1992
DOI: 10.1016/0144-8617(92)90101-u
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Structural differences between chitin polymorphs and their precipitates from solutions—evidence from CP-MAS 13C-NMR, FT-IR and FT-Raman spectroscopy

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Cited by 205 publications
(92 citation statements)
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“…Both forms can be differentiated by infrared; solid-state NMR [80] spectroscopy, and X-ray diffraction [81][82][83]. A third allomorph, γ-chitin, has also been described [84].…”
Section: Structural Properties Of Chitinmentioning
confidence: 99%
“…Both forms can be differentiated by infrared; solid-state NMR [80] spectroscopy, and X-ray diffraction [81][82][83]. A third allomorph, γ-chitin, has also been described [84].…”
Section: Structural Properties Of Chitinmentioning
confidence: 99%
“…For that, approximately 2 mg of sample was mixed with 98 mg of KBr previously oven dried, and the mixture homogenized in an agate mortar. The mixture was compressed in a hydraulic press to form a pellet of approximately 0.20 mm thick, which was then analyzed in triplicate (Focher et al, 1992).…”
Section: Characterizationmentioning
confidence: 99%
“…Peak (3,263 cm -1 ) is generally assigned to the N-H stretching restricted by the intermolecular C(2)NH … O=C(7) H-bonds and peak (3,109 cm -1 ) to the O-H stretching restricted by the intermolecular C(6) OH … H-O-C (6 0 ) H-bonds [26,27]. In addition, the spectrum of the native chitosan is characterized by a splitting of the amide I vibration at 1,660 and 1,629 cm -1 which have been assigned to the stretching of C=O groups hydrogen bonded to N-H groups of the adjacent chain, and the stretching of the C=O groups bifurcated by forming an additional hydrogen bond to the primary OH groups of the same chain, respectively [28,29]. In contrast, evident differences can be observed when comparing the IR spectra of the regenerated chitosan from [Gly]Cl solvent (Fig.…”
Section: Resultsmentioning
confidence: 99%