Second-order nonlinear optical active polymethacrylate and polyester containing a methylsulfonylbenzothiazole azo chromophore

Ju Sik Kang, Jae Hyung Kim, Chul Ju Lee, Dong Hoon Choi

Research output: Contribution to journalArticle

Abstract

We synthesized the second-order nonlinear optical (NLO) copolymers for studying the effect of temperature on the temporal stability of the electro-optic effect. Heterocyclic azo chromophore was synthesized to be anchored to methacrylate and naphthalate polymer backbone. The decaying behavior of the electro-optic response was traced at different temperatures. The rates of relaxation were considered based on the difference in the polymer structure.

Original languageEnglish
Pages (from-to)67-70
Number of pages4
JournalMolecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals
Volume349
Publication statusPublished - 2000 Dec 1
Externally publishedYes

Fingerprint

Polyesters
polyesters
Chromophores
Electrooptical effects
chromophores
electro-optics
Polymers
Methacrylates
polymers
copolymers
Copolymers
Temperature
temperature
polymethacrylic acid

ASJC Scopus subject areas

  • Condensed Matter Physics

Cite this

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abstract = "We synthesized the second-order nonlinear optical (NLO) copolymers for studying the effect of temperature on the temporal stability of the electro-optic effect. Heterocyclic azo chromophore was synthesized to be anchored to methacrylate and naphthalate polymer backbone. The decaying behavior of the electro-optic response was traced at different temperatures. The rates of relaxation were considered based on the difference in the polymer structure.",
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AU - Choi, Dong Hoon

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AB - We synthesized the second-order nonlinear optical (NLO) copolymers for studying the effect of temperature on the temporal stability of the electro-optic effect. Heterocyclic azo chromophore was synthesized to be anchored to methacrylate and naphthalate polymer backbone. The decaying behavior of the electro-optic response was traced at different temperatures. The rates of relaxation were considered based on the difference in the polymer structure.

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