Organo-soluble cellulose-p-toluenesulfonates (tosylates) with an insig
nificant incorporation of chlorodeoxy functions were prepared by react
ing cellulose dissolved in N,N-dimethyl acetamide/LiCl and used as int
ermediates in the design of cellulosics with new, unusual molecular st
ructures. Thus, the remaining OH groups were acylated and sulfated yie
lding products with controlled lipophily and amphiphily which are prom
ising polymers for self-organizing systems. The polarity reversal by t
osylation was used for C-substitution reactions. The molecular structu
res of the products were proved by FTIR, H-1- and C-13-NMR spectroscop
y.