Journal article

The radical anion of acepentalene


Authors listde Meijere, A; Schreiner, PR; Schüngel, FM; Gerson, F; Merstetter, P

Publication year1999

Pages2189-2190

JournalChemical Communications

Issue number21

ISSN1359-7345

DOI Linkhttps://doi.org/10.1039/a906972k

PublisherRoyal Society of Chemistry


Abstract
In the radical anion (1(.-)) of acepentalene, generated by photooxidation of the corresponding dianion (1(2-)), the spin population appears to be evenly distributed over the nine-membered perimeter due to a rapid interconversion between two bowl-shaped C-s forms and a relatively low lying planar C-2v transition structure (TS).



Citation Styles

Harvard Citation stylede Meijere, A., Schreiner, P., Schüngel, F., Gerson, F. and Merstetter, P. (1999) The radical anion of acepentalene, Chemical Communications(21), pp. 2189-2190. https://doi.org/10.1039/a906972k

APA Citation stylede Meijere, A., Schreiner, P., Schüngel, F., Gerson, F., & Merstetter, P. (1999). The radical anion of acepentalene. Chemical Communications(21), 2189-2190. https://doi.org/10.1039/a906972k


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