2012
DOI: 10.1080/15583724.2012.668154
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Solution NMR Spectroscopy of Food Polysaccharides

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Cited by 240 publications
(196 citation statements)
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“…Figure 3, signals in the region between 5.3 and 4.5 ppm related to H1-4 and H1-3 are well resolved and indicate α-D-glucans (Synytsya & Novak, 2014). The main signals in the anomeric region correspond to protons bound to C1 in the primary 1→4 glycosidic bond ( =5.36 ppm), and C1 in the branching 1→3 ( = 5.32 ppm), and a small signal at = 4.95 ppm, attributable to 1→6 glycosidic bonds was also observed (Cheng & Neiss, 2012;Zang , Howseman, & Shulman, 1991;Zang, Rothman, & Shulman, 1990). The signals obtained in the spectrum in the ring proton region were poorly resolved due to the overlapping chemical shifts.…”
Section: Nmr Analysismentioning
confidence: 77%
See 1 more Smart Citation
“…Figure 3, signals in the region between 5.3 and 4.5 ppm related to H1-4 and H1-3 are well resolved and indicate α-D-glucans (Synytsya & Novak, 2014). The main signals in the anomeric region correspond to protons bound to C1 in the primary 1→4 glycosidic bond ( =5.36 ppm), and C1 in the branching 1→3 ( = 5.32 ppm), and a small signal at = 4.95 ppm, attributable to 1→6 glycosidic bonds was also observed (Cheng & Neiss, 2012;Zang , Howseman, & Shulman, 1991;Zang, Rothman, & Shulman, 1990). The signals obtained in the spectrum in the ring proton region were poorly resolved due to the overlapping chemical shifts.…”
Section: Nmr Analysismentioning
confidence: 77%
“…The signals obtained in the spectrum in the ring proton region were poorly resolved due to the overlapping chemical shifts. However, it is possible to observe clearly the H4´ peak corresponding to the protons bound to the free C4 non reducing ends ( = 3.41 ppm) and other intense peaks from the H2 (=3.63 ppm), H3 ( =3.95 ppm), H4 ( =3.62 ppm), H5 ( =3.81 ppm) and H6a and H6b ( =3.86 and 3.79 ppm, respectively) (Cheng & Neiss, 2012;Nilsson, Bergquist, Nilsson, & Gorton, 1996;Zang et al, 1990;Zang et al, 1991), but better assignments will require more specific identifications. The intensities of the resonances contain information about the branched structure of the molecule.…”
Section: Nmr Analysismentioning
confidence: 94%
“…Furthermore, considerable progress has been made during the last decade toward the development of nuclear magnetic resonance (NMR) techniques for the analysis of natural [28] and synthetic polymers [29]. NMR spectroscopy represents a simple and relatively low-cost analytical technique for obtaining unambiguous structural information, making it a basic tool in polymer analysis.…”
Section: Introductionmentioning
confidence: 99%
“…Solution NMR can be applied effectively to identify the type, the number, and the proportions of different sugar residues in a polysaccharide as well as different linkage configurations and positions in the polymer (27). We used the technique and the results approved our sugar analysis (5) but the structure of the sample could not be fully determined because of some signal overlaps and low signal to noise ratio.…”
Section: Discussionmentioning
confidence: 99%