1.
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.