Abstract
A series of ternary asymmetric triazines with tunable singlet and triplet excited states were successfully synthesized on the basis of σ-spacer methodology and a facile synthetic route. The optoelectronic properties are dominated by the conjugated donor-acceptor (D-A) backbone of peripheral carbazoles (D) and triazine core (A), and can be further modulated via the partially interrupted conjugation between the core and the third substituents by the σ spacers of N-CH3, NH, O, S and OSO, which offers new opportunities to fine tune the electronic structures and properties of triazines.
Original language | English |
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Pages (from-to) | 13782-13788 |
Number of pages | 7 |
Journal | RSC Advances |
Volume | 3 |
Issue number | 33 |
DOIs | |
State | Published - 7 Sep 2013 |
Externally published | Yes |