A thermal stable aromatic polyimide (PI) with side-chain second-order nonlinear optical (NLO) chromophores has been developed. The PI was prepared by the ring-opening polyaddition of 4,4ะ-(hexafluoroisopropylidene)diphthalic anhydride with a new diamine having two N-ethyl-N-[4-[(6-chlorobenzothiazol
Characterization of a side chain polymer for second-order nonlinear optical properties
โ Scribed by P. R. Srikanth Sharma; P. Zhou; H. L. Frisch; E. A. Van Wagenen; G. M. Korenowski
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 146 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
We report the characterization of copolymers of methyl methacrylate (MMA) and 2-propenoic acid, 2-methyl-, 2-[[[[4-methyl-3-[[(2-methyl-4-nitrophenyl)amino]carbonyl]aminophenyl]carbonyl]oxy]ethyl ester (PAMEE) exhibiting nonlinear optical (NLO) properties. The linear copolymer, poly(MMA-co-PAMEE), with a NLO chromophore incorporated into PAMME exhibits a high glass transition temperature of 131ยฐC, as determined by DSC. The thin films of copolymers, which were cast on microscopic glass slides, were optically transparent, and the corona poled polymers produced relatively large and stable second harmonic generation (SHG) signals at room temperature. The nonlinear coefficient d 33 of the crosslinked copolymer containing 30 wt % PAMEE was 30.8 pm/V. The SHG signal strength remained unchanged, even after 120 days, and exhibited excellent thermal stability at 65ยฐC.
๐ SIMILAR VOLUMES
A two-step, generally applicable synthetic approach for nonlinear optical (NLO) side-chain polyimides was developed. This included the preparation of a preimidized, organosoluble polyimide with benzene moiety pendant from main chains, followed by the covalent bonding of the NLO chromophores onto the