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Chem Commun (Camb) ; (7): 830-2, 2009 Feb 21.
Artigo em Inglês | MEDLINE | ID: mdl-19322456

RESUMO

Isoelectronic benzo-1,3,2-diazaphospholium cations and benzo-1,3,2-diazaphospholide anions were prepared from the same phosphazane precursor; both species display according to computational studies similar aromaticity as the neutral benzo-1,3,2-diazaphosphole but are chemically more stable due to their ionic nature.

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