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Abstract The structure and thermodynamic properties of atactic and isotactic acrylic and methacrylic polymers containing 16–18 carbon atoms in the n ‐aliphatic side chains, and of copolymers of hexadecyl acrylate with isopropyl acrylate were studied by means of x‐ray and differential thermal analysis. The crystallization of branched acrylic and methacrylic polymers and of acrylic copolymers proceeds in the form of a hexagonal crystal, regardless of the configuration of the backbone chain. Methods of ordering branched macromolecules are proposed, and the melting points, heats and entropies of fusion determined. The role of flexibility of the backbone chains in ordering and the crystallization processes was determined. In the case of poly( n ‐alkyl acrylates) the backbone chain is involved in the crystalline lattice; this is not the case in methacrylates and copolymers of hexadecyl acrylate with isopropyl acrylate. Some similarity was assumed between the structure of biopolymers and synthetic branched polymers.
Platé et al. (Sun,) studied this question.