Loading…
New water-soluble and film-forming aminocellulose tosylates as enzyme support matrices with Cu2+-chelating properties
Within the framework of our studies on enzyme-compatible support matrix structures, we succeeded in making further derivatives of the new aminocellulose type ‘P–CH2–NH–(X)–NH2’ (P = cellulose); (X) = –(CH2)2– (EDA), –(CH2)2–NH–(CH2)2– (DETA), –(CH2)3–NH–(CH2)3– (DPTA), –(CH2)2–NH–(CH2)2–NH–(CH2)2– (...
Saved in:
Published in: | Cellulose (London) 2005-02, Vol.12 (1), p.67-84 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Within the framework of our studies on enzyme-compatible support matrix structures, we succeeded in making further derivatives of the new aminocellulose type ‘P–CH2–NH–(X)–NH2’ (P = cellulose); (X) = –(CH2)2– (EDA), –(CH2)2–NH–(CH2)2– (DETA), –(CH2)3–NH–(CH2)3– (DPTA), –(CH2)2–NH–(CH2)2–NH–(CH2)2– (TETA) accessible by nucleophilic substitution reaction with ethylenediamine (EDA) and selected oligoamines starting from 6(2)-O-tosylcellulose tosylate (DStosylate = 0.8). The 13C-NMR data show that the EDA and oligoamine residues are at C6 of the anhydroglucose unit (AGU) and that OH and tosylate are also (partially) present at C6. OH and partially tosylate are at C2/C3. All the synthesized aminocellulose tosylates were soluble in water and formed transparent films from their solutions. The aminocellulose tosylate solutions and the films prepared from them formed blue-coloured chelate complexes with Cu2+ ions, whose absorption maxima at wavelengths in the VIS region were located similarly to those of the Cu2+ chelate complexes with EDA and with the oligoamines. AFM investigations have shown that the aminocellulose films, depending on structural and environment-induced factors influencing e.g. SiO2 polymer films, exhibit ‘flat’ topographies ( |
---|---|
ISSN: | 0969-0239 1572-882X |
DOI: | 10.1007/s10570-004-4356-9 |