Phosphole P-oxide is a useful building block for φ-conjugated materials due to its nonaromatic and electron-accepting character. We have synthesized a series of ring-fused derivatives of phosphole P-oxide based on the intramolecular nucleophilic cyclization of appropriate alkyne precursors or radical phosphanylations. Some of the thus obtained compounds exhibited intriguing fluorescence properties and were applied to fluorescence imaging. A donor-acceptor-type benzo[b]phosphole P-oxide with a (diphenylamino)phenyl group exhibited large solvatochromism in its fluorescence spectra, and could hence be used as a staining agent for lipid droplets. C-Naphox and PB430, which consist of fully ring-fused φ - conjugated ladder-type scaffolds, exhibited outstanding photostability and their absorption and emission properties were suitable for super-resolution STED imaging. Moreover, using PB430-conjugated antibodies, we carried out a 3-D reconstruction of the STED images and developed a photostability-based multicolor STED imaging technique.
CITATION STYLE
Yamaguchi, S., Fukazawa, A., & Taki, M. (2017). Phosphole P-oxide-containing φ-electron materials: Synthesis and applications in fluorescence imaging. Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 75(11), 1179–1187. https://doi.org/10.5059/yukigoseikyokaishi.75.1179
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