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New Possibilities of the Acetosulfation of Cellulose
Author(s) -
Hettrich Kay,
Wagenknecht Wolfgang,
Volkert Bert,
Fischer Steffen
Publication year - 2008
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.200850216
Subject(s) - cellulose , solubility , chemistry , dissolution , reactivity (psychology) , organic chemistry , polymer , aqueous solution , polymer chemistry , medicine , alternative medicine , pathology
Regioselectively substituted cellulose sulfates in C2/3‐, C2/6‐, or C6‐position of the anhydroglucose unit are accessible by certain synthesis routes. Thereby, products with different properties and various application areas are resulted. Important characteristics of cellulose sulfates regarding their applications are solubility (e.g. in water), rheological behavior, different interaction with low or high molecular cations, thermo reversible gel formation, enzymatic degradability, anticoagulant and antiviral activity. In C6‐position substituted cellulose sulfates can be synthesized in principle by acetosulfation. The acetosulfation is a quasi‐homogeneous synthesis proceeding under gradually dissolution of the cellulose by using different reactivity of the primary and secondary OH‐groups as soon as converting cellulose acetate sulfates. After precipitation of the polymer the acetyl groups are cleaved in alkaline solution. The focus of our study was firstly the investigation of the acetosulfation in different polar aprotic solvents by various sulfating and acetylating agents. In general it should be investigated if C6 substituted cellulose sulfates can be obtained by acetosulfation with different solvents and agents. The products were characterized by 13 C‐NMR and Raman spectroscopy.