Heterogeneous Organocatalysis at Work: Functionalization of Hollow Periodic Mesoporous Organosilica Spheres with MacMillan Catalyst

被引:94
|
作者
Shi, Jiao Yi [1 ]
Wang, Chang An [1 ]
Li, Zhi Jun [1 ]
Wang, Qiong [1 ]
Zhang, Yuan [1 ]
Wang, Wei [1 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
asymmetric catalysis; heterogeneous catalysis; hollow structures; organocatalysis; mesoporous materials; DIELS-ALDER REACTION; POROUS CARBON SHELL; ORGANIC CATALYSIS; CHIRAL IMIDAZOLIDIN-4-ONE; ASYMMETRIC CATALYSIS; HYBRID MATERIALS; NANOSPHERES; SILICA; STRATEGIES; HYDROGENATION;
D O I
10.1002/chem.201100072
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report a new method for the synthesis of hollow-structured phenylene-bridged periodic mesoporous organosilica (PMO) spheres with a uniform particle size of 100-200 nm using alpha-Fe(2)O(3) as a hard template. Based on this method, the hollow-structured phenylene PMO could be easily functionalized with MacMillan catalyst (H-PhPMO-Mac) by a co-condensation process and a "click chemistry" post-modification. The synthesized H-PhPMO-Mac catalyst has been found to exhibit high catalytic activity (98% yield, 81% enantiomeric excess (ee) for endo and 81% ee for exo) in asymmetric Diels-Alder reactions with water as solvent. The catalyst could be reused for at least seven runs without a significant loss of catalytic activity. Our results have also indicated that hollow-structured PMO spheres exhibit higher catalytic efficiency than solid (non-hollow) PMO spheres, and that catalysts prepared by the co-condensation process and "click chemistry" post-modification exhibit higher catalytic efficiency than those prepared by a grafting method.
引用
收藏
页码:6206 / 6213
页数:8
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