Journal of Polymer Science Part A: Polymer Chemistry, Vol.32, No.14, 2619-2624, 1994
Preparation and Block Copolymerization of Oligodihexanoylchitin Having Hydroxy-Groups at Both Ends
The preparation of oligodihexanoylchitin (3) having hydroxy groups at the both ends was carried out by an acid hydrolysis of a parent dihexanoylchitin in a mixed solution of acetic acid and conc. hydrochloric acid (11 : 1 in volume) at a room temperature. After 13-21 h, the products were isolated and their molecular weights were calculated as 7400-1100 by GPC analyses. The structure of the product 3 was determined by H-1 and C-13-NMR and IR spectra. The IR spectra of the products yielded for longer hydrolysis times than 30 h, however, indicated the occurrence of the dehexanoylation. The block copolymerization of 3 with poly (propylene glycol) (PPG) using 4,4’-methylenedi (phenyl isocyanate) (MDI) as a coupling reagent gave the block copolymer 6. The molecular weight of 6 as obtained by GPC was 52,000.
Keywords:POLYMERS