Unperturbed dimensions of random and alternating styrene/<i>n</i>‐alkyl methacrylate copolymers

Abstract

Abstract The steric factors σ of homopolymers of ethyl, n ‐butyl, and n ‐octyl methacrylate, of equimolar random and alternating copolymers of these monomers with styrene, and of polystyrene, were determined by measuring intrinsic viscosities in a good solvent (butanone, 25°C) and extrapolating the data thus obtained to zero molecular weight of the polymer. For all comonomeric pairs under investigation, the σ 2 of an equimolar random copolymer and, particularly, of an alternating copolymer, is higher than the arithmetic mean (σ + σ )/2 of the σ 2 values of the parent homopolymers. The positive deviation from the linear dependence of σ 2 on the copolymer composition, expressed as an increment of σ 2 , is proportional to the mole fraction of alternating dyads in the copolymer chain with in the limits of experimental error. The effect of copolymer microstructure on the unperturbed dimensions of the chains has been compared for equimolar copolymers of styrene with methyl, ethyl, n ‐butyl, and n ‐octyl methacrylate by using a relative increment ξ defined as the ratio of σ 2 of the alternating copolymer to (σ + σ )/2. The dependence of ξ on the number of carbon atoms in the alcohol substituent of the methacrylate component of the copolymer seems to exhibit a maximum for ethyl methacrylate.