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On the Unusual Global Aromaticity of Two Cyclopenta-Ring-Fused Oligo(m-Phenylenes).
Summa, Francesco F; Zanasi, Riccardo; Dordevic, Sladana; Radenkovic, Slavko; Monaco, Guglielmo.
Afiliação
  • Summa FF; Dipartimento di Chimica e Biologia "A. Zambelli", University of Salerno, Fisciano, 84084, Italy.
  • Zanasi R; Dipartimento di Chimica e Biologia "A. Zambelli", University of Salerno, Fisciano, 84084, Italy.
  • Dordevic S; University of Kragujevac, Faculty of Science, 34000, Kragujevac, Serbia.
  • Radenkovic S; University of Kragujevac, Faculty of Science, 34000, Kragujevac, Serbia.
  • Monaco G; Dipartimento di Chimica e Biologia "A. Zambelli", University of Salerno, Fisciano, 84084, Italy.
Chemphyschem ; : e202400342, 2024 May 29.
Article em En | MEDLINE | ID: mdl-38807571
ABSTRACT
Some years ago, Jishan Wu reported the synthesis of 8MC and 10MC, two homologues of the cyclopenta-ring-fused oligo(m-phenylene) macrocycles mMC, each behaving as an annulene-within-an-annulene (AWA). This was a surprising result as the AWA behavior is rare. Both molecules have a partial polyradical character, enforced by the quest for restoring some aromatic character of benzene rings. However, that restoration brings back some coupling between the two annulenes. Indeed, we found that the geometry and the magnetically induced currents indicate that, while 8MC does have an AWA character, this is not the case of the larger 10MC. Limitations of the design strategy of AWA molecules should be taken into account in future attempts to prepare novel large coronenes.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Chemphyschem Assunto da revista: BIOFISICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Chemphyschem Assunto da revista: BIOFISICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália