Palladium-catalyzed Stille and Sonogashira. coupling reactions were sequent
ially applied for constructing novel pyrimidine-containing linear molecules
. The chemoselectivity of 5-bromo-2-iodopyrimidine (1) towards Pd-catalyzed
coupling reaction serves as a tool for the successful control of the arran
gement of dipolar pyrimidine moieties inside the conjugated backbone. The i
nfluence of the arrangement of dipolar pyrimidine in the linear backbone on
their absorption and photoluminescence are not stupendous. Thermogravimetr
ic analysis (TGA) indicate that all linear molecules in this study exhibit
high thermal stability. (C) 2001 Elsevier Science Ltd. All rights reserved.