Volume 14, Issue 5 pp. 472-480
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Study on thermal stability of poled non-linear optical polymers

Shen Yu-Quan

Shen Yu-Quan

Institute of Photographic Chemistry, Chinese Academy of Sciences, Beijing 100101, China

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Yang Yu-Chun

Yang Yu-Chun

Institute of Photographic Chemistry, Chinese Academy of Sciences, Beijing 100101, China

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Qiu Ling

Qiu Ling

Institute of Photographic Chemistry, Chinese Academy of Sciences, Beijing 100101, China

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Fu Xing-Fa

Fu Xing-Fa

Institute of Photographic Chemistry, Chinese Academy of Sciences, Beijing 100101, China

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Yu Shang-Xian

Yu Shang-Xian

Department of Chemistry, Beijing Normal University, Beijing 100875, China

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Gu Jiang-Nan

Gu Jiang-Nan

Department of Chemistry, Beijing Normal University, Beijing 100875, China

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Möhlmann G.R.

Möhlmann G.R.

AKZO NOBEL Research Laboratories Arnhem, P.O. Box 9300,6800 SB Arnhem, The Netherlands

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Van Der Vorst C.P.J.M.

Van Der Vorst C.P.J.M.

AKZO NOBEL Research Laboratories Arnhem, P.O. Box 9300,6800 SB Arnhem, The Netherlands

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First published: September 1996

Abstract

A logarithmic expression is proposed to describe relaxation of the polar order in side chain polymers, together with a new way of plotting temperature dependent relaxation data. This results in a straight line extending even below the glass transition temperature in the case of poled nonlinear optics (NLO) side chain polymers. A simple procedure to determine the rotational diffusion constant Dr is given and Dr values of several polymer systems have been evaluated and compared with each other. It appears that, starting from the conventional and well known poled polymer system currently applied, a further lowering of Dr by about 3 orders of magnitude is necessary in order to reach an acceptable orientational stability or lifetime of poled polymers for practical applications. Attempts have been made to introduce electron push-pull substituents into high thermostable molecular frameworks and results of preliminary measurements are reported.

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