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Synthesis and Photophysical Properties of New Conjugated Fluorophores Designed for Two-Photon-Excited Fluorescence

Novel elongated push-push fluorophores (e.g., 9) were synthesized by 2-fold Sonogashira or Wittig−Horner reactions. Modulation of the length and topology of the conjugated connectors allows tuning of their photophysical properties. In addition, their photoluminescence can be adjusted by playing on p...

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Published in:Organic letters 2002-03, Vol.4 (5), p.719-722
Main Authors: Mongin, Olivier, Porrès, Laurent, Moreaux, Laurent, Mertz, Jerome, Blanchard-Desce, Mireille
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Language:English
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cited_by cdi_FETCH-LOGICAL-a377t-3c4afe12c136888bebd34616ffc4309f80e98cc110e2fdcf231bf761b4a390a83
cites cdi_FETCH-LOGICAL-a377t-3c4afe12c136888bebd34616ffc4309f80e98cc110e2fdcf231bf761b4a390a83
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container_title Organic letters
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creator Mongin, Olivier
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description Novel elongated push-push fluorophores (e.g., 9) were synthesized by 2-fold Sonogashira or Wittig−Horner reactions. Modulation of the length and topology of the conjugated connectors allows tuning of their photophysical properties. In addition, their photoluminescence can be adjusted by playing on polarity. Derivatives combining enhanced two-photon absorption cross section (σ2) in the visible red and high fluorescence quantum yield (Φ) have been obtained. Such fluorophores hold promise for nonlinear imaging of biological systems.
doi_str_mv 10.1021/ol017150e
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title Synthesis and Photophysical Properties of New Conjugated Fluorophores Designed for Two-Photon-Excited Fluorescence
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