Search results for "Tetra"

showing 10 items of 6481 documents

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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Ionic partition diagram of tetraphenylporphyrin at the water|1,2-dichloroethane interface

2011

diagram of 5,10,15,20-tetraphenyl-21H,23H-porphine (H2TPP) at the water|1,2-dichloroethane interface using a simple Born solvation model. This zone diagram shows under which form this porphyrin is present, i.e. neutral, monoprotonated or diprotonated, and in which phase i.e. either in the aqueous or the organic phase as a function of the aqueous pH and the interface polarisation that can be controlled externally or by the distribution of supporting electrolytes. This diagram explains why the monoprotonated form has been difficult to observe when doing biphasic pH titrations

Aqueous solutionIonic partition diagramStereochemistryGeneral Chemical EngineeringSolvationElectrolytePorphyrinAnalytical Chemistrychemistry.chemical_compoundchemistryPhase (matter)TetraphenylporphyrinElectrochemistryPhysical chemistryITIESJournal of Electroanalytical Chemistry
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Calorimetric study of the solubilization of ethylenediamine, N,N-dimethylaminoethylamine and N,N,N?,N?-tetramethylethylenediamine by reversed AOT mic…

1993

Distribution constants and standard enthalpies of transfer of ethylenediamine (en), N,N-dimethylaminoethylamine (dmen) and N,N,N′,N′-tetramethylethylenediamine (tmen) partitioned between n-heptane and water containing reversed sodium bis(2-ethylhexyl) sulfosuccinate (AOT) micelles as a function of the molar concentration ratio R (R=[water]/[AOT]) were evaluated by a calorimetric method. The results show that en, dmen and tmen molecules, solubilized in the reversed micelles, are distributed between the micellar aqueous core and the micellar palisade layer. An analysis of the thermodynamic parameters of the partition process demonstrates the peculiar solvent properties of the water containing…

Aqueous solutionMolar concentrationBiophysicsEthylenediamineTetramethylethylenediamineBiochemistryMicelleMedicinal chemistrySolventPartition coefficientchemistry.chemical_compoundchemistryDiamineOrganic chemistryPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Structural and Vibrational Study of a New Mixed Dipotassium Hydrogenselenate Dihydrogenphosphate K2(HSeO4)1.5 (H2PO4)0.5.

2006

Abstract Ongoing studies of the KHSeO4–KH2PO4 system, aimed at developing novel proton conducting solids, resulted in the new compound K2(HSeO4)1.5(H2PO4)0.5 (dipotassium hydrogenselenate dihydrogenphosphate). The crystals have been prepared by slow evaporation of an aqueous solution at room temperature. The structural properties of the crystals were characterized by X-ray single analysis (performed at room temperature), which revealed that K2(HSeO4)1.5(H2PO4)0.5 (KHSeP) crystallizes in space group P 1 ¯ with lattice parameters: a = 7.417(3) A, b = 7.668(2) A, c = 7.744(5) A, α = 71.59(3)°, β = 87.71(4)° and γ = 86.04(6)°. The compound has a unit cell volume 416.8(3) A3 and two formula unit…

Aqueous solutionProtonHydrogenInfraredHydrogen bondChemistryMechanical EngineeringInorganic chemistryMetals and AlloysEvaporationSpace groupInfrared spectroscopychemistry.chemical_elementGeneral MedicineCrystal structureCrystallographyChemical bondMechanics of MaterialsMaterials ChemistryTetrahedronChemInform
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Protonation of Carbonate in Aqueous Tetraalkylammonium Salts at 25°C.

2006

Protonation constants of carbonate were determined in tetramethylammonium chloride (Me4NClaq 0.1≤I/mol kg−1 ≤4) and tetraethylammonium iodide (Et4NIaq 0.1≤I/mol kg−1 ≤1) by potentiometric ([H+]-glass electrode) measurements. Dependence of protonation constants on ionic strength was taken into account by modified specific ion interaction theory (SIT) and by Pitzer models. Literature data on the protonation of carbonate in NaClaq (0.1≤I/mol kg−1 ≤6) were also critically analysed. Both protonation constants of carbonate follow the trend Et4NI>Me4NCl > NaCl. An ion pair formation model designed to take into account the different protonation behaviours of carbonate in different supporting electr…

Aqueous solutionProtonation of carbonateSpecific ion interaction theory (SIT)Ion pair formation modelChemistryInorganic chemistryTetraalkylammonium saltProtonationDependence on ionic strengthElectrolyteIon pairsAnalytical Chemistrychemistry.chemical_compoundIonic strengthTetramethylammonium chlorideAqueous solutionPitzer equationsCarbonateSettore CHIM/01 - Chimica AnaliticaProtonation of carbonate; Dependence on ionic strength; Aqueous solution; Tetraalkylammonium salts; Ion pair formation model; Specific ion interaction theory (SIT); Pitzer equationPitzer equation
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Ionic liquids versus amine solutions in biogas upgrading: the level of volatile organic compounds

2013

Background: This article provides information related to the occurrence of volatile organic compounds before and after biogas purification, by means of both aqueous amine solutions and ionic liquids. Results & discussion: Encouraging results were obtained. Under the experimental conditions, 1-butyl-3-methylimidazolium acetate ionic liquid appeared to perform at least two-times better than aqueous amines solutions, since it captured 65 wt% of the identified volatile organic compounds, while aqueous amine solutions retained around 35 wt% only. However, in the case of octamethylcyclotetrasiloxane and dichlorobenzene, aqueous amine solutions rendered better purification performance and diminish…

Aqueous solutionRenewable Energy Sustainability and the EnvironmentChemistryta1172Inorganic chemistryOctamethylcyclotetrasiloxaneDichlorobenzenechemistry.chemical_compoundBiogasBioenergyBiofuelIonic liquidOrganic chemistryAmine gas treatingWaste Management and DisposalBiofuels
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Evaluation of biosorbents for Cu removal from wastewater in the presence of EDTA

2007

BACKGROUND: This paper evaluates the use of several biosorbents for Cu removal from aqueous solutions in the absence and presence of ethylenediaminetetraacetic acid (EDTA). The objective was to determine the applicability of the sorption process after conventional physicochemical wastewater treatment, or as primary treatment, replacing the physicochemical process. RESULTS: Fixed-bed experiments were performed at Cu influent concentrations of 2 and 20 mg dm−3 and EDTA doses between 0 and 10 mg dm−3. At low Cu concentration without EDTA, Cu uptake capacity followed the order Posidonia oceanica > chitosan > chitin > Scharlau AC > Darco AC, with a maximum, at C/C0 = 0.2, of 23.2 mg g−1. In the …

Aqueous solutionRenewable Energy Sustainability and the EnvironmentGeneral Chemical EngineeringOrganic ChemistryBiosorptionEnvironmental engineeringSorptionEthylenediaminetetraacetic acidPollutionInorganic ChemistryChitosanchemistry.chemical_compoundFuel TechnologychemistryWastewatermedicineWaste Management and DisposalEffluentBiotechnologyNuclear chemistryActivated carbonmedicine.drugJournal of Chemical Technology & Biotechnology
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Influence of chloride anions on the electrodeposition and electroactivity of the polymer matrix in polypyrrole, poly( N -methylpyrrole) and polypyrro…

2004

We report electrochemical studies on the influence of a small concentration of chloride ions on the electroactivity of the polymer matrix of polypyrrole (PPy), poly(N-methylpyrrole) [p(N-MePy)] and a poly(titanocene-propyl-pyrrole) derivative, p(Tc3Py) [Tc(CH2)3NC4H4; Tc=CpCp′TiCl2; Cp=C5H5; Cp′=C5H4] in acetonitrile (AN), tetrahydrofuran (THF) and N,N-dimethylformamide (DMF). The polymer films were obtained on Pt disc electrodes from AN solutions of the monomers containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF6) as the supporting electrolyte and then transferred to the corresponding monomer-free solution. Studies in Cl−-containing solutions have shown that the p(Tc3Py) matrix…

Aqueous solutionSupporting electrolyteInorganic chemistryCondensed Matter PhysicsElectrochemistryPolypyrroleChloridechemistry.chemical_compoundMonomerchemistryTetrabutylammonium hexafluorophosphatePolymer chemistryElectrochemistrymedicineGeneral Materials ScienceElectrical and Electronic EngineeringAcetonitrilemedicine.drugJournal of Solid State Electrochemistry
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Removal of drugs in aqueous systens by photoassisted degradation

2005

Aqueous solutions of tetracycline, lincomycin and ranitidine were irradiated with UV light in homogeneous and heterogeneous systems. Two commercial polycrystalline TiO2 powders (Degussa P25 and Merck) were used as photocatalysts. After 5A h, an appreciable photolytic degradation of tetracycline and ranitidine was observed while the degradation of lincomycin was noticeably lower. As far as the mineralization is concerned, a small decrease of the TOC values was measured in the case of tetracycline whereas negligible variations were found for lincomycin or ranitidine. The presence of the photocatalysts greatly enhanced the degradation rates of the drugs with respect to those observed during th…

Aqueous solutionTetracyclineGeneral Chemical EngineeringInorganic chemistryLincomycinchemistry.chemical_compoundAdsorptionchemistryAntibioticsveterinary antibioticsTitanium dioxideMaterials ChemistryElectrochemistryPhotocatalysismedicineSettore CHIM/07 - Fondamenti Chimici Delle TecnologieoxytetracyclinePhotodegradationmedicine.drugAntibacterial agent
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Synthesis, characterization and thermal behavior of nine new -type quaternary ammonium tetrafluoroborate or hexafluorophosphate salts prepared by met…

2008

Abstract Nine new quaternary ammonium tetrafluoroborate or hexafluoroborate salts were prepared from analogous bromide or chloride salts using anion exchange reaction in which the corresponding bromide or chloride salt was treated with HBF4 or HPF6 acid in aqueous solutions. The characterizations were performed by 1H NMR and 13C NMR spectroscopy as well as by elemental analysis. The single crystals of three tetrafluoroborate and two hexafluorophosphate salts were obtained by slow evaporation from a methanol/ethyl acetate solution and the crystal structures were determined by X-ray single crystal diffraction. Four of the compounds crystallized in the orthorhombic and one in the monoclinic cr…

Aqueous solutionTetrafluoroborateOrganic ChemistryInorganic chemistryHalideCrystal structureChlorideAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryBromideHexafluorophosphatemedicineSpectroscopymedicine.drugMonoclinic crystal systemJournal of Molecular Structure
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