Search results for "Self-assembly"

showing 10 items of 438 documents

Molecular association of small amphiphiles: Origin of ionic liquid properties in dibutyl phosphate/propylamine binary mixtures

2018

Abstract Binary mixtures of liquid surfactants, owing to the amphiphilic nature of the molecules involved, can exhibit nano-segregation and peculiar transport properties. The amphiphilicity, and consequently the resulting self-assembly, can be tuned by changing the length of the alkyl chains and the nature of the polar head group. So, in the present study, the structural and dynamic properties of dibutyl phosphate/propylamine liquid mixtures at various compositions have been investigated by Wide Angle X-ray Scattering (WAXS), FT-IR, rheometry and dielectric spectroscopy in order to study the intermolecular association taking place when alkylphosphates and alkylamines with a small apolar par…

Steric effectspropylaminePropylamine02 engineering and technologyDielectric010402 general chemistry01 natural sciencesionic liquidschemistry.chemical_compoundMaterials ChemistryMoleculePhysical and Theoretical ChemistrySpectroscopyAlkylchemistry.chemical_classificationamphiphilesIntermolecular forceself-assembly021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsDielectric spectroscopychemistryChemical physicsdibutyl phosphateIonic liquid0210 nano-technology
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Surface functionalization and surface recognition: Plasmon optical detection of molecular recognition at self assembled monolayers

1991

The synthesis of biotin- functionalized organic mercaptans and their chemisorption on gold surfaces is described. Biotin bound covalently to self assembled monolayers is recognized by streptavidin from aqueous buffer solutions. Spacer length and packing density of the biotin labels on the organic surface determine the docking kinetics. With a flexible and hydrophilic spacer very fast -diffusion controlled-docking is observed. As an alternative method of self assembly the spreading of organic mercaptans on water surfaces is established. Pressure-area diagrams of different functionalized mercaptans and disulfides are shown and their monolayer properties are discussed.

StreptavidinPolymers and PlasticsChemistryOrganic ChemistrySelf-assembled monolayerCondensed Matter PhysicsCombinatorial chemistrychemistry.chemical_compoundMolecular recognitionChemisorptionMonolayerMaterials ChemistryOrganic chemistrySurface modificationSelf-assemblyPlasmonMakromolekulare Chemie. Macromolecular Symposia
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Functionalized lipid tubules as tools for helical crystallization of proteins

1997

The development of functional supramolecular devices built by self-assembly of elementary molecules and with bioactive properties arouses considerable interest in the field of nanotechnology and new materials. We report here the formation of a new class of lipid tubules exhibiting both properties of molecular recognition and crystal formation for the protein streptavidin. These lipid tubules, made of biotin-containing dioctadecylamine molecules, are straight hollow cylinders with a constant diameter of 27 nm and variable length up to several micrometers. They are unilamellar with an inner diameter of about 16 nm, as shown by cryoelectron microscopy. Streptavidin binds to the biotinylated tu…

StreptavidinliposomesSupramolecular chemistryTWO-DIMENSIONAL CRYSTALSMEMBRANESCatalysisACETYLCHOLINE-RECEPTORVESICLESlipidschemistry.chemical_compoundTOXIN B-SUBUNITMolecular recognition2-DIMENSIONAL CRYSTALLIZATIONELECTRON-MICROSCOPYLiposomeChemistryVesicleOrganic Chemistrytechnology industry and agricultureCHOLERA-TOXINGeneral ChemistryCrystallographyMembranehelical structuresRESOLUTIONBiotinylationSelf-assemblyself-assembly tubulesMICROSTRUCTURESChemistry – A European Journal
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Decisive influence of substitution positions in molecular self-assembly

2014

Molecular self-assembly provides a versatile tool for creating functional molecular structures at surfaces. A rational design of molecular structure formation requires not only an in-depth understanding of the subtle balance between intermolecular and molecule-surface interactions, but might also involve considering chemical changes of the molecules, such as deprotonation. Here, we present a systematic investigation of a comparatively simple class of molecules, namely dihydroxybenzoic acid, which, nevertheless, enables creating a rich variety of structures when deposited onto calcite (10.4) held at room temperature. Based on non-contact atomic force microscopy measurements in ultra-high vac…

Structure formationChemistryStereochemistrySubstitution (logic)Intermolecular forceRational designGeneral Physics and AstronomyProtonation530CrystallographyDeprotonationMoleculeMolecular self-assemblyPhysical and Theoretical Chemistry
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Dual-Mode Chiral Self-Assembly of Cone-Shaped Subphthalocyanine Aromatics

2020

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/jacs.0c07291

SubphthalocyanineChemistryThermodynamic equilibriumDimerStackingSupramolecular chemistryPorphyrinoidsSelf-assemblyQuímicaGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryEnantiopure drugPolymerizationChemical physicsLiquid crystalSupramolecular PolymersSelf-assembly
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Self-assembled aggregates of amphiphilic perylene diimide-based semiconductor molecules: effect of morphology on conductivity.

2011

Abstract Two amphiphilic perylenetetracarboxylic diimide derivatives modified with different side chains at imide nitrogen, N- n -hexyl-N′-(2-hydroxyethyl)-1,7-di(4′-t-butyl)phenoxy-perylene-3,4:9,10-tetracarboxylic diimide ( PDI 1 ) and N,N′-di(2-hydroxyethyl)-1,7-di(4′-t-butyl)phenoxy-perylene-3,4:9,10-tetracarboxylic diimide ( PDI 2 ), were fabricated into organic nanostructures via solution-phase self-assembly. Their self-assembling properties in methanol and n -hexane have been comparatively studied by electronic absorption, fluorescence, and Fourier transform infrared spectroscopy (FT-IR). The morphologies and structures of the self-assemblies were examined by scanning electronic micr…

SubstituentAnalytical chemistryInfrared spectroscopySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsCrystallographychemistry.chemical_compoundColloid and Surface ChemistrychemistryDiimideSide chainMoleculeSelf-assemblyFourier transform infrared spectroscopyPeryleneJournal of colloid and interface science
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How deprotonation changes molecular self-assembly – an AFM study in liquid environment

2013

We study the influence of Alizarin Red S deprotonation on molecular self-assembly at the solid-liquid interface of the natural cleavage plane of calcite immersed in aqueous solution. To elucidate the adsorption details, we perform pH dependent high-resolution atomic force microscopy measurements. When Alizarin Red S is deposited onto calcite(10.4) in a liquid environment at an acidic pH of 5, weakly bound, ordered islands with a (3 x 3) superstructure are observed. A sharp structural transition is revealed when increasing the pH above 8. Above this pH, stable needle-like structures oriented along the [01.0] direction form on the surface. Comparing these results with potentiometric titration…

SuperstructureAqueous solutionChemistryPotentiometric titrationInorganic chemistryALIZARIN REDProtonationGeneral ChemistryCondensed Matter Physics530CrystallographyDeprotonationAdsorptionMolecular self-assemblySoft Matter
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Organic nanosheets with charged surface: two dimensional self-assembly of a non-symmetric bis-acylurea with pyridyl end group

2011

We present a novel non-symmetric bis-acylurea that self-assembles into two dimensional nanosheet superstructures. The bis-acylurea (PyrC8Bn) has a pyridyl and a benzyl end group divided by a spacer group [–NHCONHCO–(CH2)8–CONHCONH–, C8] with two hydrogen bonding sites. Upon cooling a hot solution in ethanol, the molecule self-assembles into multilayered nanosheet structures due to the intermolecular biaxial hydrogen bonding. The surface charge of the nanosheets could be switched between positive and neutral by adjusting the pH. The charged character of the nanosheets was utilized in immobilizing negatively charged gold nanoparticles. An attempt to regulate the self-assembly allowed us to fi…

SuperstructureEnd-groupCrystallographyMaterials scienceHydrogen bondColloidal goldInorganic chemistryMoleculeGeneral ChemistrySelf-assemblySurface chargeCondensed Matter PhysicsNanosheetSoft Matter
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Hierarchical Self-Assembly of Supramolecular Spintronic Modules into 1D- and 2D-Architectures with Emergence of Magnetic Properties

2004

Hierarchical self-assembly of complex supramolecular architectures allows for the emergence of novel properties at each level of complexity. The reaction of the ligand components A and B with Fe II cations generates the (2 K 2) grid-type functional building modules 1 and 2, presenting spin-tran- sition properties and preorganizing an array of coordination sites that sets the stage for a second assembly step. Indeed, binding of La III ions to 1 and of Ag I ions to 2 leads to a 1D columnar superstructure 3 and to a wall-like 2D layer 4, respectively, with concomitant modulation of the magnetic properties of 1 and 2. Thus, to each of the two levels of structural complexity generat- ed by the t…

SuperstructureSpintronicsLigandChemistryOrganic ChemistrySupramolecular chemistrySpin transitionNanotechnologyGeneral ChemistrySelf-assemblyLayer (object-oriented design)CatalysisStructural complexityChemistry - A European Journal
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Photocontrolled On-Surface Pseudorotaxane Formation with Well-Ordered Macrocycle Multilayers.

2016

The photoinduced pseudorotaxane formation between a photoresponsive axle and a tetralactam macrocycle was investigated in solution and on glass surfaces with immobilized multilayers of macrocycles. In the course of this reaction, a novel photoswitchable binding station with azobenzene as the photoswitchable unit and diketopiperazine as the binding station was synthesized and studied by NMR and UV/Vis spectroscopy. Glass surfaces have been functionalized with pyridine-terminated SAMs and subsequently with multilayers of macrocycles through layer-by-layer self assembly. A preferred orientation of the macrocycles could be confirmed by NEXAFS spectroscopy. The photocontrolled deposition of the …

Supramolecular chemistryTetralactam macrocyclesurface chemistry02 engineering and technology010402 general chemistryLinear dichroismPhotochemistry01 natural sciencessupramolecular chemistryCatalysischemistry.chemical_compoundSpectroscopyta116pseudorotaxanesphotochemistryOrganic ChemistryGeneral Chemistry021001 nanoscience & nanotechnologyXANES0104 chemical sciencesazobenzeneAzobenzenechemistryNexafs spectroscopySelf-assembly0210 nano-technologyChemistry (Weinheim an der Bergstrasse, Germany)
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