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...

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Hauptverfasser: Zango, Germán, Zirzlmeier, Johannes, Claessens, Christian G, Clark, Timothy, Martínez-Díaz, M. Victoria, Guldi, Dirk M, Torres, Tomás
Format: Artikel
Sprache:eng
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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