journal article·2011-08-09

Enhancement of the Two-Photon Initiating Efficiency of a Thioxanthone Derivative through a Chevron-Shaped Architecture

Jean-Pierre Malval, Ming Jin, Fabrice Morlet-Savary, Hélène Chaumeil, Albert Defoin, Olivier Soppera, Teodora Scheul, Michel Bouriau, Patrice L. Baldeck

Chemistry of Materials· Volume 23· Issue 15
Publisher page

Abstract

We investigated the one- and two-photon excitation properties of a new hybrid anthracene–thioxanthone ( ANTX ) system, which was assembled into a chevron-shaped molecular architecture. Such a geometrical association first preserves the high efficiency of the free radical photoinitiator and leads, in the same time, to a strong increase in the two-photon absorption (2PA) cross section by more than a factor of 30 as compared to thioxanthone ( TX ). A four-state model was required to fit the 2PA spectrum of ANTX, which clearly undergoes a strong enhancement in the low-frequency region. As a consequence, ANTX constitutes a suitable two-photon initiating chromophore with a much higher efficiency as TX used as reference. At λ exc = 710 nm for instance, we showed that the two-photon polymerization threshold of ANTX is five times lower with respect to that of TX . Additionally, we demonstrated by the fabrication of three-dimensional microstructures that this new hybrid system remains two-photon activable when excited at wavelengths near its one-photon absorption region as suggested by the sum–overstates model. We also show that this new two-photon initiator exhibits a higher reactivity than a diaminofluorene derivative, which is commonly used in two-photon polymerization.
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Research context

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

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

Affiliations

Institut de Sciences des Matériaux de Mulhouse, LRC CNRS 7228, Université de Haute Alsace, 15 rue Jean Starcky, 68057 Mulhouse, France

Institute of Functional Polymer Materials, School of Materials Science and Technology, Tongji University, 1239 Siping Road, 200092 Shanghai, China

Département de Photochimie Générale, FRE CNRS 3252, Université de Haute Alsace, ENSCMu. 3 rue Alfred Werner, 68093 Mulhouse, France

Laboratoire de Chimie Organique et Bioorganique, FRE CNRS 3253, Université de Haute Alsace, ENSCMu, 3 rue Alfred Werner, 68093 Mulhouse, France

Laboratoire Interdisciplinaire de Physique, UMR CNRS 5588, Université Grenoble 1, 38402 Saint Martin d'Hères, France

References (68)

Show source-provided references
1. Belfield K. D. · J. Phys. Org. Chem. · 2000 · 13 · 83710.1002/1099-1395(200012)13:12<837::AID-POC315>3.0.CO;2-5 ↗
2. Cumpston B. H. · Nature · 1999 · 398 · 5110.1038/17989 ↗
3. Kawata S. · Nature · 2001 · 412 · 69710.1038/35089130 ↗
4. Lee K. S. · Prog. Polym. Sci. · 2008 · 33 · 63110.1016/j.progpolymsci.2008.01.001 ↗
5. Maruo S. · Opt. Lett. · 1997 · 22 · 13210.1364/OL.22.000132 ↗
6. Sun H.-B. · 2004 · 170
7. Lee K.-S. · Polym. Adv. Technol. · 2006 · 17 · 7210.1002/pat.664 ↗
8. Belfield K. D. · Chem. Mater. · 2004 · 16 · 463410.1021/cm049872g ↗
9. Hales J. M. · J. Chem. Phys. · 2004 · 121 · 315210.1063/1.1770726 ↗
10. Belfield K. D. · J. Org. Chem. · 2000 · 65 · 447510.1021/jo991950+ ↗
11. Martineau C. · Chem.Phys.Lett. · 2002 · 362 · 29110.1016/S0009-2614(02)01073-4 ↗
12. He G. S. · Chem. Rev. · 2008 · 108 · 124510.1021/cr050054x ↗
13. Lu Y. · J. Lumin. · 2004 · 110 · 110.1016/j.jlumin.2004.02.012 ↗
14. Zhang X. · Mater. Lett. · 2005 · 59 · 348510.1016/j.matlet.2005.06.025 ↗
15. Rumi M. · J. Am. Chem. Soc. · 2000 · 122 · 950010.1021/ja994497s ↗
16. Belfield K. D. · J. Phys. Chem. B · 2007 · 111 · 1272310.1021/jp074456f ↗
17. Lemercier G. · C.R. Chimie · 2005 · 8 · 130810.1016/j.crci.2004.11.038 ↗
18. Belfield K. D. · J. Am. Chem. Soc. · 2000 · 122 · 121710.1021/ja991990v ↗
19. Li X. · J. Photochem. Photobiol., A · 2007 · 190 · 2210.1016/j.jphotochem.2007.03.007 ↗
20. Zhao Y. · J. Photochem. Photobiol., A · 2006 · 177 · 1210.1016/j.jphotochem.2005.05.006 ↗
21. Roffey C. · 1997
22. Eaton D. F. · 1986 · 14
23. Lougnot D. J. · Macromolecules · 2002 · 22 · 10810.1021/ma00191a022 ↗
24. Malval J.-P. · J. Photochem. Photobiol., A · 2007 · 192 · 6610.1016/j.jphotochem.2007.05.005 ↗
25. Fouassier J. P. · 1995
26. Schafer K. J. · J. Photochem. Photobiol., A · 2004 · 162 · 49710.1016/S1010-6030(03)00394-0 ↗
27. Scaiano J. C. · J. Am. Chem. Soc. · 1980 · 102 · 774710.1021/ja00546a018 ↗
28. Malval J.-P. · EPA Newslett. · 2009 · 79 · 37
29. Burget D. · J. Lumin. · 1992 · 54 · 17710.1016/0022-2313(92)90006-U ↗
30. Angulo G. · ChemPhysChem · 2010 · 11 · 48010.1002/cphc.200900654 ↗
31. Förster T. · Z. Naturforsch. · 1949 · 4 · 32110.1515/zna-1949-0501 ↗
32. Jin M. · Chem. Commun. · 2008 · 48 · 654010.1039/b808457b ↗
33. Lemercier G. · New J. Chem. · 2006 · 30 · 160610.1039/B608391A ↗
34. Wu J. · Dyes Pigm. · 2008 · 76 · 69010.1016/j.dyepig.2007.01.007 ↗
35. Xing J. F. · J. Photochem. Photobiol., A · 2007 · 189 · 39810.1016/j.jphotochem.2007.03.002 ↗
36. Neumann M. G. · J. Chem. Soc., Faraday Trans. · 1997 · 93 · 151710.1039/a607264j ↗
37. Encinas M. V. · Polymer · 2002 · 43 · 390910.1016/S0032-3861(02)00211-2 ↗
38. Ferreira G. C. · J. Braz. Chem. Soc. · 2006 · 17 · 90510.1590/S0103-50532006000500013 ↗
39. Balta D. K. · Macromolecules · 2007 · 40 · 413810.1021/ma0628735 ↗
40. Jin M. · Phys. Chem. Chem. Phys. · 2009 · 11 · 262210.1039/b813717j ↗
41. Meech R. · J. Photochem. · 1983 · 23 · 19310.1016/0047-2670(83)80061-6 ↗
42. Prazeres T. J. V. · J. Phys. Chem. A · 2008 · 112 · 503410.1021/jp710625j ↗
43. Connor D. V. · 1984
44. Malval J.-P. · Res. Chem. Intermed. · 2001 · 27 · 2110.1163/156856701745104 ↗
45. 2002
46. Xu C. · J. Opt. Soc. Am. B · 1996 · 13 · 48110.1364/JOSAB.13.000481 ↗
47. Montalti M. · 200610.1201/9781420015195 ↗
48. Kryskowiak E. · ChemPhysChem · 2006 · 7 · 59710.1002/cphc.200500375 ↗
49. Lippert E. · Elektrochem. Angew. Phys. Chem. · 1957 · 61 · 962
50. Abdullah K. A. · J. Photochem. · 1986 · 32 · 4910.1016/0047-2670(86)85006-7 ↗
51. Lai T. · Chem. Phys. Lett. · 1980 · 73 · 24410.1016/0009-2614(80)80366-6 ↗
52. Lai T.-i. · Chem. Phys. Lett. · 1981 · 84 · 30310.1016/0009-2614(81)80351-X ↗
53. Lim E. C. · J. Phys. Chem. · 1986 · 90 · 677010.1021/j100284a012 ↗
54. Malval J.-P. · J. Phys. Chem. C · 2009 · 113 · 2081210.1021/jp9075977 ↗
55. Strickler S. J. · J. Chem. Phys. · 1962 · 37 · 81410.1063/1.1733166 ↗
56. Orr B. J. · Mol. Phys. · 1971 · 20 · 51310.1080/00268977100100481 ↗
57. Kamada K. · Chem. Phys. Lett. · 2003 · 372 · 38610.1016/S0009-2614(03)00413-5 ↗
58. Corrêa D. S. · J. Phys. Chem. A · 2006 · 110 · 643310.1021/jp057065e ↗
59. Oliveira S. L. · Adv. Mater. · 2005 · 17 · 189010.1002/adma.200500533 ↗
60. Kogej T. · Chem.Phys.Lett. · 1998 · 298 · 110.1016/S0009-2614(98)01196-8 ↗
61. Beljonne D. · Adv. Funct. Mater. · 2002 · 12 · 63110.1002/1616-3028(20020916)12:9<631::AID-ADFM631>3.0.CO;2-W ↗
62. Martineau C. · Synth. Met. · 2003 · 138 · 35310.1016/S0379-6779(03)00111-5 ↗
63. Pruzinsky S. A. · Adv. Funct. Mater. · 2005 · 15 · 199510.1002/adfm.200500345 ↗
64. Drobizhev M. · J. Am. Chem. Soc. · 2004 · 126 · 1535210.1021/ja0445847 ↗
65. Drobizhev M. · Chem. Phys. Lett. · 2002 · 361 · 50410.1016/S0009-2614(02)00999-5 ↗
66. Drobizhev M. · Chem. Phys. Lett. · 2002 · 355 · 17510.1016/S0009-2614(02)00206-3 ↗
67. Belfield K. D. · J. Fluoresc. · 2006 · 16 · 10510.1007/s10895-005-0008-1 ↗
68. Yates S. F. · J. Org. Chem. · 2002 · 49 · 334910.1021/jo00192a019 ↗