This study utilizes the primary amide side-chain of acrylamide copolymers as an isocyanate surrogate. The isocyanate is generated through an electrochemical Hofmann rearrangement under mild conditions, resulting in the formation of O-alkyl carbamate side-chains in alcohol solvents. This represents a novel strategy for modifying amide-functionalized (co)polymers.
The primary amide side-chain of acrylamide copolymers has been utilised as an isocyanate surrogate. The isocyanate is formed under mild conditions via an electrochemical Hofmann rearrangement resulting in the formation of O-alkyl carbamate side-chains in alcohol solvents. This represents a new strategy for the modification of amide-functionalised (co)polymers.
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