Search results for "Self-Assembly"

showing 10 items of 438 documents

Archaea Analogue Thiolipids for Tethered Bilayer Lipid Membranes on Ultrasmooth Gold Surfaces

2003

biologySurface PropertiesChemistryLipid BilayersMolecular ConformationNanotechnologyBiological membraneGeneral ChemistryModel lipid bilayerbiology.organism_classificationArchaeaCatalysisMembraneBilayer lipid membranesSpectroscopy Fourier Transform InfraredMonolayerBiophysicsGoldSulfhydryl CompoundsSelf-assemblyLipid bilayerArchaeaAngewandte Chemie International Edition
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Xyloglucan self-assembled nanostructures and gels for biomedical applications

biomedical applicationsXyloglucan; self-assembly; biomedical applicationsself-assemblySettore CHIM/07 - Fondamenti Chimici Delle TecnologieXyloglucan
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Guest-Induced Folding of the N-Benzyl Substituents in an Ammonium Resorcinarene Chloride and the Formation of a Halogen-Bonded Dimer of Capsules

2016

In methanol, N-benzyl ammonium resorcinarene chloride (Bn-NARCl) crystallizes as a solvate with the benzyl groups oriented in an open flower-like manner parallel to the cation–anion seam. 1,4-Dioxane as guest triggers a “semi-closed” single-molecule capsule with two benzyl “arms” enclosing the guest. The introduction of halogen bond (XB) donor 1,4-diiodoperfluorobutane (1,4-DIOFB) additionally folds the remaining two benzyl arms thus resulting in a fully closed capsule. Two 1,4-DIOFB molecules bridge two such Bn-NARCl capsules, forming a 2:2:2 XB held dimeric assembly of single-molecule capsules. The peculiar behavior was not observed in the bromide analog under similar experimental conditi…

capsulessupramolecular self-assembly processesStereochemistryDimer010402 general chemistry01 natural sciencesChloridechemistry.chemical_compoundBromidemedicineMoleculeGeneral Materials Scienceta116halogen-bonded dimersHalogen bondta114thermodynamically disfavored conformations010405 organic chemistryGeneral ChemistryResorcinareneCondensed Matter Physics0104 chemical sciencesCrystallographychemistryHalogenSingle crystalmedicine.drugCrystal Growth & Design
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Definition of the chalcogen bond (IUPAC Recommendations 2019)

2019

Abstract This recommendation proposes a definition for the term “chalcogen bond”; it is recommended the term is used to designate the specific subset of inter- and intramolecular interactions formed by chalcogen atoms wherein the Group 16 element is the electrophilic site.

chalcogen bond; IUPAC Organic and Biomolecular Chemistry Division; IUPAC Physical and Biophysical Chemistry Division; nomenclature; noncovalent interactions; self-assembly; supramolecular chemistryGeneral Chemical EngineeringChemical nomenclature010402 general chemistrynoncovalent interaction01 natural sciencessupramolecular chemistrykemialliset sidoksetnoncovalent interactionsChalcogenGroup (periodic table)supramolekulaarinen kemiaNon-covalent interactionsIUPAC Organic and Biomolecular Chemistry DivisionIUPAC Physical and Biophysical Chemistry Divisionchalcogen bondchemistry.chemical_classification010405 organic chemistryChemistryBondSolid State & Structural Chemistry Unitself-assemblyGeneral Chemistry0104 chemical sciencesTerm (time)ChemistryCrystallographyIntramolecular forcenimikkeistötnomenclaturePure and Applied Chemistry
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Reversible self-assembly of metal chalcogenide/metal oxide nanostructures based on Pearson hardness.

2010

Nanotechnology has reached a stage of development where not individual nanoparticles but rather systems of greater complexity are the focus of concern. These complex structures incorporate two or more types of materials, an example of which is the formation of metal–semiconductor hybrids, which effectively combine the properties of both materials. The assembly of multicomponent nanoparticles from constituents with different optical, electrical, magnetic, and chemical properties can lead to novel functionalities that are independent of the individual components and may be tailored to fit a specific application. These applications include such far-reaching challenges as solar energy conversio…

chalcogenides; HSAB principle; MnO nanoparticles; surface functionalization; WS2 nanotubesMaterials scienceNanostructureChalcogenideInorganic chemistryNanoparticleIonic bondingWS2 nanotubesGeneral ChemistryCatalysisMnO nanoparticleschemistry.chemical_compoundChemical engineeringchemistryMoleculeSurface modificationchalcogenidesSelf-assemblyHSAB principleBifunctionalsurface functionalizationAngewandte Chemie (International ed. in English)
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Kinetically Controlled Stepwise Self-Assembly of AuI-Metallopeptides in Water

2018

The combination of attractive supramolecular interactions of a hydrophobic AuI-metallopeptide with the shielding effect of flexible oligoethylene glycol chains provides access to a stepwise self-assembly of a AuI-metalloamphiphile in water. Kinetic control of the supramolecular polymer morphology is achieved using a temperature-dependent assembly protocol, which yields low dispersity supramolecular polymers (metastable state I) or helical bundled nanorods (state II).

chemistry.chemical_classification010405 organic chemistryChemistryDispersitySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryKinetic controlCatalysis0104 chemical sciencesSupramolecular polymersColloid and Surface ChemistryChemical engineeringMetastabilityShielding effectNanorodSelf-assemblyJournal of the American Chemical Society
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Self-assembly of an iron(ii)-based M5L6 metallosupramolecular cage

2011

A pentanuclear M(5)L(6) coordination cage is self-assembled in solution from a rigid linear heteroditopic phen-tpy ligand and an iron (II) salt.

chemistry.chemical_classification010405 organic chemistryLigandInorganic chemistryMetals and AlloysSalt (chemistry)General Chemistry010402 general chemistry01 natural sciencesCatalysis3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCoordination cagePolymer chemistryMaterials ChemistryCeramics and CompositesSelf-assemblyCageChemical Communications
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Effects of metal–ligand coordination on the self-assembly behaviour of a crown ether functionalised perylenetetracarboxylic diimide

2012

A novel perylenetetracarboxylic diimide (PDI) derivative, N,N′-di(4′-benzo-15-crown-5-ether)-1,7-di(4-tert-butyl-phenoxy)perylene-3,4;9,10-tetracarboxylic diimide (CRPDI), has been synthesised and characterised. Dimerisation of CRPDI is induced by the presence of K+ in CHCl3 or spontaneously occurs in methanol, as revealed by absorption and emission spectroscopy. In particular, the formation of co-facial dimer in the presence of K+ proceeds in a three-stage process, as indicated by absorption spectroscopy. The belt- and rope-like nanostructures of CRPDI fabricated from methanol and CHCl3 solution in the presence of K+ are obtained by scanning electron microscopy. Furthermore, the conductivi…

chemistry.chemical_classificationAbsorption spectroscopyStereochemistryLigandDimerGeneral ChemistryMetalCrystallographychemistry.chemical_compoundchemistryDiimidevisual_artvisual_art.visual_art_mediumSelf-assemblyAbsorption (chemistry)Crown etherSupramolecular Chemistry
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Odd-even chain length-dependent order in pH-switchable self-assembled layers.

2004

The reversible self-assembly of a series of bipolar amphiphiles, alpha,omega-bis(3- or 4-amidinophenoxy)alkanes (chain length n = 5-12), on mercaptoalkanoic acid-functionalized gold surfaces (chain length n = 10, 11, 14, 15) has been studied by in-situ ellipsometry, IR reflection absorption spectroscopy (IRAS), and atomic force microscopy (AFM). The layer order, amphiphile orientation, and tendency to form bilayers depends on the position of the amidine substituent, the alkyl chain length of both the amidine amphiphile and the underlying acid self-assembled monolayer (SAM), and whether the amidine alkyl chain contained an even or odd number of methylene groups. Thus, para-substituted bisben…

chemistry.chemical_classificationAbsorption spectroscopyStereochemistryOrganic ChemistrySubstituentGeneral ChemistryCatalysisAmidinechemistry.chemical_compoundCrystallographychemistryMonolayerAmphiphileSelf-assemblyMethyleneAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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2020

The pH-responsive nature of two self-assembled NDI-peptide amphiphile conjugates is reported. The diethoxy substituted NDI showed a pH-dependent assembly behaviour, as expected. In contrast, the isopropylamino- and ethoxy-substituted NDI based supramolecular polymer was stable at acidic and basic aqueous conditions. This finding highlights how subtle changes in the molecular design of π-stacked chromophore-peptide conjugates have a drastic impact on their equilibrium structure and ultimately functional properties.

chemistry.chemical_classificationAqueous solution010405 organic chemistryPeptideGeneral ChemistryChromophore010402 general chemistry01 natural sciencesCombinatorial chemistryFluorescence0104 chemical sciencesSupramolecular polymerschemistryAmphiphileSelf-assemblyLuminescenceChemistryOpen
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