Complexations of the hydrophilic and hydrophobic moieties of benzethonium chloride by cucurbit[7]uril in aqueous solution

Abstract

The sequential complexations of the hydrophilic and hydrophobic end groups of benzethonium chloride by cucurbit[7]uril (CB[7]) in aqueous solution have been investigated using 1H NMR spectroscopy and electrospray ionization mass spectrometry. The initial binding is to the benzyldimethylammonium group, with a stability constant of (8.7 ± 3.1) × 107 (mol/L)–1. This binding constant and the complexation-induced upfield shifts of the benzyl guest protons are similar to those values observed with other cationic guests containing benzyl moieties. This equilibrium is followed by the binding of a second equivalent of the host to the hydrophobic 2-(2,4,4-trimethylpentyl) group, with a stability constant of (4.0 ± 1.9) × 103 (mol/L)–1. The relatively strong binding of this uncharged hydrophobic end of the guest molecule is consistent with the inclusion of eight heavy (nonhydrogen) atoms within the inner cavity of CB[7], with its low polarizability. The packing coefficient for the 2-(2,4,4-trimethylpentyl) group with the inner cavity is calculated to be 61%, close to Rebek’s ideal value of 55%.