G. Jochem et al., BIS(TRIPHENYLPHOSPHONIUMYLIDYL)PHOSPHANE, Zeitschrift fur Naturforschung. B, A journal of chemical sciences, 51(2), 1996, pp. 267-276
Bis(ylidyl)phosphanes can be prepared from ylides and dichlorophosphan
es or from bis(ylidyl)phosphenium chlorides and organolithium compound
s. By substituting in bis(ylidyl)phosphenium chlorides the chloride io
n for more basic anions, a large variety of bis(ylidyl)phosphanes is a
ccessible. They can be protonated at the ylidic carbon atoms, but alky
lated and oxidized at the central phosphorus atom. As shown by P-31 NM
R in solution and by Xray investigation of the crystal, the lone pair
at the tervalent phosphorus is generally oriented synperiplanar to bot
h phosphonio groups.