The radical anion of acepentalene

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Armin de Meijere, Peter R. Schreiner, Franz-Manfred Schüngel, Fabian Gerson and Pascal Merstetter


Abstract

In the radical anion (1•–) of acepentalene, generated by photooxidation of the corresponding dianion (12–), the spin population appears to be evenly distributed over the nine-membered perimeter due to a rapid interconversion between two bowl-shaped Cs forms and a relatively low lying planar C2v transition structure (TS).


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