Search results for "supramolecular chemistry"

showing 10 items of 721 documents

Binding abilities of new cyclodextrin-cucurbituril supramolecular hosts

2015

Various combined techniques (UV–vis spectrophotometry, isothermal titration calorimetry, thermogravimetry, ESI-MS mass spectrometry, polarimetry and 1H NMR spectroscopy) were used in order to study the interaction between a new combined supramolecular host, namely a bow-tie-structured cyclodextrin–cucurbituril association solely held by non-covalent interactions, and a suitably selected guest, namely the N-(p-nitrophenyl)-1,8-diaminooctane hydrochloride. In particular, the use of different techniques highlighted the peculiar features of the possible host–guest supramolecular interactions under different concentration conditions.

chemistry.chemical_classificationcucubiturilCyclodextrinsmedicine.diagnostic_testCyclodextrinHydrochloridecucurbiturilsSupramolecular chemistryIsothermal titration calorimetryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMass spectrometrycucurbiturilThermogravimetryCrystallographychemistry.chemical_compoundcyclodextrinchemistryComputational chemistryCucurbiturilSpectrophotometrymedicinecucurbiturils; Cyclodextrins; supramolecular co-polymerssupramolecular co-polymerscyclodextrins; cucurbiturils; supramolecular co-polymers
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Microwave-assisted synthesis of novel cyclodextrin–cucurbituril complexes

2011

Microwave irradiation was successfully used in order to obtain stable supramolecular aggregates between cyclodextrins and cucurbiturils, without the participation of any long-chain common ‘molecular thread’ guest. These aggregates were characterised by means of various different techniques, namely NMR, thermogravimetry, polarimetry and ESI-MS. Cross-analysis of experimental data allowed us to obtain insights on the stoichiometries of the composites and their thermal stabilities. The possible structures of the composites are briefly discussed, as well as the actual nature of their intrinsic stability.

chemistry.chemical_classificationcyclodextrinsCyclodextrinCUCURBITURILSSupramolecular chemistryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMicrowave assistedcucurbiturilThermogravimetrychemistrycyclodextrinCucurbiturilComputational chemistryMicrowave irradiationOrganic chemistrymicrowave irradiationStoichiometry
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Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions

2018

Abstract Molecular recognition of aromatic hydrocarbons by four endo -functionalized molecular tubes has been studied by 1 H NMR spectroscopy, computational methods, and single crystal X-ray crystallography. The binding selectivity is rationalized by invoking shape complementarity and dipole alignment. The non-covalent interactions are proved to predominantly be C/N-H⋅⋅⋅ π interactions.

chemistry.chemical_classificationhydrogen bond010405 organic chemistryHydrogen bondStereochemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesmolecular dynamics0104 chemical sciencesMolecular recognitionmacrocycleschemistryhydrogenProton NMRhost-guest chemistryaromatic hydrocarbonhydrocarbonsmolecular recognitionAromatic hydrocarbonSpectroscopyHost–guest chemistryta116Binding selectivityChinese Chemical Letters
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Methyl-Substituted α-Cyclodextrin as Affinity Material for Storage, Separation, and Detection of Trichlorofluoromethane

2018

Abstract The severely ozone‐depleting trichlorofluoromethane is still appearing in several recycling processes or industrial applications. A simple and selective supramolecular complex formation of per‐methylated α‐cyclodextrin (1) with the highly volatile trichlorofluoromethane (2) is reported. This interaction moreover leads to thermally stable crystals. Per‐methylated α‐cyclodextrin is successfully exploited as a reversible and selective adsorption material for liquid and airborne trichlorofluoromethane as well as an affinity material for the chemical sensing and detection of this particular volatile organic component.

chemistry.chemical_classificationoptical sensorsCyclodextrinTrichlorofluoromethaneCFC‐11CommunicationComplex formationSupramolecular chemistrymacromolecular substances02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryCommunicationssupramolecular chemistry0104 chemical scienceschemistry.chemical_compoundcyclodextrinchemistrySelective adsorptiontrichlorofluoromethaneOrganic component0210 nano-technologyGlobal Challenges
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Probing the Folding of Peptide–Polymer Conjugates Using the π-Dimerization of Viologen End-Groups

2020

The synthesis of a foldable viologen-functionalized peptide–polymer conjugate is presented. The ABA-type triblock conjugate with a PEG polymer was capped with a FHFHF pentapeptide sequence and further modified with a viologen building block at both chain ends. The pH-responsive peptide domains fold into an intermediate structure inducing close proximity of the viologen units, which upon a reduction step form π-dimers of the radical cation. Overall the intramolecular folding and intermolecular self-assembly process leads to the formation of supramolecular nanorods. Mixing of viologen-peptide–polymer conjugates with unfunctionalized conjugates leads to crosslinking of the nanorods and hydroge…

chemistry.chemical_classificationstimuli-responsive polymerspeptide conjugation010405 organic chemistrySupramolecular chemistrytechnology industry and agricultureViologenPolymersupramolecular materials010402 general chemistry01 natural sciencesPentapeptide repeat0104 chemical scienceslcsh:ChemistrychemistryRadical ionlcsh:QD1-999Intramolecular forcePolymer chemistrySelf-healing hydrogelsmedicineelectrochromismhydrogelmedicine.drugConjugateOrganic Materials
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Resorcinarene Crowns ☆

2017

Resorcinarene crowns are a class of supramolecular hosts combining a crown ether moiety to a resorcinarene platform as either a podand arm, lower rim substituent, or a bridge. Resorcinarene crowns act as cation hosts and have therefore shown potential in ion transportation and in antibacterial applications.

chemistry.chemical_classificationstomatognathic diseaseschemistry.chemical_compoundstomatognathic systemchemistryPolymer chemistrySupramolecular chemistrySubstituentMoietyResorcinareneHost–guest chemistryCrown etherIon transportation
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Giant Crown-Shaped Polytungstate Formed by Self-Assembly of CeIII-Stabilized Dilacunary Keggin Fragments

2010

Single crystals of Na40K6[Ni(H2O)6]3 [K@K7Ce24Ge12W120O456 (OH)12(H2O)64]· 178H2O are synthesized by addition of KCl to a NaOAc/AcOH buffer solution containing Ce(NO3)3, GeO2, Na2WO4, and NiCl2 followed by slow evaporation at room temperature (24% yield).

chemistry.chemical_compoundCeriumchemistryYield (chemistry)Polymer chemistrySupramolecular chemistrychemistry.chemical_elementGeneral ChemistryBuffer solutionSelf-assemblyGeneral MedicineEvaporation (deposition)CatalysisAngewandte Chemie
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Novel Applications of Dynamic NMR in Organic Chemistry

2004

Abstract This review article is oriented on NMR applications in studying various dynamic processes of organic molecules. The topic as a whole is too large to be covered exhaustively in one article or by one author. Therefore, the literature searches are limited mainly for the years 1999–2001. Further, many interesting branches joined essentially with organic chemistry such as supramolecular and organometallic chemistry are left outside this article because there exist recent reviews on these topics. Similarly, the theoretical background of dynamic NMR is not included. The nature of dynamic NMR itself is changing with the recent progress in computational possibilities to estimate the differe…

chemistry.chemical_compoundChemistryChemical shiftSupramolecular chemistryOrganic chemistryDensity functional theoryGeneral MedicineOrganometallic chemistryOrganic moleculesChemInform
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Discrete supramolecular donor-acceptor complexes

2009

The renewed interest in noncovalently associating electroactive molecules arises in part from the quest for new organic materials that convert solar energy into electrical/ chemical equivalents. In this context, the formation of charge-separated states is a key prerequisite. Charge-transfer events triggered by light have been studied in supramolecular donor–acceptor systems based on hydrogen bonds and coordinative metal bonds. Although many of the most widely utilized electroactive fragments feature large pconjugated surfaces, to date the use of p–p aromatic interactions has mainly been limited to the construction of semi-infinite ensembles of chromophores either to achieve charge transport…

chemistry.chemical_compoundChemistryHydrogen bondComputational chemistryTweezersSupramolecular chemistryMoleculePi interactionContext (language use)General ChemistryChromophoreCatalysisTetrathiafulvalene
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Novel Porphyrin-cholic Acid Conjugates as Receptors for Biologically Important Anions

2007

chemistry.chemical_compoundChemistrySupramolecular chemistryCholic acidGeneral ChemistryReceptorPorphyrinCombinatorial chemistryConjugateSupramolecular Chemistry
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