Anchoring of a [Mn(salen)Cl] complex onto mesoporous carbon xerogels

被引:36
作者
Mahata, N.
Silva, A. R.
Pereira, M. F. R.
Freire, C.
de Castro, B.
Figueiredo, J. L. [1 ]
机构
[1] Univ Porto, Dept Engn Quim, Lab Catalise & Mat, P-4200465 Oporto, Portugal
[2] Univ Porto, Fac Ciencias, Dept Quim, REQUIMTE, P-4169007 Oporto, Portugal
关键词
carbon xerogels; activation; complex immobilization; surface functional groups;
D O I
10.1016/j.jcis.2007.02.080
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carbon xerogels were synthesized by the conventional sol-gel approach using formaldehyde and resorcinol. The wet gel was dried by two different procedures followed by carbonization, leading to mesoporous carbon xerogels with considerably different pore size distributions. The materials were subsequently oxidized with air, in order to introduce functional groups on the surface, in particular phenols, anhydrides and carbonyls. The capacity of the carbon xerogels for direct immobilization of metal complexes was tested with a manganese(III) salen complex which possesses an extended ligand pi system and two reactive hydroxyl groups on the aldehyde fragment. The manganese loadings of the various samples indicate that larger amounts of Mn(III) complex were immobilized in the oxidized carbon xerogels when compared with the parent unactivated materials, suggesting that complex immobilization took place preferably by covalent bond between the surface oxygen functional groups and the ligand reactive groups, rather than by pi-pi interactions. The size and shape of the carbon xerogel pores were also shown to play an important role in the final loading of the manganese(III) salen complex. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:152 / 158
页数:7
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