Photocontrolled lactide ROP by the light-regulated release of potassium acetate from an azobenzene-bridged crown ether

An azobenzene-bridged 15-crown-5 ether (1) was successfully used as a photoswitchable cocatalyst for modulating the catalytic activity of potassium acetate (KOAc) in the ring-opening polymerization (ROP) of L-lactide (L-LA) when initiated from an exogenous alcohol. By alternating exposure to daylight and UV light, 1 transforms the K+,Ac- ion pair-like in free ions ondemand, resulting in an effective form of the catalytic complex. This allows the modulation of the L-LA ROP speed, switching the process from a slow to a fast state.

Automated summary

The azobenzene-bridged 15-crown-5 ether was successfully utilized as a photoswitchable cocatalyst to modulate the catalytic activity of potassium acetate in the ring-opening polymerization of L-lactide. By alternating exposure to daylight and UV light, the ion pair-like structure of KOAc was transformed on-demand, resulting in effective modulation of the polymerization speed from slow to fast.