Metal-organic modification of periodic mesoporous silica: Multiply bonded systems

被引:13
作者
Angloher, Stephan [1 ]
Kecht, Johann [1 ]
Bein, Thomas [1 ]
机构
[1] Univ Munich LMU, Dept Chem & Biochem, D-81377 Munich, Germany
关键词
D O I
10.1021/cm0613556
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 use of metal-organic compounds for the organic modification of mesoporous silica such as MCM-41 leads to a fast, efficient, and economic access to inorganic-organic hybrid materials. Using this method, MCM-41 was modified with short-chain alkenes such as allyl and vinyl groups, as well as styrene and different acetylenic molecules. The resulting modified mesoporous materials were characterized with respect to their structural integrity, surface area, and pore volume and the nature and concentration of the grafted species. These grafted periodic mesoporous inorganic-organic hybrid systems offer the potential for a wide range of further modifications aimed at applications in catalysis, sensing, or chemisorption.
引用
收藏
页码:5797 / 5802
页数:6
相关论文
共 38 条
[1]   Heavy metals removal from electroplating wastewater by aminopropyl-Si MCM-41 [J].
Algarra, M ;
Jiménez, MV ;
Rodríguez-Castellón, E ;
Jiménez-López, A ;
Jiménez-Jiménez, J .
CHEMOSPHERE, 2005, 59 (06) :779-786
[2]   Optimization of reaction conditions for the metalorganic modification of MCM-41 [J].
Angloher, Stephan ;
Kecht, Johann ;
Bein, Thomas .
CHEMISTRY OF MATERIALS, 2007, 19 (14) :3568-3574
[3]   Surface characterization and functionalization of MCM-41 silicas via silazane silylation [J].
Anwander, R ;
Nagl, I ;
Widenmeyer, M ;
Engelhardt, G ;
Groeger, O ;
Palm, C ;
Röser, T .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (15) :3532-3544
[4]  
Asefa T, 2001, ADV FUNCT MATER, V11, P447, DOI 10.1002/1616-3028(200112)11:6<447::AID-ADFM447>3.0.CO
[5]  
2-L
[6]   Hybrid catalysts for acetylenes polymerization prepared by anchoring [Rh(cod)Cl]2 on MCM-41, MCM-48 and SBA-15 mesoporous molecular sieves -: The effect of support structure on catalytic activity in polymerization of phenylacetylene and 4-ethynyl-N-{4-[(trimethylsilyl)-ethynyl]benzylidene}aniline [J].
Balcar, H ;
Sedlácek, J ;
Svoboda, J ;
Zilková, N ;
Rathousky, J ;
Vohlídal, J .
COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 2003, 68 (10) :1861-1876
[7]  
BEYER H, 1998, LEHRBUCH ORG CHEM, P100
[8]   HALOBORANES AND THEIR ALKYL DERIVATIVES [J].
BROWN, HC ;
KULKARNI, SU .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1982, 239 (01) :23-41
[9]   The preparation of highly ordered MCM-41 with extremely low surfactant concentration [J].
Cai, Q ;
Lin, WY ;
Xiao, FS ;
Pang, WQ ;
Chen, XH ;
Zou, BS .
MICROPOROUS AND MESOPOROUS MATERIALS, 1999, 32 (1-2) :1-15
[10]  
CAREY FA, 1995, ORG CHEMIE