This is the authors' abstract. We don't add key points for this paper.
The host−guest complexation of bromochlorofluoromethane (CHFClBr) and bromochlorodeuteriofluoromethane (CDFClBr) by a chiral thiomethylated cryptophane (cryptophane-E-(SCH 3 ) 6 ) was studied by fluorine NMR. Fluorine NMR T 1 experiments were performed on the {CHFClBr@cryptophane-E-(SCH 3 ) 6 } system. They revealed the presence of 19 F− 1 H CSA-DD cross-correlated relaxation, which was found to be more efficient inside the host cavity. The measurement of 19 F− 1 H CSA-DD cross-correlated relaxation rates at two different magnetic field strengths allowed the determination of the correlation time τ C of CHFClBr outside (τ C = 0.27 ns) and inside the cryptophane (τ C = 0.62−0.78 ns). These correlation times were confirmed by the measurement of the deuterium quadrupolar relaxation time T q in the {CDFClBr@cryptophane-E-(SCH 3 ) 6 } system. The two methods were in very good agreement and showed that the substrate was slowed upon complexation.
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Crassous et al. (2003) studied this question.