Search results for "Nmr titration"

showing 4 items of 4 documents

Encapsulation of tetramethylphosphonium cations

2009

International audience; The weak interactions and capsule formation of tetramethylphosphonium (TMP) cation with resorcinarenes 1 and 2 and the corresponding pyrogallarenes 3 and 4 were studied in the solid state by single crystal X-ray diffraction, in solution by NMR and in the gas phase by mass spectrometry. In methanol-D4, the NMR titration studies reveal that the association constants for the 1:1 complexes of TMP@3 and TMP@4 are much higher (TMP@4:390±37 M-1) than for the corresponding TMP@1 and TMP@2 (TMP@2:130±10 M-1) complexes. In the gas phase both monomeric 1:1 TMP@1-TMP@4 complexes as well as the dimeric 1:2 capsule complexes, TMP@12-TMP@42 were observed. The 1:1:2 molar mixtures o…

010405 organic chemistrySupramolecular chemistrySolid-stateGeneral Chemistry010402 general chemistryMass spectrometry01 natural sciences0104 chemical sciences3. Good healthGas phasechemistry.chemical_compoundCrystallographyMonomerchemistryPhysical SciencesNmr titrationX-ray crystallographyMethanolSupramolecular Chemistry
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Pentafluorophenyl salicylamine receptors in anion–π interaction studies

2012

A crystal structure analysis confirms the appropriateness of pentafluorophenyl salicylamine (1a) as a π-acceptor for anion–π interactions. Crystals of 1a·HCl show that the OH-group fixes the anion in a η2-type binding motif above the electron-deficient arene. Attempts to find some relevance for this weak intermolecular force in solution failed. Stronger CH–, NH– and OH–anion interactions are dominant over the weak anion–π interactions. Due to the hydrogen bonding, the non-fluorinated receptor exhibits the highest binding constants within this series.

Interaction studiesCrystallographyChemistryHydrogen bondNmr titrationInorganic chemistryIntermolecular forceChemieGeneral ChemistryCrystal structureReceptorta116IonSupramolecular Chemistry
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Recognition of N-Alkyl- and N-Aryl-Acetamides by N-Alkyl Ammonium Resorcinarene Chlorides

2014

N-alkyl ammonium resorcinarene chlorides are stabilized by an intricate array of intra- and intermolecular hydrogen bonds that leads to cavitand-like structures. Depending on the upper-rim substituents, self-inclusion was observed in solution and in the solid state. The self-inclusion can be disrupted at higher temperatures, whereas in the presence of small guests the self-included dimers spontaneously reorganize to 1:1 host-guest complexes. These host compounds show an interesting ability to bind a series of N-alkyl acetamide guests through intermolecular hydrogen bonds involving the carbonyl oxygen (C=O) atoms and the amide (NH) groups of the guests, the chloride anions (Cl(-)) and ammoni…

chemistry.chemical_classificationHydrogen bondStereochemistryArylOrganic ChemistryIntermolecular forceGeneral Chemistrymacromolecular substancesResorcinareneMedicinal chemistryCatalysischemistry.chemical_compoundchemistryAmideAmmoniumresorcinarenes; NMR titration; amides; host-guest complexes; X-ray crystallographyta116AlkylAcetamide
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Ion pair recognition by ditopic crown ether based bis-urea and uranyl salophen receptors

2016

ionition pair bindingcrown ethersuranyl salophensureatitraussupramolecular chemistryditopic receptorsionisidosanion bindinguranyylisalofeenitkemialliset sidoksetkruunueetteritsupramolekyylikemia¹H NMR titrationsNMR-spektroskopiaorgaaniset yhdisteetröntgenkristallografiaX-ray crystallography
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