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Design and synthesis of unsymmetric phosphinated diamines for high-T g, transparent polyimides
Journal article   Peer reviewed

Design and synthesis of unsymmetric phosphinated diamines for high-T g, transparent polyimides

Hou Chien Chang, Sheng Lung Chang, Ching Hsuan Lin and Sinn Wen Chen
Polymer, Vol.53(8), pp.1651-1658
03/04/2012

Abstract

Orientation,Polyimides,Transparency
Two phosphinated diamines, 1-(4-aminophenyl)-1-(3-t-butyl-4-aminophenyl) -1- (6-oxido-6H -dibenz <c,e> <1,2> oxaphosphorin-6-yl)ethane (1) and 1-(4-aminophenyl) -1-(3-methxoy-4-aminophenyl)-1-(6-oxido-6H -dibenz <c,e> <1,2> oxaphosphorin-6-yl)ethane (2), were prepared via a facile, one-pot reaction of DOPO, 4-aminoacetophenone and 2-tertbutylaniline or 2-anisidine in the presence of p-toluenesulfonic acid. Based on diamines (1-2), a series of unsymmetric polyimides (3-4) were prepared in NMP/xylene by high-temperature solution polymerization. Transparency polyimides 3-4 with flexibility, organo-solubility, high-T <sub>g</sub> values (310-384 °C), and moderate thermal properties (T <sub>d</sub> 5 wt%, nitrogen: 461-477 °C; air, 456-474 °C) can be achieved. We found that the transparency of polyimide films is related with the orientation of the biphenylene phosphinate pendant, and the orientation is influenced by the bulkiness of the ortho-substituted substituent. © 2012 Elsevier Ltd. All rights reserved.

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