2025年11月7日 N-アルキル化による環状インドール四量体の平面性および反芳香族性の制御に関する論文が Chemistry – A European Journal 誌に受理されました。
31. Cyclic Tetraindoles with a Cyclooctatetraene Core: Controlling Planarity and Antiaromatic Character via N-Alkylation, K. Fujimoto, R. Hirose, H. Masu, M. Takahashi, Chem. Eur. J. 2025, e03193. (10.1002/chem.202503193)
2025年9月1日 アントラセンおよびナフタレンジイミド誘導体を用いた固体中での緑から青へのフォトンアップコンバージョンに関する論文が Japanese Journal of Applied Physics 誌に受理されました。
30. Green to blue photon upconversion in solid-state using anthracene and naphthalene diimide derivatives, R. Kani, K. Fujimoto, K. Banno, Y. Majima, M. Takahashi, S. Izawa, Jpn. J. Appl. Phys. 2025, 64, 091004. (10.35848/1347-4065/ae0223)
(before March 2025)
29. Efficient Visible-Light-Induced π-Extension of Perylene Tetraesters: An Investigation on Regioselectivity, K. Fujimoto, S. Miyano, K. Norizuki, T. Inuzuka, T. Sengoku, M. Takahashi, Eur. J. Org. Chem. 2024, e202400734. (10.1002/ejoc.202400734)
28. Electron Transfer Enhanced by a Minimal Energetic Driving Force at the Organic-Semiconductor Interface, H. Iwasaki, K. Fujimoto, K. Banno, Q.-j. Shui, Y. Majima, M. Takahashi, S. Izawa, Angew. Chem. Int. Ed. 2024, 63, e202407368. (10.1002/anie.202407368)
27. Wavily Curved Perylene Diimides: Synthesis, Characterization, and Photovoltaic Properties, K. Fujimoto, S. Izawa, K. Yamada, S. Yagi, T. Inuzuka, K. Sanada, M. Sakamoto, M. Hiramoto, M. Takahashi, ChemPlusChem 2024, e202300748. (10.1002/cplu.202300748)
26. Blue organic light-emitting diode with a turn-on voltage of 1.47 V, S. Izawa, M. Morimoto, K. Fujimoto, K. Banno, Y. Majima, M. Takahashi, S. Naka, M. Hiramoto, Nature Communications 2023, 14, 5494. (10.1038/s41467-023-41208-7)
25. Visible-Light-Induced Reductive Coupling of Arylacetylenes with Benzothiazole Sulfones, T. Sengoku, H. Iwama, T. Shimotori, K. Fujimoto, T. Inuzuka, K. Matsune, H. Yoda, J. Org. Chem. 2023, 88, 12776−12782. (10.1021/acs.joc.3c01554)
24. Synthesis of Highly Emissive Fluorophores Based on Multiply Stacked Anthracene Arrangement, K. Santo, K. Uchida, K. Fujimoto, T. Inuzuka, K. Hirakawa, T. Sengoku, M. Takahashi, Eur. J. Org. Chem. 2023, e202201479. (10.1002/ejoc.202201479)
23. 7,12-Dihydrobenzo[de]indolo[3,2-b]quinoline: Unique Reactivity and Redox Interconversion, K. Fujimoto, K. Sasaki, S. Yamagishi, T. Inuzuka, K. Sanada, M. Sakamoto, M. Takahashi, Eur. J. Org. Chem. 2022, e202200564. (10.1002/ejoc.202200564)
22. Influence of N-Substituents on Photovoltaic Properties of Singly Bay-Linked Dimeric Perylene Diimides, S. Izawa, K. Uchida, M. Nakamura, K. Fujimoto, J. Roudin, J.-H. Lee, T. Inuzuka, T. Nakamura, M. Sakamoto, Y. Nakayama, M. Hiramoto, M. Takahashi, Chem Eur. J. 2021, 27, 14081-14091. (10.1002/chem.202102318)
21. 5,11-Diazadibenzo[hi,qr]tetracene: Synthesis, Properties, and Reactivity toward Nucleophilic Reagents, K. Fujimoto, S. Takimoto, S. Masuda, T. Inuzuka, K. Sanada, M. Sakamoto, M. Takahashi, Chem Eur. J. 2021, 27, 8951-8955. (10.1002/chem.202100944)
20. Curved Perylene Diimides Fused with Seven-Membered Rings, K. Fujimoto, S. Izawa, A. Takahashi, T. Inuzuka, K. Sanada, M. Sakamoto, Y. Nakayama, M. Hiramoto, M. Takahashi, Chem. Asian. J. 2021, 16, 690-695. (10.1002/asia.202100066)
19. Improved Synthesis of Bay-Monobrominated Perylene Diimides, K. Fujimoto, K. Uchida, M. Nakamura, T. Inuzuka, N. Uemura, M. Sakamoto, M. Takahashi, ChemistrySelect 2020, 5, 15028-15031. (10.1002/slct.202004432)
18. Regioselective Bay-Functionalization of Perylenes Toward Tailor-Made Synthesis of Acceptor Materials for Organic Photovoltaics, K. Fujimoto, S. Izawa, Y. Arikai, S. Sugimoto, H. Oue, T. Inuzuka, N. Uemura, M. Sakamoto, M. Hiramoto, M. Takahashi, ChemPlusChem 2020, 85, 285-293 . (10.1002/cplu.201900725)
17. Triplet–Triplet Annihilation-Based Upconversion Sensitized by a Reverse Micellar Assembly of Amphiphilic Ruthenium Complexes, K. Fujimoto, K. Kawai, S. Masuda, T. Mori, T. Aizawa, T. Inuzuka, T. Karatsu, M. Sakamoto, S. Yagai, T. Sengoku, M. Takahash, H. Yoda, Langmuir 2019, 35, 9740-9746. (10.1021/acs.langmuir.9b01433)
16. Selective Formation of Helical Tetrapyrrin-Fused Porphyrins by Oxidation ofβ-to-β Linked meso-Aminoporphyrin Dimers, K. Fujimoto, D. Shimizu, T. Mori, Y. Li, M. Zhou, J. Song, A. Osuka, Chem. Eur. J. 2019, 25, 1711-1715. (10.1002/chem.201805659)
15. Porphyrin-Stabilized Nitrenium Dication K. Fujimoto, D. Shimizu, A. Osuka, Chem. Eur. J. 2019, 25, 521-525. (10.1002/chem.201805491)
14. meso-Functionalization of Boron(III) Subporphyrin with Boron(III) meso-Lithiosubporphyrin, Y. Bekki, D, Shimizu, K. Fujimoto, A. Osuka, Chem. Eur. J. 2018, 24, 12708-12715. (10.1002/chem.201802339)
13. Stable Diporphyrinylaminyl Radical and Nitrenium Ion, D. Shimizu, K. Fujimoto, A. Osuka, Angew. Chem. Int. Ed. 2018, 57, 9434-9438. (10.1002/anie.201805385)
12. A 1,5-Naphthyridine-Fused Porphyrin Dimer: Intense NIR Absorption and Facile Redox Interconversion with Its Reduced Congener, K. Fujimoto, A. Osuka, Chem. Eur. J. 2018, 24, 6530-6533. (10.1002/chem.201800854)
11. Effective stabilization of a planar phosphorus(iii) center embedded in a porphyrin-based fused aromatic skeleton, K. Fujimoto, A. Osuka, Chem. Sci. 2017, 8, 8231-8239, (10.1039/c7sc03882h)
10. Diphenylphosphine-Oxide-Fused and Diphenylphosphine-Fused Porphyrins: Synthesis, Tunable Electronic Properties, and Formation of Cofacial Dimers, K. Fujimoto, Y, Kasuga, N. Fukui, A. Osuka, Chem. Eur. J. 2017, 23, 6741-6745. (10.1002/chem.201700909)
9. Metal-Free Approach to Biaryls from Phenols and Aryl Sulfoxides by Temporarily Sulfur-Tethered Regioselective C-H/C-H Coupling, T. Yanagi, S. Otsuka, Y. Kasuga, K. Fujimoto, K. Murakami, K. Nogi, H. Yorimitsu, A. Osuka, J. Am. Chem. Soc. 2016, 138, 14582-14585. (10.1021/jacs.6b10278)
8. Directly Diphenylborane-Fused Porphyrins, K. Fujimoto, J. Oh, H. Yorimitsu, D. Kim, A. Osuka, Angew. Chem. Int. Ed. 2016, 55, 3196-3199. (10.1002/anie.201511981)
7. Peripherally Silylated Porphyrins K. Kato, K. Fujimoto, H. Yorimitsu, A. Osuka, Chem. Eur. J. 2015, 21, 13522-13525. (10.1002/chem.201502563)
6. Porphyrinylboranes Synthesized via Porphyrinyllithiums, K. Fujimoto, H. Yorimitsu, A. Osuka, Chem. Eur. J. 2015, 21, 11311-11314. (10.1002/chem.201502215)
5. Dimeric 1:2 adduct of β,β’-bis(diphenylphosphino)porphyrin with silver(I) chloride, K. Fujimoto, H. Yorimitsu, A. Osuka, J. Porphyrins Phthalocyanines 2015, 19, 171-174. (10.1142/s1088424615500078)
4. Synthesis of Direct β-to-β Linked Porphyrin Arrays with Large Electronic Interactions: Branched and Cyclic Oligomers, H. Cai, K. Fujimoto, J, M. Lim, C. Wang, W. Huang, Y. Rao, S. Zhang, H. Shi, B. Yin, B. Chen, M. Ma, J. Song, D. Kim, A. Osuka, Angew. Chem. Int. Ed. 2014, 53, 11088-11091. (10.1002/anie.201407032)
3. Efficient Synthesis and Versatile Reactivity of Porphyrinyl Grignard Reagents, K. Fujimoto, H. Yorimitsu, A. Osuka, Eur. J. Org. Chem. 2014, 20, 4327-4334. (10.1002/ejoc.201402391)
2. Facile Preparation ofβ-Haloporphyrins as Useful Precursors of β-Substituted Porphyrins, K. Fujimoto, H. Yorimitsu, A. Osuka, Org. Lett. 2014, 16, 972-975. (10.1021/ol4037049)
1. Synthesis and Catalytic Activities of Porphyrin-Based PCP-Pincer Complexes, K. Fujimoto, T. Yoneda, H. Yorimitsu, A. Osuka, Angew. Chem. Int. Ed. 2014, 53, 1127-1130. (10.1002/anie.201308551)