Search results for "Side chain"

showing 10 items of 345 documents

Study of smectic elastomer films under uniaxial stress

2004

We study the mechanical properties of free-standing films of smectic liquid crystalline elastomers. Macroscopically ordered elastomer films of submicrometer thickness are prepared from freely suspended smectic A polymer films by photo crosslinking. The deformation characteristics depend criticically on the sample composition, in particular on the density of mesogenic side chains at the siloxane backbone. In materials where the siloxane backbone is only partially substituted (dilute systems), a uniaxial stretching of the films in the layer plane is accompanied by a shrinkage of the smectic layers. This layer shrinkage is to only a minor extent achieved by the induction of a molecular tilt. W…

chemistry.chemical_classificationMaterials scienceMesogenGeneral ChemistryPolymerCondensed Matter PhysicsElastomerchemistry.chemical_compoundchemistryLiquid crystalSiloxaneSide chainGeneral Materials ScienceDeformation (engineering)Composite materialLayer (electronics)Liquid Crystals
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Infrared spectroscopic study of a phenyl benzoate side group—methacrylate main chain polymeric liquid crystal

1994

Abstract The temperature dependence of the infrared dichroism of a side chain polymeric liquid crystal was investigated for two homogeneously oriented samples, one aligned with a PVA coating and the other aligned by a magnetic field. From the apparent order parameters, it was found that the rotation of the mesogenic side group was restricted. Not only the rigid part of the side group, but also the alkyl chains were found to be partly ordered. Realignment of the side groups was observed in the case of the magnetically aligned sample at the smectic-nematic transition temperature. Unlike the other absorption bands, the C˭O bond vibration band shifted to higher wavenumbers with increasing tempe…

chemistry.chemical_classificationMaterials scienceMesogenTransition temperatureGeneral ChemistryCondensed Matter PhysicsPolymeric liquid crystalCondensed Matter::Soft Condensed MatterCrystallographychemistryLiquid crystalSide chainOrganic chemistryGeneral Materials ScienceAbsorption (chemistry)Pendant groupAlkylLiquid Crystals
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Pearl-necklace structures of molecular brushes with rigid backbone under poor solvent conditions: A simulation study

2010

Bottle-brush polymers, where flexible side chains containing N=20 to 50 effective monomers are grafted to a rigid backbone, are studied by molecular dynamics simulations, varying the grafting density σ and the solvent quality. Whereas for poor solvents and large enough σ the molecular brush is a cylindrical object, homogeneous in axial direction, for intermediate values of σ an axially inhomogeneous structure of "pearl-necklace" type is formed. The "pearls," however, have a strongly nonspherical ellipsoidal shape, due to the fact that several side chains cluster together in one pearl, qualitatively consistent with predictions of Sheiko et al. [Eur. Phys. J. E 13, 125 (2004)] We analyze the …

chemistry.chemical_classificationMaterials scienceMolecular StructurePolymersTemperatureGeneral Physics and AstronomyPolymerMolecular Dynamics Simulationchemistry.chemical_compoundMolecular dynamicsMonomerChain (algebraic topology)chemistryChemical physicsComputational chemistrySolventsCluster (physics)Side chainCylinderPhysical and Theoretical ChemistryAxial symmetryThe Journal of Chemical Physics
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Sanidics: A new class of mesophases, displayed by highly substituted rigid-rod polyesters and polyamides

1990

Abstract The structure of rigid-chain polyesters and polyamides which possess flexible side chains consisting of methylene or 1,4,7-trioxaoctyl oxide units have been investigated by means of X-ray scattering. The X-ray studies were performed on fibres and monodomains. Additional information was gained from calorimetric, dilatometric and microscopic studies. The investigations revealed that these polymers display mesophases and that the structures of the mesophases differ from those observed for discotic and calamitic phases. They are characterized by the fact that in the ordered and disordered phases board-like molecules are stacked parallel on top of each other and that these stacks of mol…

chemistry.chemical_classificationMaterials scienceOxideGeneral ChemistryPolymerCondensed Matter PhysicsPolyesterCrystallographychemistry.chemical_compoundchemistryLiquid crystalPhase (matter)PolyamideSide chainMoleculeOrganic chemistryGeneral Materials ScienceLiquid Crystals
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Photoreactive Langmuir–Blodgett–Kuhn multilayer assemblies from functionalized liquid-crystalline side chain polymers, I. Homopolymers containing azo…

1991

Stable monomolecular layers of a liquid-crystalline homopolymer bearing azobenzene chromophores in the mesogenic side groups could be prepared at the water–air interface by slow compression at room temperature. From the area per monomer unit of A0≈0.25 nm2 a structural model with tightly packed azobenzene groups oriented nearly parallel to the surface normal was deduced. After transfer to a solid support in a Y-type mode the obtained Langmuir–Blodgett–Kuhn (LBK) multilayer assemblies of varying thicknesses (from a double layer to a thick film of d = 238 nm, capable of guiding optical modes) were prepared and analyzed by X-ray reflection and optical evanescent wave techniques. A monolayer th…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsAbsorption spectroscopybusiness.industrySurface plasmonAnalytical chemistryPolymerLangmuir–Blodgett filmchemistry.chemical_compoundOpticschemistryAzobenzeneMonolayerSide chainbusinessRefractive indexPolymers for Advanced Technologies
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Side-chain conjugated polymers for use in the active layers of hybrid semiconducting polymer/quantum dot light emitting diodes

2016

Three monomers, M1–M3, with modified carbazole cores and styrene functionality were prepared for use in the active layers of hybrid polymer/quantum dot light emitting diodes. Utilizing reversible addition fragmentation chain transfer polymerization, side-chain conjugated polymers, P1–P3, with narrow polydispersities and disulfide end groups were obtained. The thermal, optical, and electrochemical properties of the polymers varied depending on the substituents of the carbazole cores. Through the disulfide end groups the polymers were chemically blended with quantum dots to obtain QD/polymer hybrids, which were further used as active layers in light emitting diodes. The fabricated devices ret…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsCarbazolebusiness.industryOrganic ChemistryBioengineeringChain transfer02 engineering and technologyPolymerElectroluminescence010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundchemistryPolymerizationQuantum dotSide chainOptoelectronicsQuantum efficiency0210 nano-technologybusinessPolymer Chemistry
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Controlled Synthesis of Linear Polymers with Highly Branched Side Chains by “Hypergrafting”: Poly(4-hydroxy styrene)-graft-hyperbranched Polyglycerol

2012

Linear polymers with hyperbranched side chains are unusual macromolecular structures due to their high number of functional groups in the side chains as well as their potential cylindrical conformation in bulk or solution. In a three-step synthesis combining anionic and oxy-anionic polymerization, hyperbranched polyglycerol was “hypergrafted” from linear poly(4-hydroxy styrene) macroinitiators to yield poly(4-hydroxy styrene)-graft-hyperbranched polyglycerol. Successful grafting with control over molecular weight (10–31 kg·mol–1) and low PDIs (<1.4) was shown by various characterization techniques. All polymers have a high side chain density, due to rapid transfer of the initiating function…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsLinear polymerOrganic ChemistryPolymerGraftingStyreneInorganic Chemistrychemistry.chemical_compoundchemistryPolymerizationYield (chemistry)Polymer chemistryMaterials ChemistrySide chainMacromoleculeACS Macro Letters
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Ferroelectric block copolymers

1997

A block copolymer consisting of polystyrene and a side chain ferroelectric liquid crystalline polymer was synthesized using polymer analogous chemistry on a monodisperse poly(styrene-b-isoprene). Composition was adjusted to give lamellar microstructure after addition of the mesogenic side groups. If placed in an LC cell without orientation of domains, no ferroelectric response was observed. After shearing the thin film, presumably due to alignment of lamellae, a bistable ferroelectric switching could be detected.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsMesogenOrganic ChemistryPolymerCondensed Matter PhysicsFerroelectricitychemistry.chemical_compoundchemistryChemical engineeringLiquid crystalPolymer chemistryMaterials ChemistrySide chainCopolymerLamellar structurePolystyreneMacromolecular Symposia
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Polysiloxane-backbone block copolymers in a one-pot synthesis: a silicone platform for facile functionalization.

2012

Block copolymers consisting exclusively of a silicon-oxygen backbone are synthesized by sequential anionic ring-opening polymerization of different cyclic siloxane monomers. After formation of a poly(dimethylsiloxane) (PDMS) block by butyllithium-initiated polymerization of D3, a functional second block is generated by subsequent addition of tetramethyl tetravinyl cyclotetrasiloxane (D4(V) ), resulting in diblock copolymers comprised a simple PDMS block and a functional poly(methylvinylsiloxane) (PMVS) block. Polymers of varying block length ratios were obtained and characterized. The vinyl groups of the second block can be easily modified with a variety of side chains using hydrosilylation…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsMolecular StructureSiloxanesHydrosilylationOrganic Chemistrytechnology industry and agricultureSiliconesmacromolecular substancesPolymerRing-opening polymerizationPolymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationBlock (telecommunications)Polymer chemistryMaterials ChemistryCopolymerSide chainMacromolecular rapid communications
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Correlation between polymer architecture, mesoscale structure and photovoltaic performance in side-chain-modified poly(p-arylene-ethynylene)-alt-poly…

2011

Abstract Recent investigations have shown that an anthracene containing poly( p -arylene-ethynylene)-alt-poly( p -arylene-vinylene) statistical copolymer consisting of a well defined conjugated backbone, along which linear and branched alkoxy side chains are attached in a random manner, yields, compared to its counterparts with regular side chain substitution, an improved performance in polymer [6,6]:-phenyl-C 61 -butyric acid methyl ester (PCBM) bulk-heterojunction solar cells. The microscopic origin for the improved power conversion efficiency ( η  ≈ 3.8%) of the statistical copolymer – which is the best in its material class – has not been resolved. We conducted grazing incidence wide-an…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryEnergy conversion efficiencyAryleneStackingPolymer architecturePolymerPolymer solar cellCrystallographychemistryMaterials ChemistrySide chainCopolymerOrganic chemistryPolymer
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