Search results for "RESONANCE"

showing 10 items of 6625 documents

Conformational investigations of bis(α-aminoalkyl)phosphinic acids and studies of the stability of their complexes with Cu(II)

2008

Abstract Conformational investigations of a group of bis(α-aminoalkyl)phosphinic acids were performed by use of NMR spectroscopy and theoretical calculations. In the case of one of the studied compounds, substituted with aminobenzyl and amino(p-chlorobenzyl) moieties, a pH-dependent equilibrium between conformers, stabilized by intermolecular hydrogen bonds was observed. Potentiometric studies proved that these molecules formed stable complexes with copper(II) ions, where stoichiometry was 1:1 and 1:2 depending on pH of their aqueous solution.

Aqueous solutionStereochemistryHydrogen bondChemistryOrganic ChemistryIntermolecular forcePotentiometric titrationNuclear magnetic resonance spectroscopyAnalytical ChemistryInorganic ChemistryPolymer chemistryMoleculeConformational isomerismSpectroscopyStoichiometryJournal of Molecular Structure
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Thermal and Chemical Stability of Thiol Bonding on Gold Nanostars

2015

The stability of thiol bonding on the surface of star-shaped gold nanoparticles was studied as a function of temperature in water and in a set of biologically relevant conditions. The stability was evaluated by monitoring the release of a model fluorescent dye, Bodipy-thiol (BDP-SH), from gold nanostars (GNSs) cocoated with poly(ethylene glycol) thiol (PEG-SH). The increase in the BDP-SH fluorescence emission, quenched when bound to the GNSs, was exploited to this purpose. A maximum 15% dye release in aqueous solution was found when the bulk temperature of gold nanostars solutions was increased to T = 42 °C, the maximum physiological temperature. This fraction reduces 3-5% for temperatures …

Aqueous solutionSurface PropertiesAnalytical chemistryMetal NanoparticlesCondensed Matter PhysicSurfaces and InterfacesCondensed Matter PhysicsElectrochemistryPhotochemistryFluorescenceNanostructureschemistry.chemical_compoundchemistryColloidal goldElectrochemistryGeneral Materials ScienceChemical stabilityThermal stabilityGoldSulfhydryl CompoundsMaterials Science (all)Surface plasmon resonanceSurfaces and InterfaceEthylene glycolSpectroscopyLangmuir
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ChemInform Abstract: Synthesis and Magnetic Properties of Bis(μ-hydroxo)bis((2,2′-bipyridyl)copper(II)) Squarate. Crystal Structure of Bis(μ-hydroxo)…

1990

Abstract The compound [Cu2(bipy)2(OH)2](C4O4)·5.5H2O, where bipy and C4O42− correspond to 2,2′-bipyridyl and squarate (dianion of 3,4-dihydroxy-3-cyclo- butene-1,3-dione) respectively, has been synthesized. Its magnetic properties have been investigated in the 2–300 K temperature range. The ground state is a spin-triplet state, with a singlet-triplet separation of 145 cm−1. The EPR powder spectrum confirms the nature of the ground state. Well-formed single crystals of the tetrahydrate, [Cu2(bipy)2(OH)2](C4O4)·4H2O, were grown from aqueous solutions and characterized by X-ray diffraction. The system is triclinic, space group P 1 , with a = 9.022(2), b = 9.040(2), c = 8.409(2) A, α = 103.51(2…

Aqueous solutionTetrahydrateChemistrychemistry.chemical_elementGeneral MedicineCrystal structureTriclinic crystal systemAtmospheric temperature rangeCopperlaw.inventionCrystallographychemistry.chemical_compoundlawElectron paramagnetic resonanceGround stateChemInform
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N-Alkyl Ammonium Resorcinarene Chloride Receptors for Guest Binding in Aqueous Environment

2016

Host systems with guest binding ability in water and/or biological fluids are a current challenge in supramolecular host–guest chemistry. Here we present the first syntheses of water-soluble N-ethanol ammonium resorcinarene chlorides (NARCls) with terminal hydroxyl groups at the upper rim. The NARCls possess deep cavities and are shown to bind a variety of guest molecules such as linear and cyclic alkanes, linear halogenated alkanes, and aromatic fluorophores (naphthalene, p-(phenylazo)phenol) in water through hydrophobic interactions, as well as 1,4-dioxane (a water soluble guest) via hydrogen bonds. The receptors are monomeric in aqueous media and form 1:1 host–guest complexes with bindin…

Aqueous solutionta114010405 organic chemistryHydrogen bondDimerOrganic ChemistrySupramolecular chemistrymacromolecular substancesNuclear magnetic resonance spectroscopyResorcinarene010402 general chemistry01 natural sciencesHydrocarbonsHydrogen bonds0104 chemical sciencesHydrophobic effectchemistry.chemical_compoundMonomerHost-guest systemschemistryPolymer chemistryOrganic chemistryHydrophobic effectSupramolecular chemistryta116Asian Journal of Organic Chemistry
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Micro-Raman spectroscopy of pigments contained in different calcium carbonate polymorphs from freshwater cultured pearls

2008

The metastable calcium carbonate polymorph vaterite has recently been found to occur commonly in freshwater cultured pearls from Japan and China. Organic pigment molecules in these vaterite regions of freshwater cultured pearls were analysed by resonance and near-resonance micro-Raman spectroscopy, in single spectra and in mapping modes and are compared with their aragonitic counterparts. Four different excitation wavelengths (487.9, 514.5, 532.2 and 632.8 nm) were used, resulting in differential increase of resolution for the pigments. Although vaterite areas were always lightly coloured (light yellow, light brown or white), ten different pigments were identified and a single colour is for…

AragoniteMineralogyengineering.materialConjugated systemResonance (chemistry)Crystallographysymbols.namesakechemistry.chemical_compoundPigmentCalcium carbonatechemistryVateritevisual_artengineeringsymbolsvisual_art.visual_art_mediumGeneral Materials ScienceRaman spectroscopySpectroscopySpectroscopyJournal of Raman Spectroscopy
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Unusual oleanane-type saponins from Arenaria montana

2010

Three oleanane-type saponins, 3-O-β-d-glucopyranosylechinocystic acid 28-O-β-d-xylopyranosyl-(1→4)-[α-l-rhamnopyranosyl-(1→2)]-α-l-rhamnopyranosyl ester (1), 3-O-β-d-glucopyranosylechinocystic acid 28-O-α-l-arabinopyranosyl-(1→3)-β-d-xylopyranosyl-(1→4)-[α-l-rhamnopyranosyl-(1→2)]-α-l-rhamnopyranosyl ester (2), 3-O-β-d-glucopyranosylcaulophyllogenin 28-O-β-d-apiofuranosyl-(1→3)-β-d-xylopyranosyl-(1→4)-[β-d-apiofuranosyl-(1→3)]-α-l-rhamnopyranosyl-(1→2)-α-l-rhamnopyranosyl ester (3) were isolated from the whole plant of Arenaria montana. Their unusual structures for the Caryophyllaceae family were established mainly by 2D NMR techniques and mass spectrometry.

Arenaria montanaMagnetic Resonance SpectroscopyStereochemistryChemical structureArenaria PlantSaponinCaryophyllaceaeAntineoplastic AgentsPlant ScienceHorticultureMass spectrometryBiochemistryMass Spectrometrychemistry.chemical_compoundCell Line TumorBotanyHumansOleanolic AcidMolecular BiologyOleananeCell Proliferationchemistry.chemical_classificationDose-Response Relationship DrugMolecular StructurebiologyStereoisomerismGeneral MedicineSaponinsbiology.organism_classificationchemistryDrug Screening Assays AntitumorEchinocystic acidTwo-dimensional nuclear magnetic resonance spectroscopyPhytochemistry
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New organotin(IV) complexes with L-Arginine,Nα-t-Boc-L-Arginine and L-Alanyl-L-Arginine.Synthesis, structural investigations and cytotoxic activity

2010

Abstract Novel diorganotin(IV) derivatives of l -Arginine (HArg), N α -( tert -Butoxycarbonyl)- l -Arginine (Boc–Arg–OH) and l -Ala- l -Arg (H 2 Ala–Arg), H 2 NC( NH)NH(CH 2 ) 3 CH(NHR′)CO 2 H, where R′ = H in HArg, R′ = C(O)OC(CH 3 ) 3 in Boc–Arg–OH, R′ = H 2 NCH(CH 3 )CO in H 2 Ala–Arg and triorganotin(IV) derivatives of Boc–Arg–OH have been synthesized and structurally characterized. The complexes were investigated by FT-IR and 119 Sn Mossbauer in the solid state and by 1 H, 13 C, 119 Sn and 1 H– 1 H COSY NMR spectroscopy, in solution. The spectroscopic characterization leading to the proposed molecular structures was accomplished on the basis of these experiments. l -Arginine appears to…

ArginineStereochemistryLigandOrganic ChemistryL-Arginine; Boc-Arg-OH; L-Alanyl-L-Arginine; organotin(IV); NMR; cytotoxic activitySubstrate (chemistry)Biological activityorganotin(IV)BiochemistryL-ArginineNMRInorganic ChemistryL-Alanyl-L-Argininechemistry.chemical_compoundchemistryBoc-Arg-OHSettore CHIM/03 - Chimica Generale E InorganicaMaterials ChemistryChelationCarboxylatePhysical and Theoretical ChemistryCytotoxicityTwo-dimensional nuclear magnetic resonance spectroscopycytotoxic activity
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Rotation of methyl radicals in a solid krypton matrix

2009

Electron spin resonance (ESR) measurements were carried out to study the rotation of methyl radicals (CH(3)) in a solid krypton matrix at 17-31 K temperature range. The radicals were produced by dissociating methane by plasma bursts generated by a focused 193 nm excimer laser radiation during the krypton gas condensation on the substrate. The ESR spectrum exhibits only isotropic features at the temperature range examined, and the intensity ratio between the symmetric (A) and antisymmetric (E) spin state lines exhibits weaker temperature dependence than in a solid argon matrix. However, the general appearance of the methyl radical spectrum depends strongly on temperature due to the pronounce…

ArgonSpin statesKryptonGeneral Physics and Astronomychemistry.chemical_elementlaw.inventionchemistrylawExcited statePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsGround stateAnisotropyElectron paramagnetic resonanceHyperfine structureThe Journal of Chemical Physics
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Role of vitreous matrix on the optical activity of Ge-doped silica

2003

Abstract We report an experimental study on the relationship between the optical activity of Ge-oxygen deficient centers and dynamic properties and conformational heterogeneity of vitreous matrix in silica. We focus our attention on the absorption band at ∼5.2 eV (B 2β ) and on the two related emissions at ∼4.2 eV (α E ) and at ∼3.1 eV (β). From the temperature dependence of B 2β band we estimate a mean energy value of 26 meV for local vibrational modes coupled to the electronic transition, suggesting that the chromophore and its surrounding have access to low frequency dynamics. From the thermal behavior of the two emissions we distinguish the two competitive relaxation processes from the …

Arrhenius equationChemistryRelaxation (NMR)General ChemistryActivation energyChromophoreCondensed Matter PhysicsMolecular physicsMolecular electronic transitionsymbols.namesakeNuclear magnetic resonanceAbsorption bandExcited statesymbolsGeneral Materials ScienceTriplet stateJournal of Physics and Chemistry of Solids
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Irradiation induced Germanium Lone Pair Centers in Ge-doped Sol-gel SiO2: luminescence lifetime and temperature dependence

2010

We studied the temperature dependence of the emission profile and of the lifetime, measured at 4.3 eV, related to the germanium lone pair centers (GLPC) induced by gamma ray at 5 MGy in a Ge-doped silica sample and in an analogous sample irradiated at 10 MGy, in which by a successive thermal treatment up to 415 °C the induced GLPC has been modified (named residual GLPC in the following). The measurements were recorded in the temperature range 10-300 K using an excitation of ∼5.2 eV. The data show that the energy level scheme of the induced and the residual GLPC is very similar to that of the native defects generated during the synthesis, and the intersystem crossing process (ISC) of the ind…

Arrhenius equationPhotoluminescenceSettore FIS/01 - Fisica SperimentaleBiophysicsAnalytical chemistrychemistry.chemical_elementGermaniumGeneral ChemistryAtmospheric temperature rangeCondensed Matter PhysicsBiochemistryAtomic and Molecular Physics and OpticsGe-doped silica Luminescenza difetti di puntosymbols.namesakeIntersystem crossingNuclear magnetic resonancechemistrysymbolsIrradiationLuminescenceLone pair
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