Search results for "Supramolecular"

showing 10 items of 830 documents

Capping α-Cyclodextrin with Cyclotriveratrylene by Triple Disulfide-Bridge Formation

2013

Disulfide-bond formation is an expeditious coupling reaction to make macropolycyclic symmetrical receptors. It is used here for the preparation of unsymmetrical cavitands based on α-cyclodextrin (α-CDX) and cyclotriveratrylene (CTV) analogues. Accordingly, diastereomeric hemicryptophanes 2a and 2b were obtained in 11 % isolated yield by the iodine oxidation of a 1:1 mixture of racemic cyclotrithiophenolene (3) and the C3-symmetric trithiol derivative of permethylated α-cyclodextrin (PM α-CDX) 4. Remarkably, the target hemicryptophanes were obtained in a 5:3 diastereomeric ratio. The reaction produced mainly (34 %) a singly disulfide-bridged PM α-CDX dimer 7, however no traces of triply disu…

chemistry.chemical_classificationCyclodextrinStereochemistryDimerOrganic ChemistryDiastereomerSupramolecular chemistryCyclotriveratryleneMedicinal chemistryCoupling reactionchemistry.chemical_compoundchemistryYield (chemistry)Physical and Theoretical ChemistryDerivative (chemistry)European Journal of Organic Chemistry
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Binding properties of mono-(6-deoxy-6-amino)-β-cyclodextrin towards p-nitroaniline derivatives: a polarimetric study

2009

Abstract Polarimetry was used in order to investigate the formation of supramolecular complexes between mono-6-amino-β-cyclodextrin and various p-nitroaniline derivatives at two different pH values. Comparison with the behaviour of native β-cyclodextrin gave us the opportunity to consider the effect exerted by the presence of charged groups, having different solvation requirements, on the binding equilibrium. Data offer some support to the hypothesis of ‘dynamic co-inclusion’ of solvent molecules within the host–guest complex.

chemistry.chemical_classificationCyclodextrinStereochemistryOrganic ChemistrySupramolecular chemistrySolvationNitro compoundcyclodextrins polarimetric study host-guest complexes stability constantsSettore CHIM/06 - Chimica OrganicaBiochemistryInclusion compoundSolventchemistry.chemical_compoundchemistryDrug DiscoveryMoleculeAmine gas treatingTetrahedron
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Cyclodextrin/surfactant inclusion complexes: An integrated view of their thermodynamic and structural properties

2021

Cyclodextrins (CDs) play an important role in self-assembly systems of amphiphiles. The structure of CDs provides distinguished physicochemical properties, including the ability to form host-guest complexes. The complexation affects the properties of guest molecules and can produce supramolecular aggregates with desirable characteristics for fundamental and practical applications. Surfactants are particularly attractive host molecules due to their wide variety, availability, responsiveness to different stimuli, and high relevance in different fields, e.g. medical, cosmetic, pharmaceutical, and food industries. The tendency of organization in higher-order supramolecular aggregates arises the…

chemistry.chemical_classificationCyclodextrinSupramolecular chemistryNanotechnology02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni Culturali0104 chemical sciencesInclusion complexesColloid and Surface ChemistrychemistryPulmonary surfactantAmphiphileSurfactantMoleculeCyclodextrinThermodynamicsPhysical and Theoretical Chemistry0210 nano-technology
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Quantum dot/cyclodextrin supramolecular systems based on efficient molecular recognition and their use for sensing.

2011

A supramolecular system based on ketoprofen functionalised CdSe/ZnS nanoparticles and pyrene-modified β-CD was prepared and successfully used for molecular sensing of different analytes. In addition, a strategy for the individual recovery of all the components of the sensing assay is reported.

chemistry.chemical_classificationCyclodextrinsPyrenesCyclodextrinMolecular StructureMetals and AlloysSupramolecular chemistryNanoparticleNanotechnologyGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMolecular recognitionchemistryQuantum dotQuantum DotsMaterials ChemistryCeramics and CompositesNanoparticlesFluorescent DyesChemical communications (Cambridge, England)
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Dicopper(II) Metallacyclophanes as Multifunctional Magnetic Devices: A Joint Experimental and Computational Study

2015

Metallosupramolecular complexes constitute an important advance in the emerging fields of molecular spintronics and quantum computation and a useful platform in the development of active components of spintronic circuits and quantum computers for applications in information processing and storage. The external control of chemical reactivity (electro- and photochemical) and physical properties (electronic and magnetic) in metallosupramolecular complexes is a current challenge in supramolecular coordination chemistry, which lies at the interface of several other supramolecular disciplines, including electro-, photo-, and magnetochemistry. The specific control of current flow or spin delocaliz…

chemistry.chemical_classificationDelocalized electronSpintronicschemistrySupramolecular chemistryMoleculeNanotechnologyGeneral MedicineGeneral ChemistryElectronicsQuantum computerSpin-½Coordination complexAccounts of Chemical Research
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Supramolecular organic-inorganic hybrid assemblies with tunable particle size: interplay of three noncovalent interactions.

2013

chemistry.chemical_classificationDendrimersMaterials scienceSupramolecular chemistryNanoparticleMetal NanoparticlesNanotechnologyGeneral ChemistrySulfidesCatalysisPolyelectrolyteColloidchemistryMicroscopy Electron TransmissionOrganic inorganicCadmium CompoundsNon-covalent interactionsSelf-assemblyParticle sizeGoldParticle SizeColoring AgentsAngewandte Chemie (International ed. in English)
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Peptide metal-organic frameworks under pressure: flexible linkers for cooperative compression

2018

We investigate the structural response of a dense peptide metal-organic framework using in situ powder and single-crystal X-ray diffraction under high-pressures. Crystals of Zn(GlyTyr)2 show a reversible compression by 13% in volume at 4 GPa that is facilitated by the ability of the peptidic linker to act as a flexible string for a cooperative response of the structure to strain. This structural transformation is controlled by changes to the conformation of the peptide, which enables a bond rearrangement in the coordination sphere of the metal and changes to the strength and directionality of the supramolecular interactions specific to the side chain groups in the dipeptide sequence. Compar…

chemistry.chemical_classificationDipeptideCoordination sphereSupramolecular chemistryQuímica organometàl·licaPeptideSequence (biology)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundchemistrySide chainMetal-organic frameworkPèptids0210 nano-technologyLinker
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DLPNO-CCSD(T) scaled methods for the accurate treatment of large supramolecular complexes

2017

In this work, we present scaled variants of the DLPNO-CCSD(T) method, dubbed as (LS)DLPNO-CCSD(T) and (NS)DLPNO-CCSD(T), to obtain accurate interaction energies in supramolecular complexes governed by noncovalent interactions. The novel scaled schemes are based on the linear combination of the DLPNO-CCSD(T) correlation energies calculated with the standard (LoosePNO and NormalPNO) and modified (Loose2PNO and Normal2PNO) DLPNO-CCSD(T) accuracy levels. The scaled DLPNO-CCSD(T) variants provide nearly TightPNO accuracy, which is essential for the quantification of weak noncovalent interactions, with a noticeable saving in computational cost. Importantly, the accuracy of the proposed schemes is…

chemistry.chemical_classificationFullerene010304 chemical physicsDispersion forcesNoncovalent interactionsSupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesLondon dispersion force0104 chemical sciencesComputational MathematicsCrystallographychemistryComputational chemistryAb initio quantum chemistry methods0103 physical sciencesNon-covalent interactionsDLPNO-CCSD(T) scaled methodsDonor–acceptor supramolecular complexesAb initio calculationsQuímica FísicaLinear combination
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Cyclodextrin-[60]fullerene conjugates: synthesis, characterization, and electrochemical behavior

2006

Three different functionalized β-cyclodextrins (β-CDs) bearing the C60 moiety linked covalently have been prepared in good yields by reaction between the parent β-CD and [60]fullerene via 1,3-dipolar cycloaddition. These compounds have been fully spectroscopically characterized and their electrochemical behavior has been investigated. Surprisingly, the electrochemical properties of the C60 cage remain unaltered even after chemical functionalization, making these systems very appealing as supramolecular hosts for electron-transfer processes.

chemistry.chemical_classificationFullereneCyclodextrinOrganic ChemistrySupramolecular chemistrySettore CHIM/06 - Chimica OrganicaElectrochemistrycyclodextrin fullereneBiochemistryCombinatorial chemistryCycloadditionchemistryCovalent bondDrug Discovery13-Dipolar cycloadditionOrganic chemistryMoiety
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Insights into the Formation and Structures of Molecular Gels by Diimidazolium Salt Gelators in Ionic Liquids or “Normal” Solvents

2016

Insights are provided into the properties of molecular gels formed by diimidazolium salts both in “normal” solvents and ionic liquids. These materials can be interesting for applications in green and sustainable chemistry in which ionic liquids play a significant role, like catalysis and energy. In particular, two positional isomers of a diimidazolium cation have been examined with a wide range of anions for their ability to form gel phases. In particular, di-, tri-, and tetravalent anions bearing aliphatic or aromatic spacers were paired with the divalent cations. The properties of the organo- and ionogels formed have been analyzed by means of several different techniques, including calori…

chemistry.chemical_classificationGreen chemistryOrganic ChemistryInorganic chemistrySalt (chemistry)Settore CHIM/06 - Chimica Organica02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyResonance (chemistry)01 natural sciencesCatalysis0104 chemical sciencesSolventchemistry.chemical_compoundSupramolecular gels ionogels ionic liquidschemistryChemical engineeringIonic liquidStructural isomerThermal stabilityAbsorption (chemistry)0210 nano-technologyChemistry - A European Journal
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