A push-pull unsymmetrical subphthalocyanine dimerElectronic supplementary information (ESI) available. See DOI: 10.1039/c5sc01709b
Unsymmetrical subphthalocyanine fused dimers have been prepared from appropriate ortho -dinitrile SubPc precursors. In particular, either electron-donating or electron-accepting substituents have been introduced on each SubPc constituent unit, resulting in unprecedented push-pull π-extended curved a...
Gespeichert in:
Hauptverfasser: | , , , , , , |
---|---|
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Unsymmetrical subphthalocyanine fused dimers have been prepared from appropriate
ortho
-dinitrile SubPc precursors. In particular, either electron-donating or electron-accepting substituents have been introduced on each SubPc constituent unit, resulting in unprecedented push-pull π-extended curved aromatic macrocycles. From fluorescence experiments in solvents of different polarity we conclude a dual fluorescence, namely a delocalized singlet excited state (1.73 eV) and a polarized charge transfer state ( |
---|---|
ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/c5sc01709b |