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Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.
Constantinides, Christos P; Zissimou, Georgia A; Berezin, Andrey A; Ioannou, Theodosia A; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C; Koutentis, Panayiotis A.
Afiliação
  • Constantinides CP; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
  • Zissimou GA; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
  • Berezin AA; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
  • Ioannou TA; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
  • Manoli M; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
  • Tsokkou D; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
  • Theodorou E; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
  • Hayes SC; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
  • Koutentis PA; Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus.
Org Lett ; 17(16): 4026-9, 2015 Aug 21.
Article em En | MEDLINE | ID: mdl-26244376
ABSTRACT
Tetraphenylhexaazaanthracene, TPHA-1, is a fluorescent zwitterionic biscyanine with a closed-shell singlet ground state. TPHA-1 overcomes its weak 16π antiaromaticity by partitioning its π system into 6π positive and 10π negative cyanines. The synthesis of TPHA-1 is low yielding and accompanied by two analogous TPHA isomers the deep red, non-charge-separated, quinoidal TPHA-2, and the deep green TPHA-3 that partitions into two equal but oppositely charged 8π cyanines. The three TPHA isomers are compared.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article