Search results for "aqueous solution"

showing 10 items of 1610 documents

Deuterated Molecular Ruby with Record Luminescence Quantum Yield

2017

The recently reported luminescent chromium(III) complex 13+ ([Cr(ddpd)2]3+; ddpd=N,N’-dimethyl-N,N’-dipyridine-2-yl-pyridine-2,6-diamine) shows exceptionally strong near-IR emission at 775 nm in water under ambient conditions (F=11%) with a microsecond lifetime as the ligand design in 13+ effectively eliminates non-radiative decay pathways, such as photosubstitution, back-intersystem crossing, and trigonal twists. In the absence of energy acceptors, such as dioxygen, the remaining decay pathways are energy transfer to high energy solvent and ligand oscillators, namely OH and CH stretching vibrations. Selective deuteration of the solvents and the ddpd ligands probes the efficiency of these o…

Coordination sphereMaterials science010405 organic chemistryLigandMetal ions in aqueous solutionQuantum yieldGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesMicrosecondDeuteriumExcited stateLuminescenceAngewandte Chemie International Edition
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Electrically Conductive Phthalocyanine Assemblies. Structural and Non-Integer Oxidation Number Considerations

1990

Aggregation is a well-known phenomenon in phthalocyanine chemistry. Interactions can occur between adjacent phthalocyanine rings, both in organic and aqueous phases, resulting in coupling between the electronic states of two, or more, phthalocyanine units [1].

Coupling (electronics)chemistry.chemical_compoundAqueous solutionMaterials sciencechemistryPolymer chemistryPhthalocyanineMolecular planeElectrically conductivePhotochemistryElectric chargeInteger (computer science)Electronic states
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Exchange Coupling in Cyano-Bridged Homodinuclear Cu(II) and Ni(II) Complexes:  Synthesis, Structure, Magnetism, and Density Functional Theoretical St…

2001

The synthesis and structural characterization of several new cyano-bridged copper(II) and nickel(II) homodinuclear complexes is presented. The measure of magnetic properties for these complexes is complemented with a computational study of the exchange coupling for several model structures representing this family of compounds. The influence of several factors on the coupling constant has been examined, coordination position occupied by the bridging ligand, distortions of the coordination environment, and relative disposition of the cyanide ion with respect to the M-M vector. Comparison of experimental and calculated coupling constants allows for the rationalization of the most relevant fea…

Coupling constantCouplingMagnetismMetal ions in aqueous solutionExchange interactionchemistry.chemical_elementBridging ligandCopperInorganic ChemistryNickelCrystallographychemistryComputational chemistryPhysical and Theoretical ChemistryInorganic Chemistry
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Structural effects of macrocyclic compounds and their partition in sodium dodecylsulphate aqueous solutions

2003

The partition of 1,4,7,10,13,16-esaoxacyclooctadecane (18C6), 4,7,13,16-tetraoxa-1,10-diazacyclooctadecane (2.2), 2,5,8,11,14,17-esaoxabicyclo[16.4.0]dicosane (B18C6) and 2,5,8,15,18,21-esoxatricyclo[20.4.0.09.14]esacosane (Cy218C6) in sodium dodecyl sulfate (SDS) aqueous solutions and their effect on the structure of surfactant aggregates has been investigated by small-angle neutron scattering. Results from data analysis have shown that by increasing macrocycle concentration the SDS micelles dimensions reduce for all systems investigated. At the same time information on macrocycles partition between the micellar and the continuous phase have been obtained. It was found that an appreciable …

CryptandsAqueous solutionSANSChemistryAdditive partitionSodiumInorganic chemistryCryptandchemistry.chemical_elementMicelleSmall-angle neutron scatteringGeneral Biochemistry Genetics and Molecular BiologyCrystallographychemistry.chemical_compoundPulmonary surfactantMoleculeCrown ethersSodium dodecyl sulfateMicellesSettore CHIM/02 - Chimica FisicaJournal of Applied Crystallography
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Electron Diffraction and Imaging of Uncompressed Monolayers of Amphiphilic Molecules on Vitreous and Hexagonal Ice

1993

A new approach is described for probing domains of ordered self-assemblies of amphiphilic monolayers at the aqueous solution interface. The method has potential importance for the study of membrane structure, Langmuir-Blodgett films, and nucleation processes of two-and three-dimensional crystals. Electron diffraction (ED) patterns indicative of two-dimensional crystalline self-assembly were obtained from samples, which were examined by cryo-electron microscopy, of monolayers of water-insoluble amphiphiles on vitrified aqueour substrates. The apparent hexagonal symmetry of an ED pattern from a C(16)H(33)OH monolayer was interpreted in terms of multiple twinning. Monolayers of the CL(31)H(63)…

CrystallographyMultidisciplinaryAqueous solutionElectron diffractionChemistryStereochemistryMonolayerMicroscopyNucleationCrystalliteCrystal twinningEpitaxyScience
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The possibilities of using broadleaf cattail seeds (Typha latifolia L.) as super absorbents for removing aromatic hydrocarbons (BTEX) from an aqueous…

2018

Sorption of oil-related products (including mainly the propellants) is the very basic process that counteracts spreading these types of pollution into environment. Plenty of synthetic substances (including the monoaromatic hydrocarbons) are both from the surface and underground waters. The aim of this study was to present the research’s results on the possibilities of using the broadleaf cattail (Typha latifolia L.) seeds as a sorbent of monoaromatic hydrocarbons from an aqueous solution. In order to increase sorptive capacity, the seeds biomass was submitted for the process of mercerizing in diversified time and temperature in water and the NaOH solution. The removal of benzene, toluene, e…

CumeneEnvironmental EngineeringAqueous solutionSorbentsorptionEcological ModelingwatermercerizationSorptionBTEX010501 environmental sciences01 natural sciencesPollutionTolueneEthylbenzeneArticlechemistry.chemical_compoundchemistryEnvironmental chemistrybroadleaf cattail seedsEnvironmental ChemistryBenzene0105 earth and related environmental sciencesWater Science and TechnologyBTEXWater Air and Soil Pollution
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[1,2,3]Triazolo[1,5-a]pyridine derivatives as molecular chemosensors for zinc(ii), nitrite and cyanide anions

2009

Three recently prepared tridentate ligands TPF, TPS and TPT, based on the triazolopyridine–pyridine nucleus possessing fluorescent properties, have been tested as chemosensors for metal ions. A particular response is obtained in the case of ZnTPT+2. The Zn2+ TPT 1 : 1 complex has proved to be an efficient chemosensor for anions especially nitrite and cyanide.

CyanideMetal ions in aqueous solutionInorganic chemistrychemistry.chemical_elementGeneral ChemistryZincFluorescenceCatalysischemistry.chemical_compoundchemistryPolymer chemistryPyridineMaterials ChemistryNitriteNew Journal of Chemistry
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Cascade complex formation by phosphate in the cobalt(II)/[30]aneN10 anaerobic system

1993

Abstract The interaction of phosphate with the mono- and binuclear cobalt(II) complexes of [30]aneN 10 (1,4,7,10,13,16,19,22,25,28-decaazacyclotriacontane) has been studied by potentiometry in 0.15 mol dm −3 NaClO 4 solution at 298.15 K under anaerobic conditions. The stable species [CoH 2 ([30]aneN 10 )PO 4 ] + , [CoH 4 ([30]aneN 10 )PO 4 ] 3+ , [Co 2 H([30]aneN 10 )PO 4 ] 2+ , [Co 2 H 2 ([30]aneN 10 )PO 4 ] 3+ and [Co 2 H 3 ([30]aneN 10 )PO 4 ] 4+ , where the phosphate anion is directly bound to the metal ions or acts as a second sphere ligand, are formed and their stability constants have been determined. The results obtained allowed for the selection of suitable conditions for the study…

DIOXYGEN CARRIERS; DIOXYGEN BINDING; Co(II) COMPLEXES; POLYAMINE LIGANDS; DITOPIC POLYAMINES; OPEN-CHAIN POLYAZAALKANES; THERMODYNAMICS; ANION COORDINATION CHEMISTRY; INCLUSION COMPLEXESINCLUSION COMPLEXESMetal ions in aqueous solutionComplex formationInorganic chemistryDIOXYGEN BINDINGchemistry.chemical_elementMedicinal chemistryCo(II) COMPLEXESInorganic Chemistrychemistry.chemical_compoundOPEN-CHAIN POLYAZAALKANESANION COORDINATION CHEMISTRYTHERMODYNAMICSMaterials ChemistryDIOXYGEN CARRIERSPhysical and Theoretical ChemistryLigandPhosphatePhosphate anionchemistryDITOPIC POLYAMINESChemical equilibriumAnaerobic exerciseCobaltPOLYAMINE LIGANDS
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Isobaric vapor–liquid equilibria for the system 1-pentanol–1-propanol–water at 101.3 kPa

2001

Consistent vapor–liquid equilibrium data for the ternary system 1-pentanol–1-propanol–water is reported at 101.3 kPa at temperatures in the range of 362–393 K. The VLE data were satisfactorily correlated with UNIQUAC model. The authors wish to thank the Generalitat Valenciana (Spain) for the financial help of the Project GV-3174/95 and DGES for the financial aids of the Project PB96-0338.

DataUNIQUACTernary numeral systemAqueous solutionGeneral Chemical EngineeringUNIQUACGeneral Physics and AstronomyThermodynamicsWaterVapor–liquid equilibriaGroup contribution methodCorrelation1-propanolPropanolIngeniería Químicachemistry.chemical_compound1-Propanolchemistry1-PentanolAlcoholsIsobaric process1-pentanolPhysical and Theoretical Chemistry
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Calculation of proton activity in aqueous protolyte solutions

1980

Abstract A general and thermodynamically exact equation for the calculation of the proton (hydroxide ion) activity of aqueous solutions of monoprotic acidic (and basic) species is given. Under certain conditions, various approximate equations can be derived from the exact form; the applicability of these depends mainly on both the thermodynamic equilibrium constant, K p , of the protolytic reaction, and the stoichiometric concentration, C o , of the protolyte. Taking into account the mean ionic activity coefficients which are calculated by means of the Davies equation, diagrams are constructed exhibiting those combinations of K p and C o for which the respective approximations can be applie…

Davies equationActivity coefficientAqueous solutionProtonThermodynamic equilibriumChemistryIonic bondingThermodynamicsBiochemistryAnalytical ChemistryIonchemistry.chemical_compoundEnvironmental ChemistryHydroxideSpectroscopyAnalytica Chimica Acta
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