Adaptations of guest and host in expanded self-assembled capsules

Ajami and Rebek. 10.1073/pnas.0707759104.

Supporting Information

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SI Figure 10
SI Figure 11
SI Figure 12
SI Figure 13
SI Figure 14
SI Figure 15
SI Figure 16
SI Figure 17
SI Figure 18
SI Figure 19
SI Figure 20
SI Figure 21
SI Figure 22
SI Figure 23
SI Figure 24




SI Figure 10

Fig. 10. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated p-ethyl, propyl, butyl benzene in 1.24.1.





SI Figure 11

Fig. 11. Upfield shift of aromatic hydrogen of p-ethyl, propyl, butyl benzene in 1.24.1.





SI Figure 12

Fig. 12. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated (2-chloro ethyl)benzene and (3-chloro propyl) benzene in 1.24.1.





SI Figure 13

Fig. 13. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated N,N-dimethyl-p-toluidine in 1.24.1.





SI Figure 14

Fig. 14. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated arachidonic acid in 1.28.1.





SI Figure 15

Fig. 15. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated arachidonic acid ethyl ester in 1.28.1.





SI Figure 16

Fig. 16. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated arachidonoyl cyclopropylamide in 1.28.1.





SI Figure 17

Fig. 17. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated anadamide in 1.28.1.





SI Figure 18

Fig. 18. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated docosahexaenoic acid methyl ester in 1.28.1.





SI Figure 19

Fig. 19. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated palmitonyl ethanolamide in 1.28.1.





SI Figure 20

Fig. 20. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated 9-octadecenamide in 1.28.1.





SI Figure 21

Fig. 21. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated oleic acid ethyl ester in 1.28.1.





SI Figure 22

Fig. 22. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated 13-docosenamide in 1.28.1.





SI Figure 23

Fig. 23. 1H-NMR spectra (600 MHz, mesitylene-d12) of encapsulated capsaicin in 1.24.1.





SI Figure 24

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.

This Article

  1. PNAS October 9, 2007 vol. 104 no. 41 16000-16003
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