Search results for "self assembly"

showing 10 items of 14 documents

NEW GRAFT COPOLYMERS OF HYALURONIC ACID AND POLYLACTIC ACID: SYNTHESIS AND CHARACTERIZATION

2006

Abstract New graft copolymers have been synthesized, using hyaluronic acid (HA) as a hydrophilic backbone and polylactic acid (PLA) as an aliphatic polyester in order to obtain new polymeric derivatives of HA able to hydrophobically associate in an aqueous medium. Hyaluronic acid with low molecular weight was made soluble in organic solvent by transformation to its tetrabutylammonium (TBA) salt. Using the HA–TBA derivative, the reaction was performed in dimethylsulfoxide adding as a reagent the N -hydroxysuccinimide derivative of PLA. Two HA–PLA graft copolymers have been synthesized and characterized by FT-IR, 1 H NMR spectroscopy and gel permeation chromatography. The interaction between …

Aqueous solutionPolymers and PlasticsOrganic ChemistryChemical modificationhyaluronic acid self assemblyPolyelectrolytePolyesterHydrophobic effectGel permeation chromatographychemistry.chemical_compoundPolylactic acidchemistryPolymer chemistryMaterials ChemistryCopolymer
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Insights into the anion effect on the self assembly of perylene bisimide diimidazolium salts

2017

Abstract We studied how changing the anion affects the self-assembly of three diimidazolium salts bearing a perylene bisimide spacer. In particular we used [BF 4 − ] and [NTf 2 − ] based salts together with a mixed salt bearing both [I − ] and [BF 4 − ] anions. Thermal as well as concentration and temperature dependent spectroscopic investigations revealed that changing the anion impacts on solid state and solution aggregation, leading to articulate thermotropic behaviors and contrasting solvent effects, respectively. We also studied the electrochemical behavior of the salts to verify if changing the anion alters the redox properties of the salts. Finally, different anions also lead to very…

General Chemical EngineeringDiimidazolium saltSalt (chemistry)010402 general chemistryPhotochemistryElectrochemistry01 natural sciencesThermotropic crystalRedoxIonchemistry.chemical_compoundAnion effectPolymer chemistryChemical Engineering (all)chemistry.chemical_classification010405 organic chemistryProcess Chemistry and TechnologyDiimidazolium saltsAnion effect; Diimidazolium salts; Perylene bisimide; Self assembly; Chemical Engineering (all); Process Chemistry and TechnologySettore CHIM/06 - Chimica OrganicaSelf assembly0104 chemical scienceschemistryPerylene bisimideSelf-assemblySolvent effectsPeryleneDyes and Pigments
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The key role of hydrogen bonding in the nuclearity of three copper(II) complexes with hydrazone-derived ligands and nitrogen donor heterocycles

2011

International audience; Three new Cu(II) complexes of formula [Cu(L1)(pyz)(CH3OH)]ClO4 (1), [Cu(L1)(4,4′-bpy)(ClO4)]·0.5H2O (2) and [{Cu(L2)(ClO4)}2(μ-4,4′-bpy)] (3) have been synthesised by using pyrazine (pyz) and 4,4′-bipyridine (4,4′-bpy) and tridentate O,N,O-donor hydrazone ligands, L1H and L2H, obtained by the condensation of 1,1,1-trifluoro-2,4-pentanedione with salicyloylhydrazide and benzhydrazide, respectively. The ligands and their complexes have been characterized by elemental analyses, FT-IR, and UV–Vis spectroscopies. Single crystal X-ray structure analysis evidences the metal ion in a slightly deformed square pyramidal geometry in all the complexes. However complexes 1 and 2 …

Hydrogen bondingDenticityPyrazineStereochemistryHydrazonechemistry.chemical_elementAntiferromagnetic couplingCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical SciencesMonodentate pyz and 4Physical and Theoretical ChemistryCu(II) hydrazone complexescopper complexhydrazone ligandchemistry.chemical_classificationhydrogen bondHydrogen bondSelf assemblyCopperSquare pyramidal molecular geometry0104 chemical sciencesCrystallographychemistryCrystal structures4′-bpySingle crystalhydrogen bond; copper complex; hydrazone ligand
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Synthesis and cation-exchange properties of a bis-zwitterionic lamellar hybrid material

2008

The synthesis of a bis-zwitterionic lamellar hybrid material containing ammonium carboxylate groups is described. Cation-exchange properties of this material towards transition metal and lanthanide ions were studied as well as the regeneration and reuse of the material.

LanthanideseparationInorganic chemistry02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundTransition metalPolymer chemistryhybrid materialsMaterials ChemistryLamellar structureCarboxylateComputingMilieux_MISCELLANEOUSIon exchangeGeneral Chemistryself assembly[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryZwitterion[ CHIM.MATE ] Chemical Sciences/Material chemistrySelf-assembly0210 nano-technologyHybrid material
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A Columnar Liquid Crystal with Permanent Polar Order

2015

et al.

Materials scienceElectric fieldsCondensed matter physicsCrystalline materialsPolar orderSubphthalocyaninesGeneral ChemistryQuímicaPolarization (waves)Liquid crystalline materialsCondensed Matter::Soft Condensed MatterCondensed Matter::Materials ScienceDipoleCrystallographyLiquid crystalElectric fieldMaterials ChemistryMoleculePolarSelf assembly Columnar liquid crystalsLiquid Crystalline MaterialsColumnar phase
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Smart High-κ Nanodielectrics Using Solid Supported Polyoxometalate-Rich Nanostructures

2011

Utilizing Langmuir-Blodgett deposition and scanning probe microscopy, we have investigated the extent to which cations alter the self-assembly processes of hybrid polyoxometalates (POMs) on surfaces. The well-defined 2D hexagonal nanostructures obtained were extensively characterized and their properties were studied, and this has revealed fascinating dielectric behavior and reversible capacitive properties. The nanostructures are extremely stable under ambient conditions, and yet exhibit fascinating self-patterning upon heating. These findings present POMs as effective smart nanodielectrics and open up a new field for future POM applications. (c) 2011 American Chemical Society.

Materials scienceNanostructureMacromolecular SubstancesSurface PropertiesMolecular ConformationGeneral Physics and AstronomyNanotechnologyDielectricsurfacesSmart materialScanning probe microscopyMaterials TestingElectric ImpedanceIntelligent materialsGeneral Materials ScienceParticle SizeCation exchangesDielectric behaviorPolyoxometalateHexagonal crystal systemPolyoxometalatesGeneral EngineeringOxidesself-assemblyTungsten CompoundsSelf assemblyNanodielectricsNanostructuresHigh-κ NanodielectricSelf assembly processScanning probe microscopyLangmuir-Blodgett depositionPositive ionsPolyoxometalateSelf-assembly2D-hexagonalAmbient conditions
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An assembly of organic-inorganic composites using halloysite clay nanotubes

2018

Halloysite is natural tubular clay suitable as a component of biocompatible nanosystems with specific functionalities. The selective modification of halloysite inner/outer surfaces can be achieved by exploiting supramolecular and covalent interactions resulting in controlled colloidal stability adjusted to the solvent polarity. The functionalized halloysite nanotubes can be employed as reinforcing filler for polymers as well as carriers for the sustained release of active molecules, such as antioxidants, flame-retardants, corrosion inhibitors, biocides and drugs. The tubular morphology makes halloysite a perspective template for core-shell metal supports for mesoporous catalysts. The cataly…

Polymers and PlasticsHalloysite nanotube02 engineering and technologyReview01 natural sciencesunclassified drug adsorptionFlame retardantcovalent bondColloid and Surface ChemistryhalloysiteControlled drug deliverychemistry.chemical_classificationemulsionquantum dotSurfaces and InterfacesPolymerSelf assembly021001 nanoscience & nanotechnologynanorodPickering emulsionCorrosion inhibitoroil spillSolventSelective modification Kaolinite chemicals and drugNanorodBiocompatibility0210 nano-technologyOil water interfaceYarn Covalent interactionNanotubeMaterials scienceSupramolecular chemistrysustained drug releasecatalysiengineering.material010402 general chemistryHalloysitebioremediationPhysical and Theoretical ChemistryhydrophobicityMesoporous catalystpetroleummetal nanoparticlePhase interfacemetal bindingReinforcing fillerPickering emulsion0104 chemical sciencesOrganic-inorganic compositeNanotubeFilled polymerchemistryChemical engineeringengineeringSelf-assemblyCatalystMesoporous material
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SALI ORGANICI: “TECTONI” PER LO STUDIO DI PROCESSI DI SELF-ASSEMBLY IN SOLVENTI ORGANICI

Sali organiciQuenching amplificatoSettore CHIM/06 - Chimica OrganicaSelf assembly
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Organic Salts as Tectons for Self-assembly Processes in Solution

2022

The literature, covering the last decade, about the self-assembly processes of organic salts in conventional solvents was analyzed. In particular, data reported about imidazolium and ammonium salts have been considered. The analysis shows that these processes are highly determined by structural features of the salts. Indeed, besides the nature of the cationic head, features of the alkyl chain borne on the cation structure and its possible functionalization, as well as the nature of the anion play a pivotal role. These factors determine not only the nature of the solvent in which the process occurs but also the nature of the self-assembly mechanism. Consequently, the structure tunability of …

Settore CHIM/06 - Chimica OrganicaSelf assembly supramolecular chemistry electrostatic interactions.
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Self-assembly and intra-cluster reactions of erbium and ytterbium bis(2-ethylhexyl)sulfosuccinates in the gas phase.

2014

RATIONALE: The study of surfactant organization in vacuum allows surfactant–surfactant interaction to be unveiled in the absence of surrounding solvent molecules. Knowledge on their chemical-physical properties may also lead to the definition of more efficient gas-phase carriers, air-cleaning agents and nanoreactors. In addition, the presence of lanthanide-group ions adds unique photochemical properties to surfactants. METHODS: The structural features, stability and fragmentation patterns of charged aggregates formed by lanthanide- functionalized surfactants, ytterbium and erbium bis(2-ethylhexyl)sulfosuccinate ((AOT) 3 Yb and (AOT) 3 Er), have been investigated by electrospray ionization m…

Spectrometry Mass Electrospray IonizationSurface-Active AgentsSuccinatesself Assembly Mass spectrometry Lanthanides AOT Er YbGasesYtterbiumErbiumRapid communications in mass spectrometry : RCM
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