journal article·2000-08

Synthesis of fluorinated metalloporphyrinosilica imprinted with templates through sol–gel process

Katia J Ciuffi, Hérica C Sacco, Juliana C Biazzotto, Ednalva A Vidoto, Otaciro R Nascimento, Carlos A.P Leite, Osvaldo A Serra, Yassuko Iamamoto

Journal of Non-Crystalline Solids· Volume 273· Issue 1-3
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Abstract

Abstract We present the synthesis of a hybrid material containing fluorinated iron porphyrins through hydrolysis and polycondensation of iron porphyrin bearing a trifluorosilyl function with tetraethoxysilane in the presence of nitrogen bases acting as template molecules. The presence of metalloporphyrin Soret band is detected in the ultraviolet–visible absorption spectra of all metalloporphyrinosilica-templates. Thermogravimetric analysis and electron paramagnetic resonance of the materials also confirm the presence of metalloporphyrin in a silica network. Electron spectroscopy imaging was that of a non-crystalline microstructure. The iron and silicon distribution are homogeneous for the elements in all particle sites. The iron porphyrinosilicas-template were active as catalysts for cyclooctene epoxidation using iodozylbenzene as oxygen donor. In general, the epoxidation yield is larger for iron porphyrinosilicas-template than for manganese porphyrinosilicas-template. The manganese porphyrinosilicas-template had a smaller activity due to their manganese oxidation state. The largest catalytic yield were obtained with the iron porphyrinosilica-pyridine (85%).
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Research context

OpenAlex topics: Porphyrin and Phthalocyanine Chemistry · Porphyrin Metabolism and Disorders · Surface Chemistry and Catalysis

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

References (41)

Show source-provided references
1. Meunier · Chem. Rev. · 1992 · 92 · 141110.1021/cr00014a008 ↗
2. Dolphin · Acc. Chem. Res. · 1997 · 30 · 25110.1021/ar960126u ↗
3. Groves · 1995
4. Mansuy · Coord. Chem. Rev. · 1993 · 125 · 12910.1016/0010-8545(93)85013-T ↗
5. Iamamoto · J. Molec. Catal. · 1994 · 88 · 16710.1016/0304-5102(93)E0270-Q ↗
6. Iamamoto · J. Molec. Catal. · 1997 · 116 · 40510.1016/S1381-1169(96)00342-1 ↗
7. Lindsay Smith · 1994
8. Mansuy · 1994
9. Ishii · J. Mater. Chem. · 1999 · 9 · 99510.1039/a807703g ↗
10. Jiang · Macromolecules · 1997 · 30 · 557510.1021/ma970227n ↗
11. Cerveau · J. Mater. Chem. · 1998 · 8 · 270710.1039/a805794j ↗
12. Corriu · Polyhedron · 1998 · 17 · 92510.1016/S0277-5387(97)00261-1 ↗
13. Corriu · Angew. Chem. Int. Engl. · 1996 · 35 · 142010.1002/anie.199614201 ↗
14. Shea · J. Am. Chem. Soc. · 1992 · 114 · 670010.1021/ja00043a014 ↗
15. Jackson · Chem. Mater. · 1996 · 8 · 72710.1021/cm950417h ↗
16. J.E. Mark, C.Y.-C. Lee, P.A. Bianconi, Hybrid organic–inorganic composites, in: ACS Symposium Series, vol. 586, American Chemical Society, Washington, DC, 199510.1021/bk-1995-0585 ↗
17. Bystrom · J. Am. Chem. Soc. · 1993 · 115 · 208110.1021/ja00058a089 ↗
18. Makote · Chem. Mater. · 1998 · 10 · 244010.1021/cm9801136 ↗
19. G. Wulff, Polymeric reagents and catalysts, in: W.T. Ford (Ed.), ACS Symposium Series, vol. 308, American Chemical Society, Washington, DC, 1979
20. Hulff · J. Am. Chem. Soc. · 1986 · 108 · 108910.1021/ja00265a045 ↗
21. P. Battioni, E. Cardin, M. Louloudi, G. Schollhorn, G.A. Spyroullias, D. Mansuy, T.G. Traylor, Chem. Commun. 2037 (1996)10.1039/CC9960002037 ↗
22. Lindsey · J. Org. Chem. · 1987 · 52 · 82710.1021/jo00381a022 ↗
23. Adler · J. Inorg. Nucl. Chem. · 1970 · 32 · 244310.1016/0022-1902(70)80535-8 ↗
24. Prado-Manso · J. Molec. Catal. A · 1999 · 150 · 25110.1016/S1381-1169(99)00216-2 ↗
25. Wijesekera · 1994
26. Cardoso · Langmuir · 1998 · 14 · 3189
27. L. Reimer, U. Zepke, J. Moesch, St. Schulze-Hillert, M. Messemer, W. Probst, E. Weimer, EELS Spectroscopy: A Reference Handbook of Standard Data for Identification and Interpretation of Electron Energy Loss Spectra and for Generation of Electron Spectroscopic Images, Carl Zeiss, Oberkochen, Germany, 1992
28. Brunauer · J. Am. Chem. Soc. · 1938 · 60 · 30910.1021/ja01269a023 ↗
29. Sharefkin · Org. Synth. · 1963 · 43 · 6210.15227/orgsyn.043.0062 ↗
30. Lucas · Org. Synth. · 1963 · 483
31. Battioni · Tetrahedron Lett. · 1991 · 32 · 289310.1016/0040-4039(91)80641-I ↗
32. Biazzotto · J. Non-Cryst. Solids · 1999 · 247 · 14610.1016/S0022-3093(99)00050-2 ↗
33. Kadish · J. Am. Chem. Soc. · 1990 · 112 · 836410.1021/ja00179a021 ↗
34. Brinker · 1990
35. Cooke · J. Chem. Soc. Perkin Trans · 1995 · 2 · 157310.1039/p29950001573 ↗
36. G. Palmer, in: D. Dolphin (Ed.), The Porphyrins, vol. IV, Academic Press, New York, 1974 (Chapter 6)
37. Groves · J. Am. Chem. Soc. · 1988 · 110 · 844310.1021/ja00233a021 ↗
38. Tsang · Inorg. Chem. · 1990 · 29 · 284810.1021/ic00340a025 ↗
39. Iamamoto · J. Mol. A · 1997 · 116 · 36510.1016/S1381-1169(96)00343-3 ↗
40. Ozette · Inorg. Chem. Acta · 1998 · 272 · 410.1016/S0020-1693(97)05896-9 ↗
41. Cooke · J. Chem. Soc., Perkin Trans. · 1994 · 1 · 191310.1039/p19940001913 ↗