Search results for "Complex."

showing 10 items of 5824 documents

Local behaviour of singular solutions for nonlinear elliptic equations in divergence form

2012

We consider the following class of nonlinear elliptic equations $$\begin{array}{ll}{-}{\rm div}(\mathcal{A}(|x|)\nabla u) +u^q=0\quad {\rm in}\; B_1(0)\setminus\{0\}, \end{array}$$ where q > 1 and $${\mathcal{A}}$$ is a positive C 1(0,1] function which is regularly varying at zero with index $${\vartheta}$$ in (2−N,2). We prove that all isolated singularities at zero for the positive solutions are removable if and only if $${\Phi\not\in L^q(B_1(0))}$$ , where $${\Phi}$$ denotes the fundamental solution of $${-{\rm div}(\mathcal{A}(|x|)\nabla u)=\delta_0}$$ in $${\mathcal D'(B_1(0))}$$ and δ0 is the Dirac mass at 0. Moreover, we give a complete classification of the behaviour near zero of al…

Applied MathematicsMathematical analysisZero (complex analysis)Function (mathematics)DivergenceCombinatoricsNonlinear systemSettore MAT/05 - Analisi MatematicaFundamental solutionnonlinear equationsNabla symbolSingular solutionAnalysisMathematics
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Our Friend and Mathematician Karl Strambach

2020

This paper is dedicated to Karl Strambach on the occasion of his 80th birthday. Here we want to describe our work with Prof. Karl Strambach.

Applied Mathematicsimprimitive groupGrünwald spaces shells of curve010102 general mathematicsgroup theoryArt historyloop01 natural sciencescomplex curveLie group010101 applied mathematicsHjelmslev geometryMathematics (miscellaneous)Work (electrical)Mathematikalgebraic groupaffine connectionSettore MAT/03 - Geometria0101 mathematicsMathematicsBiographiebibliographiegeodesics
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Reduced complexity models in the identification of dynamical networks: Links with sparsification problems

2009

In many applicative scenarios it is important to derive information about the topology and the internal connections of more dynamical systems interacting together. Examples can be found in fields as diverse as Economics, Neuroscience and Biochemistry. The paper deals with the problem of deriving a descriptive model of a network, collecting the node outputs as time series with no use of a priori insight on the topology. We cast the problem as the optimization of a cost function operating a trade-off between accuracy and complexity in the final model. We address the problem of reducing the complexity by fixing a certain degree of sparsity, and trying to find the solution that “better” satisfi…

Approximation theoryMathematical optimizationSettore ING-INF/04 - AutomaticaDynamical systems theoryComputational complexity theoryNode (networking)A priori and a posteriorisparsification compressing sensing estimation networksNetwork topologyGreedy algorithmTopology (chemistry)MathematicsProceedings of the 48h IEEE Conference on Decision and Control (CDC) held jointly with 2009 28th Chinese Control Conference
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Polychromatic femtosecond fluorescence studies of metal–polypyridine complexes in solution

2011

Femtosecond-resolved broadband fluorescence studies are reported for[ M(bpy)(3)](2+) (M = Fe, Ru), RuN3 and RuN719 complexes in solution. We investigated the pump wavelength dependence of the fluorescence of aqueous [ Fe(bpy)(3)](2+) and the solvent and ligand dependence of the fluorescence of Ru-complexes excited at 400 nm. For all complexes, the (MLCT)-M-1 fluorescence appears at zero time delay with a mirror-like image with respect to the absorption. It decays in <= 30-45 fs due to intersystem crossing to the (MLCT)-M-3 states, but a longer lived component of similar to 190 fs additionally shows up in RuN719 and RuN3. No solvent effects are detected. The very early dynamics are character…

Aqueous solutionChemistryFluorescence up-conversionSettore FIS/01 - Fisica SperimentaleGeneral Physics and AstronomyIntersystem crossingMetal–polypyridine complexes; IVR; Internal conversion; Intersystem crossing; Ultrafast; Fluorescence up-conversionPhotochemistryFluorescencePhotoinduced electron transferIntersystem crossingInternal conversionUltrafastExcited stateIntramolecular forceFemtosecondIVRMetal–polypyridine complexePhysical and Theoretical ChemistrySolvent effects
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The interaction of amino acids with the major constituents of natural waters at different ionic strengths

2000

Abstract The interaction of amino acids with the major constituents of natural waters has been studied potentiometrically by determining protonation constants at different ionic strengths (e.g., I ≤5.6 mol (kg H 2 O) −1 (NaCl)) and in artificial seawater (containing Na + , K + , Ca 2+ , Mg 2+ , Cl − and SO 4 2− ) at different salinities. For glycine determinations in mixed NaCl–MgCl 2 , electrolyte solutions were also performed. The data included in this work, together with some already published, make it possible to calculate parameters for dependence on ionic strength using different models, i.e. an extended Debye–Huckel type equation and Pitzer equations. The results can be interpreted b…

Aqueous solutionChemistryInorganic chemistryIonic bondingArtificial seawaterProtonationGeneral ChemistryOceanographyIonic strengthStability constants of complexesEnvironmental ChemistryPitzer equationsSeawaterWater Science and Technology
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Complexation of the potassium ion by diaza crown compounds in aqueous solutions

1988

The conductance behavior of potassium nitrate in water with and without 1,7,10,16-tetraoxa-4,13-diazacyclooctandecane[2.2] and 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo-8.8.8-exacosane[2.2.2] macrocyclic ligands have been studied in order to analyze the complexation behavior of potassium cations in water. The absence of the complexation found in the [2.2] system is discussed in terms of the ligand structural features (presence of hydrogen bond donor and acceptor sites). The ion pair association constant of potassium cryptate as obtained from conductance measurements is also reported and discussed.

Aqueous solutionChemistryLigandHydrogen bondPotassiumInorganic chemistryBiophysicsConductancechemistry.chemical_elementPotassium nitrateBiochemistryCrown Compoundschemistry.chemical_compoundStability constants of complexesPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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A novel thermodynamic approach for the complexation study of toxic metal cations by a landfill leachate

2018

Landfill leachates can contaminate nearby aquifers. The hazards deriving from this contamination also depend on the chemical speciation of various contaminants. A novel approach is proposed here to face this problem from a chemical thermodynamics point of view. The complexing ability of the soluble fraction of a landfill leachate (collected from Bellolampo, Palermo, Italy) towards Pb2+, Cd2+ and Cu2+ has been investigated at T = 298.15 K in NaClaq at I = 0.1 mol dm−3. The soluble fraction of the landfill leachate was first characterized by different analytical techniques. Then, its acid–base properties were studied by ISE-H+ potentiometric titrations and modelled by the so-called diprotic-l…

Aqueous solutionChemistryPotentiometric titrationInorganic chemistry02 engineering and technologyGeneral Chemistry010501 environmental sciences021001 nanoscience & nanotechnology01 natural sciencesCatalysisMetalAnodic stripping voltammetryLandfill leachate sequestering ability complexation toxic metalsChemical thermodynamicsSequestrantvisual_artMaterials Chemistryvisual_art.visual_art_mediumTitrationSettore CHIM/01 - Chimica AnaliticaLeachate0210 nano-technology0105 earth and related environmental sciences
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Violurato complexes of nickel(II). Formation equilibria. Deprotonation equilibria of the coordinated ligands and related stereochemical changes

1986

The formation equilibria of nickel(II) violurato-complexes in water and dimethylsulphoxide-water (80∶20) as well as deprotonation of the coordinated ligands and related stereochemical changes are reported. The stability constants of the Ni2+-H2V− complexes logβ1=5.06, Iogβ2=9.38, logβ3=12.98 as well as the acidity constants of the [Ni(H2V)3]− complex, logβj1= 8.37, logβj2=15.76, logβj3=22.37 are determined at 25 °C and 0.1M NaClO4. A new violurato-complex of Ni2+, Na4[Ni(HV)3]5H2O, is isolated and characterized.

Aqueous solutionChemistryStereochemistryOrganic solventMetals and Alloyschemistry.chemical_elementMedicinal chemistryCatalysisInorganic ChemistryNickelchemistry.chemical_compoundDeprotonationStability constants of complexesMaterials ChemistryHydrateOrganometallic chemistryTransition Metal Chemistry
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Sequestration of organometallic compounds by natural organic matter. binding of trimethyltin(IV) by fulvic and alginic acids

2006

The binding capacity of fulvic and alginic acids towards trimethyl tin(IV) cation was quantitatively determined in order to evaluate the sequestering ability of toxic organometallic compounds by natural organic matter. Investigations were performed in the pH range of natural waters (5–8.5) where the carboxylate groups, largely present in both sequestering agents, are the main binding sites. A chemical interaction model, according to which both the protonation of polyelectrolyte ligands and the hydrolysis of the organotin cation in NaCl aqueous solution were considered, was used to define the speciation of the systems under investigation. Measurements performed at different ionic strength va…

Aqueous solutionChemistrycomplexationInorganic chemistrysequestrationProtonationGeneral ChemistryPolyelectrolyteInorganic ChemistryHydrolysischemistry.chemical_compoundspeciationIonic strengthStability constants of complexesSettore CHIM/01 - Chimica AnaliticaCarboxylatenatural organic matterorganometallic compoundhuman activitiesAlginic acidApplied Organometallic Chemistry
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Sequestration of alkyltin(IV) cations by complexation with amino-polycarboxylic chelating agents

2013

Abstract The binding capacity of four amino-polycarboxylic ligands (APCs) [nitrilotriacetate (NTA), ethylenediamine- N , N , N′ , N′ -tetraacetate (EDTA), (S,S)-ethylenediamine- N , N ′-disuccinic acid (S,S-EDDS) and diethylenetriamine- N , N , N′ , N″ , N″ -pentaacetate (DTPA)] towards mono-, di- and tri-alkyltin(IV) cations [(CH 3 )Sn 3 + , (CH 3 ) 2 Sn 2 + , (C 2 H 5 ) 2 Sn 2 + , (CH 3 ) 3 Sn + or (C 2 H 5 ) 3 Sn + ] was studied, in aqueous solutions, by ISE-H + potentiometry, at I  = 0.1 mol L − 1 (NaCl) and at T  = 298.15 K. In all the systems R x Sn (4 − x)+  − APC (R = CH 3 or C 2 H 5 ) a strong 1:1 species is formed together with protonated, hydroxo and dinuclear complexes. The valu…

Aqueous solutionComplexation in aqueous solutionStereochemistryLigandEthylenediamineProtonationAlkyltin(IV) cations; Amino-polycarboxylic ligands; Complexation in aqueous solution; Sequestration ability of complexones;Condensed Matter PhysicsMedicinal chemistryAtomic and Molecular Physics and OpticsAlkyltin(IV) cationElectronic Optical and Magnetic MaterialsIonAmino-polycarboxylic ligandchemistry.chemical_compoundSequestration ability of complexoneschemistryDiethylenetriamineMaterials ChemistryChelationSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistrySimple correlationSpectroscopy
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