Search results for "Length"

showing 10 items of 2188 documents

Collapse of Linear Polyelectrolyte Chains in a Poor Solvent: When Does a Collapsing Polyelectrolyte Collect its Counterions?

2008

To better understand the collapse of polyions in poor solvent conditions the effective charge and the solvent quality of the hypothetically uncharged polymer backbone need to be known. In the present work this is achieved by utilizing poly-2-vinylpyridine quaternized to 4.3% with ethylbromide. Conductivity and light scattering measurements were utilized to study the polyion collapse in isorefractive solvent/nonsolvent mixtures consisting of 1-propanol and 2-pentanone, respectively, at nearly constant dielectric constant. The solvent quality of the uncharged polyion could be quantified which, for the first time, allowed the experimental investigation of the effect of the electrostatic intera…

chemistry.chemical_classificationHydrodynamic radiusPolymers and PlasticsOrganic ChemistryBjerrum lengthEffective nuclear chargePolyelectrolyteInorganic ChemistrySolventchemistryChemical physicsPolymer chemistryMaterials ChemistryRadius of gyrationCounterionSolvent effectsMacromolecules
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Unexpected Structural Diversity in Alkali Metal Azide-Crown Ether Complexes: Syntheses, X-ray Structures, and Quantum-Chemical Calculations

2005

A series of alkali metal azide-crown ether complexes, [Li([12]crown-4)(N-3)], [Na([15]crown-5)(N-3)], [Na([15]crown-5)(H2O)(2)]N-3, [K([18]crown-6)(N-3)(H2O)], [Rb([18]crown-6)(N-3)(H2O)], [Cs([18]crown-6)(N-3)](2), and [Cs([18]crown-6)(N-3)(H2O)(MeOH)], has been synthesised. In most cases, single crystals were obtained, which allowed X-ray crystal structures to be derived. The structures obtained have been compared with molecular structures computed by density functional theory (DFT) calculations. This has allowed the effects of the crystal lattice on the structures to be investigated. Also, a study of the M-N-terminal metalazide bond length and charge densities on the metal (M) and termin…

chemistry.chemical_classificationHydrogen bondCoordination numberOrganic ChemistryIonic bondingEtherGeneral ChemistryCrystal structureCatalysisBond lengthchemistry.chemical_compoundCrystallographychemistryComputational chemistryDensity functional theoryazides crown ethers characterizationCrown etherChemistry - A European Journal
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Isoniazid cocrystallisation with dicarboxylic acids: vapochemical, mechanochemical and thermal methods

2016

Cocrystallisation with a series of related compounds allows for the exploration of trends and limitations set by structural differences between these compounds. In this work, we investigate how the length of a dicarboxylic acid influences the outcome of cocrystallisation with isoniazid. We have performed a systematic study on the mechanochemical, thermal and solvent vapour-assisted cocrystallisation of aliphatic dicarboxylic acids (C3–C10) with isoniazid. Our results demonstrate that the rate of mechanochemical and vapour-assisted cocrystallisation depends on the acid chain length and shows alternation between odd- and even-chain acids. The results of thermal cocrystallisation showed that t…

chemistry.chemical_classificationIsoniazid02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventChain lengthDicarboxylic acidchemistryMelting pointmedicineOrganic chemistryGeneral Materials Science0210 nano-technologyEutectic systemThermal methodsmedicine.drugCrystEngComm
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Neue extrem deformierte (Biphenylen‐)Kohlenwasserstoff‐Gerüste

1992

New Extremely Deformed (Biphenylene)Hydrocarbon Skeletons The tetracyclic carbon skeleton 2-oxo[3](1,8)biphenylenophane (4) was synthesized by cyclization of a mixture of the bis(bromomethyl) compounds 7a, b with p-tolylsulfonylmethyl isocyanide. 2-Hydroxy[3](1,8)biphenylenophane (5) and the [3](1,8)biphenylenophane hydrocarbon 6 were obtained by reduction of 4 with LiAlH4 and NaBH4, respectively. X-ray analyses of 4 and 6 illustrate the dramatic deformation of bond lengths and angles in these molecules.

chemistry.chemical_classificationKetoneStereochemistryIsocyanideCrystal structureBiphenyleneMedicinal chemistryInorganic ChemistryBond lengthchemistry.chemical_compoundHydrocarbonPolycyclic compoundchemistryCyclophaneChemische Berichte
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Polymeric alloys: Model materials for the understanding of the statistical thermodynamics of mixtures

1997

Polymeric materials find industrial applications that are comparable to those of metals and ceramics.1 In addition to the great variability via the synthesis of various monomers and the choice of the degree of polymerization (N), alloying of polymers finds increasing attention for combining favorable materials properties.1,2 But polymeric (binary) alloys (A,B) of flexible polymers with chain lengths NA, NB are also most interesting for testing theoretical concepts: changing NA, NB one controls the entropy of mixing, keeping intermolecular forces invariant. Variation of these control parameters thus allows stringent tests of the theories on miscibility, unmixing etc. Furthermore, the large s…

chemistry.chemical_classificationLength scaleBinodalMaterials sciencechemistrySpinodal decompositionCritical point (thermodynamics)Intermolecular forceThermodynamicsPolymer blendPolymerEntropy of mixing
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Dynamics of Glassy Polymer Melts in Confined Geometry: A Monte Carlo Simulation

1996

Dynamic properties of a dense polymer melt confined between two hard walls are investigated over a wide range of temperatures by dynamic Monte Carlo simulation. The temperature interval ranges from the ordinary liquid to the strongly supercooled melt. The influence of temperature, density and confinement on the polymer dynamics is studied by various mean-square displacements, structural relaxation functions and quantities derived from them (relaxation times, apparent diffusion coefficients, monomer relaxation rates), yielding the following results: The motion of the monomers and polymers close to the walls is enhanced in parallel, but reduced in perpendicular direction. This dynamic anisotr…

chemistry.chemical_classificationLength scaleMaterials scienceCondensed matter physicsDiffusionMonte Carlo methodGeneral EngineeringThermodynamicsStatistical and Nonlinear PhysicsPolymerCondensed Matter::Soft Condensed MatterchemistryRadius of gyrationRelaxation (physics)AnisotropySupercoolingJournal de Physique I
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Tracer diffusion properties of core-shell latex films studied by photoinduced grating relaxation

2007

This article reports the application of the Photo-Induced Grating Relaxation technique (also known as Forced Rayleigh Scattering) to investigate the dynamics of films prepared from structured core–shell latex particles via the transport property of the photochromic tracer molecule Aberchrome 540®. The core–shell particles were prepared with a fluoropolymer core (immiscible and impenetrable to the tracer) and a poly(butyl methacrylate) shell. The incompletely dried films (with residual water) manifest their spatial heterogeneity via non-Fickian behavior (spatial scale- dependent apparent diffusion coefficient). The diffusion data was interpreted using the two-state diffusion model, previousl…

chemistry.chemical_classificationLength scaleMaterials sciencePolymers and PlasticsPolymerStrain hardening exponentCondensed Matter PhysicsFick's laws of diffusionchemistry.chemical_compoundsymbols.namesakechemistryChemical physicsPolymer chemistryMaterials ChemistrysymbolsFluoropolymerEffective diffusion coefficientPhysical and Theoretical ChemistryDiffusion (business)Rayleigh scatteringJournal of Polymer Science Part B: Polymer Physics
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Growing range of correlated motion in a polymer melt on cooling towards the glass transition

1999

Many liquids cooled to low temperatures form glasses (amorphous solids) instead of crystals. As the glass transition is approached, molecules become localized and relaxation times increase by many orders of magnitude1. Many features of this ‘slowing down’ are reasonably well described2 by the mode-coupling theory of supercooled liquids3. The ideal form of this theory predicts a dynamical critical temperature T c at which the molecules become permanently trapped in the ‘cage’ formed by their neighbours, and vitrification occurs. Although there is no sharp transition, because molecules do eventually escape their cage, its signature can still be observed in real and simulated liquids. Unlike c…

chemistry.chemical_classificationLength scaleMultidisciplinaryMaterials scienceCondensed matter physicsCritical phenomenaPolymerAmorphous solidCondensed Matter::Soft Condensed MatterchemistryCritical point (thermodynamics)Mode couplingGlass transitionSupercoolingNature
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Structural Rearrangements in Triple-Decker-Like Complexes with Mixed Group 15/16 Ligands: Synthesis and Characterization of the Redox Couple [Cp2*Fe2…

2001

The reaction of As4Se4 with stoichiometric amounts of [Cp*Fe2(CO)4] (Cp* = C5Me5) in boiling toluene forms [Cp2*Fe2As2Se2] (1) in good yield. X-ray crystallography shows 1 to have a triple-decker structure which comprises a tetraatomic mu,eta4:4-As2Se2 ligand. Density functional theory (DFT) and extended Huckel molecular orbital (EHMO) calculations confirm that the As2Se2 ligand behaves as a four-electron pi donor. Oxidation of 1 with equimolar amounts of [(C5H5)2Fe]PF6, Br2 and I2, respectively, gave compounds 2-4. According to X-ray crystallographic investigations that were carried out on 2 and 4, the oxidation state has a considerable influence on the structure of the Fe2As2Se2 core: sig…

chemistry.chemical_classificationLigandOrganic ChemistryInorganic chemistryIodideGeneral ChemistryAntibonding molecular orbitalRedoxCatalysisBond lengthCrystallographychemistryOxidation stateDensity functional theoryMolecular orbitalChemistry
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Solute retention in reversed-phase chromatography as a function of stationary phase properties: Effect of n-alkyl chain length and ligand density

1988

Two series of bonded phases were synthesized employing LiChrospher Si 100, 10 μm and n-alkyldimethylmonochlorosilanes as silanizing reagents. In series A the n-alkyl chain length, n, of the bonded phase was varied between 1 and 20 at a constant ligand density of 3.5±0.2μmol·m−2. In series B the ligand density, d, was gradually changed from 0 to 4.1μmol·m−2 on the C1, C4, C6, C8 and C18 bonded phases, respectively.

chemistry.chemical_classificationLigandStereochemistryOrganic ChemistryClinical BiochemistryFunction (mathematics)Reversed-phase chromatographyBiochemistryAnalytical ChemistryCrystallographyChain lengthchemistryStationary phaseReagentPhase (matter)AlkylChromatographia
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