Search results for "Supramolecular"

showing 10 items of 830 documents

Solution-processed thin films based on sandwich-type mixed (phthalocyaninato)(porphyrinato) europium triple-deckers: Structures and comparative perfo…

2012

The solution-processed thin films of a series of three sandwich-type mixed (phthalocyaninato)(porphyrinato) europium complexes with different numbers of hydroxyl groups at the meso-substituted phenyl groups of porphyrin ligand 1–3 were prepared by a quasi-Langmuir–Shafer (QLS) method. Examination by spectroscopic methods revealed that J-type aggregates have been formed with the increasing degree of order of molecular stacking 1 < 2 < 3 films. The IR and XRD results reveal that, a dimeric supramolecular structure was formed depending mainly on the π–π interaction between the tetrapyrrole cores of neighboring triple-decker molecules, which, as the building blocks, self-assembled into the targ…

NanostructureHydrogen bondIntermolecular forceInorganic chemistryMetals and AlloysSupramolecular chemistrychemistry.chemical_elementCondensed Matter PhysicsPorphyrinSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographychemistryMaterials ChemistryPhthalocyanineMoleculeElectrical and Electronic EngineeringEuropiumInstrumentationSensors and Actuators B: Chemical
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Chiral helical nanostructures based on amorphous abc-triblock copolymers

1995

So far all lattices of regular microdomain structures reported in the literature, either based on binary AB, ABA or ternary ABC block copolymers, can be described using simple symmetry elements like mirror planes, symmetry centers and rotation axes. The microphase separation in a linear ternary block copolymer consisting of three immiscible components namely polystyrene, polybutadiene and polymethyl methacrylate gives rise to the formation of a chiral supramolecular assembly in which chirality is not defined on a molecular (or macromolecular) level but only by the assembly of the linear triblock copolymer molecules. The polybutadiene (7, 12 wt.-%) phase forms helical strands surrounding the…

NanostructureMaterials sciencePolymers and PlasticsOrganic ChemistryCondensed Matter PhysicsSupramolecular assemblyCrystallographychemistry.chemical_compoundPolybutadienechemistryPolymer chemistryMaterials ChemistryCopolymerLamellar structurePolystyreneChirality (chemistry)Ternary operationMacromolecular Symposia
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Chemical modification of halloysite nanotubes for controlled loading and release.

2020

Clay minerals have been used for medical purposes from ancient times. Among them, the halloysite nanotube, an aluminosilicate of the kaolin group, is an emerging nanomaterial which possesses peculiar chemical characteristics. By means of suitable modifications, such as supramolecular functionalization or covalent modifications, it is possible to obtain novel nanomaterials with tunable properties for several applications. In this context the covalent grafting of suitable organic moieties on the external surface or in the halloysite lumen has been exploited to improve the loading and release of several biologically active molecules. The resulting hybrid nanomaterials have been applied as drug…

NanotubeMaterials scienceTunable properties Controlled drug deliveryHalloysite nanotubeBiomedical EngineeringSupramolecular chemistryNanotechnology02 engineering and technologyengineering.materialChemical characteristic010402 general chemistryYarn Biologically active molecule01 natural sciencesHalloysiteNanomaterialsAluminosilicateKaoliniteGeneral Materials ScienceFunctionalizationGene transferSettore CHIM/02 - Chimica FisicaTargeted drug deliveryCovalent modificationMoleculeGeneral ChemistryGeneral MedicineSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesNanostructured materialNanotubeSelf-healing hydrogelsengineeringTissue regenerationSurface modificationClay0210 nano-technologyDrug carrierHybrid nanomaterialChemical modificationCovalent graftingJournal of materials chemistry. B
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Natural eutectogels: sustainable catalytic systems for C–C bond formation reactions

2021

Natural eutecto gels were prepared combining properties of amino acids with the ones of deep eutectic solvents. Soft materials obtained were fully characterised determining the gel-sol transition temperatures and analysing mechanical and morphological features through rheological measurements and polarised optical microscopy. All eutecto gels were tested as catalytic reaction media for the enantioselective aldol reaction and, the best performing one was also used to carry out the Michael addition. In both cases, eutecto gels proved to have a great potential as sustainable reaction media, allowing to perform processes under mild conditions, obtaining excellent yields and, in some cases, also…

Natural eutecto gelsMaterials scienceEnantioselective synthesisC-C bond formation reactionsSettore CHIM/06 - Chimica OrganicaSustainable catalytic systemssupramolecular gels ionic liquids organocatalysiPollutionCatalysisSolventQuímica OrgánicaAldol reactionRheologyMichael reactionEnvironmental ChemistryOrganic chemistryaldol reactionEnantiomeric excessEutectic system
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Selectivity of cyclodextrins as a parameter to tune the formation of pseudorotaxanes and micelles supramolecular assemblies. A systematic SANS study

2011

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively. We studied the formation of polypseudorotaxanes formed with cyclodextrins (CDs) threading a copolymer chain that forms self-assembled structures in water. The size of the CD cavity was chosen such that it is block selective with respect to the formation of inclusion complexes and therefore in terms of altering the structure of the copolymer self-assemblies in a systematic fashio…

Neutron scattering supramolecular chemistry cyclodextrin pseudorotaxaneschemistry.chemical_classificationMaterials scienceCyclodextrinSupramolecular chemistry02 engineering and technologyGeneral ChemistryNeutron scattering010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesSmall-angle neutron scatteringMicelle0104 chemical sciencesCrystallographychemistryCopolymerddc:5300210 nano-technologySelectivityDissolutionSettore CHIM/02 - Chimica Fisica
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Nanoassemblies Based on Supramolecular Complexes of Nonionic Amphiphilic Cyclodextrin and Sorafenib as Effective Weapons to Kill Human HCC Cells

2015

Sorafenib (Sor), an effective chemiotherapeutic drug utilized against hepatocellular carcinoma (HOC), robustly interacts with nonionic amphiphilic cyclodextrin (aCD, SC6OH), forming, in aqueous solution, supramolecular complexes that behave as building blocks of highly water-dispersible colloidal nanoassemblies. SC6OH/Sor complex has been characterized by complementary spectroscopic techniques, such as UV-vis, steady-state fluorescence and anisotropy, resonance light scattering and H-1 NMR. The spectroscopic evidences and experiments carried out in the presence of an adamantane derivative, which competes with drug for CD cavity, agree with the entrapment of Sor in aCD, pointing out the role…

NiacinamideErythrocytesPolymers and PlasticsCell SurvivalAdamantaneDrug CompoundingSupramolecular chemistryBioengineeringNanotechnologyAdamantaneAntineoplastic AgentsBinding CompetitiveHemolysisAmphiphilic Cyclodextrins; Nanoparticles; Sorafenib; HCC cellsHCC cellsBiomaterialschemistry.chemical_compoundSurface-Active AgentsIn vivoCell Line TumorAmphiphileMaterials ChemistryHumanschemistry.chemical_classificationCyclodextrinsAqueous solutionCyclodextrinPhenylurea CompoundsSorafenibFluorescenceCombinatorial chemistrydigestive system diseasesNanostructuresBINDING INTERACTION THERAPY PHARMACOKINETICS BIOAVAILABILITY NANOPARTICLESDrug LiberationKineticsnanoassembliecyclodextrinchemistryDelayed-Action PreparationsProton NMRHepatocytes
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Buckyballs

2013

Buckyballs represent a new and fascinating molecular allotropic form of carbon that has received a lot of attention by the chemical community during the last two decades. The unabating interest on this singular family of highly strained carbon spheres has allowed the establishing of the fundamental chemical reactivity of these carbon cages and, therefore, a huge variety of fullerene derivatives involving [60] and [70]fullerenes, higher fullerenes, and endohedral fullerenes have been prepared. Much less is known, however, of the chemistry of the uncommon non-IPR fullerenes which currently represent a scientific curiosity and which could pave the way to a range of new fullerenes. In this revi…

Non-IPR fullereneMolecular wireFullereneMacromolecular chemistryEndohedral fullereneOrganic photovoltaicSettore CHIM/06 - Chimica OrganicaAsymmetric synthesiSupramolecular chemistry
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Novel deoxycholic acid alkylamide-phenylurea-derived organogelators

2010

Abstract Three monomeric and three dimeric deoxycholic acid (DCA) alkylamido-phenylurea derivatives are designed based on known gelators and are synthesized and characterized by 1 H and 13 C NMR spectroscopy, ESI-TOF mass spectrometry, and elemental analyses. Among them, a monomeric derivative forms supramolecular gels in CHCl 3 and chlorobenzene, whereas a dimeric derivative gels THF and higher 1-alkanols containing 7–10 carbons. The morphologies of their xerogels are studied by scanning electron microscopy (SEM). No signature of macroscopic chirality of the gels is visible.

Organic ChemistryDeoxycholic acidSupramolecular chemistryCarbon-13 NMRMass spectrometryBiochemistrychemistry.chemical_compoundMonomerchemistryChlorobenzeneDrug DiscoveryOrganic chemistryChirality (chemistry)SpectroscopyTetrahedron Letters
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Anion–π Interactions in Salts with Polyhalide Anions: Trapping of I 4 2−

2010

The directionality of interaction of electron-deficient π systems with spherical anions (e.g,. halides) can be controlled by secondary effects like NH or CH hydrogen bonding. In this study a series of pentafluorophenyl-substituted salts with polyhalide anions is investigated. The compounds are obtained by aerobic oxidation of the corresponding halide upon crystallization. Solid-state structures reveal that in bromide 2, directing NH-anion interactions position the bromide ion in an η(1)-type fashion over but not in the center of the aromatic ring. The same directing forces are effective in corresponding tribromide salt 3. In the crystal, the bromide ion is paneled by four electron-deficient…

Organic ChemistryInorganic chemistryChemieSupramolecular chemistryHalideGeneral ChemistryCrystal structureCatalysischemistry.chemical_compoundCrystallographychemistryBromideHalogenPi interactionTriiodideTribromideChemistry – A European Journal
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Improving the Robustness of Organic Semiconductors through Hydrogen Bonding

2021

Molecular organization plays an essential role in organic semiconductors since it determines the extent of intermolecular interactions that govern the charge transport present in all electronic applications. The benefits of hydrogen bond-directed self-assembly on charge transport properties are demonstrated by comparing two analogous pyrrole-based, fused heptacyclic molecules. The rationally designed synthesis of these materials allows for inducing or preventing hydrogen bonding. Strategically located hydrogen bond donor and acceptor sites control the solid-state arrangement, favoring the supramolecular expansion of the π-conjugated surface and the subsequent π-stacking as proved by X-ray d…

Organic electronicsMaterials scienceHydrogenHydrogen bondIntermolecular forceSupramolecular chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAcceptor0104 chemical sciencesOrganic semiconductorchemistryChemical physicsMoleculeGeneral Materials Science0210 nano-technologyACS Applied Materials &amp; Interfaces
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