Paper
14 February 2007 Naphthalene diimides as tunable fluorophores suitable for single molecule applications
Toby D. M. Bell, Sheryll Yap, Chintan Jani, Steven J. Langford, Johan Hofkens, Frans De Schryver, Kenneth P. Ghiggino
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Abstract
The photophysics of two new substituted aminopropenyl naphthalene diimide (SANDI) dyes are reported. The molecules exhibit many of the photophysical properties required for fluorescence labeling applications including high photostability and high fluorescence quantum yields (> 0.5) in the visible region of the spectrum. Furthermore, the emission is sensitive to the number of substituents attached to the aromatic core, and to the surrounding environment. For example, in toluene as solvent, the mono-allyl SANDI has an emission maximum at 550 nm, whereas the di-allyl SANDI emits at 630 nm. The fluorescence decay times are in the range of ~8 - 12 ns and the Forster critical distance for fluorescence resonance energy transfer (FRET) between the mono- and di-allyl SANDI derivatives is 4.1 nm for a random donor-acceptor orientation. Single molecules of the di-allyl SANDI embedded in poly(methyl methacrylate) films show very low yields of photobleaching and very few fluorescence intermittencies or "blinks". These compounds are ideal candidates for applications at the single molecule level, for example, as FRET labels.
© (2007) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Toby D. M. Bell, Sheryll Yap, Chintan Jani, Steven J. Langford, Johan Hofkens, Frans De Schryver, and Kenneth P. Ghiggino "Naphthalene diimides as tunable fluorophores suitable for single molecule applications", Proc. SPIE 6444, Ultrasensitive and Single-Molecule Detection Technologies II, 644404 (14 February 2007); https://doi.org/10.1117/12.701443
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Cited by 2 scholarly publications.
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KEYWORDS
Molecules

Luminescence

Absorption

Photons

Fluorescence resonance energy transfer

Bioalcohols

Nitrogen

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