Ajami and Rebek. 10.1073/pnas.0707759104.
Fig. 10. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated p-ethyl, propyl, butyl benzene in 1.24.1.
Fig. 11. Upfield shift of aromatic hydrogen of p-ethyl, propyl, butyl benzene in 1.24.1.
Fig. 12. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated (2-chloro ethyl)benzene and (3-chloro propyl) benzene in 1.24.1.
Fig. 13. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated N,N-dimethyl-p-toluidine in 1.24.1.
Fig. 14. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated arachidonic acid in 1.28.1.
Fig. 15. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated arachidonic acid ethyl ester in 1.28.1.
Fig. 16. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated arachidonoyl cyclopropylamide in 1.28.1.
Fig. 17. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated anadamide in 1.28.1.
Fig. 18. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated docosahexaenoic acid methyl ester in 1.28.1.
Fig. 19. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated palmitonyl ethanolamide in 1.28.1.
Fig. 20. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated 9-octadecenamide in 1.28.1.
Fig. 21. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated oleic acid ethyl ester in 1.28.1.
Fig. 22. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated 13-docosenamide in 1.28.1.
Fig. 23. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated capsaicin in 1.24.1.
Fig. 24. (a) 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated oleic acid ethyl ester in 1.28.1. (b) Addition of 5 ml of methanol d4 to a. (c) Addition of 5 ml of methanol d4 to b. (d) Addition of 5 ml of methanol d4 to c. (e) Addition of 5 ml of methanol d4 to d.