1989Acta PolymericaRequires access

Binary copolymerizations of N‐acryloyloxyphthalimide with methyl acrylate, methyl methacrylate and acrylonitrile

A. F. Shaaban, A.A. Khalil, N. N. Messiha

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Abstract

Abstract N‐Acryloyloxyphthalimide was prepared by the reaction of acrylic acid with N‐hydroxyphthalimide in the presence of N,N′‐dicyclohexylcarbodiimide. The monomer reactivity ratios for the copolymerization of N‐acryloyloxyphthalimide with methyl acrylate, methyl methacrylate, and acrylonitrile, respectively, were estimated by 1H‐NMR spectroscopic data. The Q‐ and e‐ values for N‐acryloyloxyphthalimide were calculated.

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Abstract N‐Acryloyloxyphthalimide was prepared by the reaction of acrylic acid with N‐hydroxyphthalimide in the presence of N,N′‐dicyclohexylcarbodiimide. The monomer reactivity ratios for the copolymerization of N‐acryloyloxyphthalimide with methyl acrylate, methyl methacrylate, and acrylonitrile, respectively, were estimated by 1H‐NMR spectroscopic data. The Q‐ and e‐ values for N‐acryloyloxyphthalimide were calculated.

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Available abstract

Abstract N‐Acryloyloxyphthalimide was prepared by the reaction of acrylic acid with N‐hydroxyphthalimide in the presence of N,N′‐dicyclohexylcarbodiimide. The monomer reactivity ratios for the copolymerization of N‐acryloyloxyphthalimide with methyl acrylate, methyl methacrylate, and acrylonitrile, respectively, were estimated by 1H‐NMR spectroscopic data. The Q‐ and e‐ values for N‐acryloyloxyphthalimide were calculated.

Key concepts: Acrylonitrile, Methyl methacrylate, Copolymer, Methyl acrylate, Monomer, Polymer chemistry, Acrylic acid, Reactivity (psychology)

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