Search results for "Crown Ether"

showing 10 items of 71 documents

Ion-Pair Complexation with Dibenzo[21]Crown-7 and Dibenzo[24]Crown-8 bis-Urea Receptors

2016

Synthesis and ion-pair complexation properties of novel ditopic bis-urea receptors based on dibenzo[21]crown-7 (R(1) ) and dibenzo[24]crown-8 (R(2) ) scaffolds have been studied in the solid state, solution, and gas phase. In a 4:1 CDCl3 /[D6 ]DMSO solution, both receptors clearly show positive heterotropic cooperativity toward halide anions when complexed with Rb(+) or Cs(+) , with the halide affinity increasing in order I(-) <Br(-) <Cl(-) . In solution, the rubidium complexes of both receptors have higher halide affinities compared to the caesium complexes. However, Rb(+) and Cs(+) complexes of R(2) show stronger affinities toward all the studied anions compared to the corresponding catio…

010405 organic chemistryHydrogen bondion-pair receptorscrown ethersOrganic ChemistryInorganic chemistrySupramolecular chemistrychemistry.chemical_elementHalideCooperativityGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesditopic receptorsCatalysis0104 chemical sciencesRubidiumCrystallographychemistryCaesiumbis-urea receptorsSelectivityta116Chemistry - A European Journal
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A dual channel sulphur-containing a macrocycle functionalised BODIPY probe for the detection of Hg(II) in a mixed aqueous solution

2018

We report herein the synthesis and chromo-fluorogenic behaviour of a new probe 1 containing a boron-dipirromethene (BODIPY) unit electronically connected with a dithia-dioxa-aza macrocycle. Acetonitrile and water-acetonitrile 95:5 v/v solutions of the probe showed an ICT band in the visible zone and are nearly non-emissive. When acetonitrile was used as solvent, addition of Hg(II) and trivalent metal cations induced an hypsochromic shift of the absorption band and moderate emission enhancements. A highly selective response was obtained when using competitive media such as wateracetonitrile 95:5 v/v. In this case only Hg(II) induced a hypsochromic shift of the absorption band and a marked em…

:Ciências Químicas [Ciências Naturais]BodipyHeterocyclesColorimetric sensor010402 general chemistryPhotochemistry01 natural sciencesCatalysisMetalchemistry.chemical_compoundSynthesisQUIMICA ORGANICABODIPYMaterials ChemistryFluorimetric sensorDetection in aqueous solutionAcetonitrileDual channel chemosensorCrown etherchemistry.chemical_classificationAqueous solutionScience & Technology010405 organic chemistryChemistryOptical chemosensorQUIMICA INORGANICAWaterGeneral ChemistryMercuryCiências Naturais::Ciências QuímicasFluorescence3. Good health0104 chemical sciencesAbsorption bandvisual_artHg (II)Coordinationvisual_art.visual_art_mediumHypsochromic shiftfluorescenceBODIPYCrown ether
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Redox-active crown ethers derived from biphenyl. Electrochemical and spectroscopic study of binding processes with alkali, alkali-earth and mercury s…

1998

Abstract Three new electroactive ligands, 3a, 3b and 3c, that contain the biphenyl frameworks in their structure were prepared. These new ligands presented three interesting characteristics: 1) they exhibited a reversible oxidation, 2) the oxidation induced a conformational change in the crown moiety and 3) they had two different coordination centers, the crown ether and the dimethylamino groups. Electrochemical and spectroscopic studies using alkali, alkali-earth and mercury salts were carried out.

Biphenylchemistry.chemical_classificationConformational changeAlkaline earth metalChemistryOrganic ChemistryInorganic chemistrychemistry.chemical_elementAlkali metalElectrochemistryBiochemistryMercury (element)chemistry.chemical_compoundDrug DiscoveryMoietyCrown etherTetrahedron
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Resorcinarene bis-crown silver complexes and their application as antibacterial Langmuir-Blodgett films

2012

Silver complexes of a cation binding supramolecular host, resorcinarene bis-crown (CNBC5) with propyl, nonyl, decyl and undecyl alkyl chains were investigated by NMR titration, picrate extraction and single crystal X-ray diffraction. Binding studies showed that both 1 : 1 and 1 : 2 (host-Ag(+)) complexes are present in solution with only a slight effect of the lower rim alkyl chain length on the binding constants (log K 4.0-4.2 for 1 : 2 complexes). Solid state complexes of the resorcinarene bis-crowns bearing either C(3) or C(11) chains were obtained. Single crystal X-ray analyses showed that both derivatives bind silver ions by metal-arene and Ag···O coordination from the crown ether brid…

Cation bindingSilverPhenylalaninePicrateInorganic chemistrySupramolecular chemistryCrystallography X-RayBiochemistryLangmuir–Blodgett filmchemistry.chemical_compoundCoordination ComplexesPolymer chemistryAmphiphileEscherichia coliPhysical and Theoretical Chemistryta116Escherichia coli InfectionsAlkylCrown etherchemistry.chemical_classificationMolecular StructureOrganic ChemistryResorcinareneAnti-Bacterial AgentschemistryCalixarenesOrganic & Biomolecular Chemistry
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Structural effects of macrocyclic compounds and their partition in sodium dodecylsulphate aqueous solutions

2003

The partition of 1,4,7,10,13,16-esaoxacyclooctadecane (18C6), 4,7,13,16-tetraoxa-1,10-diazacyclooctadecane (2.2), 2,5,8,11,14,17-esaoxabicyclo[16.4.0]dicosane (B18C6) and 2,5,8,15,18,21-esoxatricyclo[20.4.0.09.14]esacosane (Cy218C6) in sodium dodecyl sulfate (SDS) aqueous solutions and their effect on the structure of surfactant aggregates has been investigated by small-angle neutron scattering. Results from data analysis have shown that by increasing macrocycle concentration the SDS micelles dimensions reduce for all systems investigated. At the same time information on macrocycles partition between the micellar and the continuous phase have been obtained. It was found that an appreciable …

CryptandsAqueous solutionSANSChemistryAdditive partitionSodiumInorganic chemistryCryptandchemistry.chemical_elementMicelleSmall-angle neutron scatteringGeneral Biochemistry Genetics and Molecular BiologyCrystallographychemistry.chemical_compoundPulmonary surfactantMoleculeCrown ethersSodium dodecyl sulfateMicellesSettore CHIM/02 - Chimica FisicaJournal of Applied Crystallography
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A “Cation-less” Oxalate-Based Ferromagnet Formed by Neutral Bimetallic Layers:  {[Co(H2O)2]3[Cr(ox)3]2(18-crown-6)2}∞ (ox = Oxalate Dianion; 18-crown…

2007

Neutral layers of the bimetallic oxalate complex {[Co(H2O)2]3[Cr(ox)3]2}∞ are formed in the presence of a crown ether and stabilized by hydrogen bonding. The resulting soluble ferromagnet orders at Tc = 7.4 K.

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundCrystallographychemistryFerromagnetismHydrogen bond18-Crown-6Physical and Theoretical ChemistryBimetallic stripCrown etherOxalateInorganic Chemistry
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Neutral and cationic trimethylsilylmethyl complexes of the rare earth metals supported by a crown ether: synthesis and structural characterization

2003

The synthesis of a series of thermally robust, isolable trimethylsilylmethyl complexes of the rare earth metals stabilized by 12-crown-4 [Ln(CH2SiMe3)3(12-crown-4)] (Ln = Sc, Y, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) is reported. The crystallographically characterized yttrium and lutetium complexes [Ln(CH2SiMe3)3(12-crown-4)] exhibit facial coordination of the crown ether at the neutral lanthanide trialkyl unit. The coordination geometry can be derived from a capped octahedron. VT NMR spectroscopic studies revealed a labile coordination of the crown ether in thf solution. Reaction of the diamagnetic derivatives with triethylammonium tetraphenylborate in thf results in the clean formation of th…

Lanthanidechemistry.chemical_classificationTetraphenylborateStereochemistryCationic polymerizationchemistry.chemical_elementYttriumLutetiumInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryOctahedronCrown etherCoordination geometryDalton Transactions
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Tetra-μ-chlorido-bis(18-crown-6)platinum(II)dipotassium(I)

2010

In the title compound, [K(2)PtCl(4)(C(12)H(24)O(6))(2)], the Pt(II) ion is located on an inversion centre and is coordinated by four Cl atoms, forming a square-planar geometry. The K(I) ion is coordinated by six O atoms of the crown ether and two bridging Cl atoms. The K(I) ion is displaced by 0.756 (2) Å from the mean plane of the six O atoms of the crown ether. The mol-ecules are connected by weak C-H⋯O hydrogen bonds, forming an infinite two-dimensional network parallel to the (10) plane. Intra- and inter-molecular C-H⋯Cl hydrogen bonds are also observed.

Metal-Organic Paperschemistry.chemical_classificationbiologyHydrogen bond18-Crown-6chemistry.chemical_elementGeneral ChemistryCondensed Matter Physicsbiology.organism_classificationBioinformaticsIonchemistry.chemical_compoundCrystallographychemistryTetraGeneral Materials SciencePlatinumCrown etherActa Crystallographica Section E Structure Reports Online
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Simultaneous Freezing of Chirality and In−Out Conformation of a Macropentacyclic Cryptand by Protonation

2004

Compound 1, a cryptand-derived macropentacycle, is a flexible molecule that encompasses many conformations (symmetrical, unsymmetrical, and chiral ones) depending on the observation temperature (VT 1H NMR). Selective monoprotonation of this molecule leads to a totally unsymmetrical, rigidly chiral species in solution (1H NMR). Helical chirality and in-out conformation of monoprotonated 1 are observed in the solid state by X-ray diffraction analysis, as well as the proton location. The latter is bound to the endo bridgehead nitrogen atom and involved in hydrogen-bonding interactions with the three closest sulfurs. Significant induction of chirality is triggered by reaction of 1 with the opti…

Models MolecularMagnetic Resonance SpectroscopyProtonChemistryStereochemistryCryptandMolecular ConformationDiastereomerStereoisomerismProtonationGeneral ChemistryNuclear magnetic resonance spectroscopyCrystallography X-RayBiochemistryCatalysisColloid and Surface ChemistryCrown EthersBenzene DerivativesProton NMRMoleculeDisulfidesAminesProtonsChirality (chemistry)Journal of the American Chemical Society
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Synthesis and structure of mono-bridged resorcinarene host: a ditopic receptor for ammonium guests.

2009

The synthesis and structural properties of tetramethoxy resorcinarene mono-crown-5 (1) are described. The binding characteristics of 1 toward acetylcholine and tetramethylammonium salts were investigated by 1H NMR titration. It was observed that the cavity of 1 provides a better fit to acetylcholine compared to the smaller tetramethylammonium cation, as acetylcholine is able to interact with both the crown ether moiety and the free hydroxyl groups of receptor 1 simultaneously.

Models MolecularMagnetic Resonance SpectroscopyStereochemistryPhenylalanineMolecular ConformationBiochemistrychemistry.chemical_compoundPolymer chemistrymedicineHydroxidesMoietyPhysical and Theoretical ChemistryCrown etherchemistry.chemical_classificationTetramethylammoniumBinding SitesOrganic ChemistryNuclear magnetic resonance spectroscopyResorcinareneCrown CompoundsQuaternary Ammonium CompoundschemistryProton NMRTitrationCalixarenesAcetylcholinemedicine.drugOrganicbiomolecular chemistry
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