Structured mesoporous organosilicas from an acetonitrile-water template system

被引:13
作者
Macquarrie, DJ [1 ]
Gilbert, BC
Gilbey, LJ
Caragheorgheopol, A
Savonea, F
Jackson, DB
Onida, B
Garrone, E
Luque, R
机构
[1] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
[2] Romanian Acad, Inst Phys Chem IG Murgulescu, Bucharest 060021, Romania
[3] Univ Reading, Dept Chem, Reading RG6 6AH, Berks, England
[4] Politecn Torino, Dipartimento Sci Mat & Ingn Chim, I-10129 Turin, Italy
关键词
D O I
10.1039/b505695k
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
The synthesis of templated mesoporous silicas with a narrow pore size distribution can be achieved in a water/acetonitrile/n-dodecylamine system. The benefits of using this system compared to aqueous ethanol to prepare silicas are the much enhanced wall thickness, leading to greater structural stability, as well as a lack of co-surfactancy from acetonitrile, which means that the pore size remains constant over a wide range of solvent compositions. The particles obtained from this route are cylindrical, with partially aligned mesopores, in contrast to those obtained from aqueous ethanol, which are spherical and have a wormhole structure. A further major advantage is that the amine-functionalised materials, formed by direct co- condensation, are nucleophilic, in contrast to those prepared from aqueous ethanol. This latter feature allows for the elaboration of these amine functions to attach a range of more complex functionality, examples of which are given.
引用
收藏
页码:3946 / 3951
页数:6
相关论文
共 47 条
[11]   A spin probe study of mesoporous silica formation via a neutral templating route [J].
Caldararu, H ;
Caragheorgheopol, A ;
Savonea, F ;
Macquarrie, DJ ;
Gilbert, BC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (25) :6032-6038
[12]   Design of large-pore mesoporous materials for immobilization of penicillin G acylase biocatalyst [J].
Chong, ASM ;
Zhao, XS .
CATALYSIS TODAY, 2004, 93-5 :293-299
[13]   Preparation of a novel silica-supported palladium catalyst and its use in the Heck reaction [J].
Clark, JH ;
Macquarrie, DJ ;
Mubofu, EB .
GREEN CHEMISTRY, 2000, 2 (02) :53-55
[14]   Chemically modified mesoporous solids and their use in the polymerisation of hydrocarbon monomers [J].
Clark, JH ;
Shorrock, K ;
Budarin, V ;
Wilson, K .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 2002, (03) :423-427
[15]   Combined alkyl and sulfonic acid functionalization of MCM-41-type silica -: Part 1.: Synthesis and characterization [J].
Díaz, I ;
Márquez-Alvarez, C ;
Mohino, F ;
Pérez-Pariente, J ;
Sastre, E .
JOURNAL OF CATALYSIS, 2000, 193 (02) :283-294
[16]   Combined alkyl and sulfonic acid functionalization of MCM-41-Type silica -: Part 2.: Esterification of glycerol with fatty acids [J].
Díaz, I ;
Márquez-Alvarez, C ;
Mohino, F ;
Pérez-Pariente, J ;
Sastre, E .
JOURNAL OF CATALYSIS, 2000, 193 (02) :295-302
[17]   Highly efficient "tight fit" immobilization of α-chymotrypsin in mesoporous MCM-41:: A novel approach using precursor immobilization and activation [J].
Fadnavis, NW ;
Bhaskar, V ;
Kantam, ML ;
Choudary, BM .
BIOTECHNOLOGY PROGRESS, 2003, 19 (02) :346-351
[18]   Catalytic activity of mesoporous silicate-immobilized chloroperoxidase [J].
Han, YJ ;
Watson, JT ;
Stucky, GD ;
Butler, A .
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 2002, 17 (01) :1-8
[19]   Lewis acid-driven accelerated living polymerization of lactones initiated with aluminum porphyrins. Chemoselective activation of ester groups by Lewis acid [J].
Isoda, M ;
Sugimoto, H ;
Aida, T ;
Inoue, S .
MACROMOLECULES, 1997, 30 (01) :57-62
[20]   Mesoporous zeolite as a new class of catalyst for controlled polymerization of lactones [J].
Kageyama, K ;
Ogino, S ;
Aida, T ;
Tatsumi, T .
MACROMOLECULES, 1998, 31 (13) :4069-4073