Search results for "supramolecular"

showing 10 items of 830 documents

Singlet and triplet energy transfer rate acceleration by additions of clusters in supramolecular pigment-organometallic cluster assemblies

2011

Both S(1) and T(1) energy transfer rates (porphyrin → cluster) increase from mono- to di- to tetracarboxylate[tetraphenyl-(zinc)porphyrin] adducts with [Pd(3)(dppm)(3)(CO)](2+) clusters.

Metals and AlloysSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryZincPhotochemistryPorphyrinCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdductchemistry.chemical_compoundPigmentchemistryvisual_artMaterials ChemistryCeramics and CompositesCluster (physics)visual_art.visual_art_mediumSinglet stateEnergy transfer rateChemical Communications
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Blue-emitting pyrene-based aggregates.

2015

The self-assembling features and gel formation of two pyrene imidazoles are presented. The supramolecular aggregation of these synthesised molecules results in an unusual blue-monomeric emission, which is rationalized by a combined experimental and theoretical investigation.

Metals and AlloysSupramolecular chemistrymacromolecular substancesGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMonomerchemistryPolymerizationMaterials ChemistryCeramics and CompositesBlue emittingPyreneChemical communications (Cambridge, England)
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A New Heterogeneous Catalyst Obtained via Supramolecular Decoration of Graphene with a Pd2+ Azamacrocyclic Complex

2019

A new G-(H2L)-Pd heterogeneous catalyst has been prepared via a self-assembly process consisting in the spontaneous adsorption, in water at room temperature, of a macrocyclic H2L ligand on graphene (G) (G + H2L = G-(H2L)), followed by decoration of the macrocycle with Pd2+ ions (G-(H2L) + Pd2+ = G-(H2L)-Pd) under the same mild conditions. This supramolecular approach is a sustainable (green) procedure that preserves the special characteristics of graphene and furnishes an efficient catalyst for the Cu-free Sonogashira cross coupling reaction between iodobenzene and phenylacetylene. Indeed, G-(H2L)-Pd shows an excellent conversion (90%) of reactants into diphenylacetylene under mild conditio…

Models MolecularChemical PhenomenaIodobenzeneMolecular ConformationPharmaceutical ScienceSonogashira couplingLigands010402 general chemistryHeterogeneous catalysiscross coupling01 natural sciencesArticleCoupling reactionAnalytical Chemistrylaw.inventionCatalysislcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryCoordination ComplexeslawDrug DiscoveryPolymer chemistryPhysical and Theoretical ChemistryDiphenylacetyleneMolecular Structurecatalysis010405 organic chemistryGrapheneSpectrum AnalysisOrganic ChemistrySonogashirapalladium catalystHydrogen-Ion Concentrationsupramolecular interactions0104 chemical sciencesSolutionsazamacrocycleschemistryPhenylacetyleneChemistry (miscellaneous)surface adsorptionMolecular MedicineGraphitecatalysis palladium catalyst; Sonogashira graphenePalladiumMolecules
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Simple chiral urea gelators, (R)- and (S)-2-heptylurea: their gelling ability enhanced by chirality.

2011

Abstract We present the first report on the synthesis of chiral ureas, ( R )- and ( S )-2-heptylurea, and their gelling behaviors. The ureas were prepared by the reactions of chiral amines and phenyl carbamate in the presence of triethylamine. On cooling from homogeneous solutions, the chiral ureas form gels in water and various nonpolar organic solvents, such as cyclohexane, toluene, and tetrachloromethane, while the racemate gelatinize only toluene and tetrachloromethane among the solvents we examined. The gelling ability of the enantiomeric urea is higher than the racemate, as the critical gelling concentrations in toluene, for example, were 0.2% and 0.7% (wt/wt), respectively. The enhan…

Models MolecularCyclohexaneMolecular StructureSupramolecular chemistryHydrogen BondingStereoisomerismCrystal structureCrystallography X-RayTolueneSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistrychemistryMicroscopy Electron ScanningOrganic chemistryUreaEnantiomerChirality (chemistry)TriethylamineGelsMethyl groupJournal of colloid and interface science
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Mannose-Decorated Multicomponent Supramolecular Polymers Trigger Effective Uptake into Antigen-Presenting Cells

2018

A modular route to prepare functional self-assembling dendritic peptide amphiphiles decorated with mannosides, to effectively target antigen-presenting cells, such as macrophages, is reported. The monomeric building blocks were equipped with tetra(ethylene glycol)s (TEGs) or labeled with a Cy3 fluorescent probe. Experiments on the uptake of the multifunctional supramolecular particles into murine macrophages (Mφs) were monitored by confocal microscopy and fluorescence-activated cell sorting. Mannose-decorated supramolecular polymers trigger a significantly higher cellular uptake and distribution, relative to TEG carrying bare polymers. No cytotoxicity or negative impact on cytokine producti…

Models MolecularDendrimersMannosidesBiocompatibilitySupramolecular chemistryAntigen-Presenting Cells010402 general chemistry01 natural sciencesBiochemistryPolyethylene GlycolsMiceSurface-Active Agentschemistry.chemical_compoundAmphiphileAnimalsAntigen-presenting cellMolecular BiologyCells CulturedFluorescent Dyeschemistry.chemical_classificationMicroscopy Confocal010405 organic chemistryMacrophagesOrganic ChemistryBiological TransportCarbocyaninesCell sorting0104 chemical sciencesSupramolecular polymerschemistryMannosidesBiophysicsMolecular MedicinePeptidesEthylene glycolChemBioChem
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Three-Component Entanglements Consisting of Three Crescent-Shaped Bidentate Ligands Coordinated to an Octahedral Metal Centre

2007

3,3'-biisoquinoline ligands (biiq) L, bearing aromatic substituents on their 8 and 8' positions, have been used to generate interwoven systems consisting of three crescent-shaped ligands disposed around an octahedral metal centre. Mono-ligand complexes of the type [ReL(CO)3py]+ (py: pyridine) have also been prepared, leading to sterically non-hindering complexes in spite of the endotopic nature of the chelate used. The three-component entanglements have been prepared by using either FeII or RuII as gathering metal centre. The synthetic procedure is simple and efficient, affording fully characterised complexes as their PF6 or SbCl6 salts. X-ray crystallography clearly shows that the crescent…

Models MolecularLigand field theorySteric effectsDenticityMolecular StructureLigandTrans effectStereochemistryChemistryIronOrganic ChemistryCatenaneMolecular ConformationSupramolecular chemistryGeneral ChemistryCrystallography X-RayLigandsRutheniumCatalysisCrystallographychemistry.chemical_compoundPyridineOrganometallic CompoundsQuinolinesHydrophobic and Hydrophilic InteractionsChemistry - A European Journal
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Biocompatible Hydrogelators Based on Bile Acid Ethyl Amides

2016

Four novel bile acid ethyl amides were synthetized using a well-known method. All the four compounds were characterized by IR, SEM, and X-ray crystal analyses. In addition, the cytotoxicity of the compounds was tested. Two of the prepared compounds formed organogels. Lithocholic acid derivative 1 formed hydrogels as 1% and 2% (w/v) in four different aqueous solutions. This is very intriguing regarding possible uses in biomedicine. peerReviewed

Models MolecularLithocholic acidBiocompatibilitymedicine.drug_classClinical Biochemistrysupramolecular hydrogelMolecular ConformationBiocompatible Materials02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryMicechemistry.chemical_compoundEndocrinologybiocompatibilityAmidemedicineAnimalsOrganic chemistrybile acidMolecular Biologyta116PharmacologyAqueous solutionBile acidOrganic Chemistryta1182WaterHydrogels3T3 Cellsself-assembly021001 nanoscience & nanotechnologyAmidesamide0104 chemical scienceschemistryBiochemistrySelf-healing hydrogelsLithocholic AcidSelf-assembly0210 nano-technologyDerivative (chemistry)
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Autonomous artificial nanomotor powered by sunlight

2006

Light excitation powers the reversible shuttling movement of the ring component of a rotaxane between two stations located at a 1.3-nm distance on its dumbbell-shaped component. The photoinduced shuttling movement, which occurs in solution, is based on a “four-stroke” synchronized sequence of electronic and nuclear processes. At room temperature the deactivation time of the high-energy charge-transfer state obtained by light excitation is ≈10 μs, and the time period required for the ring-displacement process is on the order of 100 μs. The rotaxane behaves as an autonomous linear motor and operates with a quantum efficiency up to ≈12%. The investigated system is a unique example of an artif…

Models MolecularLuminescenceMagnetic Resonance SpectroscopyTime FactorsRotaxaneLightRotaxanesUltraviolet RaysPhotochemistryMovementMolecular ConformationElectronsPhotochemistryAbsorptionQUIMICA ORGANICAPhenothiazinesRotaxaneElectrochemistryNanotechnologyNanomotorAbsorption (electromagnetic radiation)Molecular machinePhotolysisMultidisciplinaryChemistrybusiness.industryMolecular Motor ProteinsPhotodissociationTemperatureLinear motorKineticsNanoscienceFluid solutionSpectrophotometryPhysical SciencesSunlightOptoelectronicsQuantum efficiencyElectronicsLuminescencebusinessSupramolecular chemistry
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Crystalline supramolecular organic frameworksviahydrogen-bonding between nucleobases

2021

We report a crystalline supramolecular framework assembled by H-bonding interactions between covalently fused monomers equipped with two guanine-cytosine nucleobase pairs.

Models MolecularMacromolecular SubstancesSupramolecular chemistrymacromolecular substances010402 general chemistry01 natural sciencesCatalysisNucleobasechemistry.chemical_compoundNucleic AcidsPolymer chemistryMaterials Chemistry010405 organic chemistryHydrogen bondtechnology industry and agricultureMetals and AlloysHydrogen BondingGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMonomerchemistryCovalent bondCeramics and CompositesNucleic Acid Conformationsense organsChemical Communications
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Molecular Rearrangement of an Aza-Scorpiand Macrocycle Induced by pH: A Computational Study †

2016

Rearrangements and their control are a hot topic in supramolecular chemistry due to the possibilities that these phenomena open in the design of synthetic receptors and molecular machines. Macrocycle aza-scorpiands constitute an interesting system that can reorganize their spatial structure depending on pH variations or the presence of metal cations. In this study, the relative stabilities of these conformations were predicted computationally by semi-empirical and density functional theory approximations, and the reorganization from closed to open conformations was simulated by using the Monte Carlo multiple minimum method Financial support by the Spanish Ministerio de Economía y Competitiv…

Models MolecularMontecarlo Mètode deMonte Carlo method01 natural sciencessupramolecular chemistryMonte Carlo Multiple Minimumlcsh:ChemistryComputational chemistryaza-scorpiandsMolecular rearrangementpH controlled; supramolecular chemistry; synthetic receptors; aza-scorpiands; semi-empirical; Density Functional Theory; Monte Carlo Multiple Minimumlcsh:QH301-705.5semi-empiricalSpectroscopyDensity Functional TheoryDensity functionalsSpatial structureChemistryGeneral MedicineHydrogen-Ion ConcentrationMolecular machineComputer Science ApplicationsMonte Carlo methodpH controlledvisual_artsynthetic receptorsvisual_art.visual_art_mediumDensity functional theoryMonte Carlo MethodMacrocyclic CompoundsSupramolecular chemistry010402 general chemistryQuímica supramolecularCatalysisArticleInorganic ChemistryMetalQuantitative Biology::Subcellular ProcessesPhysical and Theoretical ChemistryMolecular BiologyAza CompoundsFuncional de densitat Teoria del010405 organic chemistryOrganic ChemistryComputational Biology0104 chemical scienceslcsh:Biology (General)lcsh:QD1-999Synthetic ReceptorsQuantum TheorySupramolecular chemistryInternational Journal of Molecular Sciences
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