Search results for "assembly"

showing 10 items of 768 documents

Cover Feature: Mannose-Decorated Multicomponent Supramolecular Polymers Trigger Effective Uptake into Antigen-Presenting Cells (ChemBioChem 9/2018)

2018

chemistry.chemical_classificationChemistryOrganic ChemistrySupramolecular chemistryMannosePolymerBiochemistryCombinatorial chemistrySupramolecular polymerschemistry.chemical_compoundFeature (computer vision)AmphiphileMolecular MedicineCover (algebra)Self-assemblyMolecular BiologyChemBioChem
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Buildup of ultrathin multilayer films by a self-assembly process: III. Consecutively alternating adsorption of anionic and cationic polyelectrolytes …

1992

A solid substrate with a positively charged planar surface is immersed in a solution containing an anionic polyelectrolyte and a monolayer of the polyanion is adsorbed. Since the adsorption is carried out at relatively high concentrations of polyelectrolyte, a large number of ionic residues remain exposed to the interface with the solution and thus the surface charge is effectively reversed. After rinsing in pure water the substrate is immersed in the solution containing a cationic polyelectrolyte. Again a monolayer is adsorbed but now the original surface charge is restored. By repeating both steps in a cyclic fashion, alternating multilayer assemblies of both polymers are obtained. The bu…

chemistry.chemical_classificationChemistrySmall-angle X-ray scatteringMetals and AlloysCationic polymerizationAnalytical chemistrySurfaces and InterfacesPolymerPolyelectrolyteSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdsorptionChemical engineeringMonolayerMaterials ChemistrySelf-assemblySurface chargeThin Solid Films
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Non-Centrosymmetric Homochiral Supramolecular Polymers of Tetrahedral Subphthalocyanine Molecules

2015

This is the peer reviewed version of the following article: Angewandte Chemie - International Edition 54.8 (2015): 2543-2547, which has been published in final form at http://dx.doi.org/10.1002/anie.201411272. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving

chemistry.chemical_classificationCircular dichroismMaterials scienceSubphthalocyanineSupramolecular chemistryStackingPorphyrinoidsGeneral MedicineGeneral ChemistrySelf-assemblyQuímicaCatalysisSupramolecular polymersCrystallographychemistryPolymerizationPolymer chemistryMoleculeSelf-assemblyChirality (chemistry)Homochiral aggregatesSupramolecular polymerization
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Multilayer Thin Films by Layer-by-Layer Assembly of Hole- and Electron-Transport Polyelectrolytes: Optical and Electrochemical Properties

2006

In this paper, we pressent the synthesis of a series of p-type and n-type semicondnctring polyelectrolytes with triarylamine, oxadiazole, thiarliazole and triazine moictes. The synthesized polymeric hole and electrom iransport materials were examined optically and electrochemically using UV/Vis spectroscopy. PL spectroscopy and CV. Based on the optical and electrochemical data, each of the energy levels were calculated and all values suggested that the were promising hole-(p-type) or alectron=transprot (n-type) materials for devices. Moreover, the synthesized ionie polymers were suitable for LBL thin film deposition from ditute polymer solutions and the multilayers were fully characterized …

chemistry.chemical_classificationConductive polymerPhotoluminescenceMaterials sciencePolymers and PlasticsOrganic ChemistryLayer by layerPolymerCondensed Matter PhysicsPolyelectrolytechemistryPolymer chemistryMaterials ChemistrySelf-assemblyPhysical and Theoretical ChemistryThin filmSpectroscopyMacromolecular Chemistry and Physics
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Inter- and intramolecular non-covalent interactions in 1-methylimidazole-2-carbaldehyde complexes of copper, silver, and gold

2014

Abstract Three new imidazole compounds, [CuBr2(mimc)2] (1), [Ag(mimc)2][CF3SO3] (2), and [AuCl3(mimc)] (3) (mimc = 1-methylimidazole-2-carbaldehyde), have been synthesized, structurally characterized, and further analyzed using the QTAIM analysis. The compounds exhibit self-assembled 3D networks arising from intermolecular non-covalent interactions such as metallophilic interactions, metal-π contacts, halogens–halogen interactions, and hydrogen bonds. These weak interactions have a strong impact on the coordination sphere of the metal atoms and on the packing of compounds 1, 2, and 3.

chemistry.chemical_classificationCoordination sphereHydrogen bondStereochemistryIntermolecular forceGeneral ChemistryCondensed Matter Physicschemistry.chemical_compoundchemistryIntramolecular forcePolymer chemistryImidazoleNon-covalent interactionsGeneral Materials ScienceSelf-assemblyta1161-MethylimidazoleSolid State Sciences
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Racemic and Optically Pure Heptahelicene-2-carboxylic Acid: Its Synthesis and Self-Assembly into Nanowire-Like Aggregates (Eur. J. Org. Chem. 5/2011)

2011

The cover picture shows heptahelicene-2-carboxylic acid, whose synthesis and self-assembly are central to the article. The background features Prague's riverbank, which is intermixed with the nanowire-like aggregates of heptahelicene-2-carboxylic acid. The alignment of the swans makes the link between self-assembly and the Prague view. Details are discussed in the article by I. G. Stara, I. Starý, A. Kuhnle et al. on p. 853 ff. Background photo by M. Bělohradský.

chemistry.chemical_classificationCrystallographyChemistryStereochemistryCarboxylic acidOrganic ChemistryNanowireCover (algebra)Self-assemblyPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion

2015

The different natures of the weakly coordinating anions – triflate or perchlorate – in the Cu2+-mediated self-assembly of cytidine monophosphate nucleotide play a fundamental role in the homochiral resolution process, yielding one-dimensional copper(II) coordination polymers of opposite helicity that can be easily inverted, in a reversible way, by changing the nature of the anion as revealed by circular dichroism experiments both in solution and in the solid state.

chemistry.chemical_classificationCytidine monophosphateCircular dichroismStereochemistryAbsolute configurationGeneral ChemistryPolymerHelicityPerchloratechemistry.chemical_compoundCrystallographychemistrySelf-assemblyTrifluoromethanesulfonateChemical Science
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Supramolecular organic-inorganic hybrid assemblies with tunable particle size: interplay of three noncovalent interactions.

2013

chemistry.chemical_classificationDendrimersMaterials scienceSupramolecular chemistryNanoparticleMetal NanoparticlesNanotechnologyGeneral ChemistrySulfidesCatalysisPolyelectrolyteColloidchemistryMicroscopy Electron TransmissionOrganic inorganicCadmium CompoundsNon-covalent interactionsSelf-assemblyParticle sizeGoldParticle SizeColoring AgentsAngewandte Chemie (International ed. in English)
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Self-assembly of a chiral three-dimensional manganese(II)-copper(II) coordination polymer with a double helical architecture

2013

The use of the anionic dicopper(ii) complex, [CuII(mpba) 2]4- [mpba = N,N′-1,3-phenylenebis(oxamate)], as tetrakis(bidentate) metalloligand toward MnII ions in the presence of oxalate and the chiral (S)-trimethyl-(1-phenylethyl)ammonium cation affords the first example of a mixed oxalato/oxamato-based chiral 3D metal-organic polymer. © 2013 The Royal Society of Chemistry.

chemistry.chemical_classificationDenticityCoordination polymerInorganic chemistrychemistry.chemical_elementGeneral ChemistryPolymerManganeseCondensed Matter PhysicsCopperOxalateIonchemistry.chemical_compoundchemistryPolymer chemistryGeneral Materials ScienceSelf-assemblyCrystEngComm
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On the behaviour of the (Z)-Phenylhydrazones of some 5-alkyl-3-benzoyl-1,2,4-oxadiazoles in solution and in the gas phase: kinetic and spectrometric …

2008

Abstract Rate constants, k A,R , for the rearrangement of the ( Z )-phenylhydrazones ( 1a – e ) of a series of 5-alkyl-3-benzoyl-1,2,4-oxadiazoles substituted at C(5) with linear alkyl chains of different length (from C 4 up to C 12 ) into the relevant 4-acylamino-2,5-diphenyl-1,2,3-triazoles ( 2a – e ) have been measured in dioxan/water in the base-catalyzed region (pS + 10.5–12.6). For each substrate log  k A,R are linearly related to pS + . The significant decrease of the slopes of these straight lines (from 0.96 down to 0.78) upon increasing the length of the linear alkyl chain at C(5) and that of the reactivity (down to 14–26%) upon increasing the substrate concentration suggest a decr…

chemistry.chemical_classificationDirect evidenceStereochemistryOrganic ChemistrySubstrate (chemistry)124-oxadiazoleKinetic energyBiochemistryCrystallographyReaction rate constantchemistryDrug DiscoveryProton NMRReactivity (chemistry)Self-assemblymononuclear rearrangementAlkyl
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