journal article·2014-06

Synthesis, prodigious two-photon absorption cross sections and electrochemical properties of a series of triphenylamine-based chromophores

Rui Li, Dandan Li, Wenwen Fei, Jingyun Tan, Shengli Li, Hongping Zhou, Shengyi Zhang, Jieying Wu, Yupeng Tian

Optical Materials· Volume 36· Issue 8
Publisher page

Abstract

Abstract A series of triphenylamine-based chromophores (L1–3) with donor-π-donor (D-π-D) model have been designed and synthesized via solid phase Wittig reaction. Their one/two-photon fluorescence and electrochemical properties have been investigated. The results show that L2 and L3 exhibited strong and wide-dispersed two-photon-excited fluorescence (TPEF) in different solvents. Chromophore L3 displays the strongest intensity two-photon absorption activity and large cross-sections (>3600 GM) in the range of 680–840 nm in THF, the largest δ up to 8899 GM in the near-IR range, and the measured maximum TPA cross-sections per molecular weight (δmax/MW) is 8.64 GM/g (L3) in THF. Significantly, it also exhibits good solubility in common organic solvents when the chromophore was modified by polyether units as peripheral groups.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

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

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

References (47)

Show source-provided references
1. Li · J. Phys. Chem. C. · 2013 · 117 · 840410.1021/jp312794t ↗
2. Zhou · Tetrahedron. Lett. · 2007 · 48 · 356310.1016/j.tetlet.2007.03.092 ↗
3. Kim · Chem. Commun. · 2009 · 153
4. Kamada · Chem. Commun. · 2012 · 48 · 798810.1039/c2cc30879g ↗
5. Kong · Sci. China Chem. · 2013 · 1 · 10610.1007/s11426-012-4794-4 ↗
6. Chantharasupawong · J. Phys. Chem. C. · 2012 · 116 · 2595510.1021/jp3096693 ↗
7. Rendón · Chem. Mater. · 2011 · 23 · 322810.1021/cm2010852 ↗
8. Lee · J. Am. Chem. Soc. · 2010 · 132 · 121610.1021/ja9090676 ↗
9. Garcia · Bioorg. Med. Chem. · 2013 · 21 · 15310.1016/j.bmc.2012.10.042 ↗
10. Cepraga · Polym. Chem. · 2013 · 4 · 6110.1039/C2PY20565C ↗
11. Balu · Biophys. J. · 2013 · 104 · 25810.1016/j.bpj.2012.11.3809 ↗
12. Koskela · Polym. Adv. Technol. · 2012 · 23 · 99210.1002/pat.2002 ↗
13. Wang · J. Phys. Chem. C. · 2011 · 115 · 77610.1021/jp1081005 ↗
14. Ogawa · Org. Biomol. Chem. · 2009 · 7 · 224110.1039/b901422e ↗
15. Zheng · Chem. Phys. Lett. · 2009 · 475 · 25010.1016/j.cplett.2009.05.040 ↗
16. Lott · Adv. Mater. · 2011 · 23 · 242510.1002/adma.201100458 ↗
17. Kim · Chem. Commun. · 2009 · 742210.1039/b916965b ↗
18. Reinhardt · Chem. Mater. · 1998 · 10 · 186310.1021/cm980036e ↗
19. Beljonne · Adv. Mater. · 2002 · 12 · 631
20. Jiang · Chem. Commun. · 2010 · 46 · 468910.1039/c0cc00803f ↗
21. Ji · Chem. Eur. J. · 2011 · 17 · 247910.1002/chem.201001449 ↗
22. Wang · Chem. Eur. J. · 2011 · 17 · 264710.1002/chem.201002821 ↗
23. Tian · J. Mater. Chem. · 2007 · 17 · 364610.1039/b703853d ↗
24. Wang · Chem. Mater. · 2011 · 23 · 442810.1021/cm201377u ↗
25. Hrobárik · J. Org. Chem. · 2011 · 76 · 872610.1021/jo201411t ↗
26. Xu · New. J. Chem. · 2009 · 33 · 245710.1039/b9nj00393b ↗
27. Fan · Dyes Pigm. · 2012 · 95 · 75710.1016/j.dyepig.2012.05.004 ↗
28. Tian · Adv. Funct. Mater. · 2007 · 17 · 169110.1002/adfm.200600916 ↗
29. Chen · J. Am. Chem. Soc. · 2007 · 129 · 722010.1021/ja071057p ↗
30. Kim · Angew. Chem. · 2008 · 120 · 524510.1002/ange.200800929 ↗
31. Crosby · J. Phys. Chem. · 1971 · 75 · 99110.1021/j100678a001 ↗
32. Xu · JOSAB · 1996 · 13 · 48110.1364/JOSAB.13.000481 ↗
33. Varnavski · J. Phys. Chem. B. · 2004 · 108 · 1048410.1021/jp0495996 ↗
34. Brousmiche · J. Phys. Chem. B. · 2004 · 108 · 859210.1021/jp049948w ↗
35. J. Mater. Chem.
36. Strehmel · 2005
37. Liu · Dyes Pigm. · 2012 · 95 · 14910.1016/j.dyepig.2012.03.020 ↗
38. Drobizhev · J. Phys. Chem. B. · 2003 · 107 · 754010.1021/jp034986l ↗
39. Patel · J. Phys. Chem. C. · 2009 · 113 · 2026410.1021/jp9079537 ↗
40. Ji · J. Org. Chem. · 2009 · 74 · 485510.1021/jo900588e ↗
41. Peng · J. Am. Chem. Soc. · 2011 · 133 · 662610.1021/ja1104014 ↗
42. Berezin · Chem. Rev. · 2010 · 110 · 264110.1021/cr900343z ↗
43. Xu · Opt. Mater. · 2007 · 29 · 72310.1016/j.optmat.2005.12.003 ↗
44. Fan · Opt. Mater. · 2012 · 34 · 60910.1016/j.optmat.2011.08.033 ↗
45. Liu · J. Lumin. · 2013 · 134 · 45910.1016/j.jlumin.2012.07.045 ↗
46. Shao · J. Org. Chem. · 2011 · 76 · 78010.1021/jo1017926 ↗
47. Xu · Chem. Commun. · 2013 · 49 · 27310.1039/C2CC36806D ↗