journal article·2013-01Open access

Synthesis and functionalization of coumarin-containing copolymers for second order optical nonlinearities

Zacaria Essaïdi, Oksana Krupka, Konstantinos Iliopoulos, Emilie Champigny, Bouchta Sahraoui, Marc Sallé, Denis Gindre

Optical Materials· Volume 35· Issue 3

Abstract

Abstract The second-order nonlinear optical properties of photocross-linkable coumarin-based copolymers were investigated using the optical second harmonic generation (SHG) with the Maker fringes technique. High quality and transparent spin-deposited thin films of various methacrylic copolymers containing 4-methylcoumarin pendant chromophores were prepared and the coumarin units were ordered and oriented by the corona poling technique. Nonlinear optical investigations were performed using a picosecond Q-switched Nd:YAG laser working at the fundamental wavelength ( λ = 1064 nm) and the second order nonlinear optical susceptibilities of the functionalized polymers were determined. The samples were irradiated using two wavelengths ( λ = 254 nm and λ > 300 nm) promoting the reversible photo-induced dimerisation of coumarin moieties within the film. The latter is shown to have a significant impact on the nonlinear optical response of the corresponding material. A large SHG response of photocross-linkable coumarin-based copolymers is obtained.
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Research context

OpenAlex topics: Liquid Crystal Research Advancements · Photochemistry and Electron Transfer Studies · Nonlinear Optical Materials Studies

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References (29)

Show source-provided references
1. Samyn · Macromol. Rapid Commun. · 2000 · 21 · 110.1002/(SICI)1521-3927(20000101)21:1<1::AID-MARC1>3.0.CO;2-X ↗
2. Prasad · 1991
3. Che · Macromolecules · 2005 · 38 · 865710.1021/ma0511393 ↗
4. Smokal · J. Optoelectron. Adv. Mater. · 2008 · 10 · 607
5. Ichimura · Chem. Rev. · 2000 · 100 · 184710.1021/cr980079e ↗
6. Gindre · Opt. Exp. · 2006 · 14 · 989610.1364/OE.14.009896 ↗
7. Chen · Chem. Mater. · 2005 · 17 · 166110.1021/cm048451w ↗
8. Gnanaguru · J. Org. Chem. · 1985 · 50 · 233710.1021/jo00213a027 ↗
9. Kim · Macromolecules · 2007 · 40 · 892410.1021/ma702080z ↗
10. Moorthy · J. Mater. Chem. · 1992 · 2 · 67510.1039/jm9920200675 ↗
11. Karthikeyan · J. Org. Chem. · 2006 · 71 · 640910.1021/jo0606498 ↗
12. Moorthy · J. Org. Chem. · 1992 · 57 · 329210.1021/jo00038a012 ↗
13. Lewis · J. Am. Chem. Soc. · 1989 · 111 · 865310.1021/ja00205a015 ↗
14. Trenor · Chem. Rev. · 2004 · 104 · 305910.1021/cr030037c ↗
15. Kim · Macromolecules · 2008 · 41 · 307510.1021/ma702809g ↗
16. Tian · J. Mater. Chem. · 2003 · 13 · 125310.1039/b302857g ↗
17. Fomine · Macromol. Chem. Phys. · 1997 · 198 · 306510.1002/macp.1997.021981007 ↗
18. Jones · J. Phys. Chem. · 1994 · 98 · 1302810.1021/j100100a035 ↗
19. Iliopoulos · J. Am. Chem. Soc. · 2010 · 132 · 1434310.1021/ja1047285 ↗
20. Obi · Chem. Mater. · 1999 · 11 · 65610.1021/cm980533v ↗
21. Jackson · Chem. Mater. · 2001 · 13 · 69410.1021/cm0011413 ↗
22. Molecule orientation techniques
23. Mortazavi · J. Opt. Soc. Am. B · 1989 · 6 · 73310.1364/JOSAB.6.000733 ↗
24. Kulyk · J. Appl. Phys. · 2007 · 102 · 11311310.1063/1.2822461 ↗
25. Jerphagnon · J. Appl. Phys. · 1970 · 41 · 166710.1063/1.1659090 ↗
26. Tsutsumi · Macromolecules · 1996 · 29 · 59210.1021/ma951077o ↗
27. Malkmus · Adv. Funct. Mater. · 2007 · 17 · 365710.1002/adfm.200700553 ↗
28. Lott · Adv. Mater. · 2011 · 23 · 242510.1002/adma.201100458 ↗
29. Gindre · Appl. Phys. Lett. · 2007 · 90 · 09410310.1063/1.2710774 ↗