Member忍久保研の構成員

講師:福井 識人
Dr. Norihito Fukui

略歴

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))
2015年4月–2018年3月日本学術振興会特別研究員(DC1)
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)
博士(理学)取得
2018年4月–2022年3月名古屋大学大学院 工学研究科 助教
2021年10月–JSTさきがけ研究者「物質探索空間の拡大による未来材料の創製」領域1期生
2022年4月–名古屋大学大学院 工学研究科 講師

業績

CVPDF
ORCiD0000-0002-0466-0116
ResearcherIDN-6736-2018
researchmap70823277

専門分野

有機化学、構造有機化学

原著論文

67. Inner-Bond-Cleavage Approach to Figure-Eight Macrocycles from Planar Aromatic Hydrocarbons

R. Yoshina, J. Hirano, E. Nishimoto, Y. Sakamoto, K. Tajima, S. Minabe, M. Uyanik, K. Ishihara, T. Ikai, E. Yashima, T. Omine, F. Ishiwari, A. Saeki, J. Kim, J. Oh, D. Kim, G. Liu, T. Yasuda, H. Shinokubo,N. Fukui,*
J. Am. Chem. Soc. 2024.

66. End-to-End Bent Perylene Bisimide Cyclophanes by Double Sulfur Extrusion

Y. Tanaka, K. Tajima, R. Kusumoto, Y. Kobori,* N. Fukui,* H. Shinokubo*
J. Am. Chem. Soc. 2024, 146, 16332–16339.

65. Homochiral and Heterochiral Self-Sorting Assemblies of Antiaromatic Ni(II) Norcorrole Dimers

S. Y. Liu, S. Li, S. Ukai, R. Nozawa, N. Fukui, R. Sugimori, R. Kishi, H. Shinokubo*
Chem. Eur. J. 2024, e202400292.

64. Changing aromatic properties through stacking: the face-to-face dimer of Ni(II) bis(pentafluorophenyl)norcorrole

Q. Wang, D. Sundholm,* J. Gauss, T. Nottoli, F. Lipparini, S. Kino, S. Ukai, N. Fukui, H. Shinokubo.
Phys. Chem. Chem. Phys. 2024, 26, 14777-14786.

63. Synthesis of sterically congested double helicene by alkyne cycloisomerization

J. Hirano, S. Miyoshi, E. Yashima, T. Ikai, H. Shinokubo, N. Fukui,*
Chem. Commun. 2024, 60, 6035-6038.

62. Close Stacking of Antiaromatic Ni(II) Norcorrole Originating from a Four-Electron Multicentered Bonding Interaction

S. Kino, S. Ukai, N. Fukui, R. Haruki, R. Kumai, Q. Wang, S. Horike, Q. M. Phung, D. Sundholm,* H. Shinokubo*
J. Am. Chem. Soc. 2024, 146, 9311-9317.

61. Excimer Formation Driven by Excited-State Structural Relaxation in a Covalent Aminonaphthalimide Dimer

R. Jing, Y. Li, K. Tajima, Y. Wan, N. Fukui,* H. Shinokubo,* Z. Kuang,* A. Xia*
J. Phys. Chem. Lett. 2024, 15, 1469-1476.

60. A Triply Linked Porphyrin−Norcorrole Hybrid with Singlet Diradical Character

K. Wang, S. Ito, S. Ren, D. Shimizu, N. Fukui, R. Kishi, Q. Liu,* A. Osuka, J. Song,* H. Shinokubo*
Angew. Chem. Int. Ed. 2024, e202401233.

59. Synthesis and properties of bay-functionalized 9,9′-bifluorenylidene derivatives

J. Hirano, H. Shinokubo, N. Fukui*
Chem. Lett. 2024, 53upad015.

58. Effect of Internal Substituents on the Properties of Dibenzo[g,p]chrysene

Y. Takeo, J. Hirano, N. Fukui,* H. Shinokubo*
Org. Lett. 2023, 25, 8484–8488.

57. Effect of internal oxygen substituents on the properties of bowl-shaped aromatic hydrocarbons

Y. Takeo, J. Hirano, D. Shimizu, N. Fukui,* H. Shinokubo*
Org. Chem. Front. 2023, 10, 5895–5901.

56. Intrinsic Photostability in Dithiolonaphthalimide Achieved by Disulfide Bond-Induced Excited-State Quenching

Z. Wang, R. Jing, Y. Li, D. Song, Y. Wan, N. Fukui,* H. Shinokubo,* Z. Kuang,* and A. Xia*
J. Phys. Chem. Lett. 2023, 14, 8485–8492.

55. Highly soluble Ni(II) dithienylnorcorrole

S. Itabuchi, R. Nozawa, T. Yoshida, N. Fukui, H. Shinokubo*
J. Porphyrins Phthalocyanines. 2023, 27, 121-125.

54. Easily Switchable 18π-, 19π-, and 20π-Conjugation of Diazaporphyrin Double-Pincer Bispalladium Complexes.

T. Sakurai, Y. Hiraoka, H. Tanaka, Y. Miyake, N. Fukui, H. Shinokubo*
Angew. Chem. Int. Ed. 2023, in press.

53. Near-Infrared-Responsive Hydrocarbons Designed by π-Extension of Indeno[1,2,3,4-pgra]perylene at the 1,2,12-Positions.

M. Kato, J. Kim, J. Oh, D. Shimizu, N. Fukui,* H. Shinokubo*
Chem. Eur. J. 2023, in press.

52. One-dimensional stacking array of 10,20-diphenyl-5,15-diazaporphyrin metal complexes.

S. Mori, T. Sakurai, T. Nishimura, N. Fukui, Y. Miyake,* H. Shinokubo*
J. Porphyrins Phthalocyanines. 2023, in press.

51. Dinaphthooxepine Bisimide Undergoes Oxygen Extrusion Reaction upon Electron Injection at Room Temperature

M. Odajima, N. Fukui,* H. Shinokubo*
Org. Lett. 2023, 25, 282–287.

50. Diazazethrene Bisimide: A Strongly Electron-Accepting π-System Synthesized via the Incorporation of both Imide Substituents and Imine-type Nitrogen Atoms into Zethrene

K. Tajima, K. Matsuo, H. Yamada, N. Fukui,* H. Shinokubo*
Chem. Sci. 2023, 14, 635-642.

49. Realization of Stacked-Ring Aromaticity in a Water-Soluble Micellar Capsule

S. Liu, N. Kishida, J. Kim, N. Fukui, R. Haruki, Y. Niwa, R. Kumai, D. Kim,* M. Yoshizawa,* H. Shinokubo*
J. Am. Chem. Soc. 2023, 145, 2135-2141.

48. Planarization of a bowl-shaped molecule by triple-decker stacking

H. Kawashima, N. Fukui, Q. M. Phung,* T. Yanai, H. Shinokubo*
Cell. Rep. Phys. Sci. 2022, 3, 101045

47. D-Mannose-appended 5,15-diazaporphyrin for photodynamic therapy

L. M. A. Ali, K. Miyagawa, N. Fukui, M. Onofre, K. Elcheikh, A. Morère, S. Clément, M. Gary-Bobo,* S. Richeter,* H. Shinokubo*
Org. Biomol. Chem. 2022, 20, 8217-8222

(Selected as a front Cover)

46. Gram-Scale Diversity-Oriented Synthesis of Dinaphthothiepine Bisimides as Soluble Precursors for Perylene Bisimides

Y. Tanaka, K. Matsuo,* H. Yamada,* N. Fukui,* H. Shinokubo*
Eur. J. Org. Chem. 2022, 31, e202200770.

45. Symmetry-breaking charge separation in a nitrogen-bridged naphthalene monoimide dimer

X. Niu, K. Tajima, J. Kong, M. Tao, N. Fukui,* Z. Kuang,* H. Shinokubo,* A.Xia*
Phys. Chem. Chem. Phys. 2022, 24, 14007-14015

44. Nitrogen Extrusion of Diazacorrphycenes to Azacorroles and Synthesis of Two Types of Copper 10-Azacorrole Complexes

A.Yagi, N. Okada, N. Fukui, H. Tanaka, T. Hatakeyama, H. Shinokubo*
Chem. Lett. 2022, 51, 321-324

43. Synthesis of Dibenzo[h,t]rubicene through Its Internally Dimethoxy-Substituted Precursor

M. Kato, N. Fukui,* H. Shinokubo*
Chem. Lett. 2022, 51, 288-291

42. Isolation and Structure Analysis of a Ni(II) Norcorrole Radical Anion

S. Ukai, N. Fukui, T. Ikeue, H. Shinokubo*
Chem. Lett. 2022, 51, 181-184

41. A Supramolecular Polymer Constituted of Antiaromatic Ni(II) Norcorroles

S. Ukai, A. Takamatsu, M. Nobuoka, Y. Tsutsui, N. Fukui, S. Ogi,* S. Seki,* S. Yamaguchi,* H, Shinokubo*
Angew. Chem. Int. Ed. 2022, 61, e202114230.

40. Indeno[1,2,3,4-pqra]perylene: A Medium-Sized Aromatic Hydrocarbon Exhibiting Full-Range Visible-Light Absorption

M. Kato, N. Fukui,* H, Shinokubo*
Chem. Eur. J. 2022, 28, e202103647.

39. Antiaromatic 1,5-Diaza-s-indacenes

K. Hanida, J. Kim, N. Fukui, Y. Tsutsui, S. Seki,* D. Kim,* H. Shinokubo*
Angew. Chem. Int. Ed. 2021, 20765-20770.

38. Determinant Factors of Three-Dimensional Aromaticity in Antiaromatic Cyclophanes

H. Kawashima, S. Ukai, R. Nozawa, N. Fukui, G. Fitzsimmons, T. Kowalczyk,* H. Fliegl,* H. Shinokubo*
J. Am. Chem. Soc. 2021, 143, 10676−10685.

37. Non-Planar Perylene Bisimide Analogues with Inserted Carbonyl and Methylene Subunits

M. Odajima, K. Tajima, N. Fukui,* H. Shinokubo*
Angew. Chem. Int. Ed. 2021, 60, 15838−15843.

36. Acridino[2,1,9,8‐klmna]acridine Bisimides: An Electron‐Deficient π‐System for Robust Radical Anions and n‐Type Organic Semiconductors

K. Tajima, K. Matsuo, H. Yamada,* S. Seki,* N. Fukui,* H. Shinokubo*
Angew. Chem. Int. Ed. 2021, 60, 14060−14067.

35. Synthesis and Properties of an 18π Aromatic Norcorrole P(V) Complex

T. Yoshida, S. A. Shafie, H. Kawashima, N. Fukui, H. Shinokubo*
Org. Lett. 2021, 23, 2826–2830.

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

K. Miyagawa, I. Hisaki, N. Fukui, H. Shinokubo*
Chem. Sci. 2021, 12, 5224–5229.

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, 10, 541–544.

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. 2021, 64, 2915–2919.

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, 49, 14383–14387.

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(2.0.1.0)

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.


著書・総説

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

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愛知県名古屋市千種区不老町
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