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Triindenotriphenylenes: Spin-Frustrated Triskelion Triradicals with Excellent Ambient Stability.
Borissov, Arseni; Chmielewski, Piotr J; Valdivia, Abel Cárdenas; García, Carlos J Gómez; Casado, Juan; Stepien, Marcin.
Afiliação
  • Borissov A; Wydzial Chemii, Uniwersytet Wroclawski, ul. F. Joliot-Curie 14, 50-383, Wroclaw, Poland.
  • Chmielewski PJ; Wydzial Chemii, Uniwersytet Wroclawski, ul. F. Joliot-Curie 14, 50-383, Wroclaw, Poland.
  • Valdivia AC; Department of Physical Chemistry, Faculty of Sciences, University of Málaga, Campus de Teatinos, 29071, Málaga, Spain.
  • García CJG; Departamento de Química Inorgánica, Universidad de Valencia, Dr Moliner 50, 46100, Burjasot, Spain.
  • Casado J; Department of Physical Chemistry, Faculty of Sciences, University of Málaga, Campus de Teatinos, 29071, Málaga, Spain.
  • Stepien M; Wydzial Chemii, Uniwersytet Wroclawski, ul. F. Joliot-Curie 14, 50-383, Wroclaw, Poland.
Angew Chem Int Ed Engl ; 63(36): e202408510, 2024 Sep 02.
Article em En | MEDLINE | ID: mdl-38881362
ABSTRACT
A triskelion-shaped triradical triindeno[1,2-a1',2'-g 1'',2''-m]triphenylen-7-yl (1) and its internally fused derivative (2) obtained by oxidative cyclization were prepared in a straightforward synthetic sequence. Both compounds were confirmed to be triradicals and to possess intramolecular antiferromagnetic exchange interactions between spins, displaying a spin-frustrated doublet ground state with doublet-quartet energy gaps of -0.14 kcal/mol for 1 and -0.06 kcal/mol for 2. Despite their open-shell character, they were sufficiently stable to be handled under ambient conditions on a timescale of days. Both compounds could be reversibly reduced to mono-, di-, and trianions and oxidized to 1+ and 22+, with strong NIR absorptions (1800 to over 3200 nm) observed for all open-shell ions.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article