Different nonlinear optical performances of polymers containing benzimidazole chromophores
Source abstract
Abstract
Abstract Two NLO azo-benzimidazolic chromophores, bis-ethanol, 2,2′-[[4-[[4-(1-ethyl-6-nitro-1H-benzimidazol-2-yl)phenyl]azo]phenyl]imino] (BZI1) and bis-ethanol, 2,2′-[[4-[[4-[(1E)-2-(1-ethyl-6-nitro-1H-benzimidazol-2-yl)ethenyl]phenyl]azo]phenyl]imino] (BZI2), properly functionalised for polycondensation reactions, have been used for the synthesis of new NLO polyurethanes and polyesters. The polymers have high thermal stability and T g ranging between 146 and 173 °C. Thin films of polymers have been prepared and oriented by electrical poling. The resonance free NLO activity has been measured at a fundamental wavelength of 1368 nm by second harmonic generation (SHG) and a maximum d 33 of 2.3 pm/V has been observed. Polymers containing the less active chromophore (BZI1, μβ = 950 × 10 −48 esu) show higher d 33 value than the analogous polymers containing BZI2 chromophore ( μβ = 1400 × 10 −48 ). A theoretical analysis suggests that this unexpected behaviour can be only partially attributed to thermodynamic effects, dynamical effects should also play a role.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nonlinear Optical Materials Research · Chemical synthesis and pharmacological studies · Crystal structures of chemical compounds
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (24)
Show source-provided references
1. Dalton · Adv. Polym. Sci. · 2002 · 158 · 110.1007/3-540-44608-7_1 ↗
2. Shi · Appl. Phys. Lett. · 1993 · 63 · 117310.1063/1.109813 ↗
3. 1995 · vol. 601
4. Van den Broeck · Polymer · 2001 · 42 · 331510.1016/S0032-3861(00)00761-8 ↗
5. Leng · Polymer · 2001 · 42 · 925310.1016/S0032-3861(01)00464-5 ↗
6. Bruno · J. Polym. Sci. A · 2002 · 40 · 146810.1002/pola.10224 ↗
7. Persico · J. Polym. Sci. A · 2003 · 41 · 184110.1002/pola.10727 ↗
8. Carella · Macromol. Chem. Phys. · 2004 · 206 · 139910.1002/macp.200500112 ↗
9. Carella · Eur. J. Org. Chem. · 2004 · 262010.1002/ejoc.200300786 ↗
10. Ambrosanio · Polymer · 1999 · 40 · 492310.1016/S0032-3861(98)00720-4 ↗
11. Casalboni · Chem. Phys. Lett. · 2000 · 319 · 10710.1016/S0009-2614(00)00103-2 ↗
12. Mortazavi · J. Opt. Soc. Am. B · 1989 · 6 · 73310.1364/JOSAB.6.000733 ↗
13. Schutzmann · J. Non-Crystalline Solids · 2005 · 351 · 181410.1016/j.jnoncrysol.2005.04.022 ↗
14. Jerphagnon · J. Appl. Phys. · 1970 · 41 · 166710.1063/1.1659090 ↗
15. Singer · Appl. Phys. Lett. · 1986 · 49 · 24810.1063/1.97184 ↗
16. Lide · 1996 · 198
17. Graf · J. Appl. Phys. · 1994 · 75 · 333510.1063/1.356142 ↗
18. Burland · Chem. Rev. · 1994 · 94 · 3110.1021/cr00025a002 ↗
19. Piekara · Proc. R. Soc. London A · 1939 · 172 · 36010.1098/rspa.1939.0109 ↗
20. Fowler · Proc. R. Soc. London A · 1935 · 149 · 110.1098/rspa.1935.0044 ↗
21. Debye · Phys. Z. · 1935 · 35 · 100
22. London · Trans. Faraday Soc. · 1937 · 33 · 810.1039/tf937330008b ↗
23. Dalton · Proc. Natl. Acad. Sci. USA · 1997 · 94 · 484210.1073/pnas.94.10.4842 ↗
24. Herminghaus · J. Opt. Soc. Am. B · 1991 · 8 · 231110.1364/JOSAB.8.002311 ↗