Search results for "Mesophase"

showing 10 items of 58 documents

Isomerisation of Liquid-Crystalline Tristriazolotriazines

2017

Star-shaped discotic liquid crystals with columnar superstructures constitute a highly interesting class of organic materials. Phenyl-substituted tris[1,2,4]triazolo-[1,3,5]triazine, prepared by a Huisgen reaction of phenyltetrazole and cyanuric chloride, represents an excellent core for discotic liquid crystals (DLCs). The thermal stability is not perfect, at temperatures above the clearing point, a successive threefold isomerization leads to a highly planar, C

010405 organic chemistryChemistryLiquid crystallineOrganic ChemistryMesophaseGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCrystallinityCrystallographyLiquid crystalX-ray crystallographyIsomerizationChemistry - A European Journal
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Ionic liquid crystals based on viologen dimers: tuning the mesomorphism by varying the conformational freedom of the ionic layer

2016

ABSTRACTWe investigated the liquid crystal behaviour of newly synthesised bistriflimide salts of symmetric viologen dimers. A smectic A phase was observed for intermediate spacer lengths and for relatively long lateral alkyl chains. The systems were characterised by thermal analysis, polarised optical microscopy, X-ray scattering and solid-state NMR. An intermediate ordered smectic phase was also exhibited by the compounds (except for systems with very short lateral chains) consisting of molten layers of alkyl chains and partially ordered ionic layers. These results, relating to the mesomorphic behaviour of viologen salts, are qualitatively compared to those of the more common imidazolium s…

4-4?-bipyridinium4-4ʹ-bipyridiniumMaterials scienceIonic liquid crystals; viologens; 4-4ʹ-bipyridiniumIonic bonding02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundLiquid crystalPhase (matter)medicineOrganic chemistryGeneral Materials ScienceBistriflimideviologensAlkylSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationviologenChemistry (all)MesophaseViologenGeneral ChemistrySettore CHIM/06 - Chimica Organica4-4ʹ-bipyridinium; Ionic liquid crystals; viologens; Condensed Matter Physics; Materials Science (all); Chemistry (all)021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesCrystallographychemistryIonic liquidIonic liquid crystalsIonic liquid crystalMaterials Science (all)0210 nano-technologymedicine.drug
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1992

A series of liquid-crystalline copolymers 1 with a chiral azobenzene moiety as photoreactive mesogenic unit was prepared. The polymers were fractionated and the mesophase behaviour of the high- and low-molecular weight fractions was examined. The copolymers display smectic A and cholesteric phases. For the cholesteric phases the pitch of the helix was determined, which ranges from 3 to 20 μm. Stable monolayers at the air-water interface were obtained from two monomers and one of the homopolymers. Multilayer assemblies of the azobenzene-containing polymers can be used to study photo-induced order/disorder transitions.

Acrylate polymerchemistry.chemical_compoundAzo compoundchemistryAzobenzeneLiquid crystalMesogenPolymer chemistrySide chainMesophasePendant groupDie Makromolekulare Chemie
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Synthesis and Characterization of Fluorescent, Low-Symmetry Triphenylene Discotic Liquid Crystals:  Tailoring of Mesomorphic and Optical Properties

1996

A series of monofunctionalized triphenylene-based discotic liquid crystals were synthesized starting from 2-hydroxy-3,6,7,10,11-pentakis(pentyloxy)triphenylene. These compounds are unique in that they possess a single electron-withdrawing group (and consequently a large dipole moment) connected directly to the polyaromatic core. All of the new liquid crystals show a significantly broader range of mesogenicity relative to the parent compound 2,3,6,7,10,11-hexakis(pentyloxy)triphenylene. Moreover, some of the new mesogens exhibit a more ordered mesophase relative to the hexagonal columnar phase (Dh) at lower temperatures. Monofunctionalization of the triphenylene core has a dramatic effect on…

ChemistryGeneral Chemical EngineeringDiscotic liquid crystalMesophaseTriphenyleneGeneral ChemistryFluorescenceDipoleCrystallographychemistry.chemical_compoundLiquid crystalMaterials ChemistrySurface modificationOrganic chemistryColumnar phaseChemistry of Materials
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Komplexierung von Übergangsmetall-Ionen mit substituierten Azamakrocyclen: Induktion columnarer Mesophasen durch molekulare Erkennung

1991

ChemistryPolymer chemistryMesophaseGeneral MedicineTransition metal ionsAngewandte Chemie
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Photoconductivity in Discotic Liquid Crystals: A New Class of High-Mobility Materials

1994

Abstract Using a time-of-flight technique, different transport mechanisms, deep trapping, multiple shallow trapping and Gaussian transport, can be observed in the different temperature and phase regions of the liquidcrystalline (LC) photoconductor hexapentyloxytriphenylene (HPT). Transient photocurrents and carrier mobilities for various temperatures, electric fields, and sample histories were examined. The ideal intrinsic Gaussian transport, observed for holes in the mesophase, puts HPT into a new class of highmobility materials with both hole mobilities on the order of 1.10−3cm2/Vs and a steplike current decay. These features result from the fact that there is obviously neither a position…

Chemistrybusiness.industryPhotoconductivityDiscotic liquid crystalMesophaseCharge (physics)TrappingCondensed Matter PhysicsOpticsChemical physicsPhase (matter)Electric fieldMoleculebusinessMolecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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Supramolecular order of stilbenoid dendrons: importance of weak interactions

2006

Stilbenoid dendrons with various donor and acceptor groups on the focal unit were synthesised by a Wittig–Horner reaction, starting from an aldehyde functionalised dendron and various substituted phosphonic acid esters. The target molecules are composed of meta-branched arms, two of them with extended conjugation (distyrylbenzene) and three flexible dodecyloxy chains; the focal group consists of a donor or acceptor substituted styryl unit. The cross-conjugation of the arms prevents the strong electronic influence of substituents on the two extended oligophenylenevinylene chromophores. However, intermolecular interactions mediated by the focal unit allow control of the supramolecular stackin…

CrystallographyChemistryHydrogen bondLiquid crystalDendrimerMaterials ChemistryStackingSupramolecular chemistryMoleculeMesophaseGeneral ChemistryPhotochemistryAcceptorJ. Mater. Chem.
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Unravelling the fine structure of stacked bipyridine diamine-derived C-3-discotics as determined by X-ray diffraction, quantum-chemical calculations,…

2011

An in depth investigation of the fine structure adopted by the helical stacks of C3-discotics 1 incorporating three 3,3'-diamino-2,2'-bipyridine units is described. In the bulk the molecules display liquid crystalline behaviour in a temperature window of >300 K and an ordered rectangular columnar mesophase (Colro) with an inter-disc distance of 3.4 Å is assigned. X-Ray diffraction on aligned samples has also revealed a helical superstructure in the liquid crystalline state, and a rotation angle of 13–16° between consecutive discs. The proposed superstructure in the bulk phase has been further substantiated by a combination of quantum-chemical calculations and solid-state NMR spectroscopy…

CrystallographyIsodesmic reactionChemistryHydrogen bondIntermolecular forceX-ray crystallographyMesophaseMoleculeGeneral ChemistryNuclear magnetic resonance spectroscopySuperstructure (condensed matter)Chemical Science
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α, ω-Dipolar amphiphiles: Influence of rigid and flexible units on aggregation behavior

1993

Mono- and α,ω-dipolar amphiphiles with hydrophilic pyridinium head groups, and flexible and rigid hydrophobic parts have been synthesized. Surface tension and conductivity measurements proved that micellar aggregates for amphiphiles 1–4 are formed. The incorporation of rigid units leads to a decrease in the critical micellar concentration (CMC): the rigid monopolar amphiphile 2 aggregates at lower concentration than the flexible monopolar amphiphile 1. A similar decrease was observed when chain ends were connected: the flexible α,ω-dipolar amphiphile 3 has a lower CMC than the flexible monopolar amphiphile 1. The more flexible amphiphiles 1–3 allow the formation of micelles of different sha…

CrystallographyLiquid crystalChemistryCritical micelle concentrationLyotropicAmphiphileMesophaseOrganic chemistryMicellar cubicLamellar structureGeneral ChemistryMicelleRecueil des Travaux Chimiques des Pays-Bas
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Liquid crystals in the series of 2,4,6-tristyryl-1,3,5-triazines

2004

Abstract Alkaline condensation reactions of 2,4,6-trimethyl-1,3,5-triazine ( 1 ) and substituted benzaldehydes ( 2a – n ) yield 2,4,6-tristyryl-1,3,5-triazines ( 3a – n ). A sufficient number and length of the alkoxy chains at the benzene rings provide liquid crystalline phases Col hd . A special structure was found for compound 3i with 9 hexyloxy chains; it exists in the solid state in a helical columnar arrangement, which is transformed by heating to a hexagonal columnar mesophase. Irradiation of the mesophases of 3i – 3m leads to partial cyclodimerization reactions, which cause different textures and lower the clearing points. The border line between the irradiated and the unirradiated z…

CrystallographyLiquid crystalChemistryYield (chemistry)Phase (matter)Organic ChemistryDrug DiscoveryAlkoxy groupMesophaseAtmospheric temperature rangeCondensation reactionColumnar phaseBiochemistryTetrahedron
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