An amphiphilic, ionic, conjugated polymer, poly(N-octadecyl-2-ethynylp
yridinium bromide) (PNO2EPB), was prepared by two different synthetic
processes. One involved a direct reaction of 2-ethynylpyridine (2EPY)
with 1-bromooctadecane (1-BO), the other involved quaternization of th
e uncharged poly(2-ethynylpyridine) (P2EPY) with 1-BO. A fully quatern
ized PNO2EPB homopolymer was produced in the former reaction, but a co
polymer of 2EPY and N-octadecyl-2-ethynylpyridinium bromide (NO2EPB) w
as obtained in the latter due to partial quaternization of P2EPY. The
structure and properties of these polymers were investigated. The stud
y of PNO2EPB formation using differential scanning calorimetry and ult
raviolet-visible spectrophotometry indicated that quaternization of 2E
PY monomer by 1-BO preceded polymerization of quaternized 2EPY monomer
. Fully quaternized PNO2EPB displays a longer conjugation length and a
n enhanced thermal stability compared with the partially quaternized P
2EPY-q-octa and the non-quaternized P2EPY. The study of compression is
otherms of monolayers of the fully quaternized polymer leads to the co
nclusion that the alkyl (octadecyl) chains of the repeating unit are p
erpendicular to the water interface while the conjugated polymer chain
s are in the plane of the interface. Copyright (C) 1996 Elsevier Scien
ce Ltd.