𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Second-derivative F.t.-i.r. spectra of native celluloses

✍ Scribed by Anthony J. Michell


Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
450 KB
Volume
197
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.

✦ Synopsis


F.t.-ir. spectra of algal, bacterial, cotton, ramie, and wood celluloses, obtained in the second-derivative mode, have improved resolution. The spectra support the hypothesis that the crystalline structures of these celluloses can be divided into algal-bacterial and cotton-ran&-wood types. Bands that differ in the spectra of the two types are different from those sensitive to the change cellulose I-+11.

INTRODIJCI?ON

The structures of the two major polymorphs (I and II) of cellulose have been studied extensively, but less attention has been given to the question of allomorphy within the cellulose I (native cellulose) family. An early X-ray diffraction study' of algal, bacterial, cotton, and ramie celluloses found significant differences in the parameters of the unit cell and differences were observed also in electron diffraction studies2p3. Solid-state n.m.r.4-8, Raman spectroscopicg, and electron diffraction studiesi showed that the crystalline structures of native celluloses can be classified into algal-bacterial and cotton-ramie-wood pulp typess. Wiley and Atalla proposed that these two types have similar conformations but are packed in different lattices, whereas otherslo have suggested that the differences within the cellulose I family are derived from the size of the unit cells.

1.r. spectroscopy was one of the earliest techniques used to examine the crystalline nature of the celluloses. Marrinan and Mann" and Liang and Marchessault" obtained two types of band patterns in the OH and CH stretching regions (3604_2SOO cm-i) for native celluloses. Marchessault and Liangi3 extended the study to the region 1700-640 cm-i. Despite some of the spectra having been recorded" on samples at the temperature of liquid nitrogen, the bands tended to be broad and poorly resolved. However, use of the second-derivative model4 can assist in resolving the spectra of celluloses. Second-derivative spectra of celluloses obtained from algae, bacteria, ramie, cotton, and wood are now reported.


πŸ“œ SIMILAR VOLUMES


Second-derivative FTIR spectra of native
✍ Anthony J. Michell πŸ“‚ Article πŸ“… 1993 πŸ› Elsevier Science 🌐 English βš– 454 KB

The greater resolution afforded by the second-derivative mode has enabled differences previously observed in bands near 3240, 750, and 710 cm-' in the FTIR spectra of Valonia and tunicin celluloses to be confirmed, and revealed new differences near 2900 and 650 cm-'. These bands are assigned largely

F.T.-I.R. spectra of oligo- and poly-nuc
✍ Anne-Marie Seuvre; Mohamed Mathlouthi πŸ“‚ Article πŸ“… 1987 πŸ› Elsevier Science 🌐 English βš– 932 KB

Fourier-transform infrared (F.t.-i.r.) spectra of some synthetic mono-, oligo-, and poly-nucleotides and a natural DNA extracted from crab gonad have been recorded. Assignments of the observed frequencies are proposed by reference to our previous interpretation of laser-Raman and F.t.-i.r. spectra o

F.t.-i.r. and laser-Raman spectra of thy
✍ Mohammed Mathlouthi; Anne-Marie Seuvre; Jack L. Koenig πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 English βš– 954 KB

F.t.-i.r. and laser-Raman spectra of thymine and thymidine in the solid state were recorded. Assignments were proposed for the frequencies observed. The influence of the deoxy sugar on the vibrations of the nucleoside are discussed as a function of its particular puckering. The aim of this work is t

F.T.-I.R. and laser-raman spectra of gua
✍ Mohamed Mathlouthi; Anne Marie Seuvre; Jack L. Koenig πŸ“‚ Article πŸ“… 1986 πŸ› Elsevier Science 🌐 English βš– 850 KB

Fourier-transform infrared (F.t.-i.r.) and laser-Raman spectra have been obtained for solid guanine. The F.t.-i.r. spectrum of guanosine in the solid state was also recorded. Assignments are proposed for the i.r. bands. The molecular basis of the spectral differences between guanine and guanosine ar