Bigger is not Better for Indolino-Oxazoline Photochemical Properties

Augustin Ayoub, Laura Le Bras, Philippe Leriche, Benoît Champagne, Lionel Sanguinet

Research output: Contribution to journalArticlepeer-review

Abstract

Indolino-oxazolidine derivatives are a new and pretty confidential family of multimodal molecular switches. Indeed, acid, electrochemical potential, and UV light irradiation can be used to convert these compounds form their colorless closed form to a colorful open form. In this publication, we have investigated the influence of the extension of the π-conjugated system beared by the indolino moiety on their halo-, electro- and photochromic properties. In this context, we have demonstrated that only their photochemical properties are strongly affected by this structural modification. Moreover, quantum chemistry calculations have allowed to rationalize our experimental observations and, noticeably, evidenced an oxidative quenching process in presence of chlorobenzene, which enhances their photoreactivity.

Original languageEnglish
Article numbere202300332
Number of pages9
JournalChemPhotoChem
Volume8
Issue number7
DOIs
Publication statusPublished - Jul 2024

Keywords

  • Electrochromism
  • Indolino-oxazolidine
  • Molecular switch
  • Photoinduced electron transfer
  • halochromism

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