The structures of uoro-2,5-bis-(pentafluorophenyl)-2,3,4-hexatriene, (
1), C18F16, -1,1,1,2,2,7,7,8,8,8-decafluoro-3,6-diphenyl-3,4,5 octatri
ene,(2), C20H10F10, and (E)-1,1,1,2,2,3,3,8,8,9, ,10-tetradecafluoro-4
,7-diphenyl-4,5,6-decatriene, (3), C22H10F14, confirm the trans confor
mation assigned by spectrophotometric methods. These trienes exhibit t
he central double-bond shortening observed in cumulenes. The phenyl ri
ngs are rotated slightly from the triene plane in (2) and (3) and are
nearly perpendicular to the triene plane in (1). The large rotation of
the perfluorophenyl rings from the triene plane is due to intramolecu
lar steric interactions with the ortho-F atoms.