Publication | Closed Access
Deprotonation of Calixarenes in Acetonitrile
30
Citations
43
References
2005
Year
Inorganic ChemistryDerivative (Chemistry)Selective TitrationEngineeringBiochemistryNatural SciencesChemical DerivativePka ValuesStructure ElucidationSpectra-structure CorrelationPhysical ChemistryQuantum ChemistryChemistryHydrogen BondingMolecular ChemistryCrystallographyEnantioselective SynthesisIon Structure
[Structure: see text]. The pKa values for calixarenes in MeCN have been determined by selective titration with bases using a spectroscopic method. These values are as follows: calix[4]arene pKa(1) = 19.06 +/- 0.22, pKa(2) > 33; calix[6]arene pKa(1) = 15.59 +/- 0.06, pKa(2) = 23.85 +/- 0.35, pKa(3) > 33; calix[8]arene pKa(1) = 17.20 +/- 0.20, pKa(2) = 20.32 +/- 0.31, pKa(3) > 33. The trends in acidity are rationalized using structures generated by a DFT model. For mono-deprotonation, the degree and nature of hydrogen bonding in the anion is the dominant factor; for di-deprotonation, spatial separation of the anionic charges becomes important.
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