OKAMOTO KAZUNORI
Graduate School 【 display / non-display 】
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Graduate school:Hiroshima University
Course:先進理工系科学研究科
Course completed:Doctor's Course
Date of completion:2025.03
Completion status:Completed
Country:Japan
Degree 【 display / non-display 】
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Degree name:博士(理学)
Classified degree field:Life Science / Functional biochemistry
Conferring institution:Hiroshima University
Acquisition way:Coursework
Date of acquisition:2025.03
Research Areas 【 display / non-display 】
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Research field:Nanotechnology/Materials / Structural organic chemistry and physical organic chemistry
Papers 【 display / non-display 】
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Language: English
Title: Impact of Transition-State Aromaticity on Selective Radical‒Radical Coupling of Triarylimidazolyl Radicals
Journal name: Journal of the American Chemical Society vol.147 (3) (p.6877 - 6885)
Date of publication: 2024.11
Author(s): Kazunori Okamoto, Sayaka Hatano, Manabu Abe*DOI: 10.1021/jacs.4c14095
Type of publication: Research paper (scientific journal)
Field of experts:Nanotechnology/Materials / Structural organic chemistry and physical organic chemistry -
Language: English
Title: Synthesis of Optically Active Folded Cyclic Dimer and Trimer
Date of publication: 2025.08
Author(s): Kumamoto, E.; Ogawa, K.; Okamoto, K.; Morisaki, Y.DOI: 10.3762/bjoc.21.124
Type of publication: Research paper (scientific journal)
Field of experts:Nanotechnology/Materials / Structural organic chemistry and physical organic chemistry -
Language: English
Title: Thermal Reaction Behavior of Triphenyl imidazolyl Radical with a Bulky Substituent
Journal name: Journal of Organic Chemistry vol.87 (10) (p.6877 - 6885)
Date of publication: 2022.05
Author(s): Kazunori Okamoto, Sayaka Hatano*, and Manabu AbeType of publication: Research paper (scientific journal)
Field of experts:Nanotechnology/Materials / Structural organic chemistry and physical organic chemistry
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Optically active higher-ordered structures, such as one-handed helical and propeller-shaped structures, can be constructed by folding the π-conjugated system using [2.2]paracyclophane as the chiral crossing unit, leading to circularly polarized luminescence (CPL) properties. Chiral cyclic dimers and trimers were synthesized using planar chiral [2.2]paracyclophane-containing enantiopure ribbon-shaped compounds as the chiral monomers. Unicursal π-conjugated systems were folded at the [2.2]paracyclophane units, and exhibited good photoluminescence quantum efficiencies and CPL anisotropy factors. Opposite chiroptical properties were observed between the dimer and trimer, despite the same absolute configuration of the planar chiral [2.2]paracyclophane units, which was reproduced by theoretical studies.