Search results for "force"

showing 10 items of 3423 documents

(Trifluoromethoxy)Phenylboronic Acids: Structures, Properties, and Antibacterial Activity.

2021

Three isomers of (trifluoromethoxy)phenylboronic acids were studied in the context of their physicochemical, structural, antimicrobial and spectroscopic properties. They were characterized by 1H, 13C, 11B and 19F NMR spectroscopy. The acidity of all the isomers was evaluated by both spectrophotometric and potentiometric titrations. The introduction of the -OCF3 group influences the acidity, depending, however, on the position of a substituent, with the ortho isomer being the least acidic. Molecular and crystal structures of ortho and para isomers were determined by the single crystal XRD method. Hydrogen bonded dimers are the basic structural motives of the investigated molecules in the sol…

Models MolecularMagnetic Resonance SpectroscopyPotentiometric titrationSubstituentMolecular ConformationPharmaceutical ScienceContext (language use)Crystal structureMicrobial Sensitivity TestsDFTMedicinal chemistryArticleOCF<sub>3</sub>Analytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug StabilityIsomerismtrifluoromethoxyDrug DiscoveryMoleculePhysical and Theoretical ChemistryMolecular StructureHydrogen bondOrganic ChemistryBoronic AcidsNMRAnti-Bacterial AgentsantibacterialchemistryChemistry (miscellaneous)Intramolecular forceX-RayMolecular MedicineisomersOCF3Derivative (chemistry)Molecules (Basel, Switzerland)
researchProduct

Synthesis and characterization of 4,6-O-butylidene-N-(2-hydroxybenzylidene)-beta-D-glucopyranosylamine: crystal structures of 4,6-O-butylidene-alpha-…

2002

4,6-O-Butylidene-N-(2-hydroxybenzylidene)-β-D-glucopyranosylamine was synthesized and characterized using analytical, spectral and single-crystal X-ray diffraction methods. 1H and 13C NMR studies showed the presence of the β-anomer, which has also been confirmed by the crystal structure. The molecular structure of this compound showed the presence of the tridentate ONO ligation-core. Both precursors, 4,6-O-butylidene-α-D-glucopyranose and 4,6-O-butylidene-β-D-glucopyranosylamine were characterized using single crystal X-ray diffraction. The α-anomeric nature of the former and β-anomeric nature of the latter were proposed based on 1H NMR studies and were confirmed by determining the crystal …

Models MolecularMagnetic Resonance SpectroscopyStereochemistryCharacterizationCyclohexane conformationCrystal structureGlycosyl amines010402 general chemistryCrystallography X-Ray01 natural sciencesBiochemistryAnalytical ChemistrySingle-crystal X-ray diffractionX-Ray DiffractionCarbohydrate ConformationMoleculePyransGlucosamineMolecular Structure010405 organic chemistryChemistryHydrogen bondOrganic ChemistryHydrogen BondingGeneral Medicine[CHIM.MATE]Chemical Sciences/Material chemistry3. Good health0104 chemical sciencesCrystallographyIntramolecular forceX-ray crystallographyProton NMRCrystal StructureSingle crystal
researchProduct

Isostructural Dinuclear Phenoxo-/Acetato-Bridged Manganese(II), Cobalt(II), and Zinc(II) Complexes with Labile Sites: Kinetics of Transesterification…

2012

Using the dinucleating phenol-based ligand 2,6-bis[3-(pyridin-2-yl)pyrazol-1-ylmethyl]-4-methylphenol] (HL(2)), in its deprotonated form, the six new dinuclear complexes [M(II)(2)(L(2))(μ-O(2)CMe)(2)(MeCN)(2)][PF(6)] (M = Mn (2a), Co (3a), Zn (4a)) and [M(II)(2)(L(2))(μ-O(2)CMe)(2)(MeCN)(2)][BPh(4)] (M = Mn (2b), Co (3b), Zn (4b)) have been synthesized. Crystallographic analyses on 2b·2MeCN, 3b·2MeCN, and 4b·2MeCN reveal that these complexes have closely similar μ-phenoxo bis(μ-carboxylato) structures. The physicochemical properties (absorption and ESI-MS spectral data, 2a,b, 3a,b, and 4a,b; (1)H NMR, 4a,b) of the cations of 2a-4a are identical with those of 2b-4b. Each metal ion is termina…

Models MolecularManganeseEsterificationStereochemistryLigandchemistry.chemical_elementCobaltManganeseZincPyrazoleCrystallography X-RayMedicinal chemistryNitrophenolsInorganic ChemistryZincchemistry.chemical_compoundOrganophosphorus CompoundsDeprotonationchemistryCoordination ComplexesIntramolecular forcePhysical and Theoretical ChemistryIsostructuralCobaltInorganic Chemistry
researchProduct

Tuning molecular self-assembly on bulk insulator surfaces by anchoring of the organic building blocks.

2013

Molecular self-assembly constitutes a versatile strategy for creating functional structures on surfaces. Tuning the subtle balance between intermolecular and molecule-surface interactions allows structure formation to be tailored at the single-molecule level. While metal surfaces usually exhibit interaction strengths in an energy range that favors molecular self-assembly, dielectric surfaces having low surface energies often lack sufficient interactions with adsorbed molecules. As a consequence, application-relevant, bulk insulating materials pose significant challenges when considering them as supporting substrates for molecular self-assembly. Here, the current status of molecular self-ass…

Models MolecularMaterials scienceAnchoringNanotechnologyInsulator (electricity)Dielectricmolecular adsorption530Molecular self-assemblyMoleculeGeneral Materials ScienceComputer Simulationnon-contact atomic forceOrganic Chemicalsinsulating surfacesMechanical EngineeringIntermolecular forceElectric Conductivityself-assemblymolecule-surface interactionsModels ChemicalMechanics of MaterialsMetalsmicroscopySelf-assemblyNon-contact atomic force microscopyAdvanced materials (Deerfield Beach, Fla.)
researchProduct

Impact of local compressive stress on the optical transitions of single organic dye molecules

2012

The ability to mechanically control the optical properties of individual molecules is a grand challenge in nanoscience and could enable the manipulation of chemical reactivity at the single-molecule level. In the past, light has been used to alter the emission wavelength of individual molecules or modulate the energy transfer quantum yield between them. Furthermore, tensile stress has been applied to study the force dependence of protein folding/unfolding and of the chemistry and photochemistry of single molecules, although in these mechanical experiments the strength of the weakest bond limits the amount of applicable force. Here, we show that compressive stress modifies the photophysical …

Models MolecularMaterials scienceBiomedical EngineeringBioengineeringNanotechnologyImidesMicroscopy Atomic ForceMolecular physicslaw.inventionAdsorptionConfocal microscopylawMoleculeGeneral Materials ScienceEmission spectrumPhysics::Chemical PhysicsElectrical and Electronic EngineeringColoring AgentsPeryleneAtomic force microscopyEquipment DesignCondensed Matter PhysicsAtomic and Molecular Physics and OpticsCompressive strengthEnergy TransferMicroscopy FluorescenceOrganic dyeStress MechanicalNature Nanotechnology
researchProduct

Mechanical Properties of Pore-Spanning Lipid Bilayers Probed by Atomic Force Microscopy

2006

AbstractWe measure the elastic response of a free-standing lipid membrane to a local indentation by using an atomic force microscope. Starting point is a planar gold-coated alumina substrate with a chemisorbed 3-mercaptopropionic acid monolayer displaying circular pores of very well defined and tunable size, over which bilayers composed of N,N,-dimethyl-N,N,-dioctadecylammonium bromide or 1,2-dioleoyl-3-trimethylammonium-propane chloride were spread. Centrally indenting these “nanodrums” with an atomic force microscope tip yields force-indentation curves, which we quantitatively analyze by solving the corresponding shape equations of continuum curvature elasticity. Since the measured respon…

Models MolecularMaterials scienceMembrane FluidityLipid BilayersBiophysicsAnalytical chemistryFOS: Physical sciencesMechanicsMicroscopy Atomic ForceCurvatureIndentation hardnessHardnessIndentationMonolayerComputer SimulationHardness TestsParticle SizeComposite materialElasticity (economics)Lipid bilayerPhysics::Biological PhysicsMembranesFlexural modulus20399 Classical Physics not elsewhere classifiedElasticityMembraneModels ChemicalStress MechanicalPorosityBiophysical Journal
researchProduct

Pore Formation by a Bax-Derived Peptide: Effect on the Line Tension of the Membrane Probed by AFM

2007

AbstractBax is a critical regulator of physiological cell death that increases the permeability of the outer mitochondrial membrane and facilitates the release of the so-called apoptotic factors during apoptosis. The molecular mechanism of action is unknown, but it probably involves the formation of partially lipidic pores induced by Bax. To investigate the interaction of Bax with lipid membranes and the physical changes underlying the formation of Bax pores, we used an active peptide derived from helix 5 of this protein (Bax-α5) that is able to induce Bax-like pores in lipid bilayers. We report the decrease of line tension due to peptide binding both at the domain interface in phase-separa…

Models MolecularMembrane FluidityProtein ConformationLipid BilayersBiophysicsPeptide bindingPeptideMicroscopy Atomic ForceProtein structureBcl-2-associated X proteinMembrane fluiditySurface TensionComputer SimulationLipid bilayerbcl-2-Associated X Proteinchemistry.chemical_classificationLiposomeMembranesbiologyChemistryCell biologyMembraneModels ChemicalLiposomesbiology.proteinPorosityBiophysical Journal
researchProduct

3,5-diphenyl-1,2,4-triazin-6(1H)-one: synthesis, and X-ray and DFT-calculated structures.

2012

The title compound, C15H11N3O, (I), was obtained by the air oxidation of 3,5-diphenyl-4,5-dihydro-1,2,4-triazin-6(1H)-one. In the crystal structure, (I) forms centrosymmetric hydrogen-bonded dimers through pairs of N—H...N hydrogen bonds. The molecular structure of (I) deviates somewhat from planarity in the crystalline state, whereas a density functional theory (DFT) study predicts a completely planar conformation (Cspoint-group symmetry) for the isolated molecule. The solid-state conformation of (I) is stabilized by intramolecular hydrogen bonds,viz.one C—H...O interaction, which forms a six-membered ring, and three C—H...N interactions that each form five-membered rings. To estimate the …

Models MolecularMolecular StructureHydrogen bondChemistryTriazinesAromaticityElectronsHydrogen BondingGeneral MedicineCrystal structureRing (chemistry)Crystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyPlanarity testingCrystallographyIntramolecular forceMoleculeDensity functional theoryActa crystallographica. Section C, Crystal structure communications
researchProduct

4-Aminopyridinium 4-aminobenzoate dihydrate and 4-aminopyridinium nicotinate.

2009

In the title compounds, 4-aminopyridinium 4-aminobenzoate dihydrate, C(7)H(6)NO(2)(-).C(5)H(7)N(2)(+).2H(2)O, (I), and 4-aminopyridinium nicotinate, C(5)H(7)N(2)(+).C(6)H(4)NO(2)(-), (II), the aromatic N atoms of the 4-aminopyridinium cations are protonated. In (I), the asymmetric unit is composed of two 4-aminopyridinium cations, two 4-aminobenzoate anions and four water molecules, and the compound crystallizes in a noncentrosymmetric space group. The two sets of independent molecules of (I) are related by a centre of symmetry which is not part of the space group. In (I), the protonated pyridinium ring H atoms are involved in bifurcated hydrogen bonding with carboxylate O atoms to form an …

Models MolecularMolecular StructureHydrogen bondWaterHydrogen BondingPyridinium CompoundsGeneral MedicineCrystal structureRing (chemistry)Crystallography X-RayNiacinGeneral Biochemistry Genetics and Molecular BiologyAdductchemistry.chemical_compoundCrystallographychemistryIntramolecular forceMoleculeCarboxylatePyridiniumActa crystallographica. Section C, Crystal structure communications
researchProduct

Carbon nanorings: A challenge to theoretical chemistry

2006

High-level quantum-chemical methods show that the binding in the inclusion complex of hexamethylbenzene (HMB) in 6-cycloparaphenilacetylene (6-CPPA) cannot be explained only in terms of electrostatic interactions - caused by the polarization associated to curved π-conjugated systems - and the inclusion of dispersion forces is definitely needed. The theoretical description of van der Waals interactions is notoriously complicated and in fact some DFT methods cannot even predict the existence of the relatively small supramolecular nanoring studied here. However, ab initio MP2 calculations agree with experimental data and show that, in the considered complex, the HMB fragment is placed at the …

Models MolecularNanoringAtomic and Molecular Physics and OpticBinding energyAb initioThermodynamicsLondon dispersion forcechemistry.chemical_compoundMolecular dynamicsAb initio quantum chemistry methodsBenzene DerivativesTheoretical chemistryHexamethylbenzeneComputer SimulationPhysical and Theoretical ChemistryPolarization (electrochemistry)Ab initio calculationChemistryCycloparaffinsCarbonAtomic and Molecular Physics and OpticsNanostructuresInclusion compoundPhysical chemistryDispersion interactionDensity functional calculation
researchProduct