Cellulose Derivatives Synthesized via Isocyanate and Activated Ester Pathways in Homogeneous Solutions of Lithium Chloride N,N-dimethylacetamide
Document Type
Article
Publication Date
1998
Department
Polymers and High Performance Materials
Abstract
Cellulose carbamate and ester derivatives were synthesized in homogeneous solutions of lithium chloride (LiCl)/N,N-dimethylacetamide (DMAc) by the reaction of cellulose with ethyl 4-isocyanatobenzoate and the activated esters of N,N-dimethylaminobenzoic acids. Comparative reactions were performed with phenyl isocyanate and the activated ester of benzoic acid. All reactions were followed spectroscopically by FTIR, H-1 NMR, and C-13 NMR. Degrees of substitution were calculated utilizing UV spectroscopy. The isocyanate reactions are facile allowing controllable degrees of substitution and high yields. By contrast, the activated ester pathway inherently results in lower degrees of substitution and lower yields due in part to undesirable side reactions.
Publication Title
Journal of Macromolecular Science: Pure and Applied Chemistry
Volume
A35
Issue
12
First Page
1915
Last Page
1927
Recommended Citation
Williamson, S. L.,
McCormick, C. L.
(1998). Cellulose Derivatives Synthesized via Isocyanate and Activated Ester Pathways in Homogeneous Solutions of Lithium Chloride N,N-dimethylacetamide. Journal of Macromolecular Science: Pure and Applied Chemistry, A35(12), 1915-1927.
Available at: https://aquila.usm.edu/fac_pubs/5128