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Axially-chiral boramidine for detailed (chir)optical studies.
Saleh, Nidal; Sucre-Rosales, Estefanía; Zinna, Francesco; Besnard, Céline; Vauthey, Eric; Lacour, Jérôme.
Afiliación
  • Saleh N; Department of Organic Chemistry, University of Geneva Quai Ernest Ansermet 30 1211 Geneva 4 Switzerland nidal.saleh@unige.ch jerome.lacour@unige.ch.
  • Sucre-Rosales E; Department of Physical Chemistry, University of Geneva Quai Ernest Ansermet 30 1211 Geneva 4 Switzerland eric.vauthey@unige.ch.
  • Zinna F; Dipartimento di Chimica e Chimica Industriale, University of Pisa Via G. Moruzzi 13 56124 Pisa Italy.
  • Besnard C; Laboratory of Crystallography, University of Geneva Quai Ernest Ansermet 24 1211 Geneva 4 Switzerland.
  • Vauthey E; Department of Physical Chemistry, University of Geneva Quai Ernest Ansermet 30 1211 Geneva 4 Switzerland eric.vauthey@unige.ch.
  • Lacour J; Department of Organic Chemistry, University of Geneva Quai Ernest Ansermet 30 1211 Geneva 4 Switzerland nidal.saleh@unige.ch jerome.lacour@unige.ch.
Chem Sci ; 15(17): 6530-6535, 2024 May 01.
Article en En | MEDLINE | ID: mdl-38699281
ABSTRACT
The inclusion of boron atoms into chiral π-conjugated systems is an effective strategy to unlock unique chiroptical properties. Herein, the preparation and characterization of a configurationally stable axially-chiral boramidine are reported, showcasing absorption in the UV domain, deep-blue fluorescence (Φ up to 94%), and ca. |10-3| gabs and glum values. Detailed photophysical studies and quantum-chemical calculations clearly elucidate the deactivation pathways of the emissive state to triplet excited states, involving increased spin-orbit coupling between the lowest singlet excited state and an upper triplet state.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2024 Tipo del documento: Article