We have prepared a series of cross-linkable oligo- and poly(dialkylfluorene
)s by nickel(0)mediated polymerization of 2,7-dibromo-9,9-dialkylfluorene (
alkyl = n-hexyl) and 4-bromo-styrene. The resulting fully soluble and proce
ssable, styryl-functionalized oligomers and polymers can be cross-linked vi
a the vinyl end-groups by curing at 175-200 degrees C, consistent with the
autopolymerization mechanism of styrene, These relatively mild conditions r
ender the materials insoluble and enable multilayering of polymers in organ
ic light emitting devices. At the same Lime, the electrical and/or optical
properties of the cross-linked polymers are preserved and no deleterious sp
ecies or undesirable byproducts are produced. Furthermore, the cross-linkin
g allows control of the supramolecular ordering of the planarized rigid rod
-type fluorene segments in the polymer backbone that leads to suppression o
f troublesome excimer/aggregate in the photo- and electrolumenescence.