Immobilized metalloporphyrins in mesoporous MCM-48 as efficient and selective heterogeneous catalysts for oxidation of cyclohexene

被引:11
作者
Khalili, Nafiseh Rahmani [1 ]
Rahimi, Rahmatollah [1 ]
Rabbani, Mahboubeh [1 ]
机构
[1] Iran Univ Sci & Technol, Dept Chem, Tehran 1684613114, Iran
来源
MONATSHEFTE FUR CHEMIE | 2013年 / 144卷 / 05期
关键词
Metalloporphyrins; MCM-48; Heterogeneous catalysts; Cyclohexene oxidation; AL; SI-MESOPOROUS MOLECULAR-SIEVES; HYDROTHERMAL STABILITY; ALLYLIC OXIDATION; HYDROGEN-PEROXIDE; SOLID CATALYSTS; SILICA; MN; EPOXIDATION; PORPHYRINS; ALMCM-48;
D O I
10.1007/s00706-012-0854-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three metalloporphyrins, Mn(III)TClPPCl, Fe(III)TClPPCl, and Co(II)TClPP (TClPP = 5,10,15,20-tetrakis(4-chlorophenyl)porphyrin), were synthesized and immobilized in MCM-48 channels. The designed heterogeneous catalysts were characterized by XRD, ICP, UV-Vis, FT-IR, N-2 adsorption-desorption, and scanning electron microscopy. These investigations showed that successful encapsulation occurred and the framework of mesoporous MCM-48 was retained without any change after incorporation of the metalloporphyrins. The effect of the support on the resistance to pore blocking was studied by comparing MCM-48 with MCM-41. The catalytic activities of the newly synthesized catalysts were examined in the oxidation of cyclohexene with t-butyl hydroperoxide as oxidant. All results confirmed that the supported catalysts presented interesting advantages such as high selectivity to the allylic products and more resistance to pore blocking. The heterogeneous catalysts were reused for several times without significant loss of their catalytic activity.
引用
收藏
页码:597 / 603
页数:7
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