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Hironori Matsushima

Researcher at University of Southern Mississippi

Publications -  6
Citations -  460

Hironori Matsushima is an academic researcher from University of Southern Mississippi. The author has contributed to research in topics: Isopropylthioxanthone & Isocyanate. The author has an hindex of 5, co-authored 6 publications receiving 429 citations.

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Segmented Polythiourethane Elastomers Through Sequential Thiol-ene and Thiol-isocyanate Reactions

TL;DR: In this article, high elastic polythiourethanes were synthesized through sequential thiol reactions involving 1,6-hexanedithiol, 1,4-butanediol diacrylate (BDDA), and several diisocyanates (ISO).
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The Thiol−Isocyanate Click Reaction: Facile and Quantitative Access to ω-End-Functional Poly(N,N-diethylacrylamide) Synthesized by RAFT Radical Polymerization

TL;DR: In this article, N,N-Diethylacrylamide (DEAm) was homopolymerized by reversible addition−fragmentation chain transfer (RAFT) radical polymerization yielding a homopolymers with a calculated degree of polymerization of 30 (PDEAm30), as determined by 1H NMR spectroscopic end-group analysis, and a polydispersity index (Mw/Mn) of 1.10.
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Thiol−Isocyanate−Ene Ternary Networks by Sequential and Simultaneous Thiol Click Reactions

TL;DR: In this article, the kinetics of the hybrid networks investigated using real-time IR indicate that both thiol-isocyanate and thiol−ene reactions were quantitatively rapid and efficient (>90% of conv...
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Thiol-isocyanate-acrylate ternary networks by selective thiol-click chemistry

TL;DR: The results indicate that the network structures and material properties are tunable over a wide range of properties, while maintaining nearly quantitative reactions, simply by controlling the component compositions.
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Non-extractable photoinitiators based on thiol-functionalized benzophenones and thioxanthones

TL;DR: In this paper, the efficiency of thiol-functionalized photoinitiators in combination with amine co-initiator was compared to benzophenone and isopropylthioxanthone with co-innitiators, and the cleavage of 2, 2-dimethoxy-1,2-diphenylethan-1-one in acrylic resins.