Phosphoniumylidyl thioxophosphanes and selenoxophosphanes, the only kn
own monomeric chalcogenoxophosphanes, react in a 2:1 ratio with triphe
nylphosphonium ylides. With loss of PPh(3) the 1,2,4-thia(or selena)di
phosphetane monosulfides (or selenides) are formed. Their prominent st
ructural feature are the very different PS bond lengths in the ring. T
hey can be oxidized to the corresponding disulfides or sulfide selenid
es. The latter rearrange to the isomer in which the selenium atom has
become a ring member.