Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/70653
標題: Thermally stable hyperbranched nonlinear optical polyimides using an "A(2)+B-3" approach
作者: Chen, Y.C.
Lo, W.C.
Juang, T.Y.
Dai, S.A.
Su, W.C.
Chou, C.C.
Jeng, R.J.
Project: Materials Chemistry and Physics
期刊/報告no:: Materials Chemistry and Physics, Volume 127, Issue 1-2, Page(s) 107-113.
摘要: 
To obtain nonlinear optical (NLO) polyimides exhibiting excellent thermal stability and large electro-optical (EO) coefficients, we synthesized a series of novel hyperbranched polyimides from a tris(ether anhydride) [1,1,1-tris[4-(3,4-dicarboxyphenoxy)phenyl]ethane trianhydride (III)] and a difunctional chromophore [(2,4-diamino-4'-(4-nitrophenyldiazenyl)azobenzene) (DNDA)], through ring-opening polyaddition at room temperature to form poly(amic acid)s (PAAs), followed by poling/curing process. The presence of the imide rings in the hyperbranched NLO polymers imparted them with excellent thermal stability. Moreover, their highly hyperbranched architectures resulted in site-isolation effects, which restricted the aggregation of the chromophore units. All of these hyperbranched polymers exhibited larger EO coefficients (14.6-17.2 pm V-1) and better temporal stability at 120 degrees C than those of linear NLO polymers. In addition, we also observed waveguide properties for hyperbranched NLO polymers (3.4-4.6 dB cm(-1) at 1310 nm). Relative to the analogous linear NLO polyimide, the hyperbranched NLO polyimides exhibited superior temporal stability, larger EO coefficients, and lower optical losses. (C) 2011 Elsevier BM. All rights reserved.
URI: http://hdl.handle.net/11455/70653
ISSN: 0254-0584
DOI: 10.1016/j.matchemphys.2011.01.042
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