01270nas a2200133   4500008004100000245013200041210006900173260000800242490000800250520070600258100002600964700002400990856012201014       2017                        eng d00aEffect of side-chain functionality on the organic field-effect transistor performance of oligo(p-phenylenevinylene) derivatives0 aEffect of sidechain functionality on the organic fieldeffect tra  cJUN0 v1343 aIn order to observe the effects of the substitution of electronegative flourine with aromatic groups in oligo(p-phenylenevinylene) compounds on their packing, morphology, and charge carrier mobility, we have synthesized napthol-substituted oligo(p-phenylenevinylene) compounds and examined their solubility, redox properties, thin film morphologies, and charge carrier properties. To date, very few examples of conjugated oligomers bearing napthol side groups have been reported in the literature. After annealing at 150 degrees C, the mobility of S1, S2, and S3 was 4.0x10(-2) cm(2) V-1 s(-1), 1.2x10(-2) cm(2) V-1 s(-1), and 2.6x10(-3) cm(2) V-1 s(-1), respectively. (c) 2017 Wiley Periodicals, Inc.1 aChini, Mrinmoy, Kumar1 aChatterjee, Shyambo  uhttps://library.ncl.res.in/content/effect-side-chain-functionality-organic-field-effect-transistor-performance-oligop