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Article Dans Une Revue Chemical Science Année : 2014

NIR electrochemical fluorescence switching from polymethine dyes

Seogjae Seo
  • Fonction : Auteur
Simon Pascal
Chihyun Park
  • Fonction : Auteur
Xu Yang
  • Fonction : Auteur
  • PersonId : 757308
  • IdRef : 223432717
Olivier Maury
Eunkyoung Kim
  • Fonction : Auteur correspondant
  • PersonId : 1117741

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Résumé

A polymethine dye was used as a fluorophore and an electroactive modulator in order to achieve reversible electrochemical fluorescence switching in the near infrared (NIR) region. An NIR emissive polymethine dye, 3H-indolium, 2-[2-[2-chloro-3-[2-[1,3-dihydro-3,3-dimethyl-1-(phenylmethyl)-2H-indol-2-ylidene]ethylidene]-5-(1,1-dimethylethyl)-1-cyclohexen-1-yl]ethenyl]-3,3-dimethyl-1-(phenylmethyl)-bromide (PM1), displayed high absorption and emission in the NIR region. In addition, it showed a relatively reversible electrochemical reaction between −0.5 and 1.1 V vs. Ag wire. In contrast, a keto group (C[double bond, length as m-dash]O) bridged polymethine analogue, 2,6-bis[2-(1,3-dihydro-1-hexyl-3,3-dimethyl-2H-indol-2-ylidene)ethylidene]-4-(1,1-dimethylethyl)cyclohexanone (PM2), showed an irreversible electrochemical reaction, possibly due to the keto group interrupting the full conjugation of the entire molecule in PM2. The reversible redox reaction of PM1 allowed electrochemical fluorescence switching in the NIR region for the first time. The NIR fluorescence switching was visually observable through a visible light cut-off filter with a cyclability of over 100.
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hal-01288845 , version 1 (05-10-2022)

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Seogjae Seo, Simon Pascal, Chihyun Park, Kyoungsoon Shin, Xu Yang, et al.. NIR electrochemical fluorescence switching from polymethine dyes. Chemical Science, 2014, 5 (4), pp.1538-1544. ⟨10.1039/C3SC53161A⟩. ⟨hal-01288845⟩
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