Nonlinear optical behavior of alkyne terminated phthalocyanines in solution and when embedded in polysulfone as thin films: Effects of aggregation
Source abstract
Abstract
Abstract We report here for the first time, on the comparative studies of the photophysical and optical limiting behavior of our two novel phthalocyanines namely 2(3), 9(10), 16(17), 23(24)-tetrakis-(4-(5-methylhex-1-yn-3-yloxy)) phthalocyanines 2, and 2(3), 9(10), 16(17), 23(24)-tetrakis-(4-(5-methylhex-1-yn-3-yloxy)) phthalocyaninato zinc (II) (3) in solution and thin films. Nonlinear optical (NLO) properties of the samples in solution and contained in polysulfone (PSU) thin films were evaluated using Z-scan technique at 532 nm and 10 ns pulsed duration. Effects of aggregation and disaggregation on the NLO performance of metal-free phthalocyanine are reported in detail. Our findings showed that the prepared Pcs show larger nonlinear absorption coefficient and lower limiting thresholds when embedded in polysulfone films compared to in solutions. The values of nonlinear susceptibility and hyperpolarizability recorded for 3-PSU in this work are respectively, ∼2.09 × 10−8 esu and ∼1.02 × 10−26 esu. These values are among the largest values reported for phthalocyanines and other macrocycles doped on polymer matrices.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Porphyrin and Phthalocyanine Chemistry · Nonlinear Optical Materials Studies · Nonlinear Optical Materials Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (54)
Show source-provided references
1. de laTorre · J. Mater. Chem. · 1998 · 8 · 167110.1039/a803533d ↗
2. de la Torre · Chem. Rev. · 2004 · 104 · 372310.1021/cr030206t ↗
3. Auger · J. Mater. Chem. · 2003 · 13 · 104210.1039/b300199g ↗
4. Ali · Chem. Rev. · 1999 · 99 · 237910.1021/cr980439y ↗
5. Iwase · J. Alloys Compd. · 1993 · 192 · 28010.1016/0925-8388(93)90249-M ↗
6. Li · Phys. Rev. A · 1994 · 49 · 114910.1103/PhysRevA.49.1149 ↗
7. Chen · Chem. Soc. Rev. · 2005 · 34 · 51710.1039/b416368k ↗
8. Guo · Dyes Pigments · 2001 · 49 · 8310.1016/S0143-7208(01)00011-0 ↗
9. Yslas · Bioorg. Med. Chem. · 2007 · 15 · 465110.1016/j.bmc.2007.03.079 ↗
10. Britton · J. Porphyr. Phthalocya. · 2011 · 15 · 123910.1142/S1088424611004142 ↗
11. Slodek · Macromol. Symp. · 2006 · 235 · 910.1002/masy.200650302 ↗
12. Yamaji · Int. Scholar. Res. Network: Phys. Chem. · 2012 · 103817
13. Nikolaitchik · J. Phys. Chem. A · 1999 · 103 · 758710.1021/jp9911651 ↗
14. Tekin · Mater. Chem. Phys. · 2013 · 138 · 27010.1016/j.matchemphys.2012.11.056 ↗
15. Mkhize · Polyhedron · 2014 · 81 · 60710.1016/j.poly.2014.07.025 ↗
16. Britton · J. Porphyr. Phthalocya. · 2013 · 17 · 69110.1142/S108842461350003X ↗
17. O’Flaherty · Adv. Mater. · 2003 · 15 · 1910.1002/adma.200390002 ↗
18. Doyle · J. Opt. A: Pure Appl. Opt. · 2008 · 10 · 7510110.1088/1464-4258/10/7/075101 ↗
19. Tekin · Opt. Commun. · 2010 · 283 · 474910.1016/j.optcom.2010.07.003 ↗
20. Sekhosana · Polyhedron · 2015 · 85 · 34710.1016/j.poly.2014.08.047 ↗
21. Lor · J. Mater. Res. · 1995 · 10 · 269310.1557/JMR.1995.2693 ↗
22. Yılmaz · Polyhedron · 2009 · 28 · 341910.1016/j.poly.2009.07.033 ↗
23. Fu · Langmuir · 2002 · 18 · 384310.1021/la011764a ↗
24. Fery-Forgues · J. Chem. Edu. · 1999 · 76 · 126010.1021/ed076p1260 ↗
25. Ogunsipe · New J. Chem. · 2004 · 7 · 82210.1039/B315319C ↗
26. Sheik-Bahae · Opt. Lett. · 1989 · 14 · 95510.1364/OL.14.000955 ↗
27. Sheik-Bahae · IEEE J. Quantum Electron. · 1990 · 26 · 76010.1109/3.53394 ↗
28. Kumar · Chem. Phys. Lett. · 2007 · 447 · 27410.1016/j.cplett.2007.09.028 ↗
29. García · J. Mater. Chem. · 2003 · 13 · 74910.1039/b210707d ↗
30. Dini · 2003 · vol. 17 · 22
31. Nas · J. Luminesc. · 2014 · 154 · 1510.1016/j.jlumin.2014.03.058 ↗
32. Patel · Indian J. Pure Appl. Phys. · 2004 · 42 · 79
33. Ceyhan · Monatsh. Chem. · 2002 · 133 · 7110.1007/s007060270007 ↗
34. Dabak · New J. Chem. · 1997 · 21 · 267
35. Stillman · 1989 · vol. 1
36. Ogunsipe · J. Mol. Struct. · 2003 · 650 · 13110.1016/S0022-2860(03)00155-8 ↗
37. Freyer · J. Photochem. Photobiol. A: Chem. · 2004 · 163 · 23110.1016/j.jphotochem.2003.12.003 ↗
38. Durmuş · Inorg. Chem. Commun. · 2007 · 10 · 33210.1016/j.inoche.2006.11.012 ↗
39. Bahr · J. Am. Chem. Soc. · 2001 · 123 · 653610.1021/ja010462s ↗
40. Gadalla · J. Phys. Chem. C · 2010 · 114 · 1785410.1021/jp104875u ↗
41. Gadalla · J. Phys. Chem. C · 2010 · 114 · 408610.1021/jp911438y ↗
42. Van Stryland · 1998 · 655
43. Dini · J. Chem. Phys. · 2003 · 119 · 485710.1063/1.1595633 ↗
44. Hosoda · Jpn. J. Appl. Phys. · 1991 · 30 · L148610.1143/JJAP.30.L1486 ↗
45. Snow · J. Am. Chem. Soc. · 1984 · 106 · 470610.1021/ja00329a012 ↗
46. T. Pritchett, Models for Saturable and Reverse Saturable Absorption in Materials for Optical Limiting; Sensors and Electron Devices Directorate, Army Research Laboratory, Oct., 2002, pp. 1–29.10.1364/NLO.2002.WE29 ↗
47. Hegde · Opt. Mater. · 2009 · 31 · 100010.1016/j.optmat.2008.11.015 ↗
48. Tutt · Prog. Quantum Electron. · 1993 · 17 · 29910.1016/0079-6727(93)90004-S ↗
49. Shirk · J. Phys. Chem. · 2000 · 104 · 143810.1021/jp993254j ↗
50. Ao · Molecules · 2015 · 20 · 555410.3390/molecules20045554 ↗
51. Shi · J. Phys. Chem. C · 2014 · 118 · 641310.1021/jp412500r ↗
52. Rao · Mater. Sci. Appl. · 2011 · 2 · 299
53. Yuwono · J. Mater. Chem. · 2003 · 13 · 147510.1039/b211976e ↗
54. Sanusi · J. Phys. Chem. C · 2014 · 118 · 705710.1021/jp501469e ↗