Combined SANS, SEC, NMR, and UV-vis studies of simultaneous living anionic copolymerization process in a concentrated solution; Elucidation of building-up processes of molecules and their self-assemblies

中性子小角散乱法と相補的な核磁気共鳴(NMR)法,ゲル浸透クロマトグラフィー法,紫外・可視分光法の同時観測法によりリビンアニオン重合反応下で成長するジブロック共重合体の自己組織化の研究

Zhao, Y.; 宮元 展義*; 小泉 智; 橋本 竹治

Zhao, Y.; Miyamoto, Nobuyoshi*; Koizumi, Satoshi; Hashimoto, Takeji

A simultaneous living anionic copolymerization of a concentrated solution of deuterated styrene (S) and nondeuterated isoprene (I) monomers in deuterated benzene as a solvent was studied by a combination of time-resolved measurements of small-angle neutron scattering (SANS), size exclusion chromatography (SEC), nuclear magnetic resonance (NMR), and ultraviolet-visible spectroscopy (UV-vis). The molecular building-up process and its consequence on the bottom-up self-assembling process during the copolymerization reaction were observed on three different length scales on the same batch of the solution, which enabled us to explore simultaneously the time changes in the local structure (living chain ends), the primary structure (propagating chains), and the higher order structure (microdomains). We found that the copolymerization process was divided into two time regions, defined by regions I and II. In region I, the copolymerization of S and I monomers took place, and all I monomers were consumed at the end of region I. In the early stage of region I (region I), the SANS profiles were almost time-independent and exhibited no scattering maximum, whereas in the late stage of region I (region I), a scattering maximum appeared at m and hardly changed with time, although the maximum intensity slightly increased with time. In region II, pure polystyrene (PS) block chains were formed. The polymerization-induced disorder-order transition (ODT) and order-order transition (OOT) were observed.