In the ring-opening polymerization (ROP) of cyclic esters and carbonates, hydrogen-bonding organocatalysis offers an interesting alternative to metal-based and enzymatic catalysis to access biocompatible and biodegradable polymers. The design of catalysts, strategies of activation and mechanistic elucidations are highlighted. Recent developments with functionalized monomers for applications in nanomaterials and biomedicine have opened perspectives to broaden the scope of future catalytic systems. In the field of sustainable chemistry, hydrogen-bonding structures devoted to ROP have become a full-fledged class of catalysts.
The mechanism of the ring-opening polymerization (ROP) of lactide catalyzed by two partner hydrogen-bonding organocatalysts was explored. New amidoindoles 4 a,c, thioamidoindoles 4 b,d, amidobenzimidazoles 5 a,c, and thioamidobenzimidazoles 5 b,c were synthesized and used as activators of the monomer. In the solid state and in solution, compounds 4 and 5 showed a propensity for self-association, which was evaluated. (Thio)Amides 4 and 5 do catalyze the ROP of lactide in the presence of a cocatalyst, tertiary amine 3 a or 3 b, which activates the growing polymer chain through hydrogen-bonding. Reactions were conducted in 2-24 h at 20 degrees C; conversion yields ranged between 22 and 100 %. A detailed study of the intermolecular interactions undertaken between the participating species showed that, as expected, simultaneous weak hydrogen bonds do exist to activate the reagents. Moreover, interactions have been revealed between the partner catalysts 4/5+3. ROP catalyzed by these partner activators is thus governed by multiple dynamic equilibria. The latter should be judiciously adjusted to fine-tune the catalytic properties of (thio)amides and organocatalysts, more generally.
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