Bimolecular hydrogen transfer in phenalene by a stepwise ene-like reaction mechanism.

نویسندگان

  • Yong-Hui Tian
  • Miklos Kertesz
چکیده

For the hydrogen transfer of phenalene, a bimolecular ene-like mechanism is proposed, which is preferable over the hypothesized unimolecular rearrangement in the literature. Unique SOMO-SOMO pi-bonding of phenalenyl reduces the barriers of pericyclic reactions significantly. Pi-bonding between radicals is being recognized as a novel type of bonding interaction. This paper adds to the use of this interaction by pointing out its effect on reaction barriers.

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عنوان ژورنال:
  • Chemical communications

دوره 46 24  شماره 

صفحات  -

تاریخ انتشار 2010