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- W2056515875 abstract "Fluorescent Probes The synthesis and photophysics of a family of BODIPY derivatives with a naphthyridine at the C8 position and alkyl, bromo, or dimethylaminoaryl groups at the C2 and C6 positions of the BODIPY core are described by Tia E. Keyes and co-workers in their Full Paper on page 763 ff. The NIR emission of the dimethylaminoaryl compounds is Stokes-shifted and strongly solvent dependent. The emission and Stokes shift are maintained in aqueous media. PEGylation of these compounds renders them water soluble and cell permeable. Their Stokes-shifted fluorescence makes them less prone to self-quenching within live cells than conventional BODIPY fluorophores." @default.
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- W2056515875 date "2013-09-01" @default.
- W2056515875 modified "2023-09-26" @default.
- W2056515875 title "Inside Cover: Naphthyridyl-Substituted 4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) Luminophores: Photophysics and Application as Molecular Imaging Probes in Live Cells (Asian J. Org. Chem. 9/2013)" @default.
- W2056515875 doi "https://doi.org/10.1002/ajoc.201390025" @default.
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