A Stable π-Expanded o-Quinodimethane via the Photochemical Dearomative Cycloaddition of Corannulene with an Isolable Dialkylsilylene DOI Creative Commons
Shintaro Ishida,

Maiko Mori,

Shunya Honda

et al.

Chemistry, Journal Year: 2025, Volume and Issue: 7(2), P. 37 - 37

Published: March 11, 2025

A stable π-expanded o-quinodimethane derivative (2) was synthesized by photochemical dearomative cycloaddition of corannulene with an isolable dialkylsilylene (1) and isolated as a dark blue solid. Compound 2 adopts very flat bowl shape in contrast to parent corannulene. Structural spectroscopic characteristics, redox properties, computational study suggest that has small but significant diradical character (y0 = 0.11). One-electron reduction provides the corresponding radical anion salt.

Language: Английский

A Stable π-Expanded o-Quinodimethane via the Photochemical Dearomative Cycloaddition of Corannulene with an Isolable Dialkylsilylene DOI Creative Commons
Shintaro Ishida,

Maiko Mori,

Shunya Honda

et al.

Chemistry, Journal Year: 2025, Volume and Issue: 7(2), P. 37 - 37

Published: March 11, 2025

A stable π-expanded o-quinodimethane derivative (2) was synthesized by photochemical dearomative cycloaddition of corannulene with an isolable dialkylsilylene (1) and isolated as a dark blue solid. Compound 2 adopts very flat bowl shape in contrast to parent corannulene. Structural spectroscopic characteristics, redox properties, computational study suggest that has small but significant diradical character (y0 = 0.11). One-electron reduction provides the corresponding radical anion salt.

Language: Английский

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