Faculty Publications
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Item Photoalignment of nematic liquid crystal by thin films of bishydrazones derived from 3,4 dipropyloxythiophene(2010) Alla, R.A.; Hegde, G.; Ravi, K.; Vasudeva Adhikari, A.V.; Vishnumurthy, K.A.; Komitov, L.Photoalignment of nematic liquid crystals (LC) promoted by thin films of bishydrazone derived from 3, 4 dipropyloxythiophene is studied. Experimental results show that bishydrazone without methyl group in their structure is promoting planar alignment parallel to the polarization direction of the actinic light whereas the ones with methyl group in the structure are promoting planar alignment perpendicular to light polarization direction. © 2010 ITE and SID.Item Nonlinear optical properties of a newly synthesized thiophene based conjugated polymer(2011) Sunitha, M.S.; Vasudeva Adhikari, A.V.; Vishnumurthy, K.A.; Philip, R.We have synthesized a new donor-acceptor (D-A) conjugated polymer containing 3,4-aralkyloxy and alkoxy substituted thiophene and 1,3,4-oxadiazole as donor and acceptor moieties respectively, through precursor polyhydrazide route. The required polyhydrazide was synthesized from 3,4-dihydroxythiophene diester through multistep reaction. The new polymer was characterized by using FTIR, 1H NMR spectroscopy, followed by Elemental analysis. The average molecular weight of the polymer was determined by Gel Permeation Chromatography. The band gap of the polymer was calculated by using UV-visible and cyclic voltametry. Further, its NLO properties in THF solution were investigated both by the Z-scan and degenerate four-wave mixing (DFWM) techniques using 532 nm, 7 nanosecond laser pulses. The results indicate that they exhibit good optical limiting behavior due to effective two-photon absorption (TPA). Values of the effective TPA coefficient (β), third-order non-linear optical susceptibility (χ(3)) and figure of merit (F) were calculated. The optical and electrochemical properties reveal that the polymer is a promising candidate for opto-electronic applications. © 2011 American Institute of Physics.Item Synthesis and characterization of a new conjugated polymer bearing pyrazole and thiophene moieties as potent NLO material(2011) Vishnumurthy, K.A.; Vasudeva Adhikari, A.V.; Sunitha, M.S.; Philip, R.In this communication we describe the design and synthesis of a new conjugated polymer (P) carrying 3,4-dialkoxythiophene, 1,3,4 oxadiazole and pyrazole units, from its monomers through condensation polymerization method. The structure of newly synthesized polymer was established by FT-IR, 1H NMR, elemental analysis and gel permeation chromatographic techniques. Further, its electrochemical, linear and nonlinear optical properties of the polymer have been investigated. The optical and electrochemical band gap was found to be 2.39 eV. Z-scan results reveal that the polymer exhibits strong optical limiting behavior due to effective three-photon absorption (3PA). The value of 3PA coefficient was found to be 1.1×10-20m3/W2, which is comparable to that of good optical limiting materials. The fluorescence quantum yield of the polymer in solution was determined using quinine sulfate as standard and it was found to be 42%. © 2011 American Institute of Physics.Item Recent developments in photoalignment technology: Alignment properties of a thiophene based bis-hydrazone derivative(2012) Hegde, G.; Srivastava, A.K.; Vasudeva Adhikari, A.V.; Vishnumurthy, K.A.; Mohd Yusoff, M.M.; Chigrinov, V.G.; Kwok, H.S.Liquid crystal photoalignment on bis-hydrazones derived from thiophene derivatives is reviewed. Proposed material shows excellent alignment properties which is highly promisable for future applications. This photoalignment is based on reorientation phenomena attributed to thiophenes.Item Design and synthesis of a new thiophene based donor-acceptor type conjugated polymer with large third order nonlinear optical activity(2011) Vishnumurthy, K.A.; Vasudeva Adhikari, A.V.; Sunitha, M.S.; Ann Mary, K.A.A.; Philip, R.In this communication we describe the design and synthesis of a new conjugated polymer (P) carrying 3,4-dialkoxythiophene, 1,3,4-oxadiazole and thienylene-vinylene units, from its monomers using Wittig condensation method. The structure of newly synthesized polymer was confirmed by FT-IR, 1H NMR, UV-vis spectral, elemental analysis and gel permeation chromatographic techniques. The polymer exhibited good thermal stability with the onset decomposition temperature around 320 °C in nitrogen atmosphere. Further, its electrochemical, linear and nonlinear optical properties have been investigated. The optical and electrochemical band gap was found to be 2.21 eV. Its third-order nonlinear optical property was investigated by Z-scan and DFWM techniques, using a Q-switched, frequency doubled Nd:YAG laser producing 7 ns laser pulses at 532 nm. Z-scan results reveal that the polymer exhibits self-defocusing nonlinearity. The operating mechanism involves reverse saturable absorption. The polymer shows strong optical limiting behavior due to effective two-photon absorption (2PA). The value of 2PA coefficient was found to be 3.0 × 10-11 mW, which is comparable to that of good optical limiting materials. The fluorescence quantum yield of the polymer in solution was determined using quinine sulfate as standard and it was found to be 35%. © 2011 Elsevier B.V. All rights reserved.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 diphenylamine-based donor-acceptor-type conjugated polymers as potential photonic materials(2011) Vishnumurthy, K.A.; Sunitha, M.S.; Philip, R.; Vasudeva Adhikari, A.V.A new series of donor-acceptor-type conjugated polymers (P1 and P2) carrying a diphenyl amine moiety were synthesized via Wittig condensation technique. The polymers structures were well established by FT-IR, 1H NMR, elemental analysis and gel permeation chromatographic techniques. They exhibited good thermal stability with an onset decomposition temperature of approximately 325 °C under nitrogen atmosphere. The optical and electrochemical properties of the polymers were studied by UV-vis, fluorescence emission spectroscopy and cyclic voltammetry. They exhibited good fluorescence in dilute solutions and showed solvatochromic behavior in various polar solvents. The electrochemical studies revealed that the polymers possess low-lying LUMO energy levels that ranging from -3.47 to -3.73 eV and high-lying HOMO energy levels that ranging from -5.57 to -5.81 eV. The thirdorder nonlinear optical properties of the polymers were investigated using the Z-scan technique. The effective two-photon absorption (TPA) coefficients (?) of the polymers were found to be 0.645 × 10-10 and 0.212 × 10-10 m/W. © 2011 Elsevier Ltd. All rights reserved.Item Electrochemical and nonlinear optical studies of new D-A type ?-conjugated polymers carrying 3,4-benzyloxythiophene, oxadiazole, and 3,4-alkoxythiophene systems(2012) Sunitha, M.S.; Vasudeva Adhikari, A.V.; Vishnumurthy, K.A.; Smijesh, N.; Philip, R.We investigated the nonlinear optical (NLO) properties of two newly synthesized conjugated polymers Pl and P2 carrying 1,3,4-oxadiazole, 3,4-dibenzyloxythiophene, and 3,4-dialkoxythiophene moieties along the main chain, as potential NLO active materials. Their structures have been well characterized. The nonlinear measurements were performed by Z-scan using 532 nm, 7 ns laser pulses. Calculated values of figure of merit and ? follow the criteria for good NLO materials. These results suggest that polymers are promising materials for applications in photonics.© 2012 The Chemical Society of Japan.Item Large third-order nonlinearity of new ?-conjugated donor-acceptor polymers with substituted thiophene and 1,3,4-oxadiazole moieties(2012) Sunitha, M.S.; Vasudeva Adhikari, A.V.; Vishnumurthy, K.A.; Safakath, K.; Philip, R.We present the synthesis of two newly designed, thiophene-based conjugated polymers (P1 and P2) carrying 1,3,4-oxadiazole, 3,4-dinaphthyloxy thiophene, and 3,4-dialkoxy thiophene moieties as potential NLO active materials. Their NLO properties have been investigated both by the Z-scan and degenerate four-wave mixing (DFWM) techniques using 532nm, 7 nanosecond laser pulses. The measured ? and ?(3) values for the polymers are found to be in the range of 1011m/W and 1011esu, respectively. The results indicate that they exhibit good optical-limiting behavior and are promising materials for nonlinear optical applications due to effective two-photon absorption (TPA). © 2012 Copyright Taylor and Francis Group, LLC.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.