Search results for "Self-Assembly"

showing 10 items of 438 documents

Multicomponent polymeric micelles based on polyaspartamide as tunable fluorescent pH-window biosensors

2010

Abstract PHEA-PEG 5000 -C 16 is a polyaspartamide polymer with appended hydrophilic PEG 5000 functions and hydrophobic n-C 16 units forming biocompatible micelles with a CAC as low as 1.8 × 10 −7  M. The protonation and acidity constants of the polymer's amino and carboxylic groups have been determined by potentiometric titrations at five different concentrations higher than CAC, finding concentration-independent values. Viscosity and polarity of the micellar core have been investigated by means of fluorescent probes, finding local values comparable to those of pure toluene and to the core of sodium dodecyl sulphate micelles, independently on the protonation degree of the polymer. The fluor…

FluorophorePolymeric micelles Fluorescent biosensor PH window Self-assemblinGInorganic chemistryPotentiometric titrationBiomedical EngineeringBiophysicsProtonationBiosensing TechniquesMicellePolyethylene Glycolschemistry.chemical_compoundElectrochemistryOrganic chemistryMicellesPolyhydroxyethyl Methacrylatechemistry.chemical_classificationEquipment DesignGeneral MedicinePolymerHydrogen-Ion ConcentrationEquipment Failure AnalysisSpectrometry FluorescencechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPyreneSelf-assemblyPeptidesBiosensorBiotechnologyBiosensors and Bioelectronics
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Of Thiols and Disulfides: Methods for Chemoselective Formation of Asymmetric Disulfides in Synthetic Peptides and Polymers.

2018

In protein or peptide chemistry, thiols are frequently chosen as a chemical entity for chemoselective modification reactions. Although it is a well-established methodology to address cysteines and homocysteines in aqueous media to form S-C bonds, possibilities for the chemoselective formation of asymmetric disulfides have been less approached. Focusing on bioreversibility in conjugation chemistry, the formation of disulfide bonds is highly desirable for the attachment of thiol-containing bioactive agents to proteins or in cross-linking reactions, because disulfide bonds can combine stability in blood with degradability inside cells. In this Concept article, recent approaches in the field of…

Free RadicalsPolymersPeptide02 engineering and technologyConjugated system010402 general chemistryMicroscopy Atomic Force01 natural sciencesCatalysisPolymerizationReactivity (chemistry)DisulfidesSulfhydryl CompoundsProtecting groupSolid-Phase Synthesis Techniqueschemistry.chemical_classificationAqueous mediumOrganic ChemistryGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryThiolQuantum TheorySelf-assembly0210 nano-technologyPeptidesChemistry (Weinheim an der Bergstrasse, Germany)
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Self-Assembly-Directed Organization of a Fullerene–Bisporphyrin into Supramolecular Giant Donut Structures for Excited-State Charge Stabilization

2021

Functional materials composed of spontaneously self-assembled electron donor and acceptor entities capable of generating long-lived charge-separated states upon photoillumination are in great demand as they are key in building the next generation of light energy harvesting devices. However, creating such well-defined architectures is challenging due to the intricate molecular design, multistep synthesis, and issues associated in demonstrating long-lived electron transfer. In this study, we have accomplished these tasks and report the synthesis of a new fullerene–bis-Zn-porphyrin e-bisadduct by tether-directed functionalization of C60 via a multistep synthetic protocol. Supramolecular oligom…

FullereneSupramolecular structures and assembliesChemistrySupramolecular chemistryGeneral ChemistryBiochemistryAcceptorArticleCatalysisElectron transferColloid and Surface ChemistryCharge transferChemical structureChemical physicsExcited stateEnergy levelMoleculePyrrolesSelf-assemblyMolecular structure
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Substrate templating guides the photoinduced reaction of C60on calcite

2014

cited By 7; International audience; A substrate-guided photochemical reaction of C60 fullerenes on calcite, a bulk insulator, investigated by non-contact atomic force microscopy is presented. The success of the covalent linkage is evident from a shortening of the intermolecular distances, which is clearly expressed by the disappearance of the moiré pattern. Furthermore, UV/Vis spectroscopy and mass spectrometry measurements carried out on thick films demonstrate the ability of our setup for initiating the photoinduced reaction. The irradiation of C60 results in well-oriented covalently linked domains. The orientation of these domains is dictated by the lattice dimensions of the underlying c…

Fullerenescanning probe microscopysurface chemistry02 engineering and technologyMicroscopy Atomic Force010402 general chemistry01 natural sciencesChemical reaction530CatalysisCalcium CarbonateScanning probe microscopychemistry.chemical_compoundSpectroscopyCalcite[PHYS]Physics [physics]Spectrum AnalysisIntermolecular forcefullerenesGeneral Chemistrycovalent networksself-assemblyPhotochemical Processes021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographychemistryChemical physicsCovalent bondSelf-assembly0210 nano-technology
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Fonctionnalisation et métallisation des diamantoïdes

2015

The thesis deals with development of synthetic methods for preparation of novel carbon-metal organohybrid based on diamondoid and palladium. The vapor pressure of various diamondoids was measured from a new measurement protocol at solid-vapor thermodynamic equilibrium state. Their volatile tendency opened a possibility to do deposition from gas phase and at various pressure (ambient, primary vacuum, and high vacuum) of diamondoids on silicon or mica substrates. SEM observations have shown that depending on the type of functional groups on the diamondoid, different crystal shapes can be produced (rods, needles, triangles, truncated octahedral form).OMCVD of palladium on functionalized diaman…

Functionalized diamondoidfunctionalized diamondoidsOMCVD de palladiumChemistry & allied sciencesPd OMCVDhybrid materialair-stable phosphineAir-stable phosphineorganic self-assemblyOrganic self-assembly[CHIM.OTHE] Chemical Sciences/Other[ CHIM.OTHE ] Chemical Sciences/Otherddc:540[CHIM.OTHE]Chemical Sciences/OtherHybrid material
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The Gelling Ability of Some Diimidazolium Salts: Effect of Isomeric Substitution of the Cation and Anion

2013

The gelling ability of some geminal imidazolium salts was investigated both in organic solvents and in water solution. Organic salts differing either in the cation or anion structure were taken into account. In particular, the effects on the gel-phase formation of isomeric substitution on the cation or anion as well as of the use of mono- or dianions were evaluated. As far as the cation structure is concerned, isomeric cations, such as 3,3′-di-n-octyl-1,1′-(1,4-phenylenedimethylene)diimidazolium and 3,3′-di-n-octyl-1,1′-(1,3-phenylenedimethylene)diimidazolium, were used. On the other hand, in addition to the bromide anion, isomeric dianions, such as the 1,5- and 2,6-naphthalenedisulfonate a…

GeminalScanning electron microscopeOrganogels Self-Assembly Imidazolium saltsInorganic chemistrySubstitution (logic)General ChemistrySettore CHIM/06 - Chimica OrganicaResonance (chemistry)IonSolventchemistry.chemical_compoundchemistryBromidePolymer chemistrySelf-assembly
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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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Hybrid Organic-Inorganic Nanostructures Fabricated from Layer-by-Layer Self-Assembled Multilayers of Hyperbranched Polyglycerols and Phosphorus Dendr…

2007

Multilayer thin films of cationic phosphorous dendrimers and anionic hyperbranched polyglycerols were fabricated by electrostatic layer-by-layer (LbL) self-assembly (SA). The film formation was monitored by surface plasmon resonance (SPR) spectroscopy and UV-visible spectroscopy, and it was found that the stepwise, alternating deposition results in a linear growth up to four bilayers. Hybrid organic-TiO2 nanostructures were generated by exposing the supramolecular multilayers to TiCl4 precursors. The amounts of TiO2 incorporated inside the scaffolds could be tuned by controlling the porosity of the multilayers with the addition of a small amount of salts. The resulting hybrid films exhibit …

GlycerolMaterials scienceMacromolecular SubstancesPolymersSurface PropertiesMolecular ConformationBiomedical EngineeringBioengineeringChemical vapor depositionDendrimerMaterials TestingPolymer chemistryNanotechnologyGeneral Materials ScienceOrganic ChemicalsParticle SizeSurface plasmon resonanceThin filmTitaniumNanocompositeLayer by layerMembranes ArtificialPhosphorusGeneral ChemistryCondensed Matter PhysicsNanostructuresChemical engineeringInorganic ChemicalsSelf-assemblyCrystallizationHybrid materialJournal of Nanoscience and Nanotechnology
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Controlled Crystallization of CaCO3on Hyperbranched Polyglycerol Adsorbed to Self-Assembled Monolayers

2005

The formation of biominerals by living organisms is governed by the cooperation of soluble and insoluble macromolecules with peculiar interfacial properties. To date, most of the studies on mineralization processes involve model systems that only account for the existence of one organic matrix and thus disregard the interaction between the soluble and insoluble organic components that is crucial for a better understanding of the processes taking place at the inorganic-organic interface. We have set up a model system composed of a matrix surface, namely, a self-assembled monolayer (SAM), and a soluble component, hyperbranched polyglycerol. The model mineral calcium carbonate displays diverse…

GlycerolPolymersBiocompatible MaterialsCalcium Carbonatelaw.inventionchemistry.chemical_compoundAdsorptionBiomimeticslawMonolayerElectrochemistryOrganic chemistryGeneral Materials ScienceCrystallizationMicellesSpectroscopyAlkylchemistry.chemical_classificationMineralsSelf-assembled monolayerSurfaces and InterfacesCondensed Matter PhysicsCalcium carbonatechemistryChemical engineeringAdsorptionSelf-assemblyCrystallizationMacromoleculeLangmuir
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Halogen bond directionality translates tecton geometry into self-assembled architecture geometry

2013

The structures of halogen-bonded infinite chains involving two diiodoperfluoroalkanes and a bent bis(pyrid-4′-yl)oxadiazole show that the geometry of the pyridyl pendant rings is translated into the angle between the formed halogen bonds.

Halogen bondhalogen bond self-assemblyBent molecular geometryOxadiazoleGeometryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsSelf assembledchemistry.chemical_compoundchemistryHalogenDirectionalityGeneral Materials Science
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