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Synthesis and characterization of thermally stable second-order nonlinear optical side-chain polyimides containing thiazole and benzothiazole push-pull chromophores

Tambe, S. M., Kittur, A. A., Inamdar, S. R., Mitchell, G. R. and Kariduraganavar, M. Y. (2009) Synthesis and characterization of thermally stable second-order nonlinear optical side-chain polyimides containing thiazole and benzothiazole push-pull chromophores. Optical Materials, 31 (6). pp. 817-825. ISSN 0925-3467

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To link to this article DOI: 10.1016/j.optmat.2008.09.005

Abstract/Summary

Push-pull nonlinear optical (NLO) chromophores containing thiazole and benzothiazole acceptors were synthesized and characterized. Using these chromophores a series of second-order NLO polyimides were Successfully prepared from 4,4'-(hexafluoroisopropylidene) diphthalic anhydride (6FDA), pyromellitic dianhydride (PMDA) and 3,3'4,4'-benzophenone tetracarboxylic dianhydride (BTDA) by a standard condensation polymerization technique. These polyimides exhibit high glass transition temperatures ranging from 160 to 188 degrees C. UV-vis spectrum of polyimide exhibited a slight blue shift and decreases in absorption due to birefringence. From the order parameters, it was found that chromophores were aligned effectively. Using in situ poling and temperature ramping technique, the optical temperatures for corona poling were obtained. It was found that the optimal temperatures of polyimides approach their glass transition temperatures. These polyimides demonstrate relatively large d(33) values range between 35.15 and 45.20 pm/V at 532 nm. (C) 2008 Elsevier B.V. All rights reserved.

Item Type:Article
Refereed:Yes
Divisions:Interdisciplinary centres and themes > Nanoscience and Materials
Faculty of Science > School of Mathematical and Physical Sciences
ID Code:1626
Uncontrolled Keywords:FUNCTIONALIZED POLYIMIDES; CROSS-LINKING; STABILITY; POLYMERS; HYPERPOLARIZABILITIES; THIOPHENE; DESIGN
Publisher:Elsevier

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