its Related Base 2-(5-Amin…

2001

International audience; A complete kinetic study of pH-dependent isomerization of 5-amino-3-imino-1,2,6,7-tetracyano-3H-pyrrolizine (HL) and 2-(5-amino-3,4-dicyano-2H-pyrrol-2-ylidene)-1,1,2-tricyanoethanide (L‘-) in the pH range from −0.5 to +13 in aqueous solution, which spans over 7 orders of magnitude for the pseudo-first-order rates (log k from −4.8 to +2.5), has revealed for the first time the existence of the corresponding conjugate species L- and HL‘. The study has allowed the determination of the acid dissociation constants of HL (pKa) and HL‘ (pKa‘), as well as all of the individual forward and reverse isomerization rates of the acidic (HL/HL‘) and basic (L-/L‘-) forms. Although L…

chemistry.chemical_classificationIsomerizationAqueous solutionBase (chemistry)ProtonStereochemistryEquilibrium[CHIM.ORGA]Chemical Sciences/Organic chemistryProtonation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesDecompositionAcid dissociation constant0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryKineticschemistryOrganic reactionsKinetic parametersPhysical and Theoretical Chemistry0210 nano-technologyIsomerizationConjugate
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Anion coordination chemistry in aqueous solution of polyammonium receptors

2006

The behavior of polyamines as receptors of selected families of anions in water is explored. First metallocyanide interaction with saturated polyammonium hosts is analyzed both in solution and in the solid state. The utility of potentiometry, multinuclear NMR, microcalorimetry and cyclic voltammetry to describe solution features of this chemistry is described for selected systems. Sulfate, phosphate, polyphosphate and nucleotide interactions with large polyammonium receptors are then reviewed. Hydrogen bond formation is discussed from a thermodynamic point of view. The influence of the presence of aromatic fragments within the structure on the binding strength is discussed. Factors affectin…

chemistry.chemical_classificationIsothermal microcalorimetryAqueous solutionHydrogen bondPolyphosphateInorganic chemistryCombinatorial chemistryCoordination complexInorganic ChemistryMetalchemistry.chemical_compoundchemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumNucleotidePhysical and Theoretical ChemistryCyclic voltammetryCoordination Chemistry Reviews
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Comparison of spin density calculation methods for various alkyl-substituted 9,10-anthraquinone anion radicals in the solution phase

1996

EPR and ENDOR spectra were recorded for 2-methyl-9,10-anthraquinone (2-methylAQ), 2-ethylAQ, 2-tertbutylAQ and 2,3-dimethylAQ anion radicals in the solution phase. The EPR spectra were simulated with the help of ENDOR data. The experimental isotropic hyperfine coupling constants (IHFCs) were compared with calculated values from semi-empirical INDO, spin-restricted AM1/CI and B3PW91 density-functional methods. The best computational methods for the IHFCs were the semi-empirical AM1/CI method and the B3PW91 density-functional method with a large basis set.

chemistry.chemical_classificationIsotropyAnalytical chemistryAnion radicalsGeneral ChemistryENDORAnthraquinoneSolution phaseAlkylanthraquinonesSpin density calculationSpectral linelaw.inventionchemistry.chemical_compoundchemistryTRIPLElawGeneral Materials ScienceEPRElectron paramagnetic resonanceBasis setAlkyl
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Robust Lanthanoid Picolinate-Based Coordination Polymers for Luminescence and Sensing Applications

2021

Picolinate-based segmented dianionic ligands L12– (5-((4-carboxyphenyl)ethynyl)picolinate) and L22– (5,5′-(ethyne-1,2-diyl)dipicolinate) have been used in the synthesis of the highly robust and luminescent europium(III) coordination polymers [(CH3)2NH2][Eu(H2O)2(L1)2] (1) and [(CH3)2NH2][Eu(L2)2]·H2O·CH3COOH (2). Both 1 and 2 exhibit high selectivity for detection of nitroaromatic compounds since they act as quenchers of the Eu3+ emission. Stern–Volmer plots, using nitrobenzene as a quencher, yielded values of KSV = 150 M–1 and 160 M–1 for 1 and 2, respectively. Luminescence studies in the presence of different metal ions indicate a high selectivity for Fe3+ detection, with KSV values of 47…

chemistry.chemical_classificationLanthanideSensing applicationsMetal ions in aqueous solutionchemistry.chemical_elementPolymerArticleInorganic ChemistryNitrobenzenechemistry.chemical_compoundchemistryPhysical chemistryPhysical and Theoretical ChemistryLuminescenceEuropiumSelectivityInorganic Chemistry
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Growth of fibrous aggregates of silica nanoparticles: Fibre growth by mimicking the biogenic silica patterning processes

2009

We describe the self-assembly of discrete SiO2 nanofibers via grafting of silicatein side chains to a polymer backbone. The covalent binding of silicatein to the backbone of the polymer is based on the affinity of the nitrilotriacetic acid (NTA) side chain, which serves as a ligand for the immobilization of His-tagged silicatein. The surface charge and the bulkiness of the protein moieties prevent the entropically favoured coil formation of the polymer and force it to adopt an open chain structure after hydrolysis of the silica precursors. The probes were characterized by scanning force microscopy (SFM) and optical light microscopy. Surface complexation of the resulting silica nanoparticles…

chemistry.chemical_classificationLigandNitrilotriacetic acidGeneral ChemistryPolymerCondensed Matter Physicschemistry.chemical_compoundchemistryChemical engineeringNanofiberPolymer chemistryMicroscopySide chainSurface chargeHigh-resolution transmission electron microscopySoft Matter
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