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

被引:32
作者
Ciuffi, KJ
Sacco, HC
Biazzotto, JC
Vidoto, EA
Nascimento, OR
Leite, CAP
Serra, OA
Iamamoto, Y
机构
[1] Univ Sao Paulo, FFCLRP, Dept Quim, BR-14040901 Ribeirao Preto, SP, Brazil
[2] Univ Franca, Franca, SP, Brazil
[3] Univ Sao Paulo, Inst Fis Sao Carlos, Sao Carlos, SP, Brazil
[4] Univ Estadual Campinas, Inst Quim, Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
D O I
10.1016/S0022-3093(00)00149-6
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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%). (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:100 / 108
页数:9
相关论文
共 39 条
[21]   Synthesis of hybrid organic-inorganic materials from interpenetrating polymer network chemistry [J].
Jackson, CL ;
Bauer, BJ ;
Nakatani, AI ;
Barnes, JD .
CHEMISTRY OF MATERIALS, 1996, 8 (03) :727-733
[22]   Synthesis and characterization of a conjugated copolymer of poly(phenylenevinylene) containing a metalloporphyrin incorporated into the polymer backbone [J].
Jiang, BW ;
Jones, WE .
MACROMOLECULES, 1997, 30 (19) :5575-5581
[23]   SYNTHESES AND SPECTROSCOPIC CHARACTERIZATION OF (T(PARA-ME2N)F4PP)H2 AND (T(PARA-ME2N)F4PP)M WHERE T(PARA-ME2N)F4PP IS THE DIANION OF MESO-TETRAKIS(ORTHO,ORTHO,META,META-TETRAFLUORO-PARA-(DIMETHYLAMINO)PHENYL)-PORPHYRIN AND M = CO(II), CU(II), OR NI(II) - STRUCTURES OF (T(PARA-ME2N)F4PP)CO AND (MESO-TETRAKIS(PENTAFLUOROPHENYL)PORPHINATO)COBALT(II), (TF5PP)CO [J].
KADISH, KM ;
ARAULLOMCADAMS, C ;
HAN, BC ;
FRANZEN, MM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (23) :8364-8368
[24]   ROTHEMUND AND ADLER-LONGO REACTIONS REVISITED - SYNTHESIS OF TETRAPHENYLPORPHYRINS UNDER EQUILIBRIUM CONDITIONS [J].
LINDSEY, JS ;
SCHREIMAN, IC ;
HSU, HC ;
KEARNEY, PC ;
MARGUERETTAZ, AM .
JOURNAL OF ORGANIC CHEMISTRY, 1987, 52 (05) :827-836
[25]  
LUCAS HJ, 1963, ORG SYNTH, P483
[26]   Template recognition in inorganic-organic hybrid films prepared by the sol-gel process [J].
Makote, R ;
Collinson, MM .
CHEMISTRY OF MATERIALS, 1998, 10 (09) :2440-2445
[27]   ACTIVATION OF ALKANES - THE BIOMIMETIC APPROACH [J].
MANSUY, D .
COORDINATION CHEMISTRY REVIEWS, 1993, 125 (1-2) :129-141
[28]  
MANSUY D, 1994, METALLOPORPHYRINS CA, pCH4
[29]  
MARK JE, 1995, ACS S SERIES, V586
[30]   METALLOPORPHYRINS AS VERSATILE CATALYSTS FOR OXIDATION REACTIONS AND OXIDATIVE DNA CLEAVAGE [J].
MEUNIER, B .
CHEMICAL REVIEWS, 1992, 92 (06) :1411-1456