Search results for "ta116"

showing 10 items of 942 documents

Fluorescence of Newo-Carborane Compounds with Different Fluorophores: Can it be Tuned?

2014

Two sets of o-carborane derivatives incorporating fluorene and anthracene fragments as fluorophore groups have been successfully synthesized and characterized, and their photophysical properties studied. The first set, comprising fluorene-containing carboranes 6-9, was prepared by catalyzed hydrosilylation reactions of ethynylfluorene with appropriate carboranylsilanes. The compound 1-[(9,9-dioctyl-fluorene-2-yl)ethynyl]carborane (11) was synthesized by the reaction of 9,9-dioctyl-2-ethynylfluorene and decaborane (B10H14). Furthermore, reactions of the lithium salt of 11 with 1 equivalent of 4-(chloromethyl)styrene or 9-(chloromethyl)anthracene yielded compounds 12 and 13. Members of the se…

AnthraceneHydrosilylationOrganic ChemistrySubstituentGeneral ChemistryFluorenePhotochemistryFluorescenceMedicinal chemistryCatalysisDilithiumchemistry.chemical_compoundchemistryDecaboraneCarboraneta116Chemistry - A European Journal
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Anthracene Fluorescence Quenching by a Tetrakis (Ketocarboxamide) Cavitand

2014

Quenching of both fluorescence lifetime and fluorescence intensity of anthracene was investigated in the presence of a newly derived tetrakis (ketocarboxamide) cavitand at various concentrations. Time-correlated single photon counting method was applied for the lifetime measurements. A clear correlation between the fluorescence lifetime of anthracene as a function of cavitand concentration in dimethylformamide solution was observed. The bimolecular collisional quenching constant was derived from the decrease of lifetime. Fluorescence intensity was measured in the emission wavelength region around 400 nm as a result of excitation at 280 nm. Effective quenching was observed in the presence of…

AnthraceneQuenching (fluorescence)Article SubjectChemistryAnalytical chemistryCavitandPhotochemistryseoksetFluorescenceAtomic and Molecular Physics and OpticsPhoton countingcarbon-tetrachlorideAnalytical Chemistrychemistry.chemical_compoundWavelengthlcsh:QC350-467Dimethylformamideta116stern-volmer plotslcsh:Optics. LightSpectroscopyExcitationJournal of Spectroscopy
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The determination of antimony and arsenic concentrations in fly ash by hydride generation inductively coupled plasma optical emission spectrometry

2011

Abstract Hydride generation inductively coupled plasma optical emission spectrometry (HG-ICP-OES) was used in the determination of As and Sb concentrations in fly ash samples. The effect of sample pre-treatment reagents and measurement parameters used for hydride generation was evaluated. Due to memory effects observed, the appropriate read delay time was adjusted to 60 s resulting in RSDs 0.6% and 2.3% for As and Sb, respectively. The most suitable volumes of pre-reduction reagents for 10 mL of sample were 4 mL of KI/ascorbic acid (5%) and 6 mL of HCl (conc.). The determination of Sb was significantly interfered by HF, but the interference could be eliminated by adding 2 mL of saturated bo…

AntimonyChromatographySpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementHydrochloric acidAscorbic acidCoal AshBiochemistryCarbonArsenicAnalytical ChemistryBoric acidchemistry.chemical_compoundBoric AcidsAntimonychemistryFly ashInductively coupled plasma atomic emission spectroscopyEnvironmental ChemistryParticulate MatterInductively coupled plasmata116SpectroscopyArsenicAnalytica Chimica Acta
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Flavonoids from Erythrina schliebenii

2017

Prenylated and O-methylflavonoids including one new pterocarpan (1), three new isoflavones (2–4), and nineteen known natural products (5–23) were isolated and identified from the root, stem bark, and leaf extracts of Erythrina schliebenii. The crude extracts and their constituents were evaluated for antitubercular activity against Mycobacterium tuberculosis (H37Rv strain), showing MICs of 32–64 μg mL–1 and 36.9–101.8 μM, respectively. Evaluation of their toxicity against the aggressive human breast cancer cell line MDA-MB-231 indicated EC50 values of 13.0–290.6 μM (pure compounds) and 38.3 to >100 μg mL–1 (crude extracts).

Antitubercular AgentsPharmaceutical ScienceMicrobial Sensitivity TestsPlant RootsTanzania01 natural sciencesErythrina schliebeniiAnalytical ChemistryMycobacterium tuberculosischemistry.chemical_compoundDrug DiscoveryBotanyHumansta116Nuclear Magnetic Resonance BiomolecularErythrinaEC50FlavonoidsPharmacologyStem barkMolecular StructureTraditional medicinebiology010405 organic chemistryOrganic ChemistryErythrina schliebeniiPterocarpanMycobacterium tuberculosisIsoflavonesbiology.organism_classification0104 chemical sciences3. Good health010404 medicinal & biomolecular chemistryComplementary and alternative medicinechemistryToxicityPlant BarkMolecular MedicineDrug Screening Assays AntitumorCancer cell linesJournal of Natural Products
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Synthesis, solid state and solution studies of cobalt(II) complexes with 2-hydroxyiminopropanoic acid

2013

Abstract This paper describes the synthesis of the Zn(II) complex with H2L = 2-hydroxyiminopropanoic acid. The final structure incorporated two linear dimeric anions with two Zn2+ atoms, which are linked by a carbonate anion into a tetranuclear unit. In each dinuclear unit, the two Zn(II) ions are coordinated by three molecules of the doubly deprotonated ligand in two different coordination modes. This result is confirmed both by X-ray crystallography and by ESI-MS investigations of the crystals dissolved in water. Equilibrium studies of the zinc(II) complexes formed by H2L in aqueous solution based on independent pH-metric titrations and zinc ion-selective electrode (ISE) titrations indica…

Aqueous solutionChemistryHydrogen bondLigandInorganic chemistrychemistry.chemical_elementProtonationZincInorganic ChemistryCrystallographyDeprotonationMaterials ChemistryMoleculeTitrationPhysical and Theoretical Chemistryta116Polyhedron
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Self-Assembly of Water-Mediated Supramolecular Cationic Archimedean Solids

2013

Understanding the self-assembly of small structural units into large supramolecular assemblies remains one of the great challenges in structural chemistry. We have discovered that tetrahedral supramolecular cages, exhibiting the shapes of Archimedean solids, can be self-assembled by hydrogen bonding interactions using tricationic N-donors (1 or 2) in cooperation with water (W). Single crystal X-ray analysis shows that cage (2)4(W)6, assembled in an aqueous solution of cation 2 and KPF6, consists of four tripodal trications linked by six water monomers and resembles the shape of a truncated tetrahedron. Similarly, cage (1)4(W6)4 spontaneously self-assembles in an aqueous solution of cation 1…

Aqueous solutionHydrogen bondChemistryCrystal chemistrySupramolecular chemistryGeneral ChemistryCondensed Matter PhysicsArchimedean solidCrystallographysymbols.namesakeTruncated tetrahedronTetrahedronsymbolsGeneral Materials ScienceSelf-assemblyta116Crystal Growth & Design
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Electrochemical reduction of graphene oxide films in aqueous and organic solutions

2013

Abstract Electrochemical reduction of graphene oxide (GO) films cast on tin oxide glass substrates were carried out in aqueous solutions and in propylene carbonate and acetonitrile. Cyclic voltammetric measurements indicate successful reduction of GO films. The reduction process begins in aqueous solutions at less negative potentials than in organic solutions. Additionally the pH value of the aqueous solutions influences the reduction potential. According to spectroscopic analysis the reduction process of the GO film can be controlled by the choice of reduction potential and electrolyte medium. The potential window in this work was made broader by increasing pH or by using organic electroly…

Aqueous solutionMaterials scienceGrapheneGeneral Chemical EngineeringInorganic chemistryOxideElectrolyteElectrochemistryTin oxidelaw.inventionchemistry.chemical_compoundchemistrylawPropylene carbonateElectrochemistryAcetonitrileta116Electrochimica Acta
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Selective recognition of fluoride anion in water by a copper(II) center embedded in a hydrophobic cavity

2014

The ability of a water-soluble pentacationic calix[6]arene-based CuII complex to bind anions in water has been explored. Quite remarkably, the complex exhibits strong and selective fluoride binding in the pH range of 6–7. The binding constant at pH 5.9 was evaluated to be 85 000 M−1, which is one of the highest values ever reported for a fluoride probe in water and at this pH. The complex also binds chloride ions, but 1000 times less efficiently. The combination of the calix[6]arene hydrophobic cavity with the CuII complex, presenting its labile site in the endo position, is the reason for the selective recognition process. The single crystal X-ray structure of the organo-soluble parent com…

Aqueous solutionMolecular modelChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryChlorideBinding constantCopperchemistry.chemical_compoundPolymer chemistrymedicineWater clusterSingle crystalFluorideta116medicine.drugChemical Science
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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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Matrix-isolation and ab initio study of the complex between formic acid and xenon

2012

Abstract We report on the identification of the complexes of formic acid (FA) and Xe in an argon matrix. The geometries, interaction energies, reaction barriers, and vibrational spectra of the FA⋯Xe complexes are calculated at the MP2 level of theory. The calculations reveal four structures for the trans-FA⋯Xe complex and four structures for the cis-FA⋯Xe complex. In the experiments, two structures of the trans-FA⋯Xe complex are observed after deposition of FA/Xe/Ar matrices, with and without OH⋯Xe interaction (H-bonded and non-H-bonded structures). The cis-FA⋯Xe complex was synthesized by vibrational excitation of the non-H-bonded trans-FA⋯Xe complex. The non-H-bonded and H-bonded structur…

Argon010304 chemical physicsHydrogen bondFormic acidOrganic ChemistryMatrix isolationAb initiochemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundMonomerXenonchemistryComputational chemistry0103 physical sciencesPhysical chemistryta116SpectroscopyExcitationJournal of Molecular Structure
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