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), w
Synthesis and properties of a second-order nonlinear optical side-chain polyimide
β Scribed by Yoshimasa Sakai; Mitsuru Ueda; Takashi Fukuda; Hiro Matsuda
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 222 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
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 4,4Π-(hexafluoroisopropylidene)diphthalic anhydride with a new diamine having two N-ethyl-N-[4-[(6-chlorobenzothiazol-2-yl)diazenyl]phenyl]-2aminoethanol units as the NLO chromophore, followed by poling during or after the thermal imidization process. The resulting PI had number and weight-average molecular weights (M n , M w ) of 25,000 and 80,000, respectively, and a relatively high glass transition temperature of 180Β°C. The second harmonic coefficient (d 33 ) of PI at the wavelength of 1.064 m was 138 pm/V (329.6 Ο« 10 Οͺ9 esu) and remained unchanged at elevated temperatures. The corona poling process of the NLO-substituted poly(amic acid) to the PI was also studied in detail by measuring the second harmonic generation (SHG) from the polymer films.
π SIMILAR VOLUMES
Aromatic polyimides with side chain nonlinear optical chromophores have been investigated through a facile two-step synthetic route. First, various poly(hydroxy imide)s have been synthesized by direct thermal imidization of diaminophenol dihydrochloride salt and aromatic dianhydride monomers. The re
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
Side-chain second-order nonlinear optical polyimides were prepared from four novel chromophore-containing diamines and 4,4Π-(hexafluoroisopropylidene) diphthalic anhydride by a traditional two-step process that included a solution polycondensation followed by a chemical imidization. The four diamine