journal article·2019-10

Azobenzene-based derivative self-assembly: Optical limiting properties and enhancement mechanism

Peng Sun, Linfeng Li, Shanyi Guang, Hongyao Xu

Optical Materials· Volume 96
Publisher page

Abstract

Abstract In order to further investigate the dependence of optical limiting properties on the molecular structures, especially the strong intermolecular effects, such as the effects of hydrogen bond, dipole-dipole interaction and the influences of their synergistic effect on the optical limiting properties, three polar D-π-A conjugated azobenzene derivatives (N1, N2 and N3) with different hydrogen-bond recognition abilities were designed and synthesized. Their molecular structure and properties were characterized and evaluated by infrared spectroscopy, thermogravimetric analysis, ultraviolet–visible spectrometry, and Z-scan technique with a Q-swithed ps Nd:YAG laser system continuum. The mechanism of optical limiting enhancement is investigated by theoretical calculation and experimental measurement based on molecular self-assembly synergistic effect of hydrogen bond and dipole-dipole interaction. The results show that the nonlinear optical properties of these polar D-π-A conjugated nonlinear optical materials were obviously affected by organic molecular structure, strong intermolecular interaction and their synergetic enhancement effect.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nonlinear Optical Materials Studies · Nonlinear Optical Materials Research · Photochromic and Fluorescence Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (43)

Show source-provided references
1. Su · Macromolecules · 2010 · 43 · 284010.1021/ma902789g ↗
2. Yan · RSC Adv. · 2013 · 3 · 802110.1039/c3ra40690c ↗
3. Sreeja · Opt. Mater. · 2017 · 66 · 46010.1016/j.optmat.2017.01.042 ↗
4. Khanzadeh · Opt. Mater. · 2017 · 66 · 66410.1016/j.optmat.2017.03.008 ↗
5. Kimiagar · Nanophotonics · 2018 · 7 · 24310.1515/nanoph-2017-0030 ↗
6. Nikbakht · Opt. Commun. · 2018 · 429 · 110.1016/j.optcom.2018.07.080 ↗
7. Santos · Carbon · 2018 · 135 · 20210.1016/j.carbon.2018.04.040 ↗
8. Yan · Polym. Sci. · 2011 · 53 · 535
9. Sreenath · Opt. Laser. Technol. · 2017 · 97 · 39010.1016/j.optlastec.2017.07.032 ↗
10. Papagiannouli · Chem. Phys. Lett. · 2012 · 554 · 10710.1016/j.cplett.2012.10.007 ↗
11. Xu · Adv. Mater. · 2009 · 21 · 127510.1002/adma.200801617 ↗
12. Jiang · Opt. Mater. · 2017 · 64 · 19310.1016/j.optmat.2016.12.019 ↗
13. He · J. Phys. Chem. C · 2009 · 113 · 1302910.1021/jp9006813 ↗
14. Kuzmina · Polyhedron · 2017 · 135 · 4110.1016/j.poly.2017.06.048 ↗
15. Nwaji · J. Photochem. Photobiol. A Chem. · 2017 · 346 · 4610.1016/j.jphotochem.2017.05.042 ↗
16. Chen · Chem. Phys. Lett. · 2009 · 474 · 17510.1016/j.cplett.2009.04.049 ↗
17. Wang · J. Mater. Chem. · 2009 · 19 · 742510.1039/b906294g ↗
18. Zheng · Adv. Funct. Mater. · 2008 · 18 · 277010.1002/adfm.200800419 ↗
19. Ouyang · J. Phys. Chem. B · 2009 · 113 · 1456510.1021/jp905390q ↗
20. Iliopoulos · Dyes Pigments · 2014 · 101 · 22910.1016/j.dyepig.2013.10.006 ↗
21. Kulyk · Org. Electron. · 2016 · 36 · 110.1016/j.orgel.2016.05.028 ↗
22. Kulyk · RSC Adv. · 2016 · 6 · 8485410.1039/C6RA19023E ↗
23. Rau · JOSA B · 2008 · 25 · 173810.1364/JOSAB.25.001738 ↗
24. Zhou · Chem. Mater. · 2005 · 17 · 520910.1021/cm0512878 ↗
25. Zheng · J. Phys. Chem. B · 2006 · 110 · 1460410.1021/jp0617874 ↗
26. Li · Polym. Chem. · 2011 · 2 · 272310.1039/c1py00205h ↗
27. Li · Macromolecules · 2009 · 42 · 158910.1021/ma8025223 ↗
28. Hua · React. Funct. Polym. · 2007 · 67 · 2510.1016/j.reactfunctpolym.2006.08.007 ↗
29. Qu · Opt. Commun. · 2001 · 196 · 31710.1016/S0030-4018(01)01375-X ↗
30. Yan · Adv. Funct. Mater. · 2012 · 22 · 34510.1002/adfm.201101565 ↗
31. Yan · J. Phys. Chem. C · 2012 · 116 · 889410.1021/jp300155g ↗
32. Zhang · J. Am. Chem. Soc. · 2007 · 129 · 352710.1021/ja0642109 ↗
33. Jordan · Small · 2008 · 4 · 207410.1002/smll.200800811 ↗
34. Harris · Proteins Struct. Funct. Bioinform. · 1999 · 35 · 27510.1002/(SICI)1097-0134(19990515)35:3<275::AID-PROT1>3.0.CO;2-V ↗
35. Cesteros · Macromolecules · 1993 · 26 · 725610.1021/ma00078a022 ↗
36. Xu · Macromolecules · 2002 · 35 · 878810.1021/ma0202843 ↗
37. Yin · Dyes Pigments · 2006 · 71 · 13810.1016/j.dyepig.2005.04.019 ↗
38. Ma · Langmuir · 2010 · 26 · 670210.1021/la9040387 ↗
39. Wang · J. Mater. Chem. · 2008 · 18 · 420410.1039/b807004k ↗
40. Su · J. Polym. Sci. A Polym. Chem. · 2008 · 46 · 452910.1002/pola.22790 ↗
41. Sheik-Bahae · IEEE J. Quantum Electron. · 2002 · 26 · 76010.1109/3.53394 ↗
42. Bhaskar · J. Am. Chem. Soc. · 2006 · 128 · 1184010.1021/ja060630m ↗
43. Frisch · 2004