Search results for "Molecule"

showing 10 items of 5162 documents

Potent affinity material for tracing acetone and related analytes based on molecular recognition by halogen bonds.

2014

Affinity materials based on halogen bonds turned out to be a powerful tool for the molecular recognition of acetone or related carbonyl compounds in the presence of ubiquitous protic molecules. The superior selectivity and sensitivity were found by the gravimetric detection of volatile organic compounds by quartz crystal microbalances.

inorganic chemicalsAnalyteMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystalchemistry.chemical_compoundMolecular recognitionchemistryHalogenMaterials ChemistryCeramics and CompositesAcetoneMoleculeOrganic chemistryGravimetric analysisSelectivityChemical communications (Cambridge, England)
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Properties of a triazolopyridine system as a molecular chemosensor for metal ions, anions, and amino acids.

2006

The characteristics as a chemosensor of the compound 3-methyl-6,8-di(2-pyridyl)-[1,2,3]triazolo[5',1':6,1]pyrido[2,3-]pyrimidine (1) have been analyzed. Interaction with Cu(2+) produces a quenching of the fluorescence, while interaction with Zn(2+) leads to a quenching of the fluorescence followed by a bathochromic shift. The crystal structure of the Zn(1)(H(2)O)(3)(ClO(4))(2) x H(2)O complex shows the coordination of Zn(2+) through the terpyridine moiety. The octahedral site is completed by three water molecules. Interactions of the Zn(2+) complex with the anions sulfate, nitrate, nitrite, and dihydrogenphosphate in ethanol produce hypsochromic shifts and restoration of the fluorescence wh…

inorganic chemicalsAnionsQuenching (fluorescence)ChemistryPyridinesMetal ions in aqueous solutionOrganic ChemistryInorganic chemistryCrystallography X-RayMedicinal chemistrychemistry.chemical_compoundSpectrometry FluorescenceMetalsCationsBathochromic shiftMoleculeMoietyTriazolopyridineHypsochromic shiftSpectrophotometry UltravioletTerpyridineAmino AcidsThe Journal of organic chemistry
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Monoamide Derivatives of EDTA Incorporating Pendent Carboxylates or Pyridyls: Synthesis, Metal Binding, and Crystal Structure of a Dinuclear Ca2+ Com…

2017

EDTA is a powerful, cheap and widely-used chelating unit for a large range of metal ions. To link it covalently to other molecules, the formation of an amide bond using one of the carboxylates is an attractive and simple approach, even though it may compromise metal ion binding as one of the four carboxylate donors is lost. Here we undertake a quantitative study of the metal ion binding of two new mono-amide derivatives of EDTA, namely AmGly1 and AmPy1, featuring an additional coordinating carboxylate or pyridyl group in the amide, respectively. The compounds are conveniently synthesised through alkylation of the tris-t-butyl ester of ethylenediamine-triacetic acid with the appropriate α-ch…

inorganic chemicalsAqueous solution010405 organic chemistryStereochemistryChemistryMetal ions in aqueous solutionGeneral ChemistryCrystal structure010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundAmidePolymer chemistryMoleculeChelationCarboxylateCoordination geometryChemistrySelect
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<i>Geminal</i> Parahydrogen-Induced Polarization: Accumulating Long-Lived Singlet Order on Methylene Proton Pairs

2020

Abstract. In the majority of hydrogenative PHIP (Parahydrogen Induced Polarization) experiments, the hydrogen molecule undergoes pairwise cis-addition to an unsaturated precursor to occupy vicinal positions on the product molecule. However, some ruthenium-based hydrogenation catalysts induce geminal hydrogenation, leading to a reaction product in which the twohydrogen atoms are transferred to the same carbon center, forming a methylene (CH2) group. The singlet order of parahydrogen is substantially retained over the geminal hydrogenation reaction, giving rise to a singlet-hyperpolarized CH2 group. Although the T1 relaxation times of the methylene protons are often short, the singlet order h…

inorganic chemicalsGeminalHydrogen010405 organic chemistrychemistry.chemical_element010402 general chemistrySpin isomers of hydrogenPhotochemistry01 natural sciencesChemical reaction0104 chemical sciencesChemical kineticschemistry.chemical_compoundchemistryMoleculeSinglet stateMethylene
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Combined NC-AFM and DFT study of the adsorption geometry of trimesic acid on rutile TiO2(110)

2010

The adsorption behavior of trimesic acid (TMA) on rutile TiO(2)(110) is studied by means of non-contact atomic force microscopy (NC-AFM) and density-functional theory (DFT). Upon low-coverage adsorption at room temperature, NC-AFM imaging reveals individual molecules, centered above the surface titanium rows. Based on the NC-AFM results alone it is difficult to deduce whether the molecules are lying flat or standing upright on the surface. To elucidate the detailed adsorption geometry, we perform DFT calculations, considering a large number of different adsorption positions. Our DFT calculations suggest that single TMA molecules adsorb with the benzene ring parallel to the surface plane. In…

inorganic chemicalsHydrogenSurface PropertiesStereochemistryMolecular Conformationchemistry.chemical_elementBiosensing TechniquesMicroscopy Atomic ForceRing (chemistry)530chemistry.chemical_compoundAdsorptionMoleculeGeneral Materials ScienceTitaniumTemperatureTricarboxylic AcidsCondensed Matter PhysicsCarbonTitanium oxideOxygenCrystallographychemistryRutileAdsorptionTrimesic acidHydrogenTitaniumJournal of Physics: Condensed Matter
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Laboratory measurements and astronomical search for the HSO radical

2016

[Context] Despite the fact that many sulfur-bearing molecules, ranging from simple diatomic species up to astronomical complex molecules, have been detected in the interstellar medium, the sulfur chemistry in space is largely unknown and a depletion in the abundance of S-containing species has been observed in the cold, dense interstellar medium. The chemical form of the missing sulfur has yet to be identified.

inorganic chemicalsMethods: laboratory: molecularHydrogenLine: identificationlaboratory: molecular [Methods]chemistry.chemical_elementContext (language use)ISM: moleculeAstrophysics7. Clean energy01 natural sciencesArticleAbundance (ecology)0103 physical sciencesPhysics::Chemical Physicsidentification [Line]Spectral resolutionSubmillimeter: ISM010303 astronomy & astrophysicsAstrophysics::Galaxy Astrophysicsmolecules [ISM]Radio lines: ISMPhysics010304 chemical physicsMolecular dataTriatomic moleculeISM [Submillimeter]AstronomyAstronomy and AstrophysicsAstronomy and AstrophysicSulfurDiatomic moleculeISM: moleculesISM [Radio lines]Interstellar mediumchemistry13. Climate actionSpace and Planetary ScienceAstronomy & Astrophysics
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Stromal Interaction Molecule 1 (STIM1) Is Involved in the Regulation of Mitochondrial Shape and Bioenergetics and Plays a Role in Oxidative Stress

2012

Calcium ions are involved in a plethora of cellular functions including cell death and mitochondrial energy metabolism. Store-operated Ca(2+) entry over the plasma membrane is activated by depletion of intracellular Ca(2+) stores and is mediated by the sensor STIM1 and the channel ORAI1. We compared cell death susceptibility to oxidative stress in STIM1 knock-out and ORAI1 knockdown mouse embryonic fibroblasts and in knock-out cells with reconstituted wild type and dominant active STIM1. We show that STIM1 and ORAI1 deficiency renders cells more susceptible to oxidative stress, which can be rescued by STIM1 and ORAI1 overexpression. STIM1 knock-out mitochondria are tubular, have a higher Ca…

inorganic chemicalsProgrammed cell deathORAI1 ProteinEukaryotic Initiation Factor-2Active Transport Cell NucleusApoptosisMitochondrionBiologymedicine.disease_causeBiochemistryMiceeIF-2 KinasemedicineAnimalsStromal Interaction Molecule 1PhosphorylationMolecular BiologyTranscription factorCells CulturedMice KnockoutEIF-2 kinaseMembrane GlycoproteinsEndoplasmic reticulumMolecular Bases of DiseaseSTIM1Cell BiologyFibroblastsEmbryo MammalianMitochondriaCell biologyOxidative Stressbiology.proteinCalciumCalcium ChannelsEnergy MetabolismIntracellularOxidative stressJournal of Biological Chemistry
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Bis[S-hexyl 3-(thiophen-2-ylmethylidene)dithiocarbazato-κ2N3,S]palladium(II)

2016

In the title complex, [Pd(C12H17N2S3)2], the PdIIatom exhibits a square-planar coordination geometry with theN,S-chelating ligands arranged in atransconfiguration. Intramolecular C—H...S hydrogen bonds are observed. In the crystal, molecules are linked by weak C—H...N hydrogen-bond interactions, forming chains parallel to thebaxis.

inorganic chemicalsQuantitative Biology::Biomoleculescrystal structureChemistryStereochemistryHydrogen bondThio-chemistry.chemical_elementGeneral MedicineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryhumanitiespalladium(II) complex0104 chemical sciencesCrystalTrans configurationlcsh:QD901-999lcsh:Crystallographydithiocarbazate ligandCoordination geometryPalladiumIUCrData
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Formation and growth of palladium nanoparticles inside porous poly(4-vinyl-pyridine) monitored by operando techniques: The role of different reducing…

2017

In this work we followed the formation of palladium nanoparticles, starting from palladium (II) acetate precursor, inside a poly(4-vinylpyridine-co-divinylbenzene) polymer in presence of different reducing agents. The formation and growth of palladium nanoparticles in presence of H-2 was followed as a function of temperature by simultaneous XANES-SAXS techniques, coupled with DRIFT spectroscopy in operando conditions. It was found that the pyridyl functional groups in the polymer plays a fundamental role in the stabilization of the palladium (II) acetate precursor, as well as in the stabilization of the palladium nanoparticles. The effect of a thermal treatment in alcohol (ethanol and 2-pro…

inorganic chemicalsReducing agentInfrared spectroscopychemistry.chemical_element02 engineering and technologyThermal treatment010402 general chemistryPhotochemistry01 natural sciencesAEROBIC ALCOHOL OXIDATIONCatalysisCatalysiCatalysisP4VPRUTHENIUM NANOPARTICLESMoleculeOrganic chemistryOperandoCATALYTIC-ACTIVITYchemistry.chemical_classificationPD NANOPARTICLESDRIFT; Operando; P4VP; Palladium nanoparticles; SAXS; XANESChemistryIN-SITUChemistry (all)SAXSGeneral ChemistryPolymerPalladium nanoparticleSELECTIVE OXIDATION021001 nanoscience & nanotechnologyPalladium nanoparticlesXANESX-RAY-SCATTERINGPARTICLE-SIZE0104 chemical sciencesDRIFTColloidal goldGOLD NANOPARTICLESVIBRATIONAL PROPERTIESDRIFT; Operando; P4VP; Palladium nanoparticles; SAXS; XANES; Catalysis; Chemistry (all)0210 nano-technologyPalladiumCatalysis Today
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Structure-based evaluation of the resonance interactions and effectiveness of the charge transfer in nitroamines

2011

Structural data for five nitroamines of general formula Me2N–G–NO2 show effectiveness of the ground-state charge transfer to be most and least efficient in N,N-dimethylnitramine and in 4-N,N-dimethylamino-β-nitrostyrene, respectively. Electron-donor power of the amino nitrogen atom in the latter compound is less than that in 4-nitro-β-N,N-dimethylaminostyrene (these two compounds are isomers). Natural population analysis shows that the charge transfer from the amino to the nitro oxygen atoms is most effective in N,N-dimethylnitramine, Me2N–NO2. The nitro oxygen atoms are not the only acceptors of the negative charge lost by the amino nitrogen atom. The nitro group in two substituted nitrobe…

inorganic chemicalsSubstituentCharge (physics)Resonance (chemistry)Ring (chemistry)Condensed Matter PhysicsMedicinal chemistryNitrobenzenechemistry.chemical_compoundchemistryComputational chemistryNitroMoleculePhysical and Theoretical ChemistryBenzeneStructural Chemistry
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