Facile Synthesis of Unimodal Polymethacrylates with Narrow Dispersity via NIR LED Light-Controlled Bromine-Iodine Transformation Reversible-Deactivation Radical Polymerization

A facile and clean strategy for synthesizing unimodal polymethacrylates with narrow dispersity (D < 1.10) is successfully developed by a near-infrared (NIR) light-emitting diode (LED) light (lambda(max) = 740 nm)-controlled in situ bromine-iodine transformation reversible-deactivation radical polymerization system without the use of NIR dyes and expensive catalysts. In this system, alkyl iodide ethyl alpha-iodophenylacetate (EIPA) initiator is generated in situ by the nucleophilic substitution reaction between an alkyl bromide compound ethyl alpha-bromophenylacetate and sodium iodide (NaI). At the same time, excessive NaI is also acted as a highly active catalyst by forming halogen bonds with terminal iodine of the polymer chains in this system to make it capable of precisely synthesizing polymethacrylates with narrow dispersities (D = 1.03-1.10). In addition, the strong penetration ability of NIR LED light is illustrated by the successful polymerization even through 11 pieces of A4 paper.

Automated summary

A facile strategy for synthesizing unimodal polymethacrylates with narrow dispersity (D < 1.10) has been successfully developed using a near-infrared (NIR) light-emitting diode (LED) controlled system, demonstrating the strong penetration ability of NIR LED light through 11 pieces of A4 paper.