TY - JOUR
T1 - Bigger is not Better for Indolino-Oxazoline Photochemical Properties
AU - Ayoub, Augustin
AU - Le Bras, Laura
AU - Leriche, Philippe
AU - Champagne, Benoît
AU - Sanguinet, Lionel
N1 - Publisher Copyright:
© 2024 The Authors. ChemPhotoChem published by Wiley-VCH GmbH.
PY - 2024/7
Y1 - 2024/7
N2 - 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.
AB - 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.
KW - Electrochromism
KW - Indolino-oxazolidine
KW - Molecular switch
KW - Photoinduced electron transfer
KW - halochromism
UR - http://www.scopus.com/inward/record.url?scp=85195600854&partnerID=8YFLogxK
U2 - 10.1002/cptc.202300332
DO - 10.1002/cptc.202300332
M3 - Article
SN - 2367-0932
VL - 8
JO - ChemPhotoChem
JF - ChemPhotoChem
IS - 7
M1 - e202300332
ER -