Journal article

The protonation of cubane revisited


Authors list: Fokin, AA; Tkachenko, BA; Gunchenko, PA; Schreiner, PR

Publication year: 2005

Pages: 146-149

Journal: Angewandte Chemie International Edition

Volume number: 44

Issue number: 1

ISSN: 1433-7851

DOI Link: https://doi.org/10.1002/anie.200461042

Publisher: Wiley


Abstract: 

Cubane's proton affinity is now understood! Protonated cubane
forms a structure with a protonated C-C bond (see scheme), which
undergoes rearrangement along the most favorable reaction path rapidly
giving 1,8‐dihydropentalene as the final product. The results confirm
the experimentally determined proton affinity of cubane.




Citation Styles

Harvard Citation style: Fokin, A., Tkachenko, B., Gunchenko, P. and Schreiner, P. (2005) The protonation of cubane revisited, Angewandte Chemie International Edition, 44(1), pp. 146-149. https://doi.org/10.1002/anie.200461042

APA Citation style: Fokin, A., Tkachenko, B., Gunchenko, P., & Schreiner, P. (2005). The protonation of cubane revisited. Angewandte Chemie International Edition. 44(1), 146-149. https://doi.org/10.1002/anie.200461042


Last updated on 2025-21-05 at 13:32