Search results for "Phene"

showing 10 items of 863 documents

ChemInform Abstract: Conjugated Compounds Based on Vinylthiazole Units.

2008

Conjugated oligomers attract increasing attention because of their interesting properties in materials science [1]. Moreover, they are model compounds for conjugated polymers. Molecules polarized by electronic effects, in particular push-pull systems having terminal donor-acceptor substitution represent a special class of such oligomers [2]. Their major applications are in the field of nonlinear optics (NLO), twophoton absorption (TPA), two-photon induced fluorescence (TPIF), and photorefractive materials (PR). Fig. 1 illustrates known 2,5-thienylenevinylenes with zwitterionic resonance structures 1 (D = NR2; A = NO2, CHO, SO2R; n = 1, 2) [3, 4]. The corresponding compounds 2 with thiazole …

chemistry.chemical_classificationStereochemistryElectron donorGeneral MedicineConjugated systemElectron acceptorRing (chemistry)Medicinal chemistrychemistry.chemical_compoundchemistryThiopheneElectronic effectMoleculeThiazoleChemInform
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Effective complexation of psychotropic phenethylammonium salts from a disodium dipyrazolate salt of macrocyclic structure

2002

The equilibrium stability constants (Ks) of ammonium pyrazolate complexes [L2−]2RN(R′)H2+ (3, R′ = H and 4, R′ = Me) formed from a macrocyclic disodium dipyrazolate salt 2[L2−] 2Na+ and ammonium salts (RNH3+X− or RN(Me)H2+X−) of psychotropic drugs and neurotransmitter catecholamines have been evaluated by electrochemical methods in DMSO solution. The resulting Ks values demonstrate that, except for (±)-amphetamine, the complexes formed by lipophilic primary [mescaline, (+)-amphetamine, (±)-p-methoxyamphetamine (PMA), (±)-3,4-methylenedioxyamphetamine (MDA)] and secondary [(±)-methamphetamine, (+)-methamphetamine and (±)-3,4-methylenedioxymethamphetamine (MDMA ‘ecstasy’)] phenethylamines are…

chemistry.chemical_classificationStereochemistrySalt (chemistry)PhenethylaminesMescalineCarbon-13 NMRElectrochemistryMedicinal chemistrychemistry.chemical_compoundchemistryEquilibrium stabilitymedicineAmmoniummedicine.drugJ. Chem. Soc., Perkin Trans. 2
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Synthesis and characterization of bisulfonated poly(vinyl alcohol)/graphene oxide composite membranes with improved proton exchange capabilities

2020

Abstract Composite membranes based on poly(vinyl alcohol) (PVA) and graphene oxide (GO) were prepared by solution-casting method to be used as proton exchange membranes (PEMs) in fuel cell (FC) applications. Bisulfonation was employed as a strategy to enhance the proton conductivity of these membranes. First, a direct sulfonation of the polymer matrix was accomplished by intra-sulfonation of the polymer matrix with propane sultone, followed by the inter-sulfonation of the polymer chains using sulfosuccinic acid (SSA) as a crosslinking agent. Furthermore, the addition of graphene oxide (GO) as inorganic filler was also evaluated to enhance the proton-conducting of the composite membranes. Th…

chemistry.chemical_classificationThermogravimetric analysisVinyl alcoholMaterials sciencePolymers and PlasticsGrapheneOrganic ChemistryProton exchange membrane fuel cellNanoparticle02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionDielectric spectroscopychemistry.chemical_compoundMembranechemistryChemical engineeringlaw0210 nano-technologyPolymer Testing
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ChemInform Abstract: New Acetylenes from Chrysanthemum coronarium L.

1990

The investigation of the aerial parts of Chrysanthemum coronarium yielded, in addition to several known compounds, two new acetylenic sulfoxides 9 and 10, and a new thiophene spiroacetal enol ether 11. Their structures were deduced by spectroscopic and chemical methods.

chemistry.chemical_classificationchemistry.chemical_compoundChemistryChrysanthemum coronariumThiopheneEnol etherOrganic chemistryGeneral MedicineChemInform
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Conjugated Compounds Based on Vinylthiazole Units

2007

Conjugated oligomers attract increasing attention because of their interesting properties in materials science [1]. Moreover, they are model compounds for conjugated polymers. Molecules polarized by electronic effects, in particular push-pull systems having terminal donor-acceptor substitution represent a special class of such oligomers [2]. Their major applications are in the field of nonlinear optics (NLO), twophoton absorption (TPA), two-photon induced fluorescence (TPIF), and photorefractive materials (PR). Fig. 1 illustrates known 2,5-thienylenevinylenes with zwitterionic resonance structures 1 (D = NR2; A = NO2, CHO, SO2R; n = 1, 2) [3, 4]. The corresponding compounds 2 with thiazole …

chemistry.chemical_classificationchemistry.chemical_compoundchemistryThiopheneElectronic effectMoleculeElectron donorGeneral ChemistryConjugated systemElectron acceptorRing (chemistry)ThiazoleMedicinal chemistryZeitschrift für Naturforschung B
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Multicomponent Synthesis of Benzothiophen-2-acetic Esters by a Palladium Iodide Catalyzed S-cyclization – Alkoxycarbonylation Sequence

2021

A catalytic carbonylative approach to the multicomponent synthesis of benzothiophene derivatives from simple building blocks [1-(2-(methylthio)phenyl)prop-2-yn-1-ols, carbon monoxide, and an alcohol)] is presented. It is based on an S-cyclization-demethylation-alkoxycarbonylation-reduction sequence promoted by the PdI2/KI catalytic system, occurring under relatively mild conditions (40 atm, 80 °C, 15 h). Benzothiophene-2-acetic esters are obtained in moderate to good yields (35–70%) starting from variously substituted substrates in combination with different alcohols as external nucleophiles (17 examples). (Figure presented.).

chemistry.chemical_classificationmulticomponent reactionIodidechemistry.chemical_elementGeneral ChemistrycarbonylationSettore CHIM/06 - Chimica OrganicapalladiumCombinatorial chemistryCatalysischemistrybenzothiophenesS-cyclizationCarbonylationPalladiumSequence (medicine)
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Efficient palladium catalyzed synthesis of heteroaromatic sulfoxides

2007

Abstract The present Letter describes the efficient synthesis of novel heteroaromatic sulfoxides by means of a palladium catalyzed heteroarylation of sulfenate anions. Triazolopyridine, pyridine and thiophene sulfoxides can be obtained under mild conditions and in high yield from the corresponding heteroaryl bromides.

chemistry.chemical_compoundChemistryYield (chemistry)Organic ChemistryDrug DiscoveryPyridineThiophenechemistry.chemical_elementTriazolopyridineBiochemistryCombinatorial chemistryCatalysisPalladiumTetrahedron Letters
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Linear free energyortho-correlations in the thiophene series. Part IX . Kinetics of esterification with diazodiphenylmethane of some 3-, 4-, and 5-su…

1981

The rate constants for the esterification of some 3-, 4-, and 5-substituted thiophene-2-carboxylic acids with diazodiphenylmethane in methanol at 25° have been measured. The reactivity of some para- and ortho-substituted benzoic acids has also been determined. Logarithmic kinetic constants for ortho-, meta-, and para-like substituted thiophene-2-carboxylic acids furnish an excellent linear free energy relationship when plotted versus Δpka (β 0.89, r 0.989, C.L. > 99.9%, n 18, i 0.04), thus confirming the peculiar behaviour of five-membered ring derivatives. The correlation with σH values offers an additional proof of the hyper-ortho character of the 2,3-relation in thiophene derivatives. pa…

chemistry.chemical_compoundDiazodiphenylmethaneReaction rate constantChemistryOrganic ChemistryKineticsThiopheneOrganic chemistryReactivity (chemistry)MethanolFree-energy relationshipRing (chemistry)Medicinal chemistryJournal of Heterocyclic Chemistry
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Crystal structure and reactivity of 2-chloro-3,5-dinitrothiophene and of 2-phenylsulphonyl-3,5-dinitrothiophene with nucleophiles

1988

The geometry obtained by a crystal structure determination of the title compounds, as compared with that of the analogous benzene derivatives, along with results of ab initio calculations, is used to interpret the different SNAr reactivities in some thiophene and benzene compounds. The smaller rotation of the nitro groups with respect to the aromatic rings observed in thiophene derivatives should be considered a relevant factor in the higher reactivity in the thiophene series.

chemistry.chemical_compoundNucleophileAb initio quantum chemistry methodsNucleophilic aromatic substitutionChemistryOrganic ChemistryThiopheneOrganic chemistryReactivity (chemistry)AromaticityCrystal structureBenzeneMedicinal chemistryJournal of Heterocyclic Chemistry
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The structure of ammonium pyrazolates in the solid state

2006

The crystals obtained by mixing equimolar amounts of diethyl 1H-pyrazole-3,5-dicarboxylate and the primary amines phenethylamine and homoveratrylamine are ammonium pyrazolate salts as determined by 13C and 15N CPMAS NMR. Copyright © 2006 John Wiley & Sons, Ltd.

chemistry.chemical_compoundPhenethylaminePrimary (chemistry)chemistryInorganic chemistryMixing (process engineering)Solid-stateGeneral Materials ScienceAmmoniumGeneral ChemistryCarbon-13 NMR
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