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Rules of Nucleophilic Additions to Zigzag Nanographene Diones*.
Ribar, Peter; Valenta, Leos; Solomek, Tomás; Jurícek, Michal.
Afiliação
  • Ribar P; Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056, Basel, Switzerland.
  • Valenta L; Department of Chemistry, University of Zurich, Winterthurerstrasse 190, 8057, Zurich, Switzerland.
  • Solomek T; Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056, Basel, Switzerland.
  • Jurícek M; Prievidza Chemical Society, M. Hodzu 10/16, 971 01, Prievidza, Slovak Republic.
Angew Chem Int Ed Engl ; 60(24): 13521-13528, 2021 Jun 07.
Article em En | MEDLINE | ID: mdl-33645878
ABSTRACT
Nucleophilic addition of carbon-centered nucleophiles to nanographene ketones represents a valuable late-stage method for the functionalization of zigzag nanographenes, but its use is rare in the chemical literature. Using two model systems, non-Kekulé triangulene-4,8-dione and Kekulé anthanthrone, we identify unexpected regioselectivities and uncover the rules that govern these reactions. Considering the large number of nanographene ketones that have been reported since the pioneering work of Eric Clar, this method enables synthesis and exploration of hitherto unknown functionalized nanographenes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Suíça