Search results for "ALK"

showing 10 items of 4314 documents

3D Conformations of Thick Synthetic Polymer Chains Observed by Cryogenic Electron Microscopy.

2019

The backbone conformations of individual, unperturbed synthetic macromolecules have so far not been observed directly in spite of their fundamental importance to polymer physics. Here we report the dilute solution conformations of two types of linear dendronized polymers, obtained by cryogenic transmission electron stereography and tomography. The three-dimensional trajectories show that the wormlike chain model fails to adequately describe the scaling of these thick macromolecules already beyond a few nanometers in chain length, in spite of large apparent persistence lengths and long before a signature of self-avoidance appears. This insight is essential for understanding the limitations o…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceScatteringGeneral EngineeringGeneral Physics and Astronomy02 engineering and technologyPolymerElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionCondensed Matter::Soft Condensed MatterchemistryChemical physicslawPolymer physicsGeneral Materials ScienceElectron microscope0210 nano-technologyScalingSelf-avoiding walkMacromoleculeACS nano
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Photooxidations of Alkenes in Fluorinated Constrained Media:  Fluoro-organically Modified NaY as Improved Reactors for Singlet Oxygen “Ene” Reactions

2007

Creating a stationary fluorinated environment inside the zeolite cavity can increase the reactivity observed for intrazeolite photooxidation of alkenes. Exchanging the zeolite with fluorinated organic cations is a much more effective strategy than simply using a fluorinated solvent for slurry irradiations. Use of cations containing C-F bonds is also more efficient than use of deuterated cations for creation of a singlet oxygen friendly environment where the quenching processes are slowed down. Doping the zeolite with fluoro-organic cation 4 resulted in an increase in the singlet oxygen lifetime to 12 micros.

chemistry.chemical_classificationQuenching (fluorescence)ZEOLITESChemistryAlkeneSinglet oxygenOrganic ChemistryInorganic chemistryINTRAZEOLITE PHOTOOXIDATIONSLIFETIMEOXIDATIONPhotochemistrySolventchemistry.chemical_compoundCHEMISTRYReactivity (chemistry)Singlet stateDEACTIVATIONOLEFINSZeoliteEne reactionThe Journal of Organic Chemistry
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Separation of lanthanides and actinides using magnetic silica particles bearing covalently attached tetra-CMPO-calix[4]arenes

2004

Calix[4]arene tetraethers in the cone conformation bearing four –NH–CO–CH2–P(O)Ph2 (= CMPO) residues on their wide rim and one, two or four ω-amino alkyl residues of various lengths at the narrow rim were synthesized. Reaction with dichlorotriazinyl (DCT) functionalized magnetic particles led to complete coverage of the available surface by covalently linked CMPO-calix[4]arenes in all cases. Magnetically assisted removal of Eu(III) and Am(III) from acidic solutions was distinctly more efficient with these particles in comparison to analogous particles bearing the same amount of analogous single-chain CMPO-functions. The best result, an increase of the extraction efficiency by a factor of 14…

chemistry.chemical_classificationRange (particle radiation)biologyOrganic ChemistryExtraction (chemistry)Actinidebiology.organism_classificationBiochemistrychemistryCovalent bondPolymer chemistryMagnetic nanoparticlesTetraOrganic chemistryPhysical and Theoretical ChemistrySelectivityAlkylOrg. Biomol. Chem.
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Efficient alkali iodide promoted 18F-fluoroethylations with 2-[18F]fluoroethyl tosylate and 1-bromo-2-[18F]fluoroethane

2003

Abstract Radiochemical 18 F-fluorination yields of several compounds using the secondary labelling precursors 2-[ 18 F]fluoroethyl tosylate ([ 18 F]FETos) and 1-bromo-2-[ 18 F]fluoroethane ([ 18 F]BFE) could be considerably enhanced by the addition of an alkali iodide. The radiochemical yield of [ 18 F]fluoroethyl choline for example could be doubled with [ 18 F]BFE and increased from 13% to ≈80% with [ 18 F]FETos. By addition of alkali iodide to the precursor, the 18 F-fluoroethylation yields of established radiopharmaceuticals, especially in the case of automated syntheses, could be significantly increased without major changes of the reaction conditions.

chemistry.chemical_classificationReaction conditionsOrganic ChemistryIodideAlkali metalBiochemistrychemistry.chemical_compoundFluoroethyl tosylatechemistryYield (chemistry)LabellingDrug DiscoveryCholineFluoroethylNuclear chemistryTetrahedron Letters
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Formation of Bridging Alkene and Conjugated Dialkenes Exclusively Generated from Alkynes on the [3,3‘-Co(1,2-C2B9H11)2]- Platform. The Unique Hydrobo…

2003

The unprecedented metal-mediated transformation of an alkyne into a B,B' bridging alkene is reported. Also, the unprecedented synthesis of a conjugated dialkene derivative of [3,3'-Co(1,2-C2B9H11)2]- generated only from an alkyne, contrary to the usual case where an alkyne and an alkene are needed, is described. This has been possible through the singular capacity of a B-H to produce hydroboration.

chemistry.chemical_classificationReaction mechanismHydroborationColloid and Surface ChemistryBridging (networking)ChemistryStereochemistryAlkeneAlkyneGeneral ChemistryConjugated systemBiochemistryCatalysisJournal of the American Chemical Society
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Oxidation of N,N-Benzylalkylamines to Nitrones by Mo(VI) and W(VI) Polyperoxo Complexes

1996

Abstract Oxidation of N,N-benzylalkylamines in chloroform by Mo(VI) and W(VI) polyperoxo complexes (PPC) of general formula Q+3{PO4[MO(O2)2]4}3− (Q+ = onium ion) yield the corresponding nitrones as oxidized products quantitatively. Only in the case of N,N-benzylmethylamine the formation of nitrone is accompanied by 25% of benzaldoxime. Oxidation of N,N-benzyltertbutylamine and N,N-benzylisopropylamine follows second order kinetics. This finding does not disqualify the hypothesis that the reaction might occur by a rate determining nucleophilic attack of the amine onto the peroxide oxygens leading, through a Bartlett-type transition state, to the probable formation of the corresponding hydrox…

chemistry.chemical_classificationReaction mechanismLigandStereochemistryPolyperoxo complexesProcess Chemistry and TechnologyN-benzylalkylaminesNPolyperoxo complexes; NN-benzylalkylamines; OxidationMedicinal chemistryPeroxideCatalysisNitroneReaction coordinateAdductchemistry.chemical_compoundHydroxylaminechemistryNucleophileOxidationPhysical and Theoretical Chemistry
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Zum Ligandenaustausch des Ferrocens mit Methyl- und Ethyl-substituierten Naphthalinen

1988

Abstract The replacement of a Cp ligand of ferrocene by each of ten unsymmetrically substituted naphthalenes yields pairs of complex ions [arene-FeCp] + , which have been identified from their 1 H NMR spectra. The influence of the substituent on the ratio of the two isomers, and its temperature dependence implies a complex reaction mechanism involving an η 2 -bound intermediate of the associated naphthalene. The proton resonances of the alkyl groups of the naphthalenes are shifted to lowfield by complexation; this effect decreases with increasing distance from the iron. The resonance shift of the arene protons has a different sign for the complexed (highfield) and the uncomplexed part (lowf…

chemistry.chemical_classificationReaction mechanismStereochemistryLigandOrganic ChemistrySubstituentNuclear magnetic resonance spectroscopyBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryFerroceneMaterials ChemistryProton NMRPhysical and Theoretical ChemistryMetalloceneAlkylJournal of Organometallic Chemistry
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The skeletal isomerization of but-1-ene catalyzed by theta-1 zeolite

2001

The complete mechanism for the skeletal isomerization of but-1-ene catalyzed by theta-1 zeolite was investigated theoretically by means of DFT calculations, and the influence of the local geometry of the active site and of electrostatic effects on the geometries of the species involved and on activation and reaction energies were analyzed. It was found that whereas the geometry and stability of alkoxide intermediates are strongly influenced by the local geometry of the active site, the ionic transition states are mainly stabilized by electrostatic effects. Both aspects result in a lowering of the activation energies of the elementary steps that form the mechanism and therefore in enhanced r…

chemistry.chemical_classificationReaction mechanismbiologyAlkeneStereochemistryGeneral Physics and AstronomyActive siteIonic bondingTransition statechemistryComputational chemistrybiology.proteinReactivity (chemistry)Physical and Theoretical ChemistryIsomerizationEne reactionPhysical Chemistry Chemical Physics
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Crosstalk between mitochondria and peroxisomes

2015

Mitochondria and peroxisomes are small ubiquitous organelles. They both play major roles in cell metabolism, especially in terms of fatty acid metabolism, reactive oxygen species (ROS) production, and ROS scavenging, and it is now clear that they metabolically interact with each other. These two organelles share some properties, such as great plasticity and high potency to adapt their form and number according to cell requirements. Their functions are connected, and any alteration in the function of mitochondria may induce changes in peroxisomal physiology. The objective of this paper was to highlight the interconnection and the crosstalk existing between mitochondria and peroxisomes. Speci…

chemistry.chemical_classificationReactive oxygen speciesFatty acid metabolismCellReviewMitochondrionBiologyPeroxisomechemistry.chemical_compoundCrosstalk (biology)medicine.anatomical_structurechemistryBiochemistryOrganellemedicineBeta oxidation
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Gold Redox Catalytic Cycles for the Oxidative Coupling of Alkynes

2011

[EN] Au(I)/Au(III) catalytic cycles are catalytically competent to perform the oxidative coupling of alkynes in the homogeneous phase at room temperature and without any protecting atmosphere. Selectfluor as oxidant, wet acetonitrile as solvent, and sodium carbonate as base are the reagents of choice. Both aromatic and alkyl alkynes can be coupled, and mechanistic studies reveal that at least two gold species having different oxidation states are implicated in the key step of the coupling.

chemistry.chemical_classificationRedox chemistryGold catalysisGeneral ChemistryPhotochemistryRedoxCatalysisCatalysisSolventDiyneschemistry.chemical_compoundQUIMICA ORGANICAchemistryReagentOxidative coupling of alkynesVoltammetryOxidative coupling of methaneSelectfluorAcetonitrileAlkyl
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