Search results for "CONDENSATION"

showing 8 items of 468 documents

Solvatochromic behaviour of new donor–acceptor oligothiophenes

2021

Oligothiophene derivatives play a central role in the formulation of materials used in devices in the field of organic electronics. In this work, we report the results of the study of UV-vis absorption and fluorescence spectra, in several solvents, of a series of oligothiophenes recently synthesized in our laboratory. The studied oligothiophenes present different structures due to several factors: the donor– acceptor (D–A) or acceptor–donor–acceptor (A–D–A) architecture, the number of thiophene rings in the backbone (ranging from three to eight), the number and position of solubilizing octyl chains in the backbone, and the type of acceptor moieties (from Knoevenagel condensation either with…

oligothiophenessolvatochromism02 engineering and technology010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesCatalysischemistry.chemical_compoundMaterials ChemistryThiopheneOrganic electronicsanodic dimerizationSolvatochromismSettore CHIM/06 - Chimica OrganicaGeneral Chemistry021001 nanoscience & nanotechnologyAcceptor0104 chemical scienceschemistryoligothiophenes; solvatochromism; anodic dimerizationKnoevenagel condensationAbsorption (chemistry)0210 nano-technologyDonor acceptorOligothiophenes fluorescence donor-acceptor systemsNew Journal of Chemistry
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Synthesis, Structure and Solvatochromism of the Emission of Cyano-Substituted Oligo(phenylenevinylene)s

2001

Strongly luminescent and highly soluble oligo(phenylenevinylene)s with five benzene rings and cyano groups in different positions of the terminal styrene units were prepared by means of Horner and Knoevenagel reactions. The substitution pattern − cyanide moieties on the vinyl or on the aromatic regions, together with the effect of auxochromic groups − has distinct influences on the electronic spectra, particularly on the fluorescence. Polar solvents induce red shifts and strongly reduce the fluorescence intensity of the vinyl-substituted oligomers. Cyano substitution increases the electron affinity of the oligomers; this effect is more pronounced for molecules with vinyl cyanides and can be…

organic chemicalsOrganic ChemistrySolvatochromismPhotochemistryOligomerStyrenechemistry.chemical_compoundBenzonitrilechemistryElectron affinity (data page)Polymer chemistryMoleculeKnoevenagel condensationPhysical and Theoretical ChemistryBenzeneEuropean Journal of Organic Chemistry
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Silseskwioksany i ich zastosowanie w syntezie materiałów polimerowych

2015

Artykuł stanowi przegląd literatury dotyczącej syntezy oraz charakterystyki materiałów polimerowych zawierających silseskwioksany (POSS). Przedstawiono metody otrzymywania hybrydowych materiałów polimerowych z udziałem funkcjonalizowanych POSS na drodze click chemistry, polikondensacji, poliaddycji, metatezy z otwarciem pierścienia ipolimeryzacji rodnikowej zarówno konwencjonalnej, jak i kontrolowanej (ATRP).

poliedryczne oligomeryczne silseskwioksany (POSS)ring opening metathesis polymerizationpolimeryzacja wolnorodnikowamateriały hybrydoweATRPpoliaddycjapolikondensacjametateza z otwarciem pierścieniaclick chemistryhybrid materialspolycondensationpolyadditionfree-radical polymerizationpolyhedral oligomeric silsesquioxane (POSS)Polimery
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Three-dimensional skyrmions in spin-2 Bose–Einstein condensates

2017

We introduce topologically stable three-dimensional skyrmions in the cyclic and biaxial nematic phases of a spin-2 Bose-Einstein condensate. These skyrmions exhibit exceptionally high mapping degrees resulting from the versatile symmetries of the corresponding order parameters. We show how these structures can be created in existing experimental setups and study their temporal evolution and lifetime by numerically solving the three-dimensional Gross-Pitaevskii equations for realistic parameter values. Although the biaxial nematic and cyclic phases are observed to be unstable against transition towards the ferromagnetic phase, their lifetimes are long enough for the skyrmions to be imprinted…

spinor condensateSUPERFLUID HE-3Angular momentumSYMMETRYFOS: Physical sciencesGeneral Physics and AstronomyBose-Einstein condensation114 Physical sciences01 natural sciencesInstability010305 fluids & plasmaslaw.inventionPHASESKNOTSlaw0103 physical sciencesField theory (psychology)magnetismikvanttifysiikka010306 general physicsVORTICESSpin-½Condensed Matter::Quantum GasesPhysicsBose–Einstein condensationBiaxial nematicCondensed matter physicsSkyrmionMONOPOLESCondensed Matter::Mesoscopic Systems and Quantum Hall EffectFIELD-THEORYSymmetry (physics)skyrmionQuantum Gases (cond-mat.quant-gas)Condensed Matter - Quantum GasesBose–Einstein condensateNew Journal of Physics
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1,2,6-Thiadiazine 1-Oxides: Unsaturated Three-Dimensional S,N-Heterocycles from Sulfonimidamides.

2020

Unprecedented three-dimensional 1,2,6-thiadiazine 1-oxides have been prepared by an aza-Michael-addition/cyclization/condensation reaction sequence starting from sulfonimidamides and propargyl ketones. The products have been further functionalized by standard cross-coupling reactions, selective bromination of the heterocyclic ring, and conversion into a β-hydroxy substituted derivative. A representative product was characterized by single-crystal X-ray structure analysis. peerReviewed

sulfonimidamidessingle-crystal X-raybioaktiiviset yhdisteet010405 organic chemistryStereochemistryChemistryOrganic ChemistryOxideHalogenation010402 general chemistryCondensation reaction01 natural sciencesBiochemistryCoupling reaction0104 chemical scienceschemistry.chemical_compoundPropargylPhysical and Theoretical ChemistrySequence (medicine)Organic letters
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Synthesis of new hybrid 1,4-thiazinyl-1,2,3-dithiazolyl radicals via Smiles rearrangement

2017

The condensation reaction of 2-aminobenzenethiols and 3-aminopyrazinethiols with 2-amino-6-fluoro-N-methylpyridinium triflate afforded thioether derivatives that were found to undergo Smiles rearrangement and cyclocondensation with sulphur monochloride to yield new hybrid 1,4-thiazine-1,2,3-dithiazolylium cations. The synthesized cations were readily reduced to the corresponding stable neutral radicals with spin densities delocalized over both 1,4-thiazinyl and 1,2,3-dithiazolyl moieties. peerReviewed

synthesis010405 organic chemistryChemistryRadical12010402 general chemistryPhotochemistryCondensation reaction01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundDelocalized electron14-thiazinyl-123-dithiazolyl radicalsThioether4-thiazinyl-1Smiles rearrangementYield (chemistry)Polymer chemistrysynteesiSmiles rearrangementTrifluoromethanesulfonateta1163-dithiazolyl radicalsDalton Transactions
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Organocatalytic Oxa-Michael/Michael/Michael/Aldol Condensation Quadruple Domino Sequence : Asymmetric Synthesis of Tricyclic Chromanes

2018

An efficient and highly stereoselective one-pot, four-component synthesis of functionalized tricyclic chromanes has been achieved through an organocatalyzed quadruple domino reaction. The reaction sequence involves an oxa-Michael/Michael/Michael/aldol condensation between alcohols, 2 equiv of acrolein, and nitrochromenes to generate the pharmaceutically important tricyclic chromanes bearing three contiguous stereogenic centers including a chiral tetrasubstituted carbon center in good domino yields (30–70%) and excellent diastereo- and enantioselectivities (>20:1 dr and >99% ee). peerReviewed

synthesisalkoholit (yhdisteet)natural productsStereochemistryasymmetric synthesisluonnontuotteet010402 general chemistry01 natural sciencesBiochemistryDominoStereocenterchemistry.chemical_compoundCascade reactionsynteesiPhysical and Theoretical Chemistryta116chemistry.chemical_classification010405 organic chemistryOrganic ChemistryAcroleindomino reactionsEnantioselective synthesistricyclic chromanes0104 chemical scienceschemistryalcohols (organic compounds)asymmetriaAldol condensationStereoselectivityasymmetryTricyclic
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Tube transport of water vapor with condensation and desorption

2013

Attenuation and delay of active tracers in tube transport is an important current problem, but its full explanation is still lacking. To this end a model is introduced, where part of a tracer undergoes condensation and evaporation, treated as a diffusion-type process, in addition to Taylor dispersion. Condensation of water was verified by high-speed imaging, and the model solution fitted the breakthrough curves of laboratory measurements with pulses of water vapor of varying relative humidity. The model provides a transfer function whose performance was verified against field measurements. peerReviewed

ta114010504 meteorology & atmospheric sciencesPhysics and Astronomy (miscellaneous)ChemistryAttenuationTaylor dispersionCondensationAnalytical chemistryEvaporationMechanics01 natural sciences010305 fluids & plasmasDesorption0103 physical sciencesRelative humidityCurrent (fluid)Water vaporPhysics::Atmospheric and Oceanic Physics0105 earth and related environmental sciences
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