Sequence-Selective Terpolymerization from Monomer Mixtures Using a Simple Organocatalyst.

One-step synthesis of block copolymer from mixed monomers is of great interest and challenge. Using a simple non-nucleophilic organobase as the catalyst, we have achieved sequence-selective terpolymerization from a mixture of phthalic anhydride (PA), an epoxide, and rac -lactide (LA). Alcohol-initiated alternating copolymerization of PA and epoxide occurs first and exclusively because PA is substantially more active than LA for reacting with base-activated hydroxyl. When PA is fully consumed, LA polymerizes from the termini of the first block while excess epoxide stays intact because of the mild basicity of the catalyst. The two polymerizations thus occur tandemly, both in chemoselective manners, so that an aromatic-aliphatic block copolyester is generated in this one-step synthesis. The effectiveness and versatility of this approach is demonstrated by the use of ethylene oxide and several monosubstituted epoxides as well as mono-, di-, or tetrahydroxy initiators.