Search results for "calixarene"

showing 10 items of 149 documents

Functionalized Calix[8]arenes, Synthesis and Self-assembly on Graphite

2005

With the intention of building hollow tubular structures by self-assembly, we have designed and successfully synthesized a series of calix[8]arene derivatives. Their phenolic units were functionalized in p-position by various groups which are able to interact via hydrogen bonding or π−π stacking. Ethynyl, amide, urea, or imide links were chosen for the covalent attachment of these functional groups, to ensure the adjustment of an optimal distance for their interaction. Two different kinds of nanostructures self-assembled on a highly oriented pyrolytic graphite (HOPG) surface were found by scanning force microscopy:  parallel aligned nanorods in which the calixarene molecules are adsorbed ed…

Materials scienceHydrogen bondGeneral Chemical EngineeringStackingGeneral Chemistrychemistry.chemical_compoundHighly oriented pyrolytic graphitechemistryCalixarenePolymer chemistryMaterials ChemistryOrganic chemistryNanorodSelf-assemblyGraphiteImideChemistry of Materials
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Size- and Structure-Selective Noncovalent Recognition of Saccharides by Tetraethyl and Tetraphenyl Resorcinarenes in the Gas Phase

2008

The noncovalent complexation of tetraethyl and tetraphenyl resorcinarenes with mono-, di-, and oligosaccharides was studied with negative-polarization electrospray ionization quadrupole ion trap and electrospray ionization Fourier-transform ion cyclotron resonance mass-spectrometric analysis. The saccharides formed 1:1 complexes with deprotonated resorcinarenes, which exhibited clear size and structure selectivity in their complexation. In the case of the monosaccharides, hexoses formed much more abundant and kinetically stable complexes than pentoses or deoxyhexoses. A comparison of the mono-, di-, and oligosaccharides revealed that both the relative abundance and stability of the complexe…

Models MolecularCellobiosePhenylalanineElectrospray ionizationCarbohydratesCrystallography X-RayMass spectrometryMass SpectrometryCatalysisSubstrate SpecificityDeprotonationPolymer chemistryCarbohydrate ConformationOrganic chemistryQuadrupole ion trapHost–guest chemistrychemistry.chemical_classificationOrganic ChemistryGeneral ChemistryOligosaccharideResorcinareneKineticschemistryGasesCalixarenesIon cyclotron resonanceChemistry - A European Journal
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Picomolar inhibition of cholera toxin by a pentavalent ganglioside GM1os-calix[5]arene

2013

Cholera toxin (CT), the causative agent of cholera, displays a pentavalent binding domain that targets the oligosaccharide of ganglioside GM1 (GM1os) on the periphery of human abdominal epithelial cells. Here, we report the first GM1os-based CT inhibitor that matches the valency of the CT binding domain (CTB). This pentavalent inhibitor contains five GM1os moieties linked to a calix[5]arene scaffold. When evaluated by an inhibition assay, it achieved a picomolar inhibition potency (IC50 = 450 pM) for CTB. This represents a significant multivalency effect, with a relative inhibitory potency of 100000 compared to a monovalent GM1os derivative, making GM1os-calix[5]arene one of the most potent…

Models MolecularCholera ToxinbindingStereochemistrydesignCalix[5]areneEpithelial cellsG(M1) GangliosideHeat-labile enterotoxinmedicine.disease_causeligandBiochemistrycrystalMultivalency effectsCholeraCausative agentsmedicinePotencyHumansoligosaccharidePhysical and Theoretical ChemistryIC50Vibrio choleraeheat-labile enterotoxinVLAGchemistry.chemical_classificationgm1 mimicsGangliosideInhibition assaysChemistryCholera toxinOrganic ChemistryOligosaccharideBinding domainLigand (biochemistry)ValenciesOrganische ChemiehexamethylenetetramineChemistryPositive ionsaffinityAntitoxinsCalixarenesrecognitionBinding domain
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Piperazine bridged resorcinarene cages.

2010

The one-pot Mannich condensation of resorcinarenes with piperazine and an excess of formaldehyde under high dilution conditions results in a helical cage, namely, a covalently linked dimer of two resorcinarenes connected via four piperazine bridges in yields ranging from 20 to 40%. The compounds were analyzed by NMR spectroscopy, ESI mass spectrometry, and single crystal X-ray diffraction. The helical cages can encapsulate small guest molecules by adapting the cavity volume by changing the helical pitch according to the guest size.

Models MolecularDimerPhenylalanineOrganic ChemistryFormaldehydeMolecular ConformationStereoisomerismNuclear magnetic resonance spectroscopyResorcinareneCrystallography X-RayBiochemistryPiperazineschemistry.chemical_compoundPiperazinechemistryCovalent bondPolymer chemistryMoleculeOrganic chemistryPhysical and Theoretical ChemistryCalixarenesSingle crystalPiperazineOrganic letters
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Selective recognition of neutral guests in an aqueous medium by a biomimetic calix[6]cryptamide receptor

2015

The design of artificial receptors that can efficiently work in water is a challenging research area. A possible biomimetic approach for the elaboration of such receptors consists of associating a hydrophobic cavity with a polar polyfunctional binding site. On this basis, a hydrophilic calix[6]cryptamide decorated with oligo(ethylene glycol) units (i.e. 8) was synthesized through an efficient [1 + 1] macrocyclization reaction as the key-step. The complexation of neutral molecules was evaluated by NMR spectroscopy through competition experiments either in apolar or aqueous media. In both media, host 8 can bind neutral species that display H-bonding acceptor and donor groups such as amides or…

Models MolecularEthylene GlycolMagnetic Resonance SpectroscopyStereochemistryAllosteric regulationMolecular ConformationCrystallography X-Ray010402 general chemistry01 natural sciencesBiochemistrychemistry.chemical_compoundBiomimetic MaterialsCalixareneUreaMoleculeaqueous mediumartificial receptorsbiomimeticsPhysical and Theoretical ChemistryBinding siteta116010405 organic chemistryHydrogen bondOrganic ChemistryWaterHydrogen BondingNuclear magnetic resonance spectroscopyAmidesAcceptor0104 chemical scienceschemistryCyclizationCalixarenesHydrophobic and Hydrophilic InteractionsEthylene glycolOrganic & Biomolecular Chemistry
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Polymorphism control of an active pharmaceutical ingredient beneath calixarene-based Langmuir monolayers.

2014

This communication demonstrates the possibility to nucleate and grow different crystalline polymorphic forms of gabapentin (GBP) using, as nucleation templates, Langmuir monolayers of an amphiphilic calixarene at different packing densities.

Models MolecularLangmuirCyclohexanecarboxylic AcidsNucleation02 engineering and technology010402 general chemistry01 natural sciencesCatalysisAmphiphileCalixareneMonolayerMaterials ChemistryOrganic chemistryAminesta116gamma-Aminobutyric AcidActive ingredientMolecular StructureChemistryMetals and AlloysGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineeringPolymorphism (materials science)Pharmaceutical PreparationsCeramics and CompositesCalixarenesGabapentin0210 nano-technologyChemical communications (Cambridge, England)
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Mechanically interlocked calix[4]arene dimers display reversible bond breakage under force.

2009

The physics of nanoscopic systems is strongly governed by thermal fluctuations that produce significant deviations from the behaviour of large ensembles1,2. Stretching experiments of single molecules offer a unique way to study fundamental theories of statistical mechanics, as recently shown for the unzipping of RNA hairpins3. Here, we report a molecular design based on oligo calix[4]arene catenanes—calixarene dimers held together by 16 hydrogen bridges—in which loops within the molecules limit how far the calixarene nanocapsules can be separated. This mechanically locked structure tunes the energy landscape of dimers, thus permitting the reversible rupture and rejoining of the individual n…

Models MolecularMacromolecular SubstancesSurface PropertiesBiomedical EngineeringMolecular ConformationThermal fluctuationsBioengineeringNanotechnologyMolecular dynamicsPhenolsCalixareneMaterials TestingMoleculeNanotechnologyGeneral Materials ScienceComputer SimulationElectrical and Electronic EngineeringParticle SizePhysicsHydrogen bondEnergy landscapeStatistical mechanicsPhysicistCondensed Matter PhysicsAtomic and Molecular Physics and OpticsNanostructuresModels ChemicalChemical physicsStress MechanicalCalixarenesCrystallizationDimerizationNature nanotechnology
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Calix[4]arene-Based Bis[2]catenanes: Synthesis and Chiral Resolution

2007

The exclusive formation of hydrogen-bonded dimers between tetraaryl and tetratosylurea calix[4]arenes has been used to prepare a series of ten "bisloop" tetraurea calix[4]arenes 3, in which adjacent phenylurea groups are covalently linked through alpha,omega-dioxyalkane chains. This dimerization with tetratosylurea 2 as template preorganizes the alkenyl residues of tetra(m-alkenyloxyphenyl) ureas 1 and enables their selective connection in high yield (up to 95 %) by olefin metathesis followed by hydrogenation. The "bisloop" calixarenes 3 also exclusively form heterodimers with 1. Thus, in a separated metathesis/hydrogenation sequence, a series of 14 cyclic bis[2]catenanes 4, in which two ca…

Models MolecularMagnetic Resonance SpectroscopyMolecular StructurebiologyChemistryStereochemistryOrganic ChemistryCatenaneCatenanesStereoisomerismSequence (biology)General ChemistryCrystallography X-Raybiology.organism_classificationMetathesisCatalysisChiral resolutionCrystallographyCovalent bondYield (chemistry)CalixareneTetraCalixarenesChemistry - A European Journal
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Orientational preferences of aromatic guests in dimeric capsules of tetraurea calix[4]arenes—MD and NMR studies

2006

Molecular dynamics (MD) simulations have been performed for complexes of a dimeric capsule of a tetraurea calixarene with a series of twelve aromatic guests. A distinct orientational preference and a restriction of the internal mobility was found which depend on the size and electronic properties of the guests. The results are in agreement with the CIS values obtained from (1)H NMR spectroscopic measurements and with complexation selectivities obtained by competition experiments.

Models MolecularMagnetic Resonance SpectroscopyPyridinesChemistryOrganic ChemistryBinding CompetitiveBiochemistrySubstrate SpecificityKineticsMolecular dynamicsCrystallographyPhenolsPyrazinesCalixareneBenzene DerivativesProton NMRThermodynamicsUreaCalixarenesPhysical and Theoretical ChemistryElectronic propertiesOrg. Biomol. Chem.
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Self-assembly of programmed building blocks into structurally uniform dendrimers.

2005

Selective and independent dimerization of tri- and tetraurea derivatives was used to build up dendritic assemblies which are uniform in size and structure. Dendrimers with the total molecular masses of about 25 000 g/mol were obtained. The existence of uniform assemblies was proved by 1H and 1H DOSY NMR experiments and also by dynamic light scattering.

Models MolecularMagnetic Resonance SpectroscopyStereochemistryChemistryOrganic solventMolecular ConformationHydrogen BondingGeneral ChemistryBiochemistrySolution structureCatalysisMolecular aggregationCrystallographyColloid and Surface ChemistryDynamic light scatteringPhenolsDendrimerCalixareneUreaSelf-assemblyCalixarenesJournal of the American Chemical Society
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