Synthesis and the third-order non-linear optical properties of new azobenzene-containing side-chain polymers
Source abstract
Abstract
Abstract A new series of aromatic azobenzol compounds containing vinyl have been designed as monomers. The azobenzene-containing side-chain polymers containing azo NLO chromophore in each side chain have been synthesized via free radical polymerization. FT-IR, elemental analysis and 1 H NMR were performed to characterize the azo monomers. The molecular weight of the polymers and their distribution were determined by gel permeation chromatography (GPC). The third-order NLO coefficient of azo monomers and their polymers were measured by degenerated four wave mixing (DFWM) technique. As a result, the enhancement of the molecular conjugation and the increase of the NLO chromophore concentration in the molecular chain contribute much to heightening the third-order NLO effect. The electronic effect of substituent on the azobenzol group and the push–pull electronic structure contributes much to enhancing the NLO property.
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Research context
OpenAlex topics: Nonlinear Optical Materials Research · Crystal structures of chemical compounds · Luminescence and Fluorescent Materials
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References (22)
Show source-provided references
1. Zhang · Adv. Mater. · 1996 · 8 · 11110.1002/adma.19960080203 ↗
2. Service · Science · 1995 · 267 · 191810.1126/science.267.5206.1918 ↗
3. Yang · Macromolecules · 1994 · 27 · 585810.1021/ma00098a045 ↗
4. Lon · Chem. Mater. · 1992 · 4 · 114810.1021/cm00024a009 ↗
5. Peng · Macromolecules · 1994 · 27 · 263810.1021/ma00087a039 ↗
6. Becker · Chem. Mater. · 1994 · 6 · 10410.1021/cm00038a002 ↗
7. Xie · Appl. Polym. Sci. · 1996 · 60 · 53710.1002/(SICI)1097-4628(19960425)60:4<537::AID-APP7>3.0.CO;2-P ↗
8. Lee · Opt. Soc. Am. (B) · 1998 · 15 · 39310.1364/JOSAB.15.000393 ↗
9. Pretre · Macromolecules · 1994 · 27 · 547610.1021/ma00097a030 ↗
10. Eckl · Macromol. Chem. Phys. · 1995 · 196 · 31510.1002/macp.1995.021960122 ↗
11. Tomov · J. Opt. Soc. Am (B) · 1991 · 8 · 147710.1364/JOSAB.8.001477 ↗
12. Fei · Opt. Lett. · 1995 · 20 · 151810.1364/OL.20.001518 ↗
13. Eganmi · Jpn. J. Appl. Phys. · 1992 · 31 · 293710.1143/JJAP.31.2937 ↗
14. Fei · Opt. Lett. · 1994 · 19 · 41110.1364/OL.19.000411 ↗
15. Lee · J. Polym. Sci.: Part A: Polym. Chem. Part A: Polym. Chem J. Polym. Sci. · 1998 · 36 · 30110.1002/(SICI)1099-0518(19980130)36:2<301::AID-POLA13>3.0.CO;2-S ↗
16. Xiaogong · Chem. Mater. · 1997 · 9 · 4510.1021/cm950560a ↗
17. Tian-an · Macromolecules · 1996 · 29 · 53510.1021/ma9512566 ↗
18. Zhiyong · Chem. Mater. · 1995 · 7 · 94110.1021/cm00053a020 ↗
19. Maloney · Chem. Phys. · 1988 · 121 · 2110.1016/0301-0104(88)87002-2 ↗
20. Yang · J. Opt. Soc. Am. B · 1989 · 6 · 75310.1364/JOSAB.6.000753 ↗
21. Boyd · 1992
22. Bredley · Jpn. J. Appl. Phys. · 1989 · 28 · 17410.1143/JJAP.28.174 ↗