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Vibrational spectroscopy of seaweed galactans

✍ Scribed by Betty Matsuhiro


Book ID
104623102
Publisher
Springer
Year
1996
Tongue
English
Weight
596 KB
Volume
326-327
Category
Article
ISSN
1573-5141

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✦ Synopsis


Information from classical infrared spectroscopy studies has been of significance for characterizing seaweed galactans . The development of Fourier transform infrared spectroscopy and of Fourier transform laser Raman spectroscopy has produced great advances in the application of vibrational spectroscopy to the structural study of polysaccharides . Computational facilities in the spectrometers allow the arithmetic manipulations of the spectra .The second-derivative mode in the FT IR spectrocopy provided more information by increasing the number and resolution of the bands in the spectra as compared to the parent ones . A review of literature data on vibrational spectroscopy of sulfated polysaccharides and new results are presented. Agar-type polymers showed two diagnostic bands in the second-derivative mode in the region 800-700 cm -1 . Carrageenans exhibited a number of bands in the region 1600-1000 cm -1 . Fourier transform laser Raman spectroscopy in the solid state gave well-defined characteristic spectra of agar and carrageenans . Both techniques can be applied to small samples in the solid state and allow differentiation in a few minutes between agar and carrageenan-type seaweed galactans . The second-derivative mode of the FT-IR spectra can be applied to distinguish agar-producing from carrageenan-producing seaweeds . The spectra on KBr pellets of dried, ground agarophyte and carrageenophyte seaweed samples showed the same bands as the corresponding polysaccharides .


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13C-nmr spectroscopy of red algal galact
✍ Anatoly I. Usov; Sergey V. Yarotsky; Alexandr S. Shashkov πŸ“‚ Article πŸ“… 1980 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 715 KB

## Abstract ^13^C‐nmr spectra of red seaweed galactans, belonging to the agar and carrageenan groups or having the β€œintermediate” type of structure, were interpreted on the basis of ^13^C‐nmr spectra of model compounds. Signal assignments have been made for most of the known extreme structures of s