No abstract

A new and convenient route to the regiocontrolled synthesis of a cellulose-based derivate copolymer (2,3-di-O-polycaprolactone-cellulose) grafting ε-caprolactone (ε-CL) from α-cellulose, cellulose-graft-polycaprolactone (cellulose-g-PCL), by a classical ring-opening polymerization (ROP) reaction, using stannous octoate (Sn(Oct) 2) as catalyst, in 68% concentration of zinc chloride aqueous solution at 120°C was presented. By controlling the hydroxyl of cellulose/ε-CL, catalyst/monomer ratio and the reaction time, the molecular architecture of the copolymers can be altered. The solubility of cellulose in zinc chloride aqueous was indicated by UV/VIS spectrometer and rheological measurements. The structures and thermal properties of cellulose-g-polycaprolactone copolymers were characterized using Fourier Transform Infrared (FT-IR), Proton Nuclear Magnetic Resonance Spectroscopy (1 H NMR), X-ray Diffraction (XRD), Thermogravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC) and Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). The interesting results confirm that zinc chloride solution can break the intra-molecular hydrogen bonds of cellulose selectively (not only O 3 H•••O 5 , but also O 2 H•••O 6), and has no effect on the inter-molecular hydrogen bonds (O 6 H•••O 3). And the grafting reactivity of hydroxyl on cellulose is C 2-OH > C 3-OH >> C 6-OH in zinc chloride solution, and this is clearly different from other researches. Most importantly, this work confirms that the method to regiocontrolled synthesis cellulose-based derivative polymers by regiobreaking hydrogen bonds is feasible. It is strongly believed that the new discovery may give a novel, environmental, simple and inexpensive method to modify cellulose chemically with various side chains grafted on a given hydroxyl, through liberating hydroxyl as reactive group from hydrogen bonds broken selectively by different solvents.