Search results for "ALK"

showing 10 items of 4314 documents

Studien zum Vorgang der Wasserstoffübertragung 46. Zur kathodischen Spaltung von Alkyl- und Cycloalkyl(triphenyl)-phosphoniumsalzen; Abhängigkeit der…

1977

Die kathodische Spaltung von Methyl-, Butyl- und einiger Cycloalkyl(triphenyl)phosphoniumsalze wurde potentiostatisch und galvanostatisch durchgefuhrt. Beim Methyl(triphenyl)-phosphoniumsalz hangt die prozentuale Zusammensetzung der Spaltprodukte: Triphenylphosphin und Methyl(diphenyl)phosphin sowohl vom Potential als auch von der Temperatur ab, die sich ihrerseits wieder gegenseitig beeinflussen. Zusatze unterschiedlich strukturierter quartarer Ammoniumsalze als Leitsalz verandern das prozentuale Verhaltnis (C6H5)3P/(C6H5)2PCH3 nicht, wohl aber der Zusatz von Essigsaure, welche die Bildung von Methyl(diphenyl)phosphin begunstigt. - Bei den Cycloalkyl(triphenyl)phosphoniumsalzen mit Cyclohe…

chemistry.chemical_classificationOrganic ChemistryPhosphonium saltchemistry.chemical_compoundchemistryPolymer chemistryPhenyl groupMethanolPhosphoniumPhysical and Theoretical ChemistryTriphenylphosphineSelectivityAlkylPhosphineJustus Liebigs Annalen der Chemie
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Conjugate addition of organolithium reagents to α,β-unsaturated carboxylic acids

1999

Abstract Conjugate addition of primary, secondary, tertiary alkyl and phenyl lithium reagents to 2-alkenoic acids affords good yields of branched saturated carboxylic acids. Methyl groups at the α- and β-carbon of the 2-alkenoic acid decrease reactivity as acceptors, and foster deprotonation, respectively. The lithium enediolate resulting from the conjugate addition can react with electrophiles. PM3 calculations are in agreement with the substituent effects.

chemistry.chemical_classificationOrganic ChemistrySubstituentchemistry.chemical_elementBiochemistryMedicinal chemistrychemistry.chemical_compoundDeprotonationchemistryReagentDrug DiscoveryElectrophileLithiumReactivity (chemistry)AlkylConjugateTetrahedron
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Synthesis and Characterization of theO-Alkylation Products of Resorcinarene

2013

O-Substitution reactions of tetramethoxyresorcinarene with alkyl halides produced a variety of partially O-alkylated resorcinarene derivatives with terminal alkyne functionality. The degree of alkylation was affected by the reactivity of the alkylating halide used. NMR spectroscopy proved to be an ideal tool for analyzing the complex reaction mixtures and the isolated products based on the symmetry and degree of alkylation of the resorcinarene derivatives. Single-crystal X-ray diffraction studies furthermore showed diversity in the self-assembly of the various O-alkylation products that was greatly affected by the degree of alkylation, as well as the nature of the alkyne moiety.

chemistry.chemical_classificationOrganic ChemistrySupramolecular chemistryAlkyneNuclear magnetic resonance spectroscopyAlkylationResorcinarenechemistryMoietyOrganic chemistrylipids (amino acids peptides and proteins)Reactivity (chemistry)Physical and Theoretical ChemistryAlkylEuropean Journal of Organic Chemistry
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Pyrrole Studies XXVII.1Utilisation of 1-Methyl-2-pyrrolyl Lithium in the Synthesis of 1-Methyl-2-substituted Pyrroles

1982

Abstract Although metallation of 1-substituted pyrroles with alkyl lithium reagents to give the lithiated derivatives has been recorded by several research groups,4–6 only limited use has been made of these derivatives in the synthesis of 1,2-disubstituted pyrroles. Subsequent to ourinitial studies,7 it was reported that tetrahydrofuran was the solvent of choice for the formation of the mono-lithiated pyrrole derivative and that the rate of the metallation was accelerated by the presence of TMEDA.6 We had noted,7 however, that prolonged reaction of n-butyl lithium with 1-methylpyrrole in a 2:1 mixture of tetrahydrofuran:hexaneat ca 18°C in the absence of TMEDA gave 1-methyl-2-pyrrolyl lithi…

chemistry.chemical_classificationOrganic Chemistrychemistry.chemical_elementMedicinal chemistrySolventchemistry.chemical_compoundchemistryDeuteriumReagentMass spectrumOrganic chemistryLithiumAlkylTetrahydrofuranPyrroleSynthetic Communications
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Dithienopyrrolobenzotriazole-based organic dyes with high molar extinction coefficient for efficient dye-sensitized solar cells

2016

Abstract Four novel organic dyes DT1-DT4 containing a dithienopyrrolobenzotriazole unit were synthesized and applied in dye sensitized solar cells, where dithienopyrrolobenzotriazole moiety was introduced as a π-spacer for the first time. The four dyes exhibited good light harvesting efficiency with high molar extinction coefficients and broad spectral response. The influence of the different electron donor on the photovoltaic performance was evaluated. The effects of the linear and branched alkyl chains in the π-bridge on the photophysical, electrochemical and photovoltaic performance were systemically investigated. The results show that branched alkyl chains are better than linear alkyl c…

chemistry.chemical_classificationOrganic solar cellProcess Chemistry and TechnologyGeneral Chemical EngineeringElectron donor02 engineering and technologyHybrid solar cellMolar absorptivity010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundDye-sensitized solar cellchemistrylawSolar cellMoiety0210 nano-technologyAlkylDyes and Pigments
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Dienediolates of unsaturated carboxylic acids in synthesis. Aldehydes and ketones from alkyl halides, by ozonolysis of β,γ-unsaturated α-alkyl carbox…

1997

Abstract A convenient two-step procedure for a two carbon homologative conversion of alkyl halides into aldehydes and methyl ketones by α-alkylation of unsaturated carboxylic acids, followed by ozonolysis is developed and applied to the synthesis of ω-chloro aldehydes. Triethylamine is superior to dimethyl sulfide or triphenylphosphine for cleavage of the ozonides, except when aldol condensation side reactions require use of protic solvents and iodide salts. Cleavage of the ozonides by triethylamine is shown to occur mainly through a reductive process.

chemistry.chemical_classificationOzonolysisTertiary amineOrganic ChemistryIodideHalideBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryAldol condensationTriphenylphosphineTriethylamineAlkylTetrahedron
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The synergy between the CsPbBr3 nanoparticle surface and the organic ligand becomes manifest in a demanding carbon–carbon coupling reaction

2020

We demonstrate here the suitability of CsPbBr3nanoparticles as photosensitizers for a demanding photoredox catalytic homo- and cross-coupling of alkyl bromides at room temperature by merely using visible light and an electron donor, thanks to the cooperative action between the nanoparticle surface and organic capping. Fil: Rosa-Pardo, Ignacio. Instituto de Ciencia Molecular; España. Universidad de Valencia; España Fil: Casadevall, Carla. Barcelona Institute Of Science And Technology. Institut Català D'investigació Química.; España Fil: Schmidt, Luciana Carina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigac…

chemistry.chemical_classificationPEROVSKITE CsPbBr3LigandChemistryMetals and AlloysReinforced carbon–carbonNanoparticleElectron donorGeneral ChemistryPhotochemistryCatalysisCoupling reactionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysis//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCARBON-CARBON COUPLING//purl.org/becyt/ford/1.4 [https]Materials ChemistryCeramics and CompositesPHOTOREDOXAlkylVisible spectrumChemical Communications
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Electrical conductivity and permittivity of water-AOT-n-heptane microemulsions

1995

Measurements of the electrical conductivity and of the complex permittivity of water-sodium bis(2-ethylhexyl) sulfosuccinate (AOT)-n-heptane microemulsions are reported. The experimental results are rationalized in terms of a hopping mechanism of AOT anions within clusters of reversed micelles. The dependence of the hopping rate and of the cluster dimensions upon the ratio [water]/[AOT] and temperature is discussed.

chemistry.chemical_classificationPermittivityAlkaneHeptaneBiophysicsAnalytical chemistryConductivityBiochemistryMicellechemistry.chemical_compoundHydrocarbonchemistryElectrical resistivity and conductivityOrganic chemistryMicroemulsionPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Mapping onto ideal chains overestimates self-entanglements in polymer melts

2017

In polymer physics it is typically assumed that excluded volume interactions are effectively screened in polymer melts. Hence, chains could be described by an effective random walk without excluded volume interactions. In this letter, we show that this mapping is problematic by analyzing the occurrence of knots, their spectrum and sizes in polymer melts, corresponding random walks and chains in dilute solution. The effective random walk severely overrates the occurrence of knots and their complexity, particularly when compared to melts of flexible chains, indicating that non-trivial effects due to remnants of self-avoidance still play a significant role for the chain lengths considered in t…

chemistry.chemical_classificationPersistence lengthMaterials sciencePolymers and PlasticsOrganic ChemistrySegment lengthFOS: Physical sciences02 engineering and technologyPolymerCondensed Matter - Soft Condensed Matter021001 nanoscience & nanotechnologyRandom walk01 natural sciencesInorganic ChemistryCondensed Matter::Soft Condensed Mattersurgical procedures operativeKnot (unit)stomatognathic systemchemistryChemical physics0103 physical sciencesMaterials ChemistrySoft Condensed Matter (cond-mat.soft)010306 general physics0210 nano-technology
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Self-organization of substituted azacrowns based on their discoid and amphiphilic nature

1989

Abstract Cyclame and hexacyclene derivatives, bearing four and six long-chain substituents respectively, were synthesized. They are discussed as monolayer-forming amphiphiles as well as liquid-crystalline-phase-forming thermotropic mesogens. The compounds investigated form ordered monolayers at the gas/water interface. In the monolayer the hydrophilic cyclic head group lies flat on the water surface, whereas the hydrophobic substituents are oriented perpendicularly with respect to the interface. Most derivatives fitted with aromatic substituents exhibit a solid condensed state exclusively. In contrast with this, solid condensed as well as expanded phases can be found when spreading the alip…

chemistry.chemical_classificationPhase transitionMaterials scienceGeneral ChemistryCondensed Matter PhysicsThermotropic crystalCrystallographychemistryGroup (periodic table)Liquid crystalAmphiphileMonolayerOrganic chemistryGeneral Materials ScienceAlkylLiquid Crystals
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