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Study of surfactant alcohols with various chemical moieties at the hydrophilic–hydrophobic interface

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Supporting Information For

Study of Surfactant Alcohols with various Chemical

Motives at the Hydrophilic/Hydrophobic Interface

Pierre-Léonard Zaffalon, Vincenza D’Anna, Hans Hagemann, Andreas Zumbuehl

Pet-CH3 (4)

Figure 1. 1H NMR spectra of Pet-CH3 (4).

Figure 2. 13C NMR spectra of Pet-CH3 (4).

 Published in "56&$GYDQFHV  ±"

which should be cited to refer to this work.

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Pes-OH-Pes (9)

Figure 12. 1H NMR spectra of Pes-OH-Pes (9).

Figure 13. 13C NMR spectra of Pes-OH-Pes (9).



(3)

Pad-OH-Pad (10)

Figure 3. 1H NMR spectra of Pad-OH-Pad (10)



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Cyclo-Pad-OH-Pad (11)

Figure 8. 1H NMR spectra of cyclo-Pad-OH-Pad (11).

Figure 9. 13C NMR spectra of cyclo-Pad-OH-Pad (11).



(5)

Pad-OTIPS-Pad (12)

Figure 4. 1H NMR spectra of Pad-OTIPS-Pad (12).

Figure 5. 13C NMR spectra of Pad-OTIPS-Pad (12)



(6)

Hexahydropyrimidin-5-ol (17)

Figure 6. 1H NMR spectra of hexahydropyrimidin-5-ol (17).

Figure 7. 13C NMR spectra of hexahydropyrimidin-5-ol (17).



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2-(benzyloxy)propane-1,3-diyl dipalmitate (19)

Figure 10. 1H NMR spectra of 2-(benzyloxy)propane-1,3-diyl dipalmitate. (19).

Figure 11. 13C NMR spectra of 2-(benzyloxy)propane-1,3-diyl dipalmitate (19).



Figure

Figure 1.  1 H NMR spectra of Pet-CH 3  (4).
Figure 12.  1 H NMR spectra of Pes-OH-Pes (9).
Figure 3.  1 H NMR spectra of Pad-OH-Pad (10)
Figure 8.  1 H NMR spectra of cyclo-Pad-OH-Pad (11).
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