Quinoidal Azaacenes: 99 % Diradical Character. (28th April 2020)

• Record Type: Journal Article
• Authors: Intorp, Sebastian N.; Hodecker, Manuel; Müller, Matthias; Tverskoy, Olena; Rosenkranz, Marco; Dmitrieva, Evgenia; Popov, Alexey A.; Rominger, Frank; Freudenberg, Jan; Dreuw, Andreas; Bunz, Uwe H. F.
• Is Part Of: Angewandte Chemie. Volume 132:Number 30(2020)
• Page Start: 12496
• Page End: 12501
• Publication Date: 2020-04-28
• Subjects: acenes -- heteroaromatics -- radicals -- structure elucidation -- synthetic methods; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201915977
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: Quinoidal azaacenes with almost pure diradical character ( y= 0.95 to y= 0.99) were synthesized. All compounds exhibit paramagnetic behavior investigated by EPR and NMR spectroscopy, and SQUID measurements, revealing thermally populated triplet states with an extremely low‐energy gap Δ E ST′ of 0.58 to 1.0 kcal mol −1 . The species are persistent in solution (half‐life≈14–21 h) and in the solid state they are stable for weeks. Abstract : Best of two worlds : Lateral fusion of azaacenes onto a quinoidal system furnishes stable diradicals with a radical character ( y ) of up to 0.99. All compounds exhibit paramagnetic behavior as determined by EPR and NMR spectroscopy and SQUID measurements, revealing thermally populated triplet states with an extremely low‐energy gap Δ E ST of 0.58 to 1.0 kcal mol −1 . The species are persistent in solution (half‐life≈14–21 h), and they are stable for weeks in the solid state.