journal article·2014-01-08

Transparent Organosilica Photocatalysts Activated by Visible Light: Photophysical and Oxidative Properties at the Gas–Solid Interface

Emmanuel Arzoumanian, Filippo Ronzani, Aurélien Trivella, Esther Oliveros, Mohamed Sarakha, Claire Richard, Sylvie Blanc, Thierry Pigot, Sylvie Lacombe

Publisher page

Abstract

The photophysical properties of several photosensitizers (PSs) included or grafted in silica monoliths were compared to their properties in solution. The effects of the solid support on their steady-state and transient absorption spectra, on their quantum yields of singlet oxygen ((1)O2) production, and on their ability to photoinduce the oxidation of dimethylsulfide (DMS) were investigated. Two cyanoanthracene derivatives (9,14-dicyanobenzo[b]triphenylene, DBTP, and 9,10-dicyanoanthracene, DCA), as well as three phenothiazine dyes (methylene blue, MB(+), new methylene blue, NMB(+), methylene violet, MV), were encapsulated in silica, analyzed and compared to two reference PSs (perinaphthenone, PN and rose bengal, RB). A DBTP derivative (3-[N-(N″-triethoxysilylpropyl-N'-hexylurea)]carboxamido-9,14-dicyanobenzo[b]triphenylene, 3) was also prepared and grafted onto silica. Thanks to the transparency and the free-standing shape of the monoliths, the complete spectroscopic characterization of the supported PSs was carried out directly at the gas-solid interface. The influence of the silica network, the PS, and the adsorption/grafting link between the PS and silica was investigated. The effects of PS concentration, gaseous atmosphere, humidity, and hydrophobicity on the production of (1)O2 were analyzed. With all PSs, (1)O2 production was very efficient (quantum yields of (1)O2 production, relative to PN, between 0.6 and 1), and this species was the only one involved in the pollutant photooxidation. The influence of the matrix on the PSs' photophysics could be considered as negligible. In contrast, the matrix effect on DMS photooxidation was extremely important: the gas diffusion inside the porous structure, and thus, the photoactivity of the materials, strictly depended on silica's surface area and porosity. Our results highlight the suitability of these silica structures as inert supports for the study of the photosensitizing properties at the gas-solid interface. Moreover, thanks to the adsorption properties of the matrix, the synthesized materials can be used as microphotoreactor for the (1)O2-mediated oxidation of volatile pollutants.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Porphyrin and Phthalocyanine Chemistry · Photodynamic Therapy Research Studies · Analytical Chemistry and Sensors

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

Affiliations

Laboratoire des IMRCP, UMR CNRS 5623, Université Toulouse III (Paul Sabatier, UPS), 118 route de Narbonne F-31062 Toulouse Cedex 9, France

IPREM, UMR CNRS 5254, Université de Pau et des Pays de l’Adour, Hélioparc, 2 rue du Président Angot, F-64053 Pau Cedex 9, France

ICCF, UMR CNRS 6296, Université Blaise Pascal, Campus des Cézeaux, 24 avenue des Landais BP 80026, F-63171 Aubière Cedex, France

References (94)

Show source-provided references
1. DeRosa M. C. · Coord. Chem. Rev. · 2002 · 233 · 35110.1016/S0010-8545(02)00034-6 ↗
2. Lacombe, S.; Pigot, T.InNew materials for sensitized photo-oxygenation;Albini, A.Ed.The Royal Society of Chemistry:Cambridge, 2010; Vol.38, p307.10.1039/9781849730860-00307 ↗
3. Miranda M. A. · Chem. Rev. · 1994 · 94 · 106310.1021/cr00028a009 ↗
4. Hoffmann N. · ChemSusChem · 2012 · 5 · 35210.1002/cssc.201100286 ↗
5. Oelgemöller M. · Pure Appl. Chem. · 2007 · 79 · 193910.1351/pac200779111939 ↗
6. Jesenská S. · J. Biomed. Mater. Res. A · 2011 · 99 · 67610.1002/jbm.a.33218 ↗
7. Rolim J. P. M. L. · J. Photochem. Photobiol. B: Biol. · 2012 · 106 · 4010.1016/j.jphotobiol.2011.10.001 ↗
8. Hocine O. · Int. J. Pharm. · 2010 · 402 · 22110.1016/j.ijpharm.2010.10.004 ↗
9. Jia X. · Curr. Drug Metab. · 2012 · 13 · 111910.2174/138920012802850074 ↗
10. Wilkinson F. · J. Phys. Chem. Ref. Data · 1995 · 24 · 66310.1063/1.555965 ↗
11. Aebisher D. · Photochem. Photobiol. · 2010 · 86 · 89010.1111/j.1751-1097.2010.00748.x ↗
12. Benabbou A. K. · J. Photochem. Photobiol. A: Chem. · 2011 · 219 · 10110.1016/j.jphotochem.2011.01.023 ↗
13. Horsa S. · J. Photochem. Photobiol. A: Chem. · 2011 · 221 · 8410.1016/j.jphotochem.2011.04.029 ↗
14. Lee J. · Environ. Sci. Technol. · 2010 · 44 · 948810.1021/es1028475 ↗
15. Nicole L. · Adv. Mater. · 2010 · 22 · 320810.1002/adma.201000231 ↗
16. Amore S. · Prog. React. Kinet. Mech. · 2001 · 26 · 15910.3184/007967401103165235 ↗
17. Ma D. · J. Phys. Chem. C · 2009 · 113 · 1597410.1021/jp905812f ↗
18. Mosinger J. · Langmuir · 2010 · 26 · 1005010.1021/la1001607 ↗
19. Wetzler D. E. · Phys. Chem. Chem. Phys. · 2006 · 8 · 224910.1039/B517756A ↗
20. Loponov K. · J. Photochem. Photobiol. A: Chem. · 2010 · 211 · 7410.1016/j.jphotochem.2010.02.005 ↗
21. Rossi L. M. · Langmuir · 2008 · 24 · 1253410.1021/la800840k ↗
22. Lang K. · Chem. Mater. · 2007 · 19 · 382210.1021/cm070351d ↗
23. Cojocaru B. · Langmuir · 2008 · 24 · 447810.1021/la800441n ↗
24. Latour V. · Catal. Today · 2005 · 101 · 35910.1016/j.cattod.2005.03.023 ↗
25. Cantau C. · ChemPhysChem · 2007 · 8 · 234410.1002/cphc.200700482 ↗
26. Lacombe S. · Langmuir · 2009 · 25 · 1116810.1021/la901504q ↗
27. Saint-Cricq P. · Chem. Commun. · 2009 · 528110.1039/b911742c ↗
28. Cantau C. · Appl. Catal. B: Environ. · 2006 · 65 · 7710.1016/j.apcatb.2005.12.019 ↗
29. Guli M. · J. Sol–Gel Sci. Technol. · 2010 · 54 · 32910.1007/s10971-010-2199-4 ↗
30. Adachi I. · Nucl. Instrum. Methods Phys. Res. Sect. Accel. Spectrometers Detect. Assoc. Equip. · 2011 · 639 · 22210.1016/j.nima.2010.08.125 ↗
31. Kumar P. · Microporous Mesoporous Mater. · 2010 · 132 · 110.1016/j.micromeso.2010.02.007 ↗
32. Latthe S. S. · J. Sol–Gel Sci. Technol. · 2009 · 53 · 20810.1007/s10971-009-2079-y ↗
33. Gao C. · Adv. Funct. Mater. · 2010 · 20 · 275010.1002/adfm.201000074 ↗
34. Gay D. S. F. · Desalination · 2010 · 258 · 12810.1016/j.desal.2010.03.026 ↗
35. Fukaya N. · J. Organomet. Chem. · 2010 · 695 · 254010.1016/j.jorganchem.2010.08.023 ↗
36. Bolshan Y. · Tetrahedron Lett. · 2007 · 48 · 492510.1016/j.tetlet.2007.05.050 ↗
37. Gu X. · Green Chem. · 2013 · 15 · 35710.1039/c2gc36683e ↗
38. Baciocchi E. · J. Am. Chem. Soc. · 2003 · 125 · 1644410.1021/ja037591o ↗
39. Bonesi S. M. · Eur. J. Org. Chem. · 2008 · 2008 · 261210.1002/ejoc.200800048 ↗
40. Ronzani F. · Phys. Chem. Chem. Phys. · 2013 · 15 · 1721910.1039/c3cp52168k ↗
41. Lamberts J. J. M. · J. Am. Chem. Soc. · 1983 · 105 · 746510.1021/ja00363a056 ↗
42. Mills A. · J. Phys. Chem. A · 2009 · 113 · 957510.1021/jp9030927 ↗
43. Schmidt R. · J. Photochem. Photobiol. A: Chem. · 1994 · 79 · 1110.1016/1010-6030(93)03746-4 ↗
44. Wainwright M. · Dyes Pigmen. · 2003 · 57 · 24510.1016/S0143-7208(03)00021-4 ↗
45. Otsuki S. · Bull. Chem. Soc. Jpn. · 1996 · 69 · 252510.1246/bcsj.69.2525 ↗
46. Wainwright M. · Int. J. Antimicrob. Agents · 2000 · 16 · 38110.1016/S0924-8579(00)00207-7 ↗
47. Brinker C. J. · 1990
48. Braun A. M. · Pure Appl. Chem. · 1990 · 62 · 146710.1351/pac199062081467 ↗
49. Martí C. · J. Photochem. Photobiol. Chem. · 1996 · 97 · 1110.1016/1010-6030(96)04321-3 ↗
50. Aminian-Saghafi T. · Helv. Chim. Acta · 1992 · 75 · 53110.1002/hlca.19920750213 ↗
51. Thomas A. H. · Photochem. Photobiol. Sci. · 2003 · 2 · 24510.1039/b209993d ↗
52. Cabrerizo F. M. · Photochem. Photobiol. · 2007 · 83 · 52610.1562/2006-09-15-RA-1041 ↗
53. Nonell, S.; Braslavsky, S. E.InMethods in Enzymology;Lester Packer, H. S., Ed.Academic Press, 2000; Vol.319, pp37–49.10.1016/S0076-6879(00)19006-8 ↗
54. Boneva M. · J. Photochem. Photobiol. A: Chem. · 1992 · 68 · 34310.1016/1010-6030(92)85243-N ↗
55. Martinez L. A. · J. Photochem. Photobiol. B: Biol. · 2000 · 58 · 9410.1016/S1011-1344(00)00109-3 ↗
56. Benoit-Marquié F. · J. Photochem. Photobiol. A: Chem. · 2000 · 132 · 22510.1016/S1010-6030(00)00196-9 ↗
57. McKelvey J. M. · Anal. Chem. · 1957 · 29 · 12310.1021/ac60121a036 ↗
58. Shendage D. M. · Org. Lett. · 2004 · 6 · 367510.1021/ol048771l ↗
59. Hegde N. D. · Appl. Surf. Sci. · 2006 · 253 · 156610.1016/j.apsusc.2006.02.036 ↗
60. Nogami M. · J. Sol–Gel Sci. Technol. · 2010 · 56 · 10710.1007/s10971-010-2282-x ↗
61. Mahadik S. A. · Appl. Surf. Sci. · 2010 · 257 · 33310.1016/j.apsusc.2010.06.062 ↗
62. Abboud J.-L. M. · Pure Appl. Chem. · 1999 · 71 · 64510.1351/pac199971040645 ↗
63. Graffion J. · Chem. Mater. · 2011 · 23 · 477310.1021/cm2019026 ↗
64. Chaker J. A. · J. Mater. Chem. · 2007 · 17 · 74410.1039/B612587E ↗
65. Benyahya S. · Adv. Synth. Catal. · 2008 · 350 · 220510.1002/adsc.200800360 ↗
66. Molina E. F. · J. Phys. Chem. B · 2012 · 116 · 793110.1021/jp302606b ↗
67. Blanc S. · Phys. Chem. Chem. Phys. · 2010 · 12 · 1128010.1039/c002705g ↗
68. Mills A. · Dyes Pigmen. · 2011 · 88 · 14910.1016/j.dyepig.2010.05.015 ↗
69. Ronzani F. · Photochem. Photobiol. Sci. · 2013 · 12 · 126010.1039/c3pp50246e ↗
70. Dunn D. A. · Photochem. Photobiol. · 1991 · 53 · 4710.1111/j.1751-1097.1991.tb08466.x ↗
71. Flors C. · J. Photochem. Photobiol. A: Chem. · 2004 · 163 · 910.1016/j.jphotochem.2004.01.001 ↗
72. Manring L. E. · J. Phys. Chem. · 1983 · 87 · 4010.1021/j100224a012 ↗
73. Olea A. F. · Phys. Chem. Chem. Phys. · 2002 · 4 · 16110.1039/b104806f ↗
74. Murasecco-Suardi P. · Helv. Chim. Acta · 1987 · 70 · 176010.1002/hlca.19870700712 ↗
75. Grajcar L. · J. Chim. Phys. · 1984 · 81 · 3310.1051/jcp/1984810033 ↗
76. Ketsle G. A. · Opt. Spectrosc. · 1979 · 47 · 494
77. Shimizu O. · J. Phys. Chem. A · 2006 · 110 · 173510.1021/jp056073s ↗
78. Kamat P. V. · J. Phys. Chem. · 1981 · 85 · 386410.1021/j150625a031 ↗
79. Oliveros E. · Helv. Chim. Acta · 1991 · 74 · 7910.1002/hlca.19910740110 ↗
80. Ragàs X. · Molecules · 2013 · 18 · 271210.3390/molecules18032712 ↗
81. Cantau C. · ChemPhysChem · 2007 · 8 · 234410.1002/cphc.200700482 ↗
82. Arnbjerg J. · J. Phys. Chem. A · 2007 · 111 · 575610.1021/jp071197l ↗
83. Scurlock R. D. · J. Phys. Chem. · 1995 · 99 · 352110.1021/j100011a019 ↗
84. Braun A. M. · 1991
85. Braslavsky S. E. · Pure Appl. Chem. · 2007 · 79 · 29310.1351/pac200779030293 ↗
86. Rodgers M. A. J. · J. Am. Chem. Soc. · 1983 · 105 · 620110.1021/ja00358a001 ↗
87. Bourdelande J. L. · J. Photochem. Photobiol. A: Chem. · 1997 · 108 · 27310.1016/S1010-6030(97)00096-8 ↗
88. Mosinger J. · J. Phys. Chem. B · 2010 · 114 · 1577310.1021/jp105789p ↗
89. Jockusch S. · Photochem. Photobiol. Sci. · 2005 · 4 · 40310.1039/b501701g ↗
90. Soggiu N. · J. Photochem. Photobiol. Chem. · 1999 · 124 · 110.1016/S1010-6030(99)00060-X ↗
91. Clennan E. L. · Acc. Chem. Res. · 2001 · 34 · 87510.1021/ar0100879 ↗
92. Lacombe S. · Photochem. Photobiol. Sci. · 2002 · 1 · 34710.1039/b202383k ↗
93. Schweitzer C. · Chem. Rev. · 2003 · 103 · 168510.1021/cr010371d ↗
94. García-Rodríguez F. · Solid State Commun. · 1999 · 111 · 71710.1016/S0038-1098(99)00237-9 ↗