Design and preparation of novel polyarylene ether materials based on Diels–Alder reaction as the crosslinker for electrooptical modulators
Source abstract
Abstract
Abstract Novel crosslinkable organic linear electro-optical (EO) material based on polyarylene ether as the main chain host polymer was designed and prepared. The host polymer with rigid aromatic has demonstrated a good compatibility with the guest chromophore. Long side chain with anthracene ensured the crosslinkable reaction and appropriate glass transition temperature of the host polymer (55 °C). The EO r 33 tensor coefficient for this novel EO material has been magnitude of 66 pm/V at 1310 nm and the excellent long term stability at 85 °C. These parameters permit to consider their application in fabrication of organic electro optical devices. The semi-empirical and DFT quantum chemical simulations were performed for 4 principal chromophores to clarify a role of cross-linker in the enhancement of the ground state dipole moments and effective hyperpolarizabilities.
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Research context
OpenAlex topics: Nonlinear Optical Materials Research · Synthesis and properties of polymers · Organic Electronics and Photovoltaics
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References (28)
Show source-provided references
1. Rational design of organic electro-optic materials10.1088/0953-8984/15/20/203 ↗
2. Liu · RSC Adv. · 2015 · 5 · 1578410.1039/C4RA13250E ↗
3. Chrunik · Optics Commun. · 2016 · 364 · 1310.1016/j.optcom.2015.11.028 ↗
4. Kityk · J. Non Cryst. Solids · 2001 · 292 · 18410.1016/S0022-3093(01)00860-2 ↗
5. Hales · Chem. Mater. · 2014 · 26 · 54910.1021/cm402893s ↗
6. McLaughlin · Appl. Phys. Lett. · 2008 · 9210.1063/1.2909599 ↗
7. Dalton · Opt. Mater. · 2003 · 21 · 1910.1016/S0925-3467(02)00107-6 ↗
8. Frattarelli · J. Am. Chem. Soc. · 2009 · 131 · 1259510.1021/ja900131y ↗
9. Ma · Adv. Mater · 2002 · 14 · 133910.1002/1521-4095(20021002)14:19<1339::AID-ADMA1339>3.0.CO;2-O ↗
10. Nobukatsu · Macromol. Chem. Phys. · 1999 · 200 · 230910.1002/(SICI)1521-3935(19991001)200:10<2309::AID-MACP2309>3.0.CO;2-D ↗
11. Liu · Mater. Lett. · 2015 · 143 · 33310.1016/j.matlet.2014.12.112 ↗
12. Nobukatsu · Macromol. Chem. Phys. · 1999 · 200 · 230910.1002/(SICI)1521-3935(19991001)200:10<2309::AID-MACP2309>3.0.CO;2-D ↗
13. Organic photonic materials
14. Dalton · J. Phys. Condens. Matter · 2003 · 15 · R89710.1088/0953-8984/15/20/203 ↗
15. Kuo · IEEE Photonics Technol. Lett. · 2006 · 18 · 2510.1109/LPT.2005.861632 ↗
16. Frattarelli · J. Am. Chem. Soc. · 2009 · 131 · 1259510.1021/ja900131y ↗
17. Fachetti · Chem. Mater. · 2003 · 15 · 3310.1021/cm020929d ↗
18. Liu · Dyes Pigment. · 2015 · 122 · 7410.1016/j.dyepig.2015.06.007 ↗
19. Liu · Opt. Mater. · 2015 · 47 · 25610.1016/j.optmat.2015.05.037 ↗
20. Huang · Polym. Chem. · 2013 · 4 · 576010.1039/c3py00694h ↗
21. Hsiue · Chem. Mater. · 1994 · 6 · 88410.1021/cm00043a004 ↗
22. Liu · J. Phys. Org. Chem. · 2011 · 24 · 43910.1002/poc.1772 ↗
23. Mani · Polymer · 1993 · 34 · 17110.1016/0032-3861(93)90302-Q ↗
24. Leng · Macromolecules · 2001 · 34 · 477410.1021/ma0100347 ↗
25. Sahraoui · Phys. Rev. B · 1999 · 59B · 922910.1103/PhysRevB.59.9229 ↗
26. Kolev · Chem. Phys. Lett. · 2007 · 443 · pp.30910.1016/j.cplett.2007.06.051 ↗
27. Bures · Eur. J. Org. Chem. · 2012 · 52910.1002/ejoc.201101226 ↗
28. Kulhanek · Chem. An Asian J. · 2013 · 8 · 46510.1002/asia.201200963 ↗