Faculty Publications
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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 new donor-acceptor type conjugated copolymers derived from thiophenes(2009) Manjunatha, M.G.; Vasudeva Adhikari, A.V.; Hegde, P.K.A new series of donor-acceptor type poly(thiophene) derivatives (P1-P3) were synthesized starting from thiodiglycolic acid and diethyl oxalate through multistep reactions. In the final step, the polymerization was carried out using Wittig reaction. This is a good synthetic route for the preparation of any desired p- and n-type copolymers. The optical and potential charge-transporting properties of the copolymers were investigated by UV-vis, fluorescence emission spectroscopy and cyclic voltammetry. The copolymers exhibited bluish-green/green fluorescence in their thin film forms. Cyclic voltammetry experiments showed that these copolymers have low-lying LUMO energy levels ranging from -2.98 to -3.11 eV and high lying HOMO energy levels ranging from -5.45 to -5.65 eV. The optical and electrochemical studies reveal that new copolymers are new promising materials for the development of efficient polymer light emitting diodes. © 2008 Elsevier Ltd. All rights reserved.Item Optical and electrochemical properties of a new donor-acceptor type conjugated polymer derived from thiophene, carbazole and 1,3,4-oxadiazole units(Trans Tech Publications Ltd ttp@transtec.ch, 2010) Manjunatha, M.G.; Vasudeva Adhikari, A.V.; Hegde, P.K.A new donor-acceptor type poly[3-{5-[3,4-didecyloxy-5-(1,3,4-oxadiazol-2- yl)thiophen-2-yl]-1,3,4-oxadiazol-2-yl}-9-dodecyl-9H-carbazole] (P) has been synthesized starting from thiodiglycolic acid and 9H-carbazole through multistep reactions. The polymer has been synthesized through precursor polyhydrazide route. The weight average molecular weight of the polymer was found to be 7210. The polymer exhibited intense green fluorescence in solid sate. Cyclic voltammetric experiments showed that the polymer has low-lying LUMO (-3.55 eV) and high lying HOMO (-5.77 eV) energy levels due to the presence of alternate donor and acceptor units. The optical and electrochemical studies reveal that the new polymer (P) is a promising material for the development of polymer light emitting diodes (PLEDs). © (2010) Trans Tech Publications.Item Nonlinear optical and optical power limiting studies on a new thiophene-based conjugated polymer in solution and solid PMMA matrix(2010) Poornesh, P.; Hegde, P.K.; Umesh, G.; Manjunatha, M.G.; Manjunatha, K.B.; Vasudeva Adhikari, A.V.An experimental investigation of the third-order nonlinear optical properties of new poly{2-{5-[3,4-ditetradecyloxy-5-(1,3,4-oxadiazol-2-yl)thiophen-2-yl]-1,3,4-oxadiazol-2-yl}pyridine} (P) in tetrahydrofuran (THF) solution and in solid poly(methylmethacrylate) (PMMA) matrix, by Z-scan technique is reported. The Z-scan traces reveal that the composite films exhibit large negative nonlinear refractive index of the order 10-10 esu. The excited-state absorption cross-section was found to be larger than the ground-state absorption indicating that the operating nonlinear process is reverse saturable absorption (RSA). The new polymer P exhibits good optical power limiting properties in the nanosecond regime in solution and as well in solid PMMA matrix. © 2009 Elsevier Ltd. All rights reserved.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 Design and Synthesis of New Amides and Thioamides Derived from 3,4-Ethylenedioxythiophene as Potential Anticonvulsants(2010) Kulandasamy, R.; Vasudeva Adhikari, A.V.; Stables, J.P.Five new series of 3,4-ethylenedioxythiophene derivatives carrying important pharamacophores, viz., amide, ester, ether and active secondary aryl moieties have been designed and synthesized through multistep reactions starting from thiodiglycolic ester and diethyl oxalate. They have been characterized by elemental and spectral data. All the target compounds have been screened for their anticonvulsant activity at three different models viz. maximal electroshock (MES), subcutaneous metrazole (scMET), and 6 Hz screen and evaluated for their neurotoxicity in rotorod model. Compound 6a emerged as lead with no neurotoxicity. All the five series of compounds are safe in the toxicity studies at the maximum dose of 300 mg/kg of body weight. Amongst the tested compounds, the ester pharmacophore with thioamide fragment has showed better activity than the other analogs.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 Nonlinear optical characterization of new thiophene-based conjugated polymers for photonic switching applications(2011) Hegde, P.K.; Vasudeva Adhikari, A.V.; Manjunatha, M.G.; Suchand Sandeep, C.S.S.; Philip, R.This research article describes a technique to synthesize new donor-acceptor-type conjugated polymers carrying 1,3,4-oxadiazolyl-naphthalene and 3,4-(ethylenedioxy/diphenyl)-thiophene moieties (P1 and P2) starting from 2,2?-sulfanediyldiacetic acid and diethyl ethanedioate through multistep reactions. The newly synthesized intermediates and the final polymers have been characterized by different spectroscopic techniques followed by elemental analysis. Their optical and electrochemical properties have been investigated by UV-visible, fluorescence spectroscopy, and cyclic voltammetric studies, respectively. Furthermore, the nonlinear optical transmission properties of these polymers have been investigated by the open aperture z-scan technique. The new polymers P1 and P2 have well-defined structures, good thermal stability, and band gaps of 1.98 and 1.88 eV, respectively. They emit bluish-green fluorescence both in solution and in film state. Interestingly, these polymers show saturable absorption behavior. The results of nonlinear optical studies reveal that they are potential candidates for photonic switching device applications. © 2011 Wiley Periodicals, Inc.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 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.