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Figure 4.3. Aqueous suspensions of (A) cellulose nanocrystals (0.8 wt %) and (B) FITC-labeled cellulose nanocrystals (0.5 wt %). (Reprinted with permission from ref 12. Copyright 2007 American Chemical Society)
a)
b)
Figure 6.10. O2-saturated β-D-glucose/2,2'-azino-bis(3-ethylbenzthiazoline-6sulphonic acid) solution containing horse radish peroxidase before (a) and 1 min after (b) the addition of glucose oxidase capsules
In Polysaccharide Materials: Performance by Design; Edgar, K., et al.; ACS Symposium Series; American Chemical Society: Washington, DC, 2010.
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H-bonding dominant
Bolas in solution Hydrophobic interaction dominant
Figure 14.6 - Schematic of bolaform self assembly in solution
Figure 14.7 - X-ray crystal structures of compounds 3d (major and minor diastereomers) and 3e.
In Polysaccharide Materials: Performance by Design; Edgar, K., et al.; ACS Symposium Series; American Chemical Society: Washington, DC, 2010.
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Figure 14.8 - Comparative X-ray structures of glycal bolaforms 3d and 3e with similar carbohydrate bolaforms
In Polysaccharide Materials: Performance by Design; Edgar, K., et al.; ACS Symposium Series; American Chemical Society: Washington, DC, 2010.
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Figure 15.3. 600 MHz 1H HR-MAS NMR spectra of WT (D), GH9C1-1 (C), GH9C3-1 (B), and GH9C2-2 (A) Arabidopsis thaliana root tissues scaled by carbohydrate region intensities. Arrows indicate significant differences in peak intensities in the acetate region of the spectra.
In Polysaccharide Materials: Performance by Design; Edgar, K., et al.; ACS Symposium Series; American Chemical Society: Washington, DC, 2010.
