Search results for "osso"

showing 10 items of 801 documents

GPU Based Molecular Dynamics Simulations of Polymer Rings in Concentrated Solution: Structure and Scaling

2011

We report on equilibrium properties of a concentrated solution of non-concatenated ring polymers by Molecular dynamics simulations using HooMD-blue, a fast implementation on graphics processor units (GPUs). We are able to identify the intermediate scaling regime for the radius of gyration Rg ∝ N as well as indication for a crossover to Rg ∝ N for rings with chain length N in our fully flexible off-lattice polymer model. This crossover takes place between a ring size of 2500 and 7500 monomers for monomer density ρ = 0.5. Our results are in agreement with recent studies for lattice and stiff off-lattice models and show once again that this scaling is not model dependent at all. Furthermore th…

chemistry.chemical_classificationPhysicsPhysics and Astronomy (miscellaneous)CrossoverPolymerComputational physicsRing sizeMolecular dynamicschemistryLattice (order)Radius of gyrationStatistical physicsGraphicsScalingProgress of Theoretical Physics Supplement
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Adsorption Transition of a Polymer Chain at a Weakly Attractive Surface: Monte Carlo Simulation of Off-Lattice Models

2002

A bead-spring model of a polymer chain with one end attached to a wall is studied by Monte Carlo simulations for chain lengths 16 ≤ N ≤ 256. Two types of adsorption potentials, 9-3 and 10-4 Lennard-Jones (LJ) potentials, between the effective monomers and the wall are assumed. For both cases the adsorption transition where the chain changes its asymptotic statistical properties from a three-dimensional to a two-dimensional configuration is located using a scaling analysis. It is shown that the crossover exponent φ = 0.50 ± 0.02 is the same for both LJ potentials. This value is compatible with recent theoretical predictions and simulation results for lattice models with short-range wall pote…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodCrossoverThermodynamicsStatistical mechanicsPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterInorganic ChemistryAdsorptionLattice (order)Materials ChemistryExponentStatistical physicsScalingMacromolecular Theory and Simulations
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A Mixed-Ligand Approach for Spin-Crossover Modulation in a Linear FeII Coordination Polymer

2014

In this work, we present a family of Fe(II) coordination polymers of general formula [Fe(btzx)(3-3x)(btix)(3x)](ClO4)2 with interesting spin-crossover properties. These coordination polymers have been synthesized using chemical mixtures of two different but closely related ligands, 1,4-bis(tetrazol-1-ylmethyl)benzene (btzx) and 1,4-bis(triazol-1-ylmethyl)benzene (btix), and the effect of a gradual substitution of the ligand in the spin transition temperature has been investigated. Several chemical mixtures have been structurally characterized by X-ray powder diffraction indicating a clear critical amount in the composition of the mixture after which mixed phases rather than a single phase c…

chemistry.chemical_classificationPolymersChemistryCoordination polymerLigandStereochemistrySpin transitionPolymerLigands3. Good healthInorganic ChemistryThermogravimetrychemistry.chemical_compoundCrystallographySpin crossoverThermogravimetryFerrous CompoundsPhysical and Theoretical ChemistryBenzenePowder DiffractionPowder diffractionInorganic Chemistry
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Photoswitchable coordination compounds

2001

Photoswitchable compounds represent an attractive class of materials in coordination chemistry. Recent progress dealing with transition metal compounds involving photo-induced changes of the magnetic and/or optical properties to long-lived metastable states are covered in the present review article. The basic photophysical phenomena together with representative examples such as nitroprusside derivatives, relevant spin crossover complexes, stilbenoid complexes and finally Prussian blue analogues are discussed. Some possible applications regarding energy and information storage are suggested at the end.

chemistry.chemical_classificationPrussian blueChemistryInformation storageNanotechnologyPhotomagnetismLIESSTCoordination complexInorganic Chemistrychemistry.chemical_compoundTransition metalPhoto isomerizationComputational chemistrySpin crossoverMaterials ChemistryPhysical and Theoretical ChemistryCoordination Chemistry Reviews
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Anomalous diffusion in polymer melts

2002

Abstract We present a study of the anomalous diffusion regimes in polymer melt dynamics performing a Monte Carlo (MC) simulation of the bond-fluctuation lattice model. Special emphasis is laid on the crossover from a Rouse-like motion to the behavior predicted by reptation theory. For the longest chains of N=400 the high statistical accuracy of the data allows for clear identification of the subdiffusive regimes in the center of mass motion and the monomer displacement. They are well compatible with those predicted by reptation theory. Furthermore a detailed analysis of the different short time anomalous diffusion regimes in the melt dynamics of polymer chains is presented and it is shown t…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesAnomalous diffusionMonte Carlo methodCrossoverGeneral Physics and AstronomyThermodynamicsPolymerDisplacement (vector)Condensed Matter::Soft Condensed MatterReptationchemistryStatistical physicsCenter of massPhysical and Theoretical ChemistryLattice model (physics)Chemical Physics
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Self-diffusion in polymer solutions using the bond-fluctuation MC-algorithm

1991

Abstract A lattice Monte Carlo study of the self-diffusion of polymer chains in an athermal solution of equal chains is presented. The examined chain lengths, N (= 20–200), and volume fractions, φ (= 0.025-0.5), cover the range from dilute solution to concentrated solution, respectively. The dynamics show a gradual crossover from Rouse to reptation-like behaviour. Analysing the data according to a scaling theory and taking into account the density dependence of the microscopic length and time-scales, an almost perfect scaling of the self-diffusion coefficient is achieved. The high statistical accuracy of the data (103–104 chains per parameter combination) was obtainable by using a transpute…

chemistry.chemical_classificationSelf-diffusionChemistryCrossoverThermodynamicsPolymerCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsVolume (thermodynamics)Cover (topology)Chain (algebraic topology)Computational chemistryMaterials ChemistryCeramics and CompositesRange (statistics)ScalingJournal of Non-Crystalline Solids
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Direct monitoring of spin state in dinuclear iron(II) coordination compounds

2001

So far there has been no direct method to determine the spin state of molecules in dinuclear iron(II) compounds. The molecular fractions of high-spin (HS) and low-spin (LS) species have been deduced from magnetic susceptibility and zero-field Mossbauer spectroscopy data irrespective of whether they belong to LS–LS, LS–HS and HS–HS pairs. However, the distinction of pairs becomes possible if Mossbauer measurements are carried out in an external magnetic field. The proposed method opens new possibilities in the study of spin crossover phenomena in dinuclear compounds.

chemistry.chemical_classificationSpin statesChemistryDirect methodGeneral Physics and AstronomyMagnetic susceptibilityCoordination complexMagnetic fieldCrystallographyNuclear magnetic resonanceSpin crossoverMössbauer spectroscopyMoleculeCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryChemical Physics Letters
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Thermal, Pressure and Light Induced Spin Transition in the Two-Dimensional Coordination Polymer [Fe(pmd)2[Cu(CN)2]2]

2008

[EN] A complete structural, calorimetric, and magnetic characterisation of the 2D coordination spin crossover polymer {Fe(pmd)(2)[Cu(CN)(2)](2)} is reported. The crystal structure has been investigated below room temperature at 180 K and 90 K, and at 30 K after irradiating the sample at low temperature with green light ( lambda = 532 nm). The volume cell contraction through the thermal spin transition is only 18 angstrom(3) which is lower than the usually observed value of around 25-30 angstrom(3) while the average Fe-N bond distances decrease by the typical value of about 0.19 angstrom. The structural data of the irradiated state indicate that the high spin state is well induced since the …

chemistry.chemical_classificationSpin statesCondensed matter physicsCoordination polymerSpin transitionThermodynamicsCrystal structurePolymerInorganic Chemistrychemistry.chemical_compoundchemistrySpin crossoverFISICA APLICADAThermalIrradiation
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Pressure-induced cooperative spin transition in ironII 2D coordination polymers: room-temperature visible spectroscopic study.

2011

For the 2D coordination polymers [Fe(3-Fpy)(2)M(II)(CN)(4)] (M(II) = Ni, Pd, Pt), the pressure-induced spin crossover behavior has been investigated at 298 K by monitoring the distinct optical properties associated with each spin state. Cooperative first-order spin transition characterized by a piezohysteresis loop ca. 0.1 GPa wide was observed for the three derivatives. Application of the mean field regular solution theory has enabled estimation of the cooperative parameter, Γ(p), and the enthalpy, ΔH(HL)(p), associated with the spin transition for each derivative. These values, found in the intervals 6.8-7.9 and 18.6-20.8 kJ mol(-1), respectively, are consistent with those previously repo…

chemistry.chemical_classificationSpin statesCondensed matter physicsEnthalpySpin transitionElastic energyPolymerSurfaces Coatings and FilmschemistryMean field theorySpin crossoverMaterials ChemistryPhysical chemistryPhysical and Theoretical ChemistrySpin-½The journal of physical chemistry. B
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Spin-State-Dependent Redox-Catalytic Activity of a Switchable Iron(II) Complex

2017

The spin state of catalytically active 3d metal centers plays a significant role for their activity in enzymatic processes and organometallic catalysis. Here we report on the catalytic activity of a Fe(II) coordination compound that can undergo a cooperative switch between low-spin (LS) and high-spin (HS) states. Catalytic measurements within 291 - 318 K temperature region reveal a drastic drop of the catalytic activity upon conversion of metallic centers from the LS to the HS form. For a thermoswitchable [Fe(NH2trz)3]Br2 complex (Tup = 305 K), an activation energy is found to be considerably lower for the LS state (158 kJ mol-1) comparing to the HS state (305 kJ mol-1). Mossbauer analysis …

chemistry.chemical_classificationSpin statesInorganic chemistry02 engineering and technologyActivation energy010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesRedox0104 chemical sciencesCoordination complexCatalysisInorganic ChemistryMetalCrystallographychemistrySpin crossovervisual_artvisual_art.visual_art_medium0210 nano-technologyEuropean Journal of Inorganic Chemistry
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