Search results for "Self-assembly"

showing 10 items of 438 documents

On the Structure and Chiral Aggregation of Liquid Crystalline Star‐Shaped Triazines H‐Bonded to Benzoic Acids

2020

The ability of a star-shaped tris(triazolyl)triazine derivative to hierarchically build supramolecular chiral columnar organizations through the formation of H-bonded complexes with benzoic acids was studied from a theoretical and experimental point of view. The combined study has been done at three different levels including the study of the structure of the triazine core, the association with benzoic acids in stoichiometry 1:3, and the assembly of 1:3 complexes in helical aggregates. Although the star-shaped triazine core crystallizes in a non-C3 conformation, the C3 -symmetric conformation is theoretically predicted to be more stable and gives rise to a favorable C3 supramolecular 1:3 co…

Supramolecular chirality010405 organic chemistryOrganic ChemistrySupramolecular chemistryStackingMesophaseGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCrystallographychemistry.chemical_compoundchemistryLiquid crystalSelf-assemblyChirality (chemistry)TriazineChemistry – A European Journal
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Aqueous Supramolecular Polymers and Hydrogels

2019

Supramolecular polymerschemistry.chemical_classificationAqueous solutionChemical engineeringChemistrySelf-healing hydrogelsSelf-assembly
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New Quadratic Self-Assembly of Double-Decker Phthalocyanine on Gold(111) Surface : From Macroscopic to Microscopic Scale

2018

Unveiling the self-organization mechanism of semiconducting organic molecules onto metallic surfaces is the first step to design hybrid devices in which the self-assembling is exploited to tailor magnetic properties. In this study, double-decker rare-earth phthalocyanines, namely, lutetium phthalocyanine (LuPc2), are deposited on Au(111) gold surface forming large-scale self-assemblies. Global and local experimental techniques, namely, grazing incidence X-ray diffraction and scanning tunneling microscopy, supplemented by density functional theory calculations with van der Waals corrections, give insight into the molecular structural arrangement of the thin film and the self organization at …

Surface (mathematics)Materials science02 engineering and technology01 natural sciencesPhysical ChemistryMicroscopic scaleOrganic moleculesMetalchemistry.chemical_compoundQuadratic equation0103 physical sciencesPhysical and Theoretical Chemistry010306 general physicsComputingMilieux_MISCELLANEOUSFysikalisk kemi021001 nanoscience & nanotechnologyCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergychemistryChemical physicsvisual_art[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]visual_art.visual_art_mediumPhthalocyanineSelf-assembly0210 nano-technologyDouble deckerDen kondenserade materiens fysik
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Interfacial Self-Assembly to Spatially Organize Graphene Oxide Into Hierarchical and Bioactive Structures

2020

Multicomponent self-assembly holds great promise for the generation of complex and functional biomaterials with hierarchical microstructure. Here, we describe the use of supramolecular co-assembly between an elastin-like recombinamer (ELR5) and a peptide amphiphile (PA) to organize graphene oxide (GO) flakes into bioactive structures across multiple scales. The process takes advantage of a reaction—diffusion mechanism to enable the incorporation and spatial organization of GO within multiple ELR5/PA layers. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), and ImageJ software were used to demonstrate the hierarchical organization of GO flakes within the ELR5/PA lay…

TechnologyMaterials scienceBiocompatibilityScanning electron microscopeMaterials Science (miscellaneous)Materials Sciencecomposite materialsFABRICATIONMaterials Science Multidisciplinaryhierarchical biomaterialsNanotechnology02 engineering and technology010402 general chemistrylcsh:Technology01 natural scienceselastin-like recombinamerlaw.inventionDESIGNlawPeptide amphiphileBIOMATERIALS0912 Materials EngineeringCHITOSANScience & Technology1007 Nanotechnologylcsh:TGrapheneSCAFFOLD021001 nanoscience & nanotechnologyMicrostructurepeptide amphiphiles0104 chemical sciencesmulticomponent self-assemblyDIFFERENTIATIONMembraneTransmission electron microscopygraphene oxideSelf-assembly0210 nano-technologyFILMFrontiers in Materials
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Plasmonic nanostructures through DNA-assisted lithography

2018

DALI combines DNA origami with conventional top-down fabrication for creating designer high-resolution plasmonic nanostructures.

TechnologyMaterials scienceFabricationmaterials scienceta221ta220Nanotechnology02 engineering and technologySpectrum Analysis Raman010402 general chemistry01 natural sciencesplasmonicssymbols.namesakenanorakenteetnanostructuresDNA origamiDNA nanotechnologyComputer SimulationnanolithographyLithographyNanoscopic scaleResearch ArticlesPlasmonMultidisciplinaryta114PhysicsSciAdv r-articlesMetamaterialself-assemblyDNA021001 nanoscience & nanotechnologyoptics0104 chemical sciencesChemistryTemplateApplied Sciences and EngineeringsymbolsNucleic Acid ConformationPrintingDNA origami0210 nano-technologyRaman spectroscopyBiotechnologyResearch Article
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Photomodulation of Two-Dimensional Self-Assembly of Azobenzene-Hexa-peri-hexabenzocoronene-Azobenzene Triads

2019

International audience; Achieving exquisite control over self-assembly of functional polycyclic aromatic hydrocarbons (PAH) and nanographene (NG) is essential for their exploitation as active elements in (nano)technological applications. In the framework of our effort to leverage their functional complexity, we designed and synthesized two hexa-peri-hexabenzocoronene (HBC) triads, pAHA and oAHA, decorated with two light-responsive azobenzene moieties at the pseudo-para and ortho positions, respectively. Their photoisomerization in solution is demonstrated by UV–vis absorption. 1H NMR measurements of oAHA suggested 23% of Z-form can be obtained at a photostationary state with UV irradiation …

Technology[CHIM.MATE] Chemical Sciences/Material chemistryGeneral Chemical EngineeringHexa-peri-hexabenzocoronene[CHIM.MATE]Chemical Sciences/Material chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundAzobenzenechemistryMaterials ChemistrySelf-assembly0210 nano-technologyddc:600
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POSS-tetraalkylammonium salts: A new class of ionic liquids

2012

A series of new polyhedral oligomeric silsesquioxane ionic liquids (POSS-ILs) based on the trimethylpropylammonium dielectric constants, which, conversely, display slight differences originating from the nature of the anions. The long alkyl-chain substituents on the POSS core infer on this series of ILs an overall hydrophobic character and solution properties comparable to those of classic cationic surfactants, resulting in an effective extractant capability of polyanions from aqueous solutions. Their solution diffusion properties, as investigated by room-temperature dynamic light scattering, solution conductivity, density, and osmometric measurements, do not provide evidence for the occurr…

Thermogravimetric analysisAqueous solutionChemistryDielectricConductivitySilsesquioxaneionic liquids; self-assembly; Structure–activity relationships; Extraction capability; SilsesquioxanesInorganic Chemistrychemistry.chemical_compoundDifferential scanning calorimetryDynamic light scatteringPOSS Ionic LiquidIonic liquidPhysical chemistryOrganic chemistrySettore CHIM/02 - Chimica Fisica
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Facile Fabrication of Natural Polyelectrolyte-Nanoclay Composites: Halloysite Nanotubes, Nucleotides and DNA Study

2020

Complexation of biopolymers with halloysite nanotubes (HNTs) can greatly affect their applicability as materials building blocks. Here we have performed a systematic investigation of fabrication of halloysite nanotubes complexes with nucleotides and genomic DNA. The binding of DNA and various nucleotide species (polyAU, UMP Na2, ADP Na3, dATP Na, AMP, uridine, ATP Mg) by halloysite nanotubes was tested using UV-spectroscopy. The study revealed that binding of different nucleotides to the nanoclay varied but was low both in the presence and absence of MgCl2, while MgCl2 facilitated significantly the binding of longer molecules such as DNA and polyAU. Modification of the nanotubes with DNA an…

Thermogravimetric analysisNanotubeclay/polymer compositesPharmaceutical Sciencehalloysite nanotubesengineering.materialHalloysiteArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryNucleotidePhysical and Theoretical ChemistryDissolutionMechanical Phenomenachemistry.chemical_classificationNanotubesNucleotidesOrganic ChemistrySorptionDNAnucleotidenanoclay self-assemblyPolyelectrolytesPolyelectrolytenanoclayChemical engineeringchemistryUltrasonic WavesChemistry (miscellaneous)engineeringMolecular MedicineClayThermodynamicsDNAMolecules
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A Multi-Component Reaction towards the Development of Highly Modular Hydrogelators

2018

Herein we report a multi‐component reaction approach for the development of a new class of hydrogelators based on the OxoTriphenylHexanOate (OTHO) backbone. A focused library of OTHOs has been synthesized and their hydrogelation features evaluated. The two most potent hydrogelators were studied by rheology revealing different stiffness, appearances and thixotropic behavior of the gels. The new gelators showcase the versatility of the OTHO backbone as a platform for the design of functionalized hydrogels with tunable gel properties. peerReviewed

Thixotropymulticomponent reactionNanotechnologypi interactions010402 general chemistry01 natural sciencesCatalysispyridine N-oxideRheologyMulti-component reactionta116geelitkemiallinen synteesi010405 organic chemistryChemistrybusiness.industryOrganic ChemistryGeneral Chemistryself-assemblyModular designgels0104 chemical sciencesSelf-healing hydrogelsSelf-assemblybusiness
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Selective dimerisation of tetraurea calix[4]arenes

2010

The formation of hydrogen-bonded dimeric capsules from tetraurea calix[4]arenes is controlled by loops, connecting adjacent urea functions, and more or less bulky substituents. The dimerisation is only possible if loops are not overlapping and if the respective residues can pass the loops. A sorting scheme based on small and bulky residues and one to four loops allows reducing the number of possible dimers from 35 to 6 in a stoichiometric mixture of 11 ureas. With three different loop sizes (O–(CH2) n –O chains with n = 10, 14, 20 connecting adjacent phenylurea functions via their meta positions), it is possible to distinguish four urea residues of different sizes (small, medium, bulky and …

Trischemistry.chemical_compoundResidue (chemistry)chemistryHydrogen bondStereochemistryCalixareneUreaGeneral ChemistrySelf-assemblyStoichiometrySupramolecular Chemistry
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