超酸」の中で発光し続ける色素の開発に成功~酸による分解という最大の弱点を克服、極限環境でのイメージング応用に光明~

2023-03-23 北海道大学,科学技術振興機構

北海道大学とJSTの研究グループは、濃硫酸を超える強酸「超酸」中でも分解せず蛍光を維持する新規BODIPY色素を開発した。従来のBODIPYは酸中でホウ素が脱離し発光を失う欠点があったが、三つのピロールを含む環状構造とホウ素の相互作用により高い酸耐性を実現。この色素は超酸中でも1日以上発光を維持し、発光色の調整や酸環境でのみ発光するセンサー機能も確認された。さらに、強酸性樹脂の染色やPFOA検出にも応用可能であり、極限環境下での蛍光イメージング・センシング技術の発展に寄与する成果としてNature Communicationsに掲載された。

超酸」の中で発光し続ける色素の開発に成功~酸による分解という最大の弱点を克服、極限環境でのイメージング応用に光明~
超酸性材料中での従来BODIPY色素(左)と超酸耐性BODIPY(右)の蛍光発光の違い

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超酸耐性を有する環状BODIPYs Superacid-resistant macrocyclic BODIPYs

Keita Watanabe,Gentaro Honda,Yuki Terauchi,Shunsuke Mamiya,Yuya Inaba,Tasuku Nakajima,Jian Ping Gong,Yusaku Yamaguchi,Yuichi Kitagawa,Yasuchika Hasegawa,Yuki Ide,Min Gao,Tomoki Yoneda & Yasuhide Inokuma
Nature Communications  Published:19 March 2026
DOI:https://doi.org/10.1038/s41467-026-70499-9

Abstract

Boron-dipyrromethenes (BODIPYs) are versatile fluorophores with intense fluorescence and broad applications in bioimaging and sensing. However, they undergo deboronation under acidic conditions, which causes fluorescence degradation. Herein, we designed exceptionally acid-stable BODIPYs by harnessing the synergistic boron-chelation effect of calix[3]pyrrole-like macrocycles. We show that their characteristic optical properties are retained in strongly acidic media, including superacids, without undergoing deboronation. Macrocyclic BODIPYs exhibit sharp absorption and protonation-induced fluorescence switching, with quantum yields of up to 0.90 and narrow Stokes shifts. Notably, no deboronation was observed even in non-diluted fluorosulfuric acid, and visible fluorescence was sustained for over a day. Beyond their unusual acid resistance, the macrocyclic BODIPYs had higher thermal- and photostability compared with conventional BODIPYs. Peripheral substitution allowed the modulation of absorption and emission wavelengths, and fluorous-tagging through axial ligand exchange enabled fluorescence switching in response to perfluorooctanoic acid in a fluorous solvent. We used superacid-resistant BODIPYs as acid indicators for the fluorescence staining of Nafion beads and sulfonylated gels, which are too acidic to sustain the fluorescence emission of conventional BODIPYs. Our findings expand the scope of BODIPYs into strongly acidic, non-aqueous environments, opening opportunities for fluorescence imaging and sensing in materials and biological systems.

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