R
Raita Goseki
Researcher at Tokyo Institute of Technology
Publications - 80
Citations - 2203
Raita Goseki is an academic researcher from Tokyo Institute of Technology. The author has contributed to research in topics: Living anionic polymerization & Polymer. The author has an hindex of 25, co-authored 78 publications receiving 1774 citations. Previous affiliations of Raita Goseki include National Institute of Advanced Industrial Science and Technology.
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Advances in Living Anionic Polymerization: From Functional Monomers, Polymerization Systems, to Macromolecular Architectures
TL;DR: In this article, the development in living anionic polymerization since 1990 has been discussed, including functional styrene derivatives, new monomers and promising additives, the regio-and stereoselective polymerization, special polymers having rigid-rod-like or helical conformations, the synthesis of complex branched polymers composed of comb-like segments via live anionic poly(macromonomer)s, and the precise synthesis of macromolecular architectures including multiblock polymers, exact graft polymers and multicomponent μ-star poly
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Hierarchical Self-Assembled Structures from POSS-Containing Block Copolymers Synthesized by Living Anionic Polymerization
Tomoyasu Hirai,Melvina Leolukman,Sangwoo Jin,Raita Goseki,Yoshihito Ishida,Masa Aki Kakimoto,Teruaki Hayakawa,Moonhor Ree,Padma Gopalan +8 more
TL;DR: In this article, two kinds of polyhedral oligomeric silsesquioxane (POSS)-containing block copolymers (BCPs) were synthesized by living anionic polymerization.
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Degradable epoxy resins prepared from diepoxide monomer with dynamic covalent disulfide linkage
TL;DR: In this paper, the authors demonstrate the efficient degradation of epoxy resins with disulfide linkages synthesized from bis(4-glycidyloxyphenyl)disulfide and several diamines.
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Enhancing Mechanochemical Activation in the Bulk State by Designing Polymer Architectures
TL;DR: In this paper, the authors designed linear and star polymers with a mechanophore at the center of each architecture, and investigated the effect of molecular weight and branched structures on mechanoresponsiveness in the solid state.
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Polymer–Inorganic Composites with Dynamic Covalent Mechanochromophore
TL;DR: In this paper, a rational macromolecular design to suppress the deactivation of activated dynamic mechanophores and improve sensitivity by limiting their molecular motion is proposed, which can be quantitatively evaluated by electron paramagnetic resonance spectroscopy.