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    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.
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    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.
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    Synthesis and two-photon absorption property of new ? -conjugated donor-acceptor polymers carrying different heteroaromatics
    (2013) Sunitha, M.S.; Vishnumurthy, K.A.; Vasudeva Adhikari, A.V.
    In this communication, we report the synthesis of three newly designed fluorescent polymers P1-P3, starting from simple thiophene derivatives through precursor polyhydrazide route. The new polymers, carrying donor and acceptor heterocyclic moieties with different spacer groups were found to be thermally stable and good of nonlinear optical (NLO) materials with two photon absorption property. The structures of newly synthesized monomers and polymers were confirmed by FTIR, NMR spectral and elemental analyses. Further, polymers were characterized by GPC and TGA studies. Their linear optical and electrochemical properties were evaluated by UV-vis, fluorescence spectroscopic and cyclic voltammetric (CV) studies, respectively, whereas their NLO properties were studied by Z-scan technique using Nd: YAG laser at 532 nm with 7 ns pulse. The electrochemical band gap of P1-P3 was determined to be 1.98, 1.91 and 2.05 eV, respectively. The NLO results reveal that polymers P1-P3 show good optical limiting property with TPA coefficient values 2.9 × 10 - 11 m/W, 8.0 × 10 - 11 m/W and 1.4 × 10 - 11 m/W, respectively. © 2013 Indian Academy of Sciences.
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    Synthesis of nonlinear heteroaromatic donor–acceptor conjugated polymers: Structural, theoretical, electrochemical, and optical properties
    (John Wiley and Sons Inc, 2025) Sunitha, M.S.; Naik, P.; Vishnumurthy, K.A.; Vasudeva Adhikari, A.V.
    This study presents a new class of donor–acceptor (D–A) type NLO-active polymeric materials (P1–4), bearing 3,4-disubstituted thiophene as electron donor and 1,3,4-oxadiazole as electron acceptor units, along with various aromatic spacers, namely: phenylenevinylene (P1), 3,4-ethylenedioxythiophene-EDOT (P2), naphthalene (P3), and biphenyl group (P4). Their optical and electrochemical behavior was thoroughly examined using cyclic voltammetry, UV–visible absorption spectroscopy, fluorescence emission spectroscopy, and Z-scan technique for nonlinear optical assessments. Additionally, Density Functional Theory analysis and Molecular Electrostatic Potential mapping were carried out to understand the charge distribution and electronic structure in the repeating units of polymers. The influence of the incorporated conjugated ?-linkers on their molecular geometry and optoelectronic properties was analyzed to reveal the relationship between molecular structures and optoelectronic characteristics. Interestingly, P1–4 exhibited distinctive electrochemical band gaps, and noteworthy optical limiting behavior attributed to efficient two-photon absorption, demonstrating their potential for optoelectronic and photonic applications. Among the new polymers P1–4, P2 displayed the highest two-photon absorption coefficient. Highlights: A class of D–A type polymers with varied aromatic ?-spacers were synthesized. New polymers were characterized as potential optical limiting materials. Electronic and charge distribution properties were studied by DFT and MESP. Optical and electrochemical studies showed suitability for nonlinear optics. TPA values are comparable to those typically found in top-tier NLO materials. © 2025 Society of Plastics Engineers.