2026/04/01 更新

写真a

カニ リュウノスケ
可児 龍之介
KANI RYUNOSUKE
所属
総合研究院 フロンティア材料研究所 助教
職名
助教
連絡先
メールアドレス
外部リンク

学位

  • 博士(工学) ( 2023年9月   岐阜大学 )

研究分野

  • ナノテク・材料 / 有機機能材料

学歴

  • 岐阜大学   大学院 工学研究科   工学専攻

    2020年10月 - 2023年9月

      詳細を見る

  • 岐阜大学   自然科学技術研究科   物質・ものづくり工学専攻

    2019年4月 - 2020年9月

      詳細を見る

  • 岐阜大学   工学部   化学・生命工学科 物質化学コース

    2015年4月 - 2019年3月

      詳細を見る

経歴

  • 東京科学大学   総合研究院   フロンティア材料研究所   助教

    2024年9月 - 現在

      詳細を見る

  • 東京科学大学   科学技術創成研究院   フロンティア材料研究所   研究員

    2023年10月 - 2024年8月

      詳細を見る

    国名:日本国

    researchmap

所属学協会

  • 有機EL討論会

    2024年4月 - 現在

      詳細を見る

  • 応用物理学会

    2024年4月 - 現在

      詳細を見る

論文

  • Green to blue photon upconversion in solid-state using anthracene and naphthalene diimide derivatives

    Ryunosuke Kani, Keisuke Fujimoto, Koki Banno, Yutaka Majima, Masaki Takahashi, Seiichiro Izawa

    Japanese Journal of Applied Physics   64 ( 9 )   091004 - 091004   2025年9月

     詳細を見る

    担当区分:筆頭著者   掲載種別:研究論文(学術雑誌)   出版者・発行元:IOP Publishing  

    Abstract

    Conventional photon upconversion (PUC) methods using intersystem crossing suffer from low efficiency of incident light utilization due to lowering light absorption to avoid suppression of triplet exciton deactivation by sensitizer aggregation. In this study, to overcome the difficulty, a combination of donor and acceptor materials was investigated to develop a blue PUC that relies on triplet formation by charge separation and recombination at the solid-state interface. An anthracene derivative was used for the donor and naphthalene diimide with visible light absorption was designed and synthesized for the acceptor. The key design principle of the acceptor material was controlling the energy level to proceed with charge separation and recombination emission at the interface with the anthracene. Using this study as a strategy for material selection opens the possibility of achieving solid-state PUC that exhibits a variety of emission wavelengths.

    DOI: 10.35848/1347-4065/ae0223

    researchmap

    その他リンク: https://iopscience.iop.org/article/10.35848/1347-4065/ae0223/pdf

  • A Rapid and Dual Optical CO2‐responsive Polydimethylsiloxane Elastomer with a Fluorinated Cyanine Dye

    Ryunosuke Kani, Yohei Miwa, Yasuhiro Kubota, Toshiyasu Inuzuka, Shoichi Kutsumizu, Kazumasa Funabiki

    Chemistry – An Asian Journal   2023年12月

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

    <jats:title>Abstract</jats:title><jats:p>We found that our optically CO<jats:sub>2</jats:sub>‐responsive polydimethylsiloxane (PDMS) elastomer rapidly and reversibly underwent both visible and fluorescent color changes in the presence of CO<jats:sub>2</jats:sub> gas. Unlike conventional optically CO<jats:sub>2</jats:sub>‐responsive polymeric materials, it functions in totally dry gaseous conditions. The visible color and fluorescence of the elastomer sheet change after only 1 min of exposure to CO<jats:sub>2</jats:sub>, and the sheet exhibits excellent repeatability in terms of color switching that persists for at least 20 times.</jats:p>

    DOI: 10.1002/asia.202300798

    researchmap

  • Synthesis of 1‐Trifluoromethylated Propargyl Alcohols by Two Successive Reactions of Cyclopentylmagnesium Bromide in a One‐Pot Manner

    Ryunosuke Kani, Toshiyasu Inuzuka, Yasuhiro Kubota, Kazumasa Funabiki

    Asian Journal of Organic Chemistry   2022年2月

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

    <jats:title>Abstract</jats:title><jats:p>We have developed a functional‐group‐tolerant one‐pot route to various 3‐substituted 1‐trifluoromethylpropargyl alcohols utilizing two reactions of cyclopentylmagnesium bromide with trifluoroacetic acid esters and terminal alkynes. This new synthetic method involves three successive reactions in a one‐pot process: 1) deprotonation of terminal alkynes with cyclopentylmagnesium bromide, 2) reduction of 2,2,2‐trifluoroethyl trifluoroacetate with cyclopentylmagnesium bromide, and 3) nucleophilic addition of in‐situ‐generated alkynyl Grignard reagents to in‐situ‐formed trifluoroacetaldehyde, leading to the corresponding 3‐substituted 1‐trifluoromethylated propargyl alcohols. This method can be applied to various fluorine‐containing esters as well as terminal alkynes bearing alkyl and aryl groups to give 1‐polyfluoroalkylated propargyl alcohols. The obtained 1‐trifluoromethylpropargyl alcohols with aromatic groups can be converted in good to excellent yields to 1,5‐diaryl‐3‐trifluoromethyl‐dihydropyrazoles, some of the most important motifs in medicine for the treatment of pain and inflammation associated with osteoarthritis in dogs.</jats:p>

    DOI: 10.1002/ajoc.202100700

    researchmap

  • Aromatic fluorine atom-induced highly amine-sensitive trimethine cyanine dye showing colorimetric and ratiometric fluorescence change

    Ryunosuke Kani, Yasuhiro Kubota, Toshiyasu Inuzuka, Kazumasa Funabiki

    RSC Advances   2022年

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

    <jats:p>The prepared ring-perfluorinated trimethine cyanine dye 2a has a significantly higher response to <jats:italic>n</jats:italic>-hexylamine than the non-fluorinated dye 2b, and exhibited a dual change in the solution and on filter paper and fluorescence color at widely shifted wavelengths, visible to the naked eye.</jats:p>

    DOI: 10.1039/d2ra04387d

    researchmap

  • Highly diastereo- and enantioselective organocatalytic synthesis of trifluoromethylated erythritols based on the in situ generation of unstable trifluoroacetaldehyde

    Kazumasa Funabiki, Toshiya Gotoh, Ryunosuke Kani, Toshiyasu Inuzuka, Yasuhiro Kubota

    Organic & Biomolecular Chemistry   2021年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    <p>A highly diastereo- and enantioselective organocatalytic method to synthesise erythritols bearing a trifluoromethyl group has been investigated.</p>

    DOI: 10.1039/d0ob02067b

    researchmap

  • One‐Pot Successive Turbo Grignard Reactions for the Facile Synthesis of α‐Aryl‐α‐Trifluoromethyl Alcohols

    Ryunosuke Kani, Toshiyasu Inuzuka, Yasuhiro Kubota, Kazumasa Funabiki

    European Journal of Organic Chemistry   2020年8月

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

    <jats:p>A novel straightforward one‐pot methodology for two successive turbo Grignard reagent (<jats:italic>i</jats:italic>PrMgCl<jats:bold>·</jats:bold>LiCl) reactions, was developed for a facile synthesis of α‐aryl‐α‐trifluoromethyl alcohols, motifs of value in pharmaceutical chemistry. The method displayed broad functional group tolerance, including reducible groups. Dual roles of <jats:italic>i</jats:italic>PrMgCl<jats:bold>·</jats:bold>LiCl were exploited in the tandem reaction with commercially available iodoarenes or iodoheteroarenes and 2,2,2‐trifluoroethyl trifluoroacetate. The process encompasses three successive reactions in a one‐pot process: the <jats:italic>i</jats:italic>PrMgCl<jats:bold>·</jats:bold>LiCl‐mediated iodine/magnesium‐exchange reaction of iodoarenes or iodoheteroarenes; nucleophilic addition of various generated aryl or heteroarylmagnesium reagents to 2,2,2‐trifluoroethyl trifluoroacetate; and the reduction of in‐situ generated aryl trifluoromethyl ketones with <jats:italic>i</jats:italic>PrMgCl<jats:bold>·</jats:bold>LiCl, to produce the corresponding α‐aryl or α‐heteroaryl‐α‐trifluoromethyl alcohols bearing various substituents, including reducible functional groups in good to excellent yields.</jats:p>

    DOI: 10.1002/ejoc.202000550

    researchmap

  • One‐Pot and Reducible‐Functional‐Group‐Tolerant Synthesis of α‐Aryl‐ and α‐Heteroaryl‐α‐Trifluoromethyl Alcohols via Tandem Trifluoroacetylation and MPV Type Reduction

    Kazumasa Funabiki, Ayaka Hayakawa, Ryunosuke Kani, Toshiyasu Inuzuka, Yashuhiro Kubota

    European Journal of Organic Chemistry   2019年9月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    <jats:p>We have developed a new one‐pot synthesis of α‐aryl‐ and α‐heteroaryl‐α‐trifluoromethyl alcohols carrying not only arenes with electron‐withdrawing groups but also electron‐deficient nitrogen‐containing heteroarenes, which are of increasing interest because these compounds are some of the most important units in current fluorine‐containing inhibitors or antagonists. This new method includes three tandem reactions in a one‐pot synthesis: (1) the in situ generation of functionalized aromatic and electron‐deficient heteroaromatic Grignard reagents, (2) trifluoroacetylation of the generated Grignard reagents with diphenylmethyl trifluoroacetate, and (3) successive Meerwein–Ponndorf–Verley type reduction. It offers several advantages, including no need for expensive transition metals and gaseous trifluoromethylating reagents, toleration of not only reducible functional groups on the aryl groups but also electron‐deficient nitrogen‐containing heterocycles, easy scalability, and the ability to suppress the formation of the bis‐aldol product as a by‐product by changing the ester moiety of the trifluoroacetate from an isopropyl to a diphenylmethyl group.</jats:p>

    DOI: 10.1002/ejoc.201901049

    researchmap

▼全件表示

受賞

  • 学業成績優秀者表彰

    2024年3月   岐阜大学 工学研究科 工学専攻  

     詳細を見る

  • 笹川科学研究助成

    2023年3月   日本科学協会  

     詳細を見る

  • 融合フロンティア次世代リサーチャー

    2021年10月   東海国立大学機構  

     詳細を見る

  • 学業成績優秀者表彰

    2021年3月   岐阜大学 自然科学技術研究科 物質・ものづくり工学専攻  

     詳細を見る

  • 優秀ポスター賞

    2019年11月   第42回フッ素化学討論会  

     詳細を見る

  • 学業成績優秀者表彰

    2019年3月   岐阜大学 工学部 化学・生命工学科 物質化学コース  

     詳細を見る

▼全件表示