Search results for "monomer"

showing 10 items of 857 documents

Theoretical modeling of Langmuir monolayers

1999

Abstract We study coarse-grained continuum models for Langmuir monolayers by self-consistent field theory and by Monte Carlo simulations. Amphiphilic molecules are represented by stiff chains of monomers with one end grafted to a planar surface. In particular, we discuss the origin of successive fluid–fluid transitions, the possible origin of tilt order and the factors which determine the direction of tilt.

Condensed Matter::Soft Condensed MatterAmphiphilic moleculechemistry.chemical_compoundLangmuirColloid and Surface ChemistryMonomerPlanarchemistryChemical physicsMonolayerMonte Carlo methodPhysical chemistryColloids and Surfaces A: Physicochemical and Engineering Aspects
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Spin crossover behaviour in the iron(II)-2,2-dipyridilamine system: Synthesis, X-ray structure and magnetic studies

2005

Abstract The monomeric compounds [Fe(dpa)2(X)2] · solv [X = NCS−(solv = 0.5H2O) (1), N ( CN ) 2 - (2) and dpa = 2,2-dipyridilamine] have been synthesised and characterised. They crystallise in the P21/n and in the Cc monoclinic systems, respectively. Four of six nitrogen atoms coordinated to the Fe(II) ions belong to two dpa ligands which lie in cis conformation. The remaining positions are occupied by two nitrogen atoms of the pseudo-halide ligands. The magnetic susceptibility measurements at ambient pressure have revealed that compound 1 exhibits an incomplete spin crossover behaviour (T1/2 ≈ 88 K), whereas compound 2 remains in the high-spin configuration. Pressure studies performed on c…

Condensed matter physicsX-raychemistry.chemical_elementNitrogenMagnetic susceptibilityIonInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistrySpin crossoverMaterials ChemistryPhysical and Theoretical ChemistryMonoclinic crystal systemAmbient pressureInorganica Chimica Acta
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Polymer-based symmetric electrochromic devices

1999

Abstract The fact that conjugated polymers repeatedly undergo electrochemical doping/undoping processes, which are accompained by color changes, makes these materials very attractive, and much effort has been devoted to their use in advanced devices. There is renewed interest in electroactive polymers that reversibly undergo both p- and n-doping because of their potential application in symmetric electrochemical devices. We employed fused molecules, dithienothiophenes, as monomers to obtain polymers with a narrow band gap suitable for n- and p-doping. The performance results of two symmetric electrochromic devices having as electrodes both poly(dithieno[3,4-b:3',4'-d]thiophene) (pDTT1) and …

Conductive polymerchemistry.chemical_classificationMaterials scienceRenewable Energy Sustainability and the EnvironmentDopingNanotechnologyPolymerConjugated systemElectrochromic devicesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMonomerchemistryThiopheneElectroactive polymersOrganic chemistrySolar Energy Materials and Solar Cells
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Reactivity of Nickel(II) Porphyrins in oCVD Processes—Polymerisation, Intramolecular Cyclisation and Chlorination

2019

Abstract Oxidative chemical vapour deposition of (5,15‐diphenylporphyrinato)nickel(II) (NiDPP) with iron(III) chloride as oxidant yielded a conjugated poly(metalloporphyrin) as a highly coloured thin film, which is potentially useful for optoelectronic applications. This study clarified the reactive sites of the porphyrin monomer NiDPP by HRMS, UV/Vis/NIR spectroscopy, cyclic voltammetry and EPR spectroscopy in combination with quantum chemical calculations. Unsubstituted meso positions are essential for successful polymerisation, as demonstrated by varying the porphyrin meso substituent pattern from di‐ to tri‐ and tetraphenyl substitution. DFT calculations support the proposed radical oxi…

Conjugated systemporphyrins010402 general chemistryPhotochemistry01 natural sciencesCatalysischemical vapor depositionnickelchemistry.chemical_compoundReactivity (chemistry)Full Paper010405 organic chemistryOrganic ChemistryRegioselectivityGeneral ChemistryFull PapersPorphyrin0104 chemical sciencesMonomerthin filmschemistryPolymerizationpolymerizationChemical Vapor Deposition | Hot PaperOxidative coupling of methaneCyclic voltammetryChemistry – A European Journal
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Molecular-dynamics simulation of a glassy polymer melt: Incoherent scattering function

1999

We report results of molecular-dynamics simulations for a glassy polymer melt consisting of short, linear bead-spring chains. It was shown in previous work that this onset of the glassy slowing down is compatible with the predictions of the mode coupling theory. The physical process of `caging' of a monomer by its spatial neighbors leads to a distinct two step behavior in the particle mean square displacements. In this work we analyze the effects of this caging process on the Rouse description of the melt's dynamics. We show that the Rouse theory is applicable for length and time scales above the typical scales for the caging process. Futhermore, the monomer displacement is compared with si…

CouplingQuantitative Biology::BiomoleculesWork (thermodynamics)Materials scienceThermodynamicsBinary numberCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicsMonomerchemistryParticleCage effectDisplacement (fluid)The European Physical Journal B
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Dynamics of a supercooled polymer melt above the mode-coupling critical temperature: cage versus polymer-specific effects

2000

This paper reports results of molecular dynamics simulations for a glassy polymer melt consisting of short, non-entangled chains. The temperature region studied covers the supercooled state of the melt above the mode-coupling critical temperature. The analysis focuses on the interplay of simple-liquid and polymer-specific effects. One can clearly distinguish two regimes: a regime of small and one of large monomer displacements. The first regime corresponds to motion of a monomer in its local environment. It is dominated by the cage effect and well described by the idealized mode-coupling theory. The second regime is governed by the late-β/early-α process. In this regime the connectivity of …

Couplingchemistry.chemical_classificationChemistryDynamics (mechanics)ThermodynamicsPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicsMonomerGeneral Materials ScienceCage effectSupercoolingDisplacement (fluid)Journal of Physics: Condensed Matter
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Magnetic Molecular Conductors Based on Bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) and the Tris(chlorocyananilato)ferrate(III) Complex

2019

Electrocrystallization of the bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) organic donor in the presence of the [Fe(ClCNAn)3]3– tris(chlorocyananilato)ferrate(III) paramagnetic anion in different stoichiometric ratios and solvent mixtures afforded two different hybrid systems formulated as [BEDT-TTF]4[Fe(ClCNAn)3]·3H2O (1) and [BEDT-TTF]5[Fe(ClCNAn)3]2·2CH3CN (2) (An = anilato). Compounds 1 and 2 present unusual structures without the typical segregated organic and inorganic layers, where layers of 1 are formed by Λ and Δ enantiomers of the anionic paramagnetic complex together with mixed-valence BEDT-TTF tetramers, while layers of 2 are formed by Λ and Δ enantiomers of the paramagnetic…

Crystal structure010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundParamagnetismMolecular interactionsMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistry[CHIM.MATE]Chemical Sciences/Material chemistryMolecules3. Good health0104 chemical sciencesSolventCrystallographyMonomerchemistryRadical ionOligomersCrystal structuresSolventsStoichiometryTetrathiafulvaleneInorganic Chemistry
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Spin Cross-Over (SCO) Complex Based on Unsymmetrical Functionalized Triazacyclononane Ligand: Structural Characterization and Magnetic Properties

2019

International audience; The unsymmetrical ligand 1-(2-aminophenyl)-4,7-bis(pyridin-2-ylmethyl)-1,4,7-triazacyclononane (L6) has been prepared and characterized by NMR spectroscopy. The L6 ligand is based on the triazamacrocycle (tacn) ring that is functionalized by two flexible 2-pyridylmethyl and one rigid 2-aminophenyl groups. Reaction of this ligand with Fe(ClO4)2·xH2O led to the complex [Fe(L6)](ClO4)2 (1), which was characterized as the first Fe(II) complex based on the unsymmetrical N-functionalized tacn ligand. The crystal structure revealed a discrete monomeric [FeL6]2+ entity in which the unsymmetrical N-functionalized triazacyclononane molecule (L6) acts as hexadentate ligand. As …

Crystal structure010402 general chemistryRing (chemistry)01 natural scienceslcsh:Chemistrychemistry.chemical_compoundSpin crossoverPyridineMagnetic propertiesMacrocycle ligands; Iron complex; High spin and Low spin; Spin Cross-Over; Magnetic propertiesMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryIron complex010405 organic chemistryLigand[CHIM.MATE]Chemical Sciences/Material chemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographyMonomerchemistrylcsh:QD1-999Chemistry (miscellaneous)Macrocycle ligandsHigh spin and Low spinSpin Cross-OverMagnetochemistry
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Topochemical Reactions of Monomers with Conjugated Triple-Bonds VII Mechanism of Transition from Monomer to Polymer Phase During Solid-State Polymeri…

1972

The lattice-controlled solid-state polymerisation of three different modifications of 2,4-hexadiin-1,6-diol-bis(phenylurethane) was investigated by X-ray and optical methods. The polymerisation is a homogeneous reaction. The polymer grows in the form of single chains within the crystal of the monomer. The chains extend along a definite crystallographic direction. Monomer and polymer are isomorphous and monomer-polymer single crystals of various compositions are obtained up to a quantitative conversion in the case of modification I or III. Phase separation into a mesomorphic polymer and oriented monomer phase was observed on annealing partially polymerised single-crystals of modification II …

Crystalchemistry.chemical_classificationchemistry.chemical_compoundMonomerPolymerizationchemistryTransition pointPhase (matter)Polymer chemistryGeneral ChemistryPolymerConjugated systemTriple bondIsrael Journal of Chemistry
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Synthesis and Electrochemistry of Aluminum Porphycenes. Crystal and Molecular Structure of Methyl-σ-Bonded Aluminum Etioporphycene

1997

The synthesis and characterization of three monomeric aluminum porphycenes with anionic or σ-bonded axial ligands is reported. The investigated compounds are represented as ( EtioPc ) Al ( CH 3) and ( EtioPc ) AlX where EtioPc represents the dianion of etioporphycene and X = Cl − or OH −. Each synthesized complex was characterized by mass spectrometry. 1 H NMR, IR and UV-visible spectroscopies as well as by electrochemistry. Comparisons are made between the properties of complexes in the aluminum etioporphycene series and related chloro- or methyl σ-bonded Al ( III ) porphyrins containing octaethylporphyrin ( OEP ) or tetraphenylporphyrin ( TPP ) macrocycles. Comparisons are also made betw…

Crystalchemistry.chemical_compoundCrystallographyMonomerchemistryDimerTetraphenylporphyrinInorganic chemistryX-ray crystallographyProton NMRMoleculeGeneral ChemistryElectrochemistryJournal of Porphyrins and Phthalocyanines
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