Thermally stable second-order nonlinear optical addition-type polyimides functionalized by diamine chromophore
β Scribed by Wei Wu; Dong Wang; Peiwang Zhu; Peng Wang; Cheng Ye
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 180 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
A series of chromophore-functionalized polyimide prepolymers with excellent processibility were prepared by a Michael addition reaction of diamine chromophore 2 with structurally different bismaleimide (BMI) monomers. The effects of the BMI moiety's structure and thermal curing condition on glass transition temperature (T g ) and thermal stability of the polyimides were studied by DSC, TGA, and FTIR. Among the five cured polyimides, PI 3 , bearing a sulfone moiety, exhibited the highest T g and thermal decomposition temperature (T d ). Its corresponding prepolymer, PP 3 , was selected to evaluate NLO properties in a simultaneously poling and thermal polymerization process. A relatively large poling-order parameter was observed. The second-order nonlinear coefficient, d 33 , was 25 pm/V at 1064 nm fundamental wavelength. The second harmonic generation signal was almost without decay up to 170Β°C.
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Thermally stable copolyimides were prepared from two novel second-order nonlinear optical chromophores containing diamines, 4-nitro-4Π-[N-(4,6-di-β€-aminoethylamino)-1,3,5-triazin-2-yl]aminoazobenzene (M1) and 4-nitro-4Π-[N-(4,6-di-4-aminophenylamino)-1,3,5-triazin-2-yl]aminoazobenzene (M2); two codi
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