Search results for "MBL"

showing 10 items of 1636 documents

Nanoparticle Vesicles Through Self Assembly of Cyclodextrin- and Adamantyl-Modified Silica

2010

Stable nanoparticle vesicles were for the first time prepared from adamantyl- and cyclodextrin (CD)-modified silica nanoparticles forming host-guest interactions in aqueous solution. Adamantyl-functionalized nanoparticles were obtained from thiol-isocyanate reaction of thiol-modified nanoparticles with 1-adamantyl isocyanate. The CD modified silica particles were isolated from a reaction of mono-6-para-toluenesulfonyl-β-cyclodextrin with the thiol functionalized silica under microwave conditions in basic media. The obtained particles were characterized in respect of agglomeration and self-assembly behavior in aqueous solution by dynamic light scattering and transmission electron microscopy.…

chemistry.chemical_classificationAqueous solutionNanostructureMaterials sciencePolymers and PlasticsCyclodextrinVesicleOrganic ChemistryNanoparticleInclusion compoundchemistry.chemical_compoundDynamic light scatteringchemistryChemical engineeringPolymer chemistryMaterials ChemistrySelf-assemblyMacromolecular Rapid Communications
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Molecular Self-Assembly of Enantiopure Heptahelicene-2-Carboxylic Acid on Calcite (1014)

2012

Chirality can have a decisive influence on the molecular structure formation upon self-assembly on surfaces. In this paper, we study the structures formed by enantiopure (M)-heptahelicene-2-carboxylic acid ((M)-[7]HCA) on the calcite (10 (1) over bar4) cleavage plane under ultrahigh vacuum conditions. Previous noncontact atomic force microscopy studies have revealed that the racemic mixture of (M)-[7]HCA and (P)-[7]FICA (1:1) self-assembles into well-defined molecular double rows that are oriented along the calcite [01 (1) over bar0] direction. Here, we investigate the enantiopure (M)[7]HCA compound, resulting in distinctly different molecular structures upon deposition onto calcite (10 (1)…

chemistry.chemical_classificationCalciteStereochemistryCarboxylic acid530Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundGeneral EnergyEnantiopure drugchemistryMoleculeRacemic mixtureMolecular self-assemblyPhysical and Theoretical ChemistryEnantiomerChirality (chemistry)
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Scanning tunneling microscopy investigation of tricycloquinazoline liquid crystals on gold

2000

Self-assembled monolayers (SAMs) of hexaalkylthioether derivatives of tricycloquinazoline (TCQ) on Au(111) and tungsten diselenide (WSe2) were investigated by scanning tunneling microscopy (STM). The Au(111) surfaces were found to be etched by the thioether containing solutions. Corroded surfaces which are similar to gold surfaces that were coated with SAMs of thiols or disulfides were revealed by STM. Atomic adsorption spectroscopy proved that an amount of gold that corresponds to ca. 30% of a monolayer was dissolved in the assembly solutions. On gold, the aromatic cores of the molecules were found to be in face-on orientation. The alkyl substituents were in most cases folded upwards and s…

chemistry.chemical_classificationChemistryMetals and AlloysSelf-assembled monolayerSurfaces and InterfacesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionCrystallographychemistry.chemical_compoundAdsorptionLiquid crystallawMonolayerMaterials ChemistryOrganic chemistryTungsten diselenideSelf-assemblyScanning tunneling microscopeAlkylThin Solid Films
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Helicate Extension as a Route to Molecular Wires

2008

We describe the preparation of a helicate containing four closely spaced, linearly arrayed copper(I) ions. This product may be prepared either directly by mixing copper(I) with a set of precursor amine and aldehyde subcomponents, or indirectly through the dimerization of a dicopper(I) helicate upon addition of 1,2-phenylenediamine. A notable feature of this helicate is that its length is not limited by the lengths of its precursor subcomponents: each of the two ligands wrapped around the four copper(I) centers contains one diamine, two dialdehyde, and two monoamine residues. This work thus paves the way for the preparation of longer oligo- and polymeric structures. DFT calculations and elec…

chemistry.chemical_classificationChemistryOrganic ChemistryInorganic chemistryDynamic covalent chemistrychemistry.chemical_elementGeneral ChemistryElectrochemistryCopperCatalysisCoordination complexMolecular wirechemistry.chemical_compoundDelocalized electronCrystallographyDiamineddc:540Self-assemblyChemistry - A European Journal
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Synthesis and Coordination Chemistry of Lower Rim Cavitand Ligands

2001

chemistry.chemical_classificationChemistryOrganic ChemistryPolymer chemistryOrganic chemistryCavitandSelf-assemblyPhysical and Theoretical ChemistryCoordination complexEuropean Journal of Organic Chemistry
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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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