Search results for " complex"

showing 10 items of 3391 documents

Symbolic control for underactuated differentially flat systems

2006

In this paper we address the problem of generating input plans to steer complex dynamical systems in an obstacle-free environment. Plans considered admit a finite description length and are constructed by words on an alphabet of input symbols, which could be e.g. transmitted through a limited capacity channel to a remote system, where they can be decoded in suitable control actions. We show that, by suitable choice of the control encoding, finite plans can be efficiently built for a wide class of dynamical systems, computing arbitrarily close approximations of a desired equilibrium in polynomial time. Moreover, we illustrate by simulations the power of the proposed method, solving the steer…

Channel capacityNonlinear systemCapacity planningSettore ING-INF/04 - AutomaticaDynamical systems theoryControl theoryUnderactuationControl systemdynamic systemSymbolic controlMotion controlTime complexityMathematicsProceedings 2006 IEEE International Conference on Robotics and Automation, 2006. ICRA 2006.
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On the use of fractional calculus for the probabilistic characterization of random variables

2009

In this paper, the classical problem of the probabilistic characterization of a random variable is re-examined. A random variable is usually described by the probability density function (PDF) or by its Fourier transform, namely the characteristic function (CF). The CF can be further expressed by a Taylor series involving the moments of the random variable. However, in some circumstances, the moments do not exist and the Taylor expansion of the CF is useless. This happens for example in the case of $\alpha$--stable random variables. Here, the problem of representing the CF or the PDF of random variables (r.vs) is examined by introducing fractional calculus. Two very remarkable results are o…

Characteristic function (probability theory)FOS: Physical sciencesAerospace EngineeringMathematics - Statistics TheoryOcean EngineeringProbability density functionComplex order momentStatistics Theory (math.ST)Fractional calculusymbols.namesakeIngenieurwissenschaftenFOS: MathematicsTaylor seriesApplied mathematicsCharacteristic function serieMathematical PhysicsCivil and Structural EngineeringMathematicsGeneralized Taylor serieMechanical EngineeringStatistical and Nonlinear PhysicsProbability and statisticsMathematical Physics (math-ph)Condensed Matter PhysicsFractional calculusFourier transformNuclear Energy and EngineeringPhysics - Data Analysis Statistics and ProbabilitysymbolsFractional calculus; Generalized Taylor series; Complex order moments; Fractional moments; Characteristic function series; Probability density function seriesddc:620Series expansionFractional momentProbability density function seriesSettore ICAR/08 - Scienza Delle CostruzioniRandom variableData Analysis Statistics and Probability (physics.data-an)
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Uniformization with infinitesimally metric measures

2019

We consider extensions of quasiconformal maps and the uniformization theorem to the setting of metric spaces $X$ homeomorphic to $\mathbb R^2$. Given a measure $\mu$ on such a space, we introduce $\mu$-quasiconformal maps $f:X \to \mathbb R^2$, whose definition involves deforming lengths of curves by $\mu$. We show that if $\mu$ is an infinitesimally metric measure, i.e., it satisfies an infinitesimal version of the metric doubling measure condition of David and Semmes, then such a $\mu$-quasiconformal map exists. We apply this result to give a characterization of the metric spaces admitting an infinitesimally quasisymmetric parametrization.

Characterization (mathematics)Space (mathematics)conformal modulus01 natural sciencesMeasure (mathematics)funktioteoriaCombinatoricsMathematics - Metric Geometry0103 physical sciencesFOS: Mathematics0101 mathematicsComplex Variables (math.CV)MathematicsMathematics - Complex VariablesMathematics::Complex Variables010102 general mathematicsquasiconformal mappingMetric Geometry (math.MG)metriset avaruudetmetric doubling measureMetric spaceDifferential geometryUniformization theoremMetric (mathematics)quasisymmetric mapping30L10 (Primary) 30C65 28A75 51F99 (Secondary)mittateoria010307 mathematical physicsGeometry and TopologyUniformization (set theory)
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Sequestration of organomettalic compounds by synthetic and naturally occuring polycarboxylate ligands. Binding of monomethylmercury(II) by polyacryli…

2007

The sequestering capacity of synthetic and naturally occurring polycarboxylate ligands towards mono- methylmercury(II) was evaluated by stability quantitative data on the interaction of CH3Hgþ with different molecular weight synthetic polyacrylates (2 and 20 kDa average M.wt) and alginate (70– 100 kDa) extracted from brown algae Macrocystis pyrifera. The influence of ionic medium was evaluated by measurements on the CH3Hgþ-polyacrylate systems in NaNO3 medium at different ionic strengths (0.10, 0.25, 0.50 and 0.75mol Lÿ1), and a Debye–Hu¨ ckel type equation was used for the dependence of complex formation constants on ionic strength. Measurements on the CH3Hgþ - alginate system were carried…

Chemical Health and SafetybiologyChemistryHealth Toxicology and MutagenesisComplex formationIonic bondingmonomethylmercury; sequestration by organic matter; polyacrylic and alginic acidsToxicologybiology.organism_classificationBrown algaemonomethylmercuryBinding abilityType equationpolyacrylic and alginic acidsmonomethylmercury sequestration by organic matter polyacrylic and alginic acids speciation equilibrium analysis complex species formationIonic strengthOrganic chemistrySettore CHIM/01 - Chimica Analiticasequestration by organic matterNuclear chemistryGroup 2 organometallic chemistry
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Theoretical study of new acceptor and donor molecules based on polycyclic aromatic hydrocarbons

2011

Functionalized polcyclic aromatic hydrocarbons (PAHs) are an interesting class of molecules in which the electronic state of the graphene-like hydrocarbon part is tuned by the functional group. Searching for new types of donor and acceptor molecules, a set of new PAHs has recently been investigated experimentally using ultraviolet photoelectron spectroscopy (UPS). In this work, the electronic structure of the PAHs is studied numerically with the help of B3LYP hybrid density functionals. Using the DELTA-SCF method, electron binding energies have been determined which affirm, specify and complement the UPS data. Symmetry properties of molecular orbitals are analyzed for a categorization and a…

Chemical Physics (physics.chem-ph)Materials scienceCondensed Matter - Mesoscale and Nanoscale PhysicsKoopmans' theoremFOS: Physical sciencesElectronic structureCharge-transfer complexAcceptorAtomic and Molecular Physics and OpticsCondensed Matter::Materials ScienceElectron affinity (data page)Chemical physicsPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Molecular orbitalPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsHOMO/LUMOSpectroscopyBasis setJournal of Molecular Spectroscopy
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Effects of substitutions on cyclopentadienyl rings in complexes with molybdenum-mercury bonds. 95Mo and 199Hg NMR studies

1995

NMR data for 95Mo and 199Hg nuclei have been obtained for new di- and trimetallic complexes Cp′(CO)3MoHgX containing molybdenum-mercury bonds and bulky and/or potentially bifunctional substituted cyclopentadienyl ligands; Cp′=C5HMe2Ph2, C5Me4Bz, C5Bz5, C5H4PPh2 and C5Me4PPh2 (Bz=CH2C6H5; Me =CH3; Ph=C6H5); X=Cp′(CO)3Mo, Cl, Br, 1, SCN. They are discussed within the context of our earlier results reported for analogous complexes with the cyclopentadienyl ligands bearing methyl groups. With the exception of phenyl substituted rings, a rather narrow range of 95Mo chemical shifts is found for the compounds with the same number of different substituents on cyclopentadienyl ligands. An outstandin…

Chemical shiftchemistry.chemical_elementPhotochemistryMedicinal chemistryNmr dataMercury (element)Inorganic Chemistrychemistry.chemical_compoundchemistryCyclopentadienyl complexMolybdenumIntramolecular forceMaterials ChemistryNarrow rangePhysical and Theoretical ChemistryBifunctionalInorganica Chimica Acta
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1,3-Dipolar cycloaddition of diaryldiazomethanes across N-ethoxy-carbonyl-N-(2,2,2-trichloroethylidene)amine and reactivity of the resulting 2-azabut…

2016

Abstract 1,3-dipolar cycloaddition of diaryldiazomethanes Ar2C N2 across Cl3C–CH N–CO2Et 1 yields Δ3-1,2,4-triazolines 2. Thermolysis of 2 leads, via transient azomethine ylides 3, to diaryldichloroazabutadienes [Ar(Ar')C N–CH CCl2] 4. Treatment of 4a (Ar = Ar' = C6H5) and 4c (Ar = Ar' = p-ClC6H4) with NaSR in DMF yields 2-azabutadienes [Ar2C N–C(H) C(SR)2] 5. In contrast, nucleophilic attack of NaStBu on 4 affords azadienic dithioethers [Ar2C N–C(StBu) C(H)(StBu)] (7a Ar = C6H5; 7b Ar' = p-ClC6H4). The reaction of 4a with NaSEt conducted in neat EtSH produces [Ph2C N–C(H)(SEt)–CCl2H] 8, which after dehydrochloration by NaOMe and subsequent addition of NaSEt is converted to [Ph2C N–C(SEt) C…

Chemistry(all)StereochemistryGeneral Chemical Engineering124-TriazolineCrystal structure010402 general chemistry01 natural sciencesMedicinal chemistrychemistry.chemical_compoundThioetherNucleophile[CHIM]Chemical SciencesReactivity (chemistry)ThioetherCycloadditionComputingMilieux_MISCELLANEOUS2-Azabutadienes010405 organic chemistryGeneral ChemistryCycloaddition0104 chemical sciences3. Good healthchemistry13-Dipolar cycloadditionAzomethine ylidesChemical Engineering(all)Alkoxy groupPiperidineCopperMacrocyclic complexComptes Rendus Chimie
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Periodic behaviour in heterogeneous chemical reactions

1992

Abstract The authors present an analytical and numerical analysis for a solid-gas oxidation process represented by a set of coupled reaction rates equations. The equations describe the time evolution of four elementary process that govern the overall heterogeneous kinetics. The description formation of a new oxide unit considers: (1) an internal interface (oxide-metal) reaction by which an activated complex is formed; (2) the dissolution of the complex produce a chemical element σ; (3) the diffusion of σ through the oxide layer; and (4) an external interface (oxide-gas) reaction. The results reported here delinate the parameter region where chemical oscillations are present.

ChemistryActivated complexNumerical analysisKineticsTime evolutionOxideThermodynamicsGeneral ChemistryCondensed Matter PhysicsChemical reactionchemistry.chemical_compoundPhysical chemistryGeneral Materials ScienceDiffusion (business)DissolutionSolid State Ionics
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Chlorodicyclopentadienyloxoniobium(V) complexes revisited: The origin of the asymmetry in the 1H- and 13C-NMR spectra, X-ray crystal structures and a…

2000

Abstract 1H- and 13C-NMR spectra of chlorodicyclopentadienyloxoniobium(V) complex I and its four 1,1′-dialkyl substituted derivatives II–V have been recorded and assigned based on DQF 1H,1H-COSY and PFG 1H,13C-HMQC and HMBC experiments. Non-equivalences of all cyclopentadienyl protons and carbons in II–V (as reflected by their different 1H- and 13C-NMR chemical shifts) are explained by synchronous and out-of-phase rotations of the substituted cyclopentadienyl rings. A non-equivalence of the methyls in III (1,1′-di-isopropyl) is explained by a detailed inspection of the rotamers of the isopropyl groups. The X-ray structural data show that III and IV (1-methyl-1′-tert-butyl) crystallize in th…

ChemistryChemical shiftOrganic ChemistryAb initioSpace groupCrystal structureTriclinic crystal systemBiochemistryInorganic ChemistryCrystallographyCyclopentadienyl complexMaterials ChemistryPhysical and Theoretical ChemistryConformational isomerismMonoclinic crystal system
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Chemical Reactivity in AOT Microemulsions:  Kinetics of Water Replacement in a Square-Planar Palladium(II) Aquo Complex by Monoalkylthioureas

1998

The kinetics of water replacement in the cationic palladium(II) aquo complex [Pd(Et4dien)(H2O)]2+, where Et4dien = Et2N(CH2)2NH(CH2)2NEt2, by thiourea, methylthiourea, and ethylthiourea have been studied at 25.0 °C in heptane−AOT−water microemulsion over a wide range of the molar ratio R (=[H2O]/[AOT]) at the constant surfactant concentration of 0.13 mol dm-3. The reaction rates are significantly higher in microemulsions than in bulk water and decrease rapidly as the parameter R increases. The kinetic data, interpreted quantitatively by applying the pseudophase model to the microemulsion, indicate that there is a weak partitioning of the nucleophiles between the water core and the AOT inter…

ChemistryKineticsInorganic chemistrychemistry.chemical_elementSurfaces Coatings and FilmsPartition coefficientReaction ratechemistry.chemical_compoundThioureaPulmonary surfactantMaterials ChemistryMicroemulsionPhysical and Theoretical ChemistryMetal aquo complexPalladiumThe Journal of Physical Chemistry B
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