| Literature DB >> 29995309 |
Romain Bouvier1, Raphaël Durand1, Ludovic Favereau1, Monika Srebro-Hooper2, Vincent Dorcet1, Thierry Roisnel1, Nicolas Vanthuyne3, Yuly Vesga4, Julie Donnelly4, Florencio Hernandez4, Jochen Autschbach5, Yann Trolez1, Jeanne Crassous1.
Abstract
Enantiopure P- and M-carbo[6]helicenes substituted with one or two tetracyanobutadiene moieties at positions 2 and 15 have been prepared. Grafting of these electron-accepting groups onto the π-helical core resulted in strong charge-transfer effects, which greatly affected the UV/Vis, electronic circular dichroism (ECD), and two-photon absorption (TPA) responses. The ECD signal was found to be reversibly switched by applying a redox stimulus.Entities:
Keywords: charge transfer; chiroptical activity; helicenes; tetracyanobutadiene; two-photon absorption
Year: 2018 PMID: 29995309 DOI: 10.1002/chem.201802763
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236