Search results for "DEP"

showing 10 items of 10555 documents

Complexation of enantiomerically pure tetraalkylammonium cations by ethyl resorcinarene

2013

Molecular recognition via weak interactions of three enantiopure tetraalkylammonium cations 2–4 by ethyl resorcinarene 1 was studied in the solid state using single-crystal X-ray diffraction, in solution by proton nuclear magnetic resonance spectroscopy (1H NMR) titration and in the gas phase using electrospray ionisation mass spectrometry. The 1H NMR titration studies reveal the association constants for the 1:1 complexes to vary according to the size and electronic properties of the alkyl groups of the guest cations. In the solid state, the resorcinarene is deprotonated and the X-ray structure confirms the 1:1 complex 2+@1−  to be held together by multiple cation…π and C–H…π interactions.…

chemistry.chemical_classificationGeneral ChemistryResorcinareneMass spectrometryCrystallographyMolecular recognitionEnantiopure drugDeprotonationchemistryProton NMROrganic chemistryTitrationta116AlkylSupramolecular Chemistry
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Biochemical and Kinetic Analyses of NS5B RNA-Dependent RNA Polymerase of the Hepatitis C Virus

1998

The biochemical properties of the RNA-dependent RNA polymerase (RdRp) of the hepatitis C virus were analyzed. A hexahistidine affinity-tagged NS5B fusion protein was expressed with recombinant baculoviruses in insect cells and purified to near homogeneity. Enzymatic activity of the purified protein was inhibited by KCl or high concentrations of NaCl and was absolutely dependent on Mg2+, which could be replaced by Mn2+. NS5B was found to be processive and able to copy long heteropolymeric templates with an elongation rate of 150-200 nucleotides/min at 22 degreesC. Kinetic constants were determined for all four nucleoside triphosphates and different templates. In case of a heteropolymeric RNA…

chemistry.chemical_classificationHepatitis C virusvirusesRNARNA-dependent RNA polymeraseHepacivirusBiologyViral Nonstructural ProteinsRibonucleosidemedicine.disease_causeRNA-Dependent RNA PolymeraseMolecular biologySubstrate Specificitychemistry.chemical_compoundKineticsBiochemistrychemistryRNA polymeraseVirologymedicineHumansNucleotideNS5BNucleosideVirology
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The effect of pH on polymorph formation of the pharmaceutically active compound tianeptine.

2012

The anti-depressant pharmaceutical tianeptine has been investigated to determine the dynamics of polymorph formation under various pH conditions. By varying the pH two crystalline polymorphs were isolated. The molecular and crystal structures have been determined to identify the two polymorphs. One polymorph is an amino carboxylic acid and the other polymorph is a zwitterion. In the solid state the tianeptine moieties are bonded through hydrogen bonds. The zwitterion was found to be less stable and transformed to the acid form. During this investigation an amorphous form was identified.

chemistry.chemical_classificationHydrogen bondChemistryThiazepinesCarboxylic acidPharmaceutical ScienceCrystal structureAntidepressive Agents TricyclicHydrogen-Ion Concentrationlaw.inventionAmorphous solidCrystallographychemistry.chemical_compoundX-Ray DiffractionlawActive compoundZwitterionSpectroscopy Fourier Transform InfraredmedicineTianeptineCrystallizationCrystallizationPowder Diffractionmedicine.drugInternational journal of pharmaceutics
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New molecular catalysts for ATP cleavage. Criteria of size complementarity

2000

The interaction of the cyclophane receptor 2,5,8,11,14,17-hexaaza[18]metacyclophane (L) with the nucleotides ATP, ADP and AMP is described. L yields one of the largest rate enhancements for hydrolytic ATP cleavage observed in macrocyclic polyamines. The process is specific for the formation of ADP and involves a high degree of geometrical complementarity between host and guest species. The analogue compound 24-hydroxy-2,5,8,11,14,17-hexaaza[18]metacyclophane (L11) shows also a high degree of ATP activation. However, in this case deprotonation of the hydroxy group results in almost complete quenching of the ATPase activity above pH 7.0.

chemistry.chemical_classificationHydrolysischemistry.chemical_compoundDeprotonationQuenching (fluorescence)chemistryStereochemistryNucleotideReceptorCleavage (embryo)CyclophaneCatalysis
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Coordination versatility of pyridine-functionalized N-heterocyclic carbenes: a detailed study of the different activation procedures. Characterizatio…

2005

Three different reaction procedures for the coordination of N-n-butyl-N'-(2-pyridylmethyl)imidazolium salt have produced new N-heterocyclic complexes of Rh and Ir. The direct reaction of the imidazolium salt with [IrCl(cod)](2) provides a NHC-Ir(III)-H complex, while transmetalation from a silver-NHC complex and deprotonation with NEt(3) give new NHC complexes of M(I) and M(III) when reacting with [MCl(cod)](2) or [MCl(coe)(2)](2) (M = Rh, Ir). The crystal structures of the biscarbene Rh(III) and Ir(III) complexes are described. The catalytic properties of the compounds obtained have been tested in the hydrosilylation of acetylenes, the cyclization of acetylenic carboxylic acids, and hydrog…

chemistry.chemical_classificationHydrosilylationSalt (chemistry)Hydrogen transferCrystal structureMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundTransmetalationDeprotonationchemistryPyridineOrganic chemistryPhysical and Theoretical ChemistryInorganic chemistry
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An approach to erythrophleum alkaloids. Synthesis of methyl (−)-4-epi-cassamate

1986

Abstract A synthetic approach to Erythrophleum alkaloids, involving as a key-step the regiospecific deprotonation of the ketone 5a, is described.

chemistry.chemical_classificationKetonebiologyChemistryStereochemistryAlkaloidErythrophleumOrganic Chemistrybiology.organism_classificationBiochemistrychemistry.chemical_compoundDeprotonationDrug DiscoveryOrganic chemistryEpimerStereoselectivityEnantiomerDiterpeneTetrahedron Letters
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Boosting Vis/NIR Charge-Transfer Absorptions of Iron(II) Complexes by N-Alkylation and N-Deprotonation in the Ligand Backbone.

2017

Reversing the 3MLCT / 3MC excited state order in iron(II) complexes is a challenging objective, yet would finally result in longsought luminescent transition metal complexes with an earthabundant central ion. One approach to achieve this goal is based on low-energy charge transfer absorptions in combination with a strong ligand field. Coordinating electron rich and electron poor tridentate oligopyridine ligands with large bite angles at iron(II) enables both low-energy MLCT absorption bands around 590 nm and a strong ligand field. Variations of the electron rich ligand by introducing longer alkyl substituents destabilizes the iron(II) complex towards ligand substitution reactions while hard…

chemistry.chemical_classificationLigand field theory010405 organic chemistryChemistryLigandBand gapOrganic ChemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesDeprotonationTransition metalExcited stateDensity functional theoryAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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Perovskite solar cells prepared by flash evaporation

2015

A simple vacuum deposition method for the preparation of high quality hybrid organic-inorganic methylammonium lead iodide perovskite thin films is reported. When sandwiched in between organic charge transporting layers, such films lead to solar cells with a power conversion efficiency of 12.2%.

chemistry.chemical_classificationMaterials scienceF100IodideInorganic chemistryEnergy conversion efficiencyF200Metals and AlloysFlash evaporationGeneral ChemistryHybrid solar cellCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryChemical engineeringVacuum depositionMaterials ChemistryCeramics and CompositesThin filmPerovskite (structure)Chemical Communications
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Solvent Determines Nature of Effective Interactions between Nanoparticles in Polymer Brushes

2015

We study the effective interaction between two parallel rod-like nanoparticles in swollen and collapsed polymer brushes as a function of penetration depth by 2D self-consistent field calculations. In vertical direction, the interaction is always attractive. In lateral direction, the behavior under good and poor solvent conditions is qualitatively different. In swollen brushes (good solvent), nanoparticles always repel each other. In collapsed brushes (poor solvent), we identify two different regimes: an immersed regime, where the nanoparticles are fully surrounded by the brush, and an interfacial regime, where they are located in the interface between brush and solvent. In the immersed regi…

chemistry.chemical_classificationMaterials scienceField (physics)BrushNanoparticleNanotechnologyPolymerSurfaces Coatings and Filmslaw.inventionSolventchemistrylawChemical physicsVertical directionMaterials ChemistryPhysical and Theoretical ChemistryPenetration depthThe Journal of Physical Chemistry B
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Processing and adjusting the hydrophilicity of poly(oxymethylene) (co)polymers: nanoparticle preparation and film formation

2016

Handling the insoluble POM: the preparation of nanoparticles based on hyperbranched-linear-hyperbranched ABA triblock copolymers with variable hydrophilicity and composed of short hyperbranched polyglycerol (hbPG) as the A-blocks and linear poly(oxymethylene) (POM) as a B-block is described. The POM-hbPG-nanoparticles with diameters in the range of 190 to 250 nm were generated in a convenient process, combining the solvent evaporation process with the miniemulsion technique, a water borne handling for POM-copolymers. Furthermore, the film formation properties of the nanoparticles were investigated by deposition on silicon and subsequent sintering, which leads to films with a thickness in th…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSiliconOrganic ChemistryNanoparticleSinteringchemistry.chemical_elementBioengineering02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesContact angleMiniemulsionchemistryChemical engineeringPolymer chemistryCopolymerDeposition (phase transition)0210 nano-technology
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