助教:福井 識人
Dr. Norihito Fukui


2013年3月京都大学 理学部 卒業
2015年3月 京都大学大学院 理学研究科修士課程 修了 (指導教官:大須賀 篤弘 教授、依光 英樹 准教授(当時))
2018年3月京都大学大学院 理学研究科 博士後期課程 修了 (指導教官:大須賀 篤弘 教授)
2018年4月–名古屋大学大学院 工学研究科 助教






34. Redox-induced reversible [2+2] cycloaddition of an etheno-fused diporphyrin

K. Miyagawa, I. Hisaki, N. Fukui, H. Shinokubo*
Chem. Sci. 2021, in press.

33. Dinaphtho[1,8-bc:1',8'-fg][1,5]dithiocine Bisimide

Y. Tanaka, K. Tajima, N. Fukui,* H. Shinokubo*
Asian J. Org. Chem. 2021, in press.

Invited paper for Early Career Special Collection

32. Dual Emission of a Free‐Base 5‐Oxaporphyrinium Cation from its cis‐ and trans‐NH Tautomers

A. Takiguchi, S. Kang, N. Fukui,* D. Kim,* H. Shinokubo*
Angew. Chem. Int. Ed. 2020, in press.

31. Synthesis and electron-transport property of stable antiaromatic NiII norcorrole with the smallest meso-substituent

S. Ukai, Y. Hee Koo, N. Fukui, S. Seki,* H. Shinokubo*
Dalton Trans. 2020, in press.

30. as-Indaceno[3,2,1,8,7,6-ghijklm]terrylene as a near-infrared absorbing C70-fragment

29. Dinaphthothiepine Bisimide and Its Sulfoxide: Soluble Precursors for Perylene Bisimide

S. Hayakawa, K. Matsuo, H. Yamada,* N. Fukui,* H. Shinokubo*
J. Am. Chem. Soc. 2020, 142, 11663−11668.

Press Release (Japanese)
Highlighted in a newspaper(日刊工業新聞)
Highlighted in Synfacts
explanatory video (Japanese)

28. A 2-to-2′ 18-to-18′ doubly linked Ni(ii) norcorrole dimer: an effectively conjugated antiaromatic dyad

S.-Y. Liu, H. Kawashima, N. Fukui, H. Shinokubo*
Chem. Commun. 2020, 56, 6846−6849.

27. Reactions of Antiaromatic Norcorrole Ni(II) Complex with Carbenes

S.-Y. Liu, T. Fukuoka, N. Fukui, J.-Y. Shin, H. Shinokubo*
Org. Lett. 2020, 22, 4400–4403.

26. Synthesis and properties of 5-aza-15-thiaporphyrins

D. Yamashita, H. Omori, N. Fukui, H. Shinokubo*
J. Porphyr. Phthalocyanines. 2020, 24, 84−89.

25. Inserting Nitrogen: An Effective Concept to Create Nonplanar and Stimuli-Responsive Perylene Bisimide Analogues

S. Hayakawa, A. Kawasaki, Y. Hong, D. Uraguchi, T. Ooi, D. Kim,* T. Akutagawa,* N. Fukui,* H. Shinokubo*
J. Am. Chem. Soc. 2019, 141, 19807−19816.

Highlighted in Chem-Station
Press Release (Japanese)

24. Aggregation-Induced Emission of Nitrogen-Bridged Naphthalene Monoimide Dimers

K. Tajima, N. Fukui,* H. Shinokubo*
Org. Lett. 2019, 21, 9516−9520.

23. 5,5,15,15-Tetraoxo-5,15-Dithiaporphyrinas a Highly Electron-Deficient Porphyrinic Ligand

A. Yagi, T. Kondo, D. Yamashita, N. Wachi, H. Omori, N. Fukui, T. Ikeue, H. Shinokubo*
Chem. Eur. J. 2019, 25, 15580−15585.

22. Synthesis of Hydroxyisooxophlorins by Oxidative Degradation of meso-Hydroxyporphyrins

A. Takiguchi, N. Fukui, H. Shinokubo,*
Org. Lett. 2019, 21, 3950-3953.

21. Synthesis of meso‐Alkyl‐Substituted Norcorrole Ni(II) Complexes and Conversion to 5‐Oxaporphyrins(

S. Liu, H. Tanaka, R. Nozawa, N. Fukui, H. Shinokubo*
Chem. Eur. J. 2019, 25, 7618-7622.

Selected as a Hot Paper

20. Macroscopically Anisotropic Structures Produced by Light-induced Solvothermal Assembly of Porphyrin Dimers)

Y. Yamamoto, Y. Nishimura, S. Tokonami, N. Fukui, T. Tanaka, A. Osuka, H. Yorimitsu, and T. Iida
Sci. Rep. 2018, 8, 11108.

19. Diarylamine-Fused Subporphyrins: Proof of Twisted Intramolecular Charge Transfer (TICT) Mechanism

Koki Kise, Yongseok Hong, Norihito Fukui, Daiki Shimizu, Dongho Kim,* and Atsuhiro Osuka*
Chem. Eur. J. 2018, 24, 8306–8310.

18. Singly and Doubly Sulfone-inserted Porphyrin Arch-Tape Dimers

Norihito Fukui and Atsuhiro Osuka*
Bull. Chem. Soc. Jpn. 2018, 91, 1131–1137.

Selected as a BCSJ Award Article

17. Singly and Doubly 1,2-Phenylene-Inserted Porphyrin Arch-Tape Dimers: Synthesis and Highly Contorted Structures

Norihito Fukui and Atsuhiro Osuka*
Angew. Chem. Int. Ed. 2018, 57, 6304–6308.

16. Metalation Control of Open-shell Character in meso-meso Linked Porphyrin meso-Oxy Radical Dimers

Yuta Jun-i, Norihito Fukui, Ko Furukawa,* and Atsuhiro Osuka*
Chem. Eur. J. 2018, 24, 1528–1532.

15. A meso-meso β-β β-β Triply Linked Subporphyrin Dimer

Yasuhiro Okuda, Norihito Fukui, Jinseok Kim, Hua-Wei Jiang, Graeme Copley, Masaaki Kitano, Dongho Kim,* and Atsuhiro Osuka*
Angew. Chem. Int. Ed. 2017, 56, 12317–12321.

14. Porphyrin Arch-Tapes: Synthesis, Contorted Structures, and Full Conjugation

Norihito Fukui, Taeyon Kim, Dongho Kim,* and Atsuhiro Osuka*
J. Am. Chem. Soc. 2017, 139, 9075–9088.

Selected as a JACS Spotlight

Highlighted in Synfacts

13. Diphenylphosphine-Oxide-Fused and Diphenylphosphine-Fused Porphyrins: Synthesis, Tunable Electronic Properties, and Formation of Cofacial Dimers

Keisuke Fujimoto, Yuko Kasuga, Norihito Fukui, and Atsuhiro Osuka*
Chem. Eur. J. 2017, 23, 6741–6745.

12. Aromatic Metamorphosis of Dibenzofurans into Triphenylenes Starting with Nickel-Catalyzed Ring-Opening C-O Arylation

Yuto Kurata, Sinya Otsuka, Norihito Fukui, Keisuke Nogi, Hideki Yorimitsu,* and Atsuhiro Osuka
Org. Lett. 2017, 19, 1274–1277.

11. meso-to-meso PtII-bridged NiII-porphyrin dimers

Norihito Fukui, Hua-Wei Jiang, and Atsuhiro Osuka*
Org. Chem. Front. 2017, 4, 767–772.

10. Highly planar diarylamine-fused porphyrins and their remarkably stable radical cations

Norihito Fukui, Wonhee Cha, Daiki Shimizu, Juwon Oh, Ko Furukawa,* Hideki Yorimitsu,* Dongho Kim,* and Atsuhiro Osuka*
Chem. Sci. 2017, 8, 189–199.

Highlighted in Synfacts

9. meso-meso Linked Diarylamine-Fused Porphyrin Dimers

Norihito Fukui, Hideki Yorimitsu,* and Atsuhiro Osuka*
Chem. Eur. J. 2016, 22, 18476–18483.

8. Pictet–Spengler Synthesis of Quinoline-Fused Porphyrins and Phenanthroline-Fused Diporphyrins

Ke Gao, Norihito Fukui, Seok Il Jung, Hideki Yorimitsu,* Dongho Kim,* and Atsuhiro Osuka*
Angew. Chem. Int. Ed. 2016, 55, 13038–13042.

Highlighted in Synfacts

7. Regioselective phenylene-fusion reactions of Ni(II)-porphyrins controlled by an electron-withdrawing meso-substituent

Norihito Fukui, Seung-Kyu Lee, Kenichi Kato, Daiki Shimizu, Takayuki Tanaka, Sangsu Lee, Hideki Yorimitsu,* Dongho Kim,* and Atsuhiro Osuka*
Chem. Sci. 2016, 7, 4059–4066.

6. meso,β-Oligohaloporphyrins as Useful Synthetic Intermediates of Diphenylamine-Fused Porphyrin and meso-to-meso β-to-β Doubly Butadiyne-Bridged Diporphyrin

Norihito Fukui, Hideki Yorimitsu,* and Atsuhiro Osuka*
Angew. Chem. Int. Ed. 2015, 54, 6311–6314.

5. Palladium-Catalyzed [3+2] Annulation of meso-Bromoporphyrin with Silylacetylenes and Desilylation of 8a-Silyl-7,8-dehydropurpurin

Norihito Fukui, Seiji Arai, Hiroshi Shinokubo, Hideki Yorimitsu,* and Atsuhiro Osuka*
Heterocycles 2015, 90, 252–260.

4. Control of the conformational dynamics of meso-meso vinylene-bridged Zn(II) porphyrin dimers through diamine coordination

Minjung Son, Young Mo Sung, Sumito Tokuji, Norihito Fukui, Hideki Yorimitsu, Atsuhiro Osuka,* and Dongho Kim*
Chem. Commun. 2014, 50, 3078–3080.

3. Synthesis of 7,8-Dehydropurpurin Dimers and Their Conversion into Conformationally Constrained β-to-β Vinylene-Bridged Porphyrin Dimers

Norihito Fukui, Hideki Yorimitsu,* Jong Min Lim, Dongho Kim,* and Atsuhiro Osuka*
Angew. Chem. Int. Ed. 2014, 53, 4395–4398.

2. Amination of meso-Bromoporphyrins and 9-Haloanthracenes with Diarylamines Catalyzed by a Palladium–PEPPSI Complex

Yuko Suzuki, Norihito Fukui, Kei Murakami, Hideki Yorimitsu,* and Atsuhiro Osuka*
Asian J. Org. Chem. 2013, 2, 1066–1071.

Selected as the Front Cover

1. Oxidative Fusion Reactions of meso-(Diarylamino)porphyrins

Norihito Fukui, Won-Young Cha, Sangsu Lee, Sumito Tokuji, Dongho Kim,* Hideki Yorimitsu,* and Atsuhiro Osuka*
Angew. Chem. Int. Ed. 2013, 52, 9728–9732.


3. ポルフィリン類の直接官能基化

福井 識人、忍久保 洋
直接的芳香族カップリング反応の設計と応用(監修:三浦雅博、平野康次)、14章 2019, シーエムシー出版

2. Organic Transformations by the Hydrosilane-Alkoxide System

Norihito Fukui
J. Synth. Org. Chem. Jpn. 2019, 77, 512–513.

1. Embedding heteroatoms: an effective approach to create porphyrin-based functional materials

Norihito Fukui, Keisuke Fujimoto, Hideki Yorimitsu, and Atsuhiro Osuka*
Dalton Trans. 2017, 46, 13322–13341.

Access & Contact

工学研究科 1号館 8階