Faculty Publications
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Item Nonlinear optical studies on a new poly{2-(biphenyl-4-yl)-5-[3,4- didecyloxy-5-(1,3,4-oxadiazol-2-yl)thiophen-2-yl]-1,3,4-oxadiazole}(Trans Tech Publications Ltd ttp@transtec.ch, 2010) Hegde, P.K.; Vasudeva Adhikari, A.V.; Manjunatha, M.G.; Suchand Sandeep, C.S.; Philip, R.Measurements of nonlinear optical properties of a newly synthesized thiophene based polymer are reported. The nonlinear transmission measurements were performed on the polymer dissolved in N,N-dimethylformamide by employing the single beam Z-scan technique using a Q-switched laser output at 532-nm. The polymer shows strong optical limiting behavior, where the transmittance decreases when the pump fluence is increased. It was found that an effective three-photon absorption (3PA) model at the excitation wavelength gives the best fit to the obtained experimental data. The value of the 3PA coefficient has been numerically calculated. This study clearly reveals the potential of new polymeric material has, for optical limiting applications. © (2010) Trans Tech Publications.Item A new donor-acceptor type conjugative poly{2-[4-(1-cyanoethenyl)phenyl]-3- (3,4-didodecyloxythiophen-2-yl)prop-2-enenitrile}: Synthesis and NLO studies(2010) Hegde, P.K.; Vasudeva Adhikari, A.V.; Manjunatha, M.G.; Suchand Sandeep, C.S.; Philip, R.This research article describes a technique to synthesize a new donor-acceptor type conjugated polymer carrying cyanophenylenevinylene and 3,4-didodecyloxy thiophene moieties, as an effective optical limiting material. It also includes the evaluation of its linear and nonlinear optical properties and electrochemical studies. The new polymer, viz., poly{2-[4-(1-cyanoethenyl) phenyl]-3-(3,4-didodecyloxythiophen-2-yl)prop-2-enenitrile} (P1) has been synthesized starting from 2,2?-sulfanediyldiacetic acid and diethyl ethanedioate through multistep reactions. In the final step, the polymerization was brought about by Knovenagel condensation. The newly synthesized intermediate, monomer and the polymer (P1) have been characterized by different spectroscopic techniques followed by elemental analysis. Its optical and electrochemical properties are investigated by UV-vis, fluorescence spectroscopy and cyclic voltammetric studies, respectively. The red colored polymer has a well defined structure, good thermal stability and a band gap of 1.78 eV. It emits green fluorescence both in solution and in film state. The third-order nonlinear optical property (NLO) of the polymer was studied by the Z-scan technique. The measurements were performed at 532 nm with 5 ns laser pulses using samples in solution form. An absorptive nonlinearity of the optical limiting type was found in this polymer, which is due to the combined action of saturable absorption and excited state absorption processes. These studies revealed that polymer P1 is a promising material for optical limiting applications. © 2010 Elsevier B.V.Item Nonlinear optical studies on new conjugated poly{2,2 l-(3,4- dialkoxythiophene-2,5-diyl) bis[5-(2-thienyl)-1,3,4-oxadiazole]}s(2010) Hegde, P.K.; Vasudeva Adhikari, A.V.; Manjunatha, M.G.; Suchand Sandeep, C.S.; Philip, R.Three new donor-acceptor type poly{2,2 1-(3,4-dialkoxythiophene- 2,5-diyl)bis[5-(2-thienyl)-1,3,4-oxadiazole]}s (P1, P2, and P3) were synthesized starting from thiodiglycolic acid and diethyl oxalate through multistep reactions. The polymerization was carried out using chemical polymerization technique. The optical and charge-transporting properties of the polymers were investigated by UV-visible, fluorescence emission spectroscopic and cyclic voltammetric studies. The polymers showed bluish-green fluorescence in solutions. The electrochemical band gaps were determined to be 2.03, 2.09, and 2.17 eV for P1, P2, and P3, respectively. The nonlinear optical properties of new polymers were investigated at 532 nm using single beam Z-scan and degenerate four-wave mixing (DFWM) techniques with nanosecond laser pulses. The polymers exhibited strong optical limiting behavior due to "effective" three-photon absorption. Values of the effective three-photon absorption (3PA) coefficients, thirdorder nonlinear susceptibilities (? (3)), and figures (F) of merit were calculated. © 2010 Wiley Periodicals, Inc.Item Synthesis, electrochemical and optical studies of new cyanopyridine based conjugated polymers as potential fluorescent materials(Elsevier Ltd, 2011) Vishnumurthy, K.A.; Sunitha, M.S.; Safakath, K.; Philip, R.; Vasudeva Adhikari, A.V.In this communication we describe the design and synthesis of four new conjugated polymers (P1-P4) carrying cyanopyridine in their backbone via Wittig condensation technique. Their structures were well established by FTIR, 1H NMR, elemental analysis and gel permeation chromatographic techniques. They exhibited good thermal stability with the onset decomposition temperature around 300-350 °C in nitrogen atmosphere. Further, their electrochemical, linear and third-order non-linear optical properties have been investigated. The polymers showed low electrochemical band gaps in the range of 1.77-1.99 eV and displayed very good fluorescence emission property in various polar solvents. The fluorescence quantum yields of polymers P1-P4 in tetrahydrofuran (THF) were found to be 35, 42, 38 and 34%, respectively. The effective two-photon absorption coefficients (?) for the polymers were determined by Z-Scan technique and were found to be 1.34 × 10 -11, 1.24 × 10-11, 3.04 × 10-11 and 1.85 × 10-11 m/W for polymers P1-P4, respectively. © 2011 Elsevier Ltd. All rights reserved.Item New optical limiting polymeric materials with different ?-electron conjugation bridge structures: Synthesis and characterization(2012) Vishnumurthy, K.A.; Sunitha, M.S.; Vasudeva Adhikari, A.V.In this communication we describe the design and synthesis of five new conjugated polymers (P1-P5) with various ?-electron conjugation bridges. Their structures were established by FTIR, 1H NMR spectroscopy, elemental analysis. The molecular weights of the polymers were estimated by gel permeation chromatographic technique. Further, their electrochemical, linear and nonlinear optical properties were investigated. The electrochemical band gaps of P1-P5 were found to be 1.72-2.35 eV. Their third-order nonlinear optical activities were studied by open aperture Z-scan technique, using a Q-switched, frequency doubled Nd:YAG laser producing 7 nano second laser pulses at 532 nm. Z-scan results reveal that the polymers exhibit self-defocusing nonlinearity and their operating mechanism involves reverse saturable absorption. The polymers showed strong optical limiting behavior due to effective two-photon absorption (2PA) with 2PA coefficients of the order of 10 -11 m/W, which is comparable to that of good optical limiting materials in the literature. © 2012 Elsevier Ltd. All rights reserved.Item Synthesis and characterization of thiophene-based donor-acceptor type polyimide and polyazomethines for optical limiting applications(2013) Vishnumurthy, K.A.; Sunitha, M.S.; Vasudeva Adhikari, A.V.In this communication we describe the design and synthesis of four new conjugated polymers (P1-P4) based on 3,4-ditetradecyloxythiophene. The required diamine monomer was prepared by a unique catalyst-free reduction process using hydrazine hydrate. The structures of the intermediates and polymers were established by FTIR, 1H NMR spectroscopy. Molecular weights of polymers were determined by gel permeation chromatographic (GPC) method. Their electrochemical properties were investigated by cyclic voltammetry and linear optical properties were determined by UV-Visible absorption and fluorescence emission spectroscopic techniques. Further, their nonlinear optical properties were evaluated by Z-scan technique using Nd:YAG laser. These polymers showed strong optical limiting behavior with two-photon absorption (2PA) coefficients of the order of 10-10 m/W, which are comparable to that of good optical limiting materials reported in the literature. Also, it has been observed that the optical nonlinearity enhanced with the increase in donor-acceptor strength of the polymer backbone. © 2012 Springer-Verlag.
