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Tomoyuki Ohishi

Researcher at Tokyo Institute of Technology

Publications -  30
Citations -  1003

Tomoyuki Ohishi is an academic researcher from Tokyo Institute of Technology. The author has contributed to research in topics: Polymer & Covalent bond. The author has an hindex of 14, co-authored 30 publications receiving 814 citations. Previous affiliations of Tomoyuki Ohishi include Kyushu University.

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Mechanophores with a Reversible Radical System and Freezing‐Induced Mechanochemistry in Polymer Solutions and Gels

TL;DR: The diarylbibenzofuranone-based mechanophore radical system enabled, through electron paramagnetic resonance spectroscopy, in-situ quantitative evaluation of scission of the mechanophores and estimation of mechanical energy induced along polymer chains by external forces.
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Mechanochromic Dynamic Covalent Elastomers: Quantitative Stress Evaluation and Autonomous Recovery

TL;DR: This work visualize stress by color changes, as well as quantitatively estimate the stress in situ, in segmented polyurethane elastomers with diarylbibenzofuranone-based dynamic covalent mechanophores with in situ electron paramagnetic resonance measurements, accompanied by drastic color changes.
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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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Network Reorganization of Dynamic Covalent Polymer Gels with Exchangeable Diarylbibenzofuranone at Ambient Temperature

TL;DR: The reorganization of gel networks with diarylbibenzofuranone (DABBF)-based dynamic covalent linkages in response to the ambient temperature was systematically investigated from the perspective of both macroscopic and microscopic changes.