Search results for "condensation"

showing 10 items of 468 documents

Biosilica-based immobilization strategy for label-free OWLS sensors

2013

Abstract In the last years, a new group of enzymes, so-called silicateins, have been identified and characterized, which form the axial filaments of the spicules of the siliceous sponges, consisting of amorphous silica. Silicateins are able to catalyze the polycondensation and deposition of silica at mild conditions (low temperature and physiological pH). By means of these enzymes it is possible for the first time to produce silica nanostructures biocatalytically, which opens new ways for construction of biosensors. The cDNAs encoding the responsible enzymes have been isolated and the proteins can be produced in a recombinant way. Here we demonstrate the silicatein-mediated biosilica format…

chemistry.chemical_classificationNanostructureCondensation polymerChemistryMetals and AlloysNanotechnologyCondensed Matter Physicsmedicine.disease_causeSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionEnzymeChemical engineeringlawMaterials ChemistrymedicineRecombinant DNAOptical waveguide lightmode spectroscopyElectrical and Electronic EngineeringInstrumentationEscherichia coliBiosensorLabel freeSensors and Actuators B: Chemical
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Synthesis and Physicochemical Characterization ofmeso-Functionalized Corroles: Precursors of Organic-Inorganic Hybrid Materials

2005

Cobalt(III) corroles exhibit an infinite selectivity for the coordination of carbon monoxide towards dioxygen and dinitrogen. This peculiar property thus allows their use as sensing devices for CO detection. Here are described the syntheses and physico-chemical characterization of meso mono-, bis- and tris(triethoxysilyl)-functionalized corroles, precursors of organic–inorganic materials. The corrole ring formation was achieved in every case using the “2+1” method involving the reaction of two equivalents of an encumbered dipyrromethane with one equivalent of an aromatic aldehyde in the presence of a catalytic amount of trifluoroacetic acid. The functionalization of the corrole by triethoxy…

chemistry.chemical_classificationOrganic ChemistryCondensation reactionIsocyanateAldehydeCatalysischemistry.chemical_compoundchemistryTrifluoroacetic acidOrganic chemistryPhysical and Theoretical ChemistryCorroleHybrid materialSelectivityEuropean Journal of Organic Chemistry
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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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1989

A series of combined main-chain side-group liquid-crystalline polymers was synthesized by melt polycondensation from trans-1,4-cyclohexanedicarboxylic acid, chloro-1,4-phenylene diacetate and 6-(4-methoxy-4′-biphenylyloxy)hexyl-1,4-phenylene diacetate. These polyesters combine the features of rigid-rod main-chain LC-polymers and of side-group LC-polymers. Polymers with small fractions of mesogenic side-groups (5 and 10 mol-%) have lower melting points than the parent polymer poly(chloro-1,4-phenylene 1,4-cyclohexanedicarboxylate) but are still liquid crystalline up to their decomposition at T ≥ 400°C. In polymers with larger fractions of mesogenic side-groups (50 and 100 mol-%) partial isom…

chemistry.chemical_classificationPolyesterCondensation polymerMaterials sciencechemistryLiquid crystalMesogenPolymer chemistryMelting pointThermomechanical analysisPolymerDynamic mechanical analysisDie Makromolekulare Chemie
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Molecular Weight Distribution of Hyperbranched Polymers Generated by Self-Condensing Vinyl Polymerization in Presence of a Multifunctional Initiator

1999

The molecular weight distribution (MWD) is derived for polymers generated by self-condensing vinyl polymerization (SCVP) of a monomer having a vinyl and an initiator group (“inimer”) in the presence of a multifunctional initiator. If the monomer is added slowly to the initiator solution (semi-batch process), this leads to hyperbranched polymers with a multifunctional core. If monomer and initiator are mixed simultaneously (batch process), even at vinyl group conversions as high as 99%, the total MWD consists of polymers which have grown via reactions between inimer molecules (i.e., the normal SCVP process) and those which have reacted with the initiator. Consequently, the weight distributio…

chemistry.chemical_classificationPolymers and PlasticsBulk polymerizationOrganic ChemistryPolymerSelf-condensationInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryWeight distributionMaterials ChemistryMolar mass distributionMoleculeMacromolecules
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Polymeric nitrones, 1. Synthesis and modification of polymeric nitrones derived from polymerizable aldehydes

1999

The model compound N,C-diphenylnitrone[N-(benzylidene)aniline-N-oxide] (3) was prepared by condensation of benzaldehyde with phenylhydroxylamine to study its thermal stability. X-ray diffraction analysis of a single crystal established the conformation of the nitrone group. A new monomer 4-(methacryloyloxy)benzaldehyde-phenylnitrone (8) was also prepared and could not be polymerized with 2,2′-azobisisobutyronitrile (AIBN) as initiator at 70°C. Under these conditions the nitrone reacted exclusively in an intermolecular 1,3-dipolar cycloaddition to give oligomeric tetrahydro-1,2-oxazoline derivates. The kinetics of the cycloaddition was investigated. Additionally, different (meth)acryl- and s…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationCondensed Matter PhysicsCondensation reactionAldehydeCycloadditionNitroneBenzaldehydechemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryPhenylhydroxylamineMacromolecular Chemistry and Physics
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Hyperbranched methacrylates by self-condensing group transfer polymerization

1997

The synthesis of hyperbranched methacrylates was achieved by self-condensing group transfer polymerization of 2-(2-methyl-1-triethylsiloxy-1-propenyloxy)ethyl methacrylate (1). “Back-biting” is shown to be the predominant side reaction. In spite of this, the compact nature of the hyperbranched molecules was demonstrated through SEC-viscosity measurements and comparison with a linear analogue. The degree of branching can be controlled by copolymerization with conventional monomers, e.g. MMA, and the living polymers can be used as macroinitiators for star-shaped polymers.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySide reactionPolymerSelf-condensationBranching (polymer chemistry)Methacrylatechemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerMacromolecular Rapid Communications
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Zur C-17-Oxidation von Clavinalkaloiden mit primärer alkoholischer Hydroxylgruppe

1975

Die Oppenauer-Oxidation von 1 mit Cyclohexanon fuhrt zu dem Aldolkondensationsprodukt 4 und der Carbonsaure 3. Analog konnte Lysergsaure (8) in geringer Menge aus 6 gewonnen und im Reaktionsgemisch von 7 nachgewiesen werden. Damit wurden erstmals Clavinalkaloide mit primarer alkoholischer Hydroxylgruppe chemisch zu den entsprechenden Carbonsauren oxidiert. C-17-Oxidation of Clavine Alkaloids with a Primary Alcoholic Hydroxyl Group. 1 is converted by Oppenauer oxidation with cyclohexanone to the aldol condensation product 4 and to the carboxylic acid 3. Lysergic acid (8) was obtained in a small yield by the analogous reaction of 6 and was found in the reaction mixture of 7. Thus clavine alka…

chemistry.chemical_classificationPrimary (chemistry)StereochemistryCarboxylic acidClavine AlkaloidsPharmaceutical ScienceCyclohexanoneOppenauer oxidationLysergic acidchemistry.chemical_compoundchemistryYield (chemistry)Drug DiscoveryAldol condensationArchiv der Pharmazie
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A new synthesis of soluble poly(1,4-phenylenevinylene)s and poly(2,5-pyrimidinylenevinylene)s

1991

Abstract Alkoxy-substituted 4-methylbenzylideneanilines 2a-f and their pyrimidine analogues 2g,h show an efficient selfcondensation in the alkaline medium KOC(CH 3 ) 3 /DMF. The totally stereoselective reaction yields 3a-h which are transformed by acidic work-up to 4a-h . A narrow distribution of the molecular weight can be achieved.

chemistry.chemical_classificationPyrimidine analoguechemistryOrganic ChemistryDrug DiscoveryPolymer chemistryOrganic chemistryStereoselectivityPolymerSelf-condensationBiochemistryTetrahedron Letters
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Antimicrobial activity of methylene blue and toluidine blue O covalently bound to a modified silicone polymer surface

2009

Methylene Blue or Toluidine Blue O were covalently bound to an activated silicone polymer by means of an amide condensation reaction. UV-visible absorption spectra confirmed that the dye was surface bound. The new polymers with covalently attached dye display significant bactericidal activity against Escherichia coli and Staphylococcus epidermidis with a 99.999% reduction in viable bacteria after four minutes exposure to a low power laser.

chemistry.chemical_classificationRMAbsorption spectroscopybiologyGeneral ChemistryPolymerPhotochemistrybiology.organism_classificationCondensation reactionmedicine.disease_causeRSchemistry.chemical_compoundchemistryCovalent bondStaphylococcus epidermidisAmidePolymer chemistryMaterials ChemistrymedicineEscherichia coliMethylene blueJournal of Materials Chemistry
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