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Chemical and Functional Properties of Food Saccharides

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© 2004 by CRC Press LLC<br />

FIGURE 14.2 Typical 1 H-NMR spectrum (300 MHz) <strong>of</strong> solutions <strong>of</strong> a depolymerized chitosan<br />

with F A 0.43 (10 mg/ml) in D 2O at pH 3 <strong>and</strong> 90∞C. The resonance at 0 ppm is the<br />

internal reference TSP [sodium-(trimethylsilyl)-propionate-d 4], whereas the resonances at 4.8<br />

<strong>and</strong> 4.6 ppm are H-1 <strong>of</strong> D-units <strong>and</strong> A-units, respectively. For further assignments <strong>of</strong> the<br />

resonances in the spectrum, see Vårum, K.M. et al., Carbohydr. Res., 211, 17, 1991.<br />

14.2.2 SEQUENCE<br />

High-field 1 H <strong>and</strong> 13 C NMR spectroscopy has been used to determine sequences <strong>of</strong><br />

the monomers in chitosans. However, it should be noted that high-resolution spectra<br />

are required to obtain information on sequence parameters <strong>of</strong> chitosans. 7,8 The units<br />

in the chitosan chain have been found to be r<strong>and</strong>omly distributed in water-soluble,<br />

partially N-acetylated chitosans prepared from chitin by alkaline de-N-acetylation. 7,8<br />

14.2.3 MOLECULAR MASS<br />

As polysaccharides in general, chitosans are polydisperse with respect to molecular<br />

weight. Because <strong>of</strong> this, the “molecular weight” <strong>of</strong> a chitosan is an average over the

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