Abstract
AbstractPreparation and characterization (by IR and 1H NMR spectroscopy) of isomeric methacrylic acid and acrylic acid derivatives of the herbicide 3‐amino‐1,2,4‐traizole are described. Their radical polymerization and copolymerization with styrene or methyl methacrylate give polymers containing the herbicide moiety as pendant groups bound via acyl groups at the amino group or at the ring nitrogen. The reactivity ratios were determined for the isomeric methacrylic compounds.
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