Bigger is not Better for Indolino‐Oxazoline Photochemical Properties

Author:

Ayoub Augustin1,Le Bras Laura2,Leriche Philippe1,Champagne Benoît2,Sanguinet Lionel1ORCID

Affiliation:

1. Univ Angers CNRS, MOLTECH-ANJOU, SFR MATRIX F- 49000 Angers France

2. Theoretical Chemistry Laboratory Unit of Theoretical and Structural Physical Chemistry Namur Institute of Structured Matter University of Namur Rue de Bruxelles, 61; B 5000 Namur

Abstract

AbstractIndolino‐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.

Funder

Universite Angers

Wallonie-Bruxelles International

Publisher

Wiley

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