Search results for "stereo"

showing 10 items of 6147 documents

Combined NC-AFM and DFT study of the adsorption geometry of trimesic acid on rutile TiO2(110)

2010

The adsorption behavior of trimesic acid (TMA) on rutile TiO(2)(110) is studied by means of non-contact atomic force microscopy (NC-AFM) and density-functional theory (DFT). Upon low-coverage adsorption at room temperature, NC-AFM imaging reveals individual molecules, centered above the surface titanium rows. Based on the NC-AFM results alone it is difficult to deduce whether the molecules are lying flat or standing upright on the surface. To elucidate the detailed adsorption geometry, we perform DFT calculations, considering a large number of different adsorption positions. Our DFT calculations suggest that single TMA molecules adsorb with the benzene ring parallel to the surface plane. In…

inorganic chemicalsHydrogenSurface PropertiesStereochemistryMolecular Conformationchemistry.chemical_elementBiosensing TechniquesMicroscopy Atomic ForceRing (chemistry)530chemistry.chemical_compoundAdsorptionMoleculeGeneral Materials ScienceTitaniumTemperatureTricarboxylic AcidsCondensed Matter PhysicsCarbonTitanium oxideOxygenCrystallographychemistryRutileAdsorptionTrimesic acidHydrogenTitaniumJournal of Physics: Condensed Matter
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Domain formation in monolayers

1995

For phospholipids at the air/water interface we demonstrate that molecular chirality in some, but not in all, cases influences the domain shapes. In other cases chirality in the head group region can cause a chiral structure considering the tail arrangement. This indicates head group ordering. Minute changes of the molecular structure may change domain morphology from circular to dendritic. This can be related to slight changes of the lattice structure. In case of a dendritic domain the chains are more tilted, the deviation from hexagonal symmetry is more pronounced, and hence the lattice anisotropy is larger. This can be understood also in view of recent simulations considering diffusion-l…

inorganic chemicalsMacromolecular SubstancesSurface PropertiesHigh Energy Physics::LatticeBiophysicsBiophysical PhenomenaDomain formationMonolayerpolycyclic compoundsheterocyclic compoundsMolecular BiologyPhospholipidsPhysics::Atmospheric and Oceanic PhysicsSurface diffusionMolecular StructureChemistryorganic chemicalsHigh Energy Physics::PhenomenologyWaterStereoisomerismCell BiologyCrystallographyMicroscopy FluorescenceDomain (ring theory)health occupationsChirality (chemistry)OilsMolecular Membrane Biology
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Synthesis, Characterization, and Cu(2+) Coordination Studies of a 3-Hydroxy-4-pyridinone Aza Scorpiand Derivative.

2016

The synthesis, acid-base behavior, and Cu(2+) coordination chemistry of a new ligand (L1) consisting of an azamacrocyclic core appended with a lateral chain containing a 3-hydroxy-2-methyl-4(1H)-pyridinone group have been studied by potentiometry, cyclic voltammetry, and NMR and UV-vis spectroscopy. UV-vis and NMR studies showed that phenolate group was protonated at the highest pH values [log K = 9.72(1)]. Potentiometric studies point out the formation of Cu(2+) complexes of 1:2, 2:2, 4:3, 1:1, and 2:1 Cu(2+)/L1 stoichiometries. UV-vis analysis and electrochemical studies evidence the implication of the pyridinone moieties in the metal coordination of the 1:2 Cu(2+)/L1 complexes. L1 shows …

inorganic chemicalsMagnetic Resonance SpectroscopyStereochemistryPyridinesPyridonesPotentiometric titrationProtonationChemistry Techniques Synthetic010402 general chemistry010403 inorganic & nuclear chemistryElectrochemistryCrystallography X-Ray01 natural sciencesMedicinal chemistryAntioxidantsCoordination complexInorganic Chemistrychemistry.chemical_compoundStructure-Activity RelationshipCoordination ComplexesHumansChelationPhysical and Theoretical ChemistryCell ProliferationChelating Agentschemistry.chemical_classificationLigandHydrogen-Ion Concentration0104 chemical scienceschemistryPotentiometrySpectrophotometry UltravioletCyclic voltammetryDerivative (chemistry)CopperHeLa CellsInorganic chemistry
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Amino-Acid-Based Polymerizable Surfactants for the Synthesis of Chiral Nanoparticles

2016

Amino-acid-based chiral surfactants with polymerizable moieties are synthesized, and a versatile approach to prepare particles thereof with a chiral surface functionality is presented. As an example of an application, the synthesized particles are tested for their ability as nucleating agents in the enantioselective crystallization of amino acid conglomerate systems, taking rac-asparagine as a model system. Particles resulting from chiral surfactants with different tail groups are compared and the results demonstrate that only the chiral nanoparticles made of the polymerizable surfactant are able to act efficiently as nucleation agent in enantioselective crystallization.

inorganic chemicalsMaterials sciencePolymers and PlasticsPolymersNucleationNanoparticleModel system02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationlaw.inventionSurface-Active AgentsPulmonary surfactantlawMaterials ChemistryOrganic chemistryAmino AcidsCrystallizationchemistry.chemical_classificationMolecular Structureorganic chemicalsOrganic Chemistrytechnology industry and agricultureEnantioselective synthesisStereoisomerism021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesAmino acidchemistryNanoparticles0210 nano-technologyChirality (chemistry)Macromolecular Rapid Communications
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Prolin-benzylester als chirale Hilfsgruppen in asymmetrischen 1,3-dipolaren Cycloadditionen mit Nitriloxiden

1990

Proline Benzyl Esters as Chiral Auxiliaries in Asymmetric 1,3-Dipolar Cycloadditions N-Acryloylproline benzyl ester (1b) reacts with nitrile oxides at temperatures from −78 to 0°C to give isoxazolines 4/5 with diastereomeric ratios of ca. 3:1 and with the (5S) isomer as the predominating. The corresponding N-methacryloylproline benzyl ester (1c) gives inferior results. The diastereoselectivity is not influenced by the temperature and the substituents of the nitrile oxides. To prove the absolute configuration of the predominating stereoisomer, a reaction sequence is developed which makes use of an enantioselective hydrolysis with pig liver esterase as the key step to generate an optically ac…

inorganic chemicalsNitrileChemistryStereochemistryorganic chemicalsOrganic ChemistryEnantioselective synthesisDiastereomerAbsolute configurationEsterasechemistry.chemical_compoundHydrolysis13-Dipolar cycloadditionPhysical and Theoretical ChemistryTriethylamineLiebigs Annalen der Chemie
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Bis[S-hexyl 3-(thiophen-2-ylmethylidene)dithiocarbazato-κ2N3,S]palladium(II)

2016

In the title complex, [Pd(C12H17N2S3)2], the PdIIatom exhibits a square-planar coordination geometry with theN,S-chelating ligands arranged in atransconfiguration. Intramolecular C—H...S hydrogen bonds are observed. In the crystal, molecules are linked by weak C—H...N hydrogen-bond interactions, forming chains parallel to thebaxis.

inorganic chemicalsQuantitative Biology::Biomoleculescrystal structureChemistryStereochemistryHydrogen bondThio-chemistry.chemical_elementGeneral MedicineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryhumanitiespalladium(II) complex0104 chemical sciencesCrystalTrans configurationlcsh:QD901-999lcsh:Crystallographydithiocarbazate ligandCoordination geometryPalladiumIUCrData
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Synthesis of 2,4,6-trisubstituted tetrahydropyrans via 6-exo selenoetherification of unsaturated alcohols

2001

Stereoselectivity, regioselectivity and yields in the 6-exo selenoetherification of four unsaturated diols were found to depend on the stereochemistry of the diols and on the presence of an oxygen atom close to the intermediate seleniranium ring. Silica gel was useful in order to obtain good yields. Reactions performed both under kinetic and thermodynamic control led to the same products. Stereoselectivity, regioselectivity and yields in the 6-exo selenoetherification of four unsaturated diols were found to depend on several factors such as the stereochemistry of the diols, the nature of the R group, the nature of the counter anion of the PhSe+ species and the presence of silica gel.

inorganic chemicalsSilica gelOrganic ChemistryRegioselectivityTetrahydropyranRing (chemistry)Biochemistrychemistry.chemical_compoundOxygen atomchemistryDrug Discoverypolycyclic compoundsOrganic chemistrytetrahydropyranStereoselectivityTetrahedron Letters
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closo-borane conjugated regulatory peptides retain high biological affinity: synthesis of closo-borane conjugated Tyr(3)-octreotate derivatives for B…

2008

Despite the improvements in cancer therapy during the past years, high-grade gliomas and many other types of cancer are still extremely resistant to current forms of therapy. Boron neutron capture therapy (BNCT) provides a promising way to destroy cancer cells without damaging healthy tissue. However, BNCT in practice is still limited due to the lack of boron-containing compounds that selectively deliver boron to cancer cells. Since many neuroendocrine tumors show an overexpression of the somatostatin receptor, it was our aim to synthesize compounds that contain a large number of boron atoms and still show high affinity toward this transmembrane receptor. The synthetic peptide Tyr (3)-octre…

inorganic chemicalsStereochemistryBiomedical EngineeringPharmaceutical ScienceBioengineeringPeptideBoron Neutron Capture TherapyCHO CellsConjugated systemBoranePeptides CyclicCell Linechemistry.chemical_compoundCricetulusCricetinaeNeoplasmsMoietyAnimalsHumansBinding siteBoranesPharmacologychemistry.chemical_classificationOctreotateBinding SitesSomatostatin receptorOrganic ChemistryCell MembranechemistryCancer cellBiotechnologyBioconjugate chemistry
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Prediction of properties of chiral compounds by molecular topology

1998

Abstract A common assumption in chemistry is that chiral behavior is associated with 3-D geometry. However, chiral information is related to symmetry, which allows the topological handling of chiral atoms by weighted graphs and the calculation of new descriptors that give a weight to the corresponding entry in the main diagonal of the topological matrix. In this study, it is demonstrated that, operating in this way, chiral topological indices are obtained that can differentiate the pharmacological activity between pairs of enantiomers. The 50% inhibitory concentration (IC50) values of the D2 dopamine receptor and the σ receptor for a group of 3-hydroxy phenyl piperidines are specifically pr…

inorganic chemicalsStereochemistryIn Vitro TechniquesMain diagonalStructure-Activity RelationshipMatrix (mathematics)PiperidinesComputational chemistryMaterials ChemistryAnimalsHypnotics and SedativesReceptors sigmaheterocyclic compoundsPhysical and Theoretical ChemistrySpectroscopyGroup (mathematics)Chemistryorganic chemicalsStereoisomerismComputer Graphics and Computer-Aided DesignDopamine D2 Receptor AntagonistsCharacter (mathematics)Models ChemicalDrug DesignCentral Nervous System StimulantsMolecular topologyEnantiomerSymmetry (geometry)Chirality (chemistry)Journal of Molecular Graphics and Modelling
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Nano-sized I12L6 Molecular Capsules Based on the [N⋅⋅⋅I+⋅⋅⋅N] Halogen Bond

2017

Summary Self-assembly of pre-organized subunits with a concave overall shape is an effective strategy for the synthesis of supramolecular capsules. We report the synthesis of a cavitand-based hexameric capsule held together solely by 12 robust [N⋅⋅⋅I + ⋅⋅⋅N] halogen bonds and its characterization in solution and in the gas phase via 1 H NMR spectroscopy, diffusion-ordered nuclear magnetic resonance spectroscopy (DOSY), and electrospray ionization mass spectrometry. The [N⋅⋅⋅I + ⋅⋅⋅N] halogen-bonded hexameric capsule was efficiently synthesized from the isolobal metallosupramolecular Ag + capsule by application of the [N⋅⋅⋅Ag + ⋅⋅⋅N] → [N⋅⋅⋅I + ⋅⋅⋅N] cation-exchange reaction.

inorganic chemicalsStereochemistrycapsuleGeneral Chemical EngineeringElectrospray ionizationSupramolecular chemistrysupramolecular capsule010402 general chemistry01 natural sciencesBiochemistrysupramolecular chemistryresorcinarene cavitandMaterials ChemistryEnvironmental ChemistryHalonium ionhalonium-ion-based nanotechnologyta116silver-to-iodine cation exchangeHalogen bond010405 organic chemistryChemistryBiochemistry (medical)CavitandIsolobal principleself-assemblyGeneral ChemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesCrystallographyhalonium ionProton NMRhalogen bondChem
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