Search results for "Effects"

showing 10 items of 2634 documents

Spontaneous Self-Assembly of a 1,8-Naphthyridine into Diverse Crystalline 1D Nanostructures: Implications on the Stimuli-Responsive Luminescent Behav…

2014

The previously reported organic solid-state fluorophore 7-(3,4-dimethoxyphenyl)-2-ethoxy-4-phenyl-1,8-naphthyridine-3-carbonitrile 1 was found to spontaneously self-organize into diverse 1D crystalline nanostructures by choosing appropriate liquid phase self-assembly conditions. Experimental results, as well as DFT quantum calculations (at the M06-2X/6-31+G(d) level), shed light on the aggregation mechanism. This was found in good agreement with molecules being primarily joined together through intermolecular alignment caused by electrostatic interactions, as well as minimization of the steric repulsions. This alignment provokes the preferential growth of the crystalline materials into 1D a…

Steric effectsMaterials scienceFluorophoreIntermolecular forceNanowireGeneral ChemistryCondensed Matter PhysicsFluorescenceCrystallographychemistry.chemical_compoundchemistryChemical physicsMoleculeGeneral Materials ScienceSelf-assemblyLuminescenceCrystal Growth & Design
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Effects of steric encumbrance of iridium( iii ) complex core on performance of solution-processed organic light emitting diodes

2020

Iridium(iii) complexes are the most frequently applied commercialized green and red emitters for organic light emitting diode (OLED) displays. Throughout years a significant research effort has been devoted to modify these compounds, in order to make them suitable for cost-effective solution-processing techniques, such as inkjet printing. To achieve this, the inherent tendency of the complex molecules to form poorly emissive aggregates needs to be suppressed. In many cases this has been achieved by an encapsulation of the iridium(iii) complex core with dendritic structures, composed of either passive or charge-transporting fragments. In order to validate this approach, we acquired three str…

Steric effectsMaterials scienceGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technologyTrapping010402 general chemistry7. Clean energy01 natural sciences:NATURAL SCIENCES:Physics [Research Subject Categories]OLEDMoleculeIridiumInkjet printingCommon emitterbusiness.industryGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSolution processedOrganic light emitting diodes (OLED)chemistryCharge trappingIridium compoundsOptoelectronics0210 nano-technologybusinessRSC Advances
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Influence of a sterically hindered amine on the photo-oxidation of low density/linear low density polyethylene blends

1990

Abstract Low density/linear low density polyethylene blends show a rate of degradation of the mechanical properties during photo-oxidation which increases with the content of the linear polymer. The use of a sterically hindered amine as UV stabilizer greatly improves the resistance of these blends to UV irradiation. The effectiveness of the stabilizer increases with the content of linear low density polyethylene.

Steric effectsMaterials sciencePolymers and PlasticsLinear polymerCondensed Matter PhysicsLinear low-density polyethyleneChemical engineeringMechanics of MaterialsPolymer chemistryMaterials ChemistryLow densityDegradation (geology)Amine gas treatingIrradiationStabilizer (chemistry)Polymer Degradation and Stability
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Effect of structural engineering of π-spacers on anti-aggregation of D–A–π–A dyes

2019

In this paper, the encapsulated insulated molecular wire (EIMW) and 2′,7′-bis(hexyloxy)spiro[cyclopenta[2,1-b:3,4-b′]dithiophene-4,9′-fluorene] (SPDF) were specifically designed as efficient anti-aggregation π-bridges for two novel D–A–π–A metal-free sensitizers (IBT1 and IBT2). Compared with the reference dye IBT3 with 3,3′-dihexyl-2,2′-bithiophene (DHBT) as an anti-aggregation π-bridge, both the dyes IBT1 with EIMW and IBT2 with SPDF as π-bridges can suppress intermolecular aggregation more efficiently. The π-bridge of SPDF shows the strongest anti-aggregation ability due to the rigid ‘T’ configuration among these dyes. Meanwhile, the π-bridge of EIMW shows better anti-aggregation ability…

Steric effectsMaterials sciencebusiness.industryIntermolecular forceAnti aggregation02 engineering and technologyGeneral ChemistryStructural engineering010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesMolecular wireMaterials Chemistry0210 nano-technologybusinessJournal of Materials Chemistry C
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Dual-stimuli pseudorotaxane switches under kinetic control

2021

A series of dumbbell-shaped sec-ammonium salts with bulky (pseudo)stoppers (‘speed bumps’) were tested for their ability to form pseudorotaxanes with a redox-switchable, tetrathiafulvalene (TTF)-decorated [24]crown-8 ether. Depending on the size of the pseudostoppers, fast (less than ten minutes), slow (hours to days) and very slow (no pseudorotaxanes observed) threading has been observed. NMR spectroscopy as well as tandem mass spectrometry indicate the formation of non-threaded face-to-face complexes prior to pseudorotaxanes formation. Both isomers can be distinguished by their substantially different stability in collision-induced dissociation (CID) experiments. Two external stimuli affe…

Steric effectsMechanical bond010405 organic chemistryOrganic ChemistryEtherNuclear magnetic resonance spectroscopy547010402 general chemistry01 natural sciencesDissociation (chemistry)pseudostoppers0104 chemical scienceschemistry.chemical_compoundCrystallographyDeprotonationchemistrysec-ammonium salts500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische ChemieMoietyTetrathiafulvalenepseudorotaxanes
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Electrostatic Contribution to the Surface Pressure of Charged Monolayers Containing Polyphosphoinositides

2008

Structural and functional studies of lateral heterogeneity in biological membranes have underlined the importance of membrane organization in biological function. Most inquiries have focused on steric determinants of membrane organization, such as headgroup size and acyl-chain saturation. This manuscript reports a combination of theory and experiment that shows significant electrostatic contributions to surface pressures in monolayers of phospholipids where the charge spacing is smaller than the Bjerrum length. For molecules with steric cross sections typical of phospholipids in the cell membrane (approximately 50 A(2)), only polyphosphoinositides achieve this threshold. The most abundant s…

Steric effectsModels MolecularMembrane FluiditySurface PropertiesLipid BilayersStatic ElectricityBiophysics010402 general chemistryBjerrum length01 natural sciences03 medical and health sciencesPhosphatidylinositol PhosphatesMonolayerMembrane fluidityPressureComputer SimulationLipid bilayer030304 developmental biology0303 health sciencesChromatographyMembranesHydrogen bondChemistryBiological membrane0104 chemical sciencesModels ChemicalChemical physicsIonic strength
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The role of fluorine in the stereoselective tandem Aza-Michael addition to acrylamide acceptors: An experimental and theoretical mechanistic study

2007

Aza-Michael additions of alpha-amino esters to fluorinated acceptors take place in a highly stereoselective manner, to give partially modified Psi-[NHCH2]retropeptides incorporating a hydrolytically stable trifluoroalanine mimic. The reaction mechanism has been investigated experimentally and theoretically, in order to explain the effect of the trifluoromethyl group on the reactivity and the origins of the experimentally observed stereocontrol. The reaction is a two-step process, involving a tandem aza-Michael addition followed by a stereoselective hydrogen transfer. Both steps are base-catalyzed. The high level of stereocontrol is the result of a combination of electrostatic interactions a…

Steric effectsModels MolecularReaction mechanismMagnetic Resonance SpectroscopyStereochemistrychemistry.chemical_elementStereoisomerismCatalysisMass Spectrometrychemistry.chemical_compoundComputational chemistrycalculationsReactivity (chemistry)density functionalAcrylamideTrifluoromethyldiastereoselectivity fluorine chemistryOrganic ChemistryStereoisomerismGeneral ChemistryFluorinechemistryFluorineMichael reactionpeptidesStereoselectivityMichael reaction
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Weak Interactions Modulating the Dimensionality in Supramolecular Architectures in Three New Nickel(II)-Hydrazone Complexes, Magnetostructural Correl…

2011

Three different ONO donor acetyl hydrazone Schiff bases have been synthesized from the condensation of acetic hydrazide with three different carbonyl compounds: salicylaldehyde (HL(1)), 2-hydroxyacetophenone (HL(2)), and 2, 3-dihydroxybenzaldehyde (HL(3)). These tridentate ligands are reacted with Ni(OOCCF(3))(2)·xH(2)O to yield three new Ni(II) complexes having distorted octahedral geometry at each Ni center: [Ni(L(1))(OOCCF(3))(CH(3)OH)](2) (1), [Ni(L(2))(OOCCF(3))(H(2)O)](2) (2), and [Ni(L(3))(L(3)H)](OOCCF(3))(H(2)O)(1.65)(CH(3)OH)(0.35) (3). The ligands and the complexes have been characterized by elemental analysis and IR and UV-vis spectroscopy, and the structures of the complexes ha…

Steric effectsModels MolecularStereochemistryMacromolecular SubstancesDimerSupramolecular chemistryHydrazoneAlkenes[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryCrystallography X-RayLigands01 natural sciencesCatalysisPhase TransitionInorganic Chemistrychemistry.chemical_compoundMagneticsNickelOctahedral molecular geometryMagnetic propertiesOrganometallic Compounds[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical SciencesPhysical and Theoretical Chemistrychemistry.chemical_classificationMolecular StructureCatalysts010405 organic chemistryChemistryHydrogen bondLigandHydrazonesHydrocarbons0104 chemical sciencesCrystallographySalicylaldehydeOligomersEpoxy Compounds
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Two dimensional self-assembly of bis-acylureas having various functional end groups.

2011

We present the synthesis and morphology study of thirteen bis-acylurea molecules with various functional end groups. The bis-acylureas have two acylurea groups, -NH-CO-NH-CO-, divided by a pentamethylene spacer, -(CH(2))(5)-, and two symmetric functional end groups, such as, aliphatic, benzyl, mono- and bi-thiophenyl, sulfur-containing, and propargyl (HC[triple bond]CCH(2)-) moieties. The bis-acylureas were synthesized by the coupling reactions of ureas with pimeloyl chloride or pimelic acid. Upon cooling from hot isotropic solutions, the bis-acylureas spontaneously form supermolecules. In the cases of aliphatic, benzyl, mono- and bi-thiophenyl functional groups, two dimensional supramolecu…

Steric effectsModels MolecularStereochemistrySupramolecular chemistryHydrogen BondingCrystal structureSupermoleculeCrystallography X-RaySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundCrystallographyEnd-groupColloid and Surface ChemistrychemistryPropargylFunctional groupMoleculeUreaJournal of colloid and interface science
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DNA interaction of new copper(II) complexes with sulfonamides as ligands

2007

New copper(II) complexes with sulfonamide ligands have been prepared and characterized. Sulfonamide ligands were prepared through a reaction between 8-aminoquinoline and either 2-mesitylene (Hqmesa), 4-tert-butylbenzene (Hqtbsa), or alpha-toluene (Halphaqtsa) sulfonyl chlorides. The structural analysis carried out for complex [Cu(alphaqtsa)(2)] indicated that the local environment of the Cu(II) cation is between a square planar and a tetrahedral geometry, with stacking of the benzene rings of the sulfonyl ligands between neighbor molecules. Powder EPR spectra at room temperature gave rhombic spectra for the [Cu(alphaqtsa)(2)] and [Cu(qmesa)(2)] complexes and an axial spectrum for the [Cu(qt…

Steric effectsMolecular Conformationchemistry.chemical_elementAscorbic AcidCrystallography X-RayPhotochemistryBiochemistryMedicinal chemistrylaw.inventionInorganic ChemistrylawOrganometallic CompoundsMoleculeSinglet stateElectron paramagnetic resonancechemistry.chemical_classificationSulfonylSulfonamidesMolecular StructureTetrahedral molecular geometryDNACopperIntercalating AgentsSulfonamidechemistryReactive Oxygen SpeciesCopperPlasmidsJournal of Inorganic Biochemistry
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