Search results for " solution"

showing 10 items of 3084 documents

Common best proximity points and global optimal approximate solutions for new types of proximal contractions

2015

Let $(\mathcal{X},d)$ be a metric space, $\mathcal{A}$ and $\mathcal{B}$ be two non-empty subsets of $\mathcal{X}$ and $\mathcal{S},\mathcal{T}: \mathcal{A} \to \mathcal{B}$ be two non-self mappings. In view of the fact that, given any point $x \in \mathcal{A}$, the distances between $x$ and $\mathcal{S}x$ and between $x$ and $\mathcal{T}x$ are at least $d(\mathcal{A}, \mathcal{B}),$ which is the absolute infimum of $d(x, \mathcal{S} x)$ and $d(x, \mathcal{T} x)$, a common best proximity point theorem affirms the global minimum of both the functions $x \to d(x, \mathcal{S}x)$ and $x \to d(x, \mathcal{T}x)$ by imposing the common approximate solution of the equations $\mathcal{S}x = x$ and $…

common best proximity pointproximally commuting mappingsSettore MAT/05 - Analisi Matematicaoptimal approximate solution
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Electrocatalytic properties of manganese and cobalt polyporphine films toward oxygen reduction reaction

2018

International audience; Novel member of polymetalloporphines, namely manganese polymetalloporphine of type I (pMnP-I) obtained by ion exchange from magnesium polyporphine of type I (pMgP-I) is reported for the first time and compared to its cobalt analogue (pCoP-I). Both polymer films have been obtained via two-step procedure: demetaladon of the pMgP-I electrode film via its exposure to trifluoroacetic acid solution, resulting in formation of the metal-free polyporphine of type I (pH(2)P-I) followed by electrochemically induced incorporation of Co or Mn ions from the acetonitrile solution of cobalt and manganese perchlorates. A further oxidative transformation of pCoP-I, polymer films has l…

conjugated porphyrin polymerGeneral Chemical EngineeringInorganic chemistryFOS: Physical scienceschemistry.chemical_element02 engineering and technologyElectrolyteManganesepositive potentialsphthalocyanines010402 general chemistry01 natural sciencescatalystsAnalytical ChemistryCatalysisporphine[CHIM.ANAL]Chemical Sciences/Analytical chemistryframeworksElectrochemistry[CHIM]Chemical Sciencesdioxygen reductionCondensed Matter - Materials SciencemetalloporphyrinsAqueous solutionIon exchangeMagnesiumElectroactive polymersMaterials Science (cond-mat.mtrl-sci)Oxygen electroreductionelectropolymerizationfuel-cell cathode021001 nanoscience & nanotechnologyMetalloporphines0104 chemical sciencesPolymer film coated electrodechemistry0210 nano-technologyPlatinumCobaltMg(II) porphineJournal of Electroanalytical Chemistry
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Copper Octacarboxyphthalocyanine Aggregation in Buffered Solutions

2008

Results of spectral UV-Vis absorption investigations on association of copper octa-carboxyphthalocyanine, CuPcOC, are reported. Influence of pH on association is discussed. In pH < 5.5 only ag gre gates are present. Monomer appears above pH = 5.5 and at pH Greater-than or equal to 6.2 only monomeric Pc forms exist. CuPcOC exhibits higher tendency to wards association in phosphate buffer solutions than in redistilled water. In pH 5.9–6.0 monomers, dimers and trimers coexist in equilibrium in 1.0×10–6 – 1.2×10–5 mol/dm3 concentration range at 25°C. The average assembling number n = 3 was determined for pH 5.6, 5.9 and 6.0 solutions. The spectrum of aggregate was calculated with two maxima at …

copper octacarboxyphthalocyanineUV-Vis spectrabuffered solutionsaggregationPolish Journal of Chemistry
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Dimerization of Copper Octacarboxyphthalocyanine in Aqueous Solutions

2005

Spectral absorption UV-Vis investigations on association of copper(II) octacarboxyphthalocyanine in aqueous solutions are reported. In 5.0x10-7-5.0x10-5 mol/dm3 concentration range monomers and dimers are mainly present. The calculated dimerization constant 106dm3/mol at 25°C and the hypsochromic spectral shift for the dimer 1164 cm-1 (688 nm_ 637 nm) indicate a stack-like association of molecules and suggestpi-pi interactions between Pc macrocycles in dimer and higher aggregates, in contrast to hydrogen bonding between carboxylic groups of adjacent Pc molecules.

copper octacarboxyphthalocyaninedimerizationUV/Vis spectraassociationaqueous solutionPolish Journal of Chemistry
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Multiple solutions for semilinear Robin problems with superlinear reaction and no symmetries

2021

We study a semilinear Robin problem driven by the Laplacian with a parametric superlinear reaction. Using variational tools from the critical point theory with truncation and comparison techniques, critical groups and flow invariance arguments, we show the existence of seven nontrivial smooth solutions, all with sign information and ordered.

critical groupSettore MAT/05 - Analisi Matematicacritical point theoryConstant sign and nodal solutionsuperlinear reactionflow invariance
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Large Magnetic Polyoxometalates Containing the Cobalt Cubane ‘[CoIIICo3II(OH)3(H2O)6–m(PW9O34)]3− (m = 3 or 5) as a Subunit

2018

A synthetic procedure is presented to construct new magnetic polyoxometalates (POMs) containing one or two subunits of ‘[CoIIICo3II(OH)3(H2O)6−m(PW9O34)]3−' (m = 3 or 5). The substitution of the water ligands present in these subunits by oxo or hydroxo ligands belonging to other POM fragments, gives rise to four, larger POM anions: [Co7(OH)6(H2O)6(PW9O34)2]9− (2), [Co7(OH)6(H2O)4(PW9O34)2]n9n- (2′), [Co11(OH)5(H2O)5(W6O24)(PW9O34)3]22− (3) and [{Co4(OH)3(H2O)(PW9O34)}2{K⊂(H2W12O41)2}{Co(H2O)4}2]17− (4). The crystal structures, magnetic characterization and stabilities in aqueous solutions of these POM derivatives are also presented.

crystal structureAqueous solution010405 organic chemistryMagnetismProtein subunitchemistry.chemical_elementCrystal structureGeneral Chemistry010402 general chemistrycobalt01 natural sciences0104 chemical scienceslcsh:Chemistrychemistry.chemical_compoundCrystallographylcsh:QD1-999chemistryCubanemagnetismpolyoxometalatePolyoxometalatecubane clusterCobaltFrontiers in Chemistry
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A Simple Complex on the Verge of Breakdown: Isolation of the Elusive Cyanoformate Ion

2014

Cyanide Hitches a Ride Cyanide is a by-product of the biosynthesis of ethylene in plants and it has been somewhat puzzling how the ion is safely removed before it can shut down enzymatic pathways by coordination to catalytic iron centers. A proposed mechanism has implicated the cyanoformate ion—essentially, a weak adduct of cyanide and carbon dioxide—as the initial product, although its lifetime was uncertain. Murphy et al. (p. 75 ; see the Perspective by Alabugin and Mohamed ) crystallized this previously elusive adduct and found that its solution-phase stability varies inversely with the dielectric properties of the medium. The results bolster a picture in which the adduct shuttles the cy…

crystal structureEthyleneMagnetic Resonance SpectroscopyFormateskemiallinen sitoutuminenCyanideMineralogykiderakenneMedicinal chemistryIonCatalysisAdductchemistry.chemical_compoundsyanoformaattiX-Ray DiffractionCatalytic DomainNitrilesta116MultidisciplinaryAqueous solutionCyanidesMolecular StructureChemistrychemical bondingCarbon DioxideEthylenesThermodynamicsAmino Acid OxidoreductasescyanofrmateCrystallizationShut downScience
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Synthesis and self-assembly of a PEGylated-graphene aerogel

2016

Abstract In the frame of this work, we present, for the first time, the synthesis and self-assembly of an aerogel built by graphene oxide-polyethylene glycol. The synthetic route involves at first the coupling of GO with an amino-terminated polyethylene glycol sample by carbodiimide in aqueous environment, and the subsequent conversion of the hydrogel achieved into an aerogel via freeze-drying. The 3D PEGylated graphene-based aerogel, characterized by spectroscopic, morphological, structural and mechanical analyses, displays an ultralight and highly porous (99.7%) network and possesses high mechanical properties together with a good biocompatibility.

del-assemblyMaterials sciencesynthesisBiocompatibility02 engineering and technologyPolyethylene glycol010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundEngineering (all)lawHighly porousB.Stress/strain curveD.Raman spectroscopycharacterizationComposite materialGraphene oxideCarbodiimidePEGylated-grapheneAqueous solutionGraphenetechnology industry and agricultureGeneral EngineeringAerogel021001 nanoscience & nanotechnologyB.Porosity/void0104 chemical scienceschemistryCeramics and CompositesSelf-assembly0210 nano-technologyA.Functional compositeComposites Science and Technology
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Value Co-Creation Opportunities: Managerial Transformation of Digitisation Risks into Success Factors

2018

This chapter examines the challenges and risks managers in the healthcare sector perceive in relation to the development and implementation of digitised services in a healthcare case organisation. Using data collected from managers, focus group interviews and observation method within the case organisation, the authors present an analysis that demonstrates that the risks and success factors that influence the development and implementation of digital healthcare services are related to (1) setting a clear digital strategy and implementation plan, (2) integration of digital services with the overall process and ICT, (3) committed resources and engagement of personnel, and (4) the organisation…

digitointijohtaminenKnowledge managementhealtcareProcess (engineering)Plan (drawing)Digital strategyterveysalaHealth careCo-creationdigital solutionsmenestystekijätriskitmanagerial transformationmahdollisuudetdigitisationbusiness.industryarvonluontiterveydenhuoltohealtcare servicesFocus groupvalue co-creationWork (electrical)Information and Communications Technologysähköiset palvelutbusinessmanagement
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Preparation and physico-chemical study of inclusion complexes between idebenone and modified beta-cyclodextrins

1996

The inclusion properties of modifiedβ-cyclodextrins (trimethyl-β-cyclodextrin, dimethyl-β-cyclodextrin and hydroxypropyl-β-cyclodextrin) towards idebenone were compared with naturalβ-cyclodextrin. The inclusion complexes were prepared by different methods (coprecipitation, kneading, and freeze-drying) and characterized by differential scanning calorimetry, X-ray diffractometry, UV, CD and NMR spectroscopy. The results obtained by CD and NMR spectroscopy indicate a different orientation of idebenone in dimethyl-β-cyclodextrin with respect to other cyclodextrins. Stability constants of the complexes were determined in water at various temperatures and consequently thermodynamic parameters wer…

dissolution studyAqueous solutioncyclodextrinsChemistryCoprecipitationtechnology industry and agricultureGeneral ChemistryNuclear magnetic resonance spectroscopyCondensed Matter Physicscyclodextrins; idebenone; characterization of complexes; dissolution studycarbohydrates (lipids)idebenonecharacterization of complexesDifferential scanning calorimetrypolycyclic compoundsmedicineIdebenoneOrganic chemistrylipids (amino acids peptides and proteins)Free drugInclusion (mineral)DissolutionFood Sciencemedicine.drugNuclear chemistry
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