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Synthesis and Photophysical Properties of Soluble N-Doped Rubicenes via Ruthenium-Catalyzed Transfer Hydrogenative Benzannulation.
Shuler, William G; Parvathaneni, Sai P; Rodriguez, Jacob B; Lewis, Taylor N; Berges, Adam J; Bardeen, Christopher J; Krische, Michael J.
Afiliação
  • Shuler WG; Department of Chemistry, University of Texas at Austin, 105 E 24th St. (A5300), Austin, TX, 78712-1167, USA.
  • Parvathaneni SP; Department of Chemistry, University of Texas at Austin, 105 E 24th St. (A5300), Austin, TX, 78712-1167, USA.
  • Rodriguez JB; Department of Materials Science and Engineering, University of California, 501 Big Springs Road, Riverside, CA, 92521, USA.
  • Lewis TN; Department of Chemistry, University of California, 501 Big Springs Road, Riverside, CA, 92521, USA.
  • Berges AJ; Department of Chemistry, University of California, 501 Big Springs Road, Riverside, CA, 92521, USA.
  • Bardeen CJ; Department of Materials Science and Engineering, University of California, 501 Big Springs Road, Riverside, CA, 92521, USA.
  • Krische MJ; Department of Chemistry, University of California, 501 Big Springs Road, Riverside, CA, 92521, USA.
Chemistry ; 27(15): 4898-4902, 2021 Mar 12.
Article em En | MEDLINE | ID: mdl-33576516
Ruthenium-catalyzed butadiene-mediated benzannulation enabled the first synthesis of 3,10-(di-tert-butyl)rubicene and its N-doped derivatives as well as preliminary studies on their photophysical properties. Unlike the parent rubicene and 3,10-(di-tert-butyl)rubicene, which adopt classical herringbone-type packing motifs in the solid state, the N-doped congener 7 b displayed columnar packing with an alternating co-facial arrangement of aromatic and heteroaromatic substructures.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article