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Phase Structure of the Exact Graft Copolymer Synthesized by Iterative Methodology Based on Living Anionic Polymerization
Author(s) -
Lin YuHsuan,
Chen HsinLung,
Goseki Raita,
Hirao Akira
Publication year - 2017
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201700150
Subject(s) - copolymer , polymer chemistry , materials science , polystyrene , polymerization , phase (matter) , molecule , chemistry , polymer , composite material , organic chemistry
Exact graft copolymer (EGC) is a type of copolymer with precisely defined molecular parameters, including the number of grafts per molecule ( n ), the length of the grafts ( l g ), and the separation distance between the junction points (ε) in the backbone. In the present study, the phase structure of the EGC composed of poly(2‐vinyl pyridine) backbone and polystyrene graft with n = 2 and n = 3 under fixed ε and l g is systematically investigated to seek a general understanding on the effect of the graft architecture on the domain spacing of the microphase‐separated structure and the order–disorder transition temperature ( T ODT ). It is found that the T ODT associated with the fluctuation‐induced ODT of the EGC increases with increasing n due to the increase of the total molecular weight. Nevertheless, the domain spacing does not exhibit a monotonic change with n , as the EGC with n = 2 shows the largest domain spacing compared with that of EGC with n = 3 and the corresponding linear diblock copolymer. The experimental observation on the domain spacing is explained by a thermodynamic model considering the packing mode of the constituting chains under the junction constraint.