Search results for " metal"

showing 10 items of 2159 documents

Kronenethersubstituierte 1,4-Distyrylbenzole und ihre Komplexierung mit Alkalipikraten

2000

Crown Ether Substituted 1,4-Distyrylbenzenes and their Complexation with Alkali Picrates The 1,4-distyrylbenzenes 8 and 9, which contain two crown ether units, each, were prepared by Wittig—Horner reactions. Their complexation tendencies with alkali picrates (Li—Cs) in water/dichloromethane were investigated. Potas sium ions give the strongest complexes. Generally monomo-lecular 1:1-complexes are formed; however, [K-8] + [Pik]—, [K-9]+ [Pik]— and [Rb-8] + [Pik]— generate aggregates, for which a stairway structure is proposed.

chemistry.chemical_classificationchemistry.chemical_compoundchemistryOrganic chemistryAlkali metalMedicinal chemistryCrown CompoundsCrown etherDichloromethaneJournal für praktische Chemie
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Lithium Ion Recognition with Nanofluidic Diodes through Host-Guest Complexation in Confined Geometries

2018

[EN] The lithium ion recognition is receiving significant attention because of its application in pharmaceuticals, lubricants and, especially, in energy technology. We present a nanofluidic device for specific lithium ion recognition via host guest complexation in a confined environment. A lithium-selective receptor molecule, the aminoethyl-benzo-12-crown-4 (BC12C4-NH2), is designed and functionalized on single conical nanopores in polyethylene terephthalate (PET) membranes. The native carboxylic acid groups on the pore walls are covalently linked with the crown ether moieties and the process is monitored from the changes in the current voltage (I-V) curves. The B12-crown-4 moieties are kno…

chemistry.chemical_classificationchemistry.chemical_elementIon current02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryAlkali metal01 natural sciencesChloride0104 chemical sciencesAnalytical ChemistryIonchemistry.chemical_compoundMembranechemistryFISICA APLICADAmedicineLithium chlorideLithium0210 nano-technologyCrown ethermedicine.drug
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Asymmetric hydrogenation of an α-unsaturated carboxylic acid catalyzed by intact chiral transition metal carbonyl clusters – diastereomeric control o…

2020

Twenty clusters of the general formula [(μ-H)2Ru3(μ3-S)(CO)7(μ-P–P*)] (P–P* = chiral diphosphine of the ferrocene-based Walphos or Josiphos families) have been synthesised and characterised. The clusters have been tested as catalysts for asymmetric hydrogenation of tiglic acid [trans-2-methyl-2-butenoic acid]. The observed enantioselectivities and conversion rates strongly support catalysis by intact Ru3 clusters. A catalytic mechanism involving an active Ru3 catalyst generated by CO loss from [(μ-H)2Ru3(μ3-S)(CO)7(μ-P–P*)] has been investigated by DFT calculations. peerReviewed

chemistry.chemical_classificationkarboksyylihapotCarboxylic acidAsymmetric hydrogenationDiastereomerTiglic acidasymmetric hydrogenationMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryFerroceneTransition metalkatalyysicarboxylic acidDalton Transactions
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Thermal Analysis, Mechanical and Rheological Behaviour of Melt Manufactured Polyethylene/Liquid Crystal Polymer Blends

2011

Modification of properties of conventional thermoplastics with thermotropic liquid crystal polymers, from one hand, allows decrease their viscosities, substantially facilitating processing conditions, and, from another hand, allows increase their exploitation properties. Orientation of the labile structure of liquid crystal polymer in extrusion or injection moulding causes specific reinforcement (so-called self-reinforcement) to occur in the blends containing liquid crystal polymer. Up to now the effect of self-reinforcement is mostly investigated in the blends, containing considerable amount of liquid crystal polymer. In this research the effect of minor amounts of liquid crystalline co-po…

chemistry.chemical_classificationpolyethylenelcsh:TN1-997Hydroxybenzoic acidMaterials scienceThermoplasticthermotropic liquid crystalline polymersynthesisPolymerPolyethyleneThermotropic crystalchemistry.chemical_compoundrheological propertieschemistryLiquid crystalUltimate tensile strengthGeneral Materials ScienceInjection mouldingstructuremechanicalComposite materiallcsh:Mining engineering. MetallurgyMedžiagotyra
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Untersuchungen zum oxidativen Abbau nativer Cellulose, 2. Einfluß der Alkalibehandlung auf die Viskositäts-Molekulargewichts-Beziehungen

1974

Um die Kinetik des oxidativen Abbaus nativer Cellulose viskosimetrisch verfolgen zu konnen, mussen neue [η]-M-Eichbeziehungen aufgestellt werden, da die Behandlung der Cellulose mit konzentriertem Alkali den Staudingerindex [η] erniedrigt, ohne das Molekulargewicht M zu verandern. Es wurden zwei Reihen oxidativ abgebauter, verschieden lange mit Alkali vorbehandelter Cellulosen hergestellt und an diesen die Konstanten der Kuhn-Mark-Houwink-Gleichung fur die Cellulosenitrate in Aceton und die Cellulosen in Cuoxam (Cu(NH3)4(OH)2) durch Vergleich mit Lichtstreuungsmessungen bestimmt. For kinetic studies of cellulose degradation by molecular oxygen it is necessary to establish new [η]-M-relation…

chemistry.chemical_compoundCellulose degradationChemistrySodium hydroxideIntrinsic viscosityPolymer chemistryAcetoneMolecular oxygenCelluloseAlkali metalDie Makromolekulare Chemie
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Properties of Multi Phase Interfaces on the Tungsten Trioxide Particles in the Thin Films

2000

A wide spectrum of physical and chemical properties of thin films of tungsten trioxide compounds depend on composition, constitution and structure of the film, interaction with environment, and the type of external influences/excitations. The reason is the non-stoichiometric nature of transition metal oxides and properties of d-electrons. The short range order of non-stoichiometric compounds or phases of WO3 has a strong perovskite arrangement of tungsten and oxygen ions [1, 2]. The smallest crystalline clusters of perovskite short range order consist 6÷9 of [WO6]-octahedrons. One of the structural peculiarities-features of tungsten trioxide, related to non-stoichiometry, is a variety of [W…

chemistry.chemical_compoundChemical speciesMaterials sciencechemistryTransition metalchemistry.chemical_elementPhysical chemistryTungstenThin filmTungsten trioxideAtomic unitsStoichiometryIon
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Calix Crowns Derived from para-Bridged Calix[4]arenes

2000

Two calix[4]arenes, bridged by aliphatic chains of five and eight carbon atoms spanning two opposite para positions, have been converted into their 1,3-crown ether derivatives by reaction with tetraethylene and pentaethylene glycol ditosylates. Of the two possible 1,3-crown derivatives, only the formation of those isomers is observed in which the phenolic units connected at the para positions are etherified. This has been established in one case by a single-crystal X-ray analysis. Preliminary results for the extraction of selected alkali and alkaline-earth metals are reported.

chemistry.chemical_compoundChemistryOrganic ChemistryExtraction (chemistry)Organic chemistrychemistry.chemical_elementEtherPhysical and Theoretical ChemistryAlkali metalBiochemistryCarbonOrganic Letters
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Über katalytische einflüsse bei der polykondensation des p-kresoldialkohols

1952

Wird natriumfreier p-Kresoldialkohol in Silber- oder Platingeraten bei 130°C kondensiert, so ist durch den Geruch kein Formaldehyd wahrnehmbar. p-Kresoldialkohol enthalt oft von seiner Darstellung uber das Natriumsalz her geringe Mengen an Natrium, dessen Anteil im Bereich von 0,0 bis 5,00/00 liegt (0,000 bis 0,037 Mol Natrium je Mol Phenolalkohol). Die bei der Hartung des p-Kresoldialkohols in Platin- oder Silbergeraten beobachteten Gewichtsverluste und die Formaldehydabspaltung sind umso hoher, je groser der Natriumgehalt ist. Natriumfreier p-Kresoldialkohol in Gefasen aus Jenaer Gerateglas 20 und aus gewohnlichem Glas gehartet zeigt in Ubereinstimmung mit der Abgabefahigkeit an Alkali de…

chemistry.chemical_compoundChemistrySodiumPolymer chemistryFormaldehydechemistry.chemical_elementPhenolAlkali metalSodium saltDie Makromolekulare Chemie
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ChemInform Abstract: Cobalt Clusters with Cubane-Type Topologies Based on Trivacant Polyoxometalate Ligands.

2016

Four novel cobalt-substituted polyoxometalates having cobalt cores exhibiting cubane or dicubane topologies have been synthesized and characterized by IR, elemental analysis, electrochemistry, UV–vis spectroscopy, X-ray single-crystal analysis, and magnetic studies. The tetracobalt(II)-substituted polyoxometalate [Co4(OH)3(H2O)6(PW9O34)]4– (1) consists of a trilacunary [B-α-PW9O34]9– unit which accommodates a cubane-like {CoII4O4} core. In the heptacobalt(II,III)-containing polyoxometalates [Co7(OH)6(H2O)6(PW9O34)2]9– (2), [Co7(OH)6(H2O)4(PW9O34)2]n9n– (3), and [Co7(OH)6(H2O)6(P2W15O56)2]15– (4), dicubane-like {CoII6CoIIIO8} cores are encapsulated between two heptadentate [B-α-PW9O34]9– (in…

chemistry.chemical_compoundCrystallographychemistryCubanePolyoxometalatechemistry.chemical_elementGeneral MedicineType (model theory)ElectrochemistrySpectroscopyAlkali metalCobaltExchange modelChemInform
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Electroactivation of Transition Metal Redox Couples for the Carbonylation of Alcohols to Dialkylcarbonates

1998

Electrochemical systems which promote the carbonylation of methanol to dimethylcarbonate, based on the anodic activation of transition metal redox couples, or the Br−/Br2 couple, are poorly active for the carbonylation of ethanol to diethylcarbonate at room temperature and atmospheric pressure. Positive results have been obtained by combined addiction of PdBr2 and Bu4NBr to the system. In this way yields up to 50% in diethylcarbonate were obtained, with very good conductivities in long range electrolyses.

chemistry.chemical_compoundEthanolchemistryTransition metalAtmospheric pressureInorganic chemistryMethanolElectrochemistryPhotochemistryCarbonylationRedoxAnode
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