6533b7d1fe1ef96bd125ce83
RESEARCH PRODUCT
N-Alkyl Ammonium Resorcinarene Salts as High-Affinity Tetravalent Chloride Receptors.
Sandip BhowmikKari RissanenRobin H. A. RasToni MäkeläN. Kodiah BeyehN. Kodiah BeyehFangfang Pansubject
PicrateInorganic chemistryta221chemistry.chemical_elementSalt (chemistry)receptors010402 general chemistry01 natural sciencesChlorideMedicinal chemistryCatalysishost-guest systemschemistry.chemical_compoundnoncovalent interactionsChlorinemedicineAmmoniumta116Alkylta218chemistry.chemical_classificationta214ta114010405 organic chemistryOrganic ChemistryGeneral ChemistryResorcinarene0104 chemical scienceschemistrychlorineTrifluoromethanesulfonateanionsmedicine.drugdescription
N-Alkyl ammonium resorcinarene salts (NARYs, Y=triflate, picrate, nitrate, trifluoroacetates and NARBr) as tetravalent receptors, are shown to have a strong affinity for chlorides. The high affinity for chlorides was confirmed from a multitude of exchange experiments in solution (NMR and UV/Vis), gas phase (mass spectrometry), and solid-state (X-ray crystallography). A new tetra-iodide resorcinarene salt (NARI) was isolated and fully characterized from exchange experiments in the solid-state. Competition experiments with a known monovalent bis-urea receptor (5) with strong affinity for chloride, reveals these receptors to have a much higher affinity for the first two chlorides, a similar affinity as 5 for the third chloride, and lower affinity for the fourth chloride. The receptors affinity toward chloride follows the trend K1 ≫K2 ≫K3 ≈5>K4, with Ka =5011 m(-1) for 5 in 9:1 CDCl3/[D6]DMSO.
year | journal | country | edition | language |
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2016-01-01 | Chemistry (Weinheim an der Bergstrasse, Germany) |