MOF-5/n-Bu4NBr: an efficient catalyst system for the synthesis of cyclic carbonates from epoxides and CO2 under mild conditions

被引:443
作者
Song, Jinliang [1 ]
Zhang, Zhaofu [1 ]
Hu, Suqin [1 ]
Wu, Tianbin [1 ]
Jiang, Tao [1 ]
Han, Buxing [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, Ctr Mol Sci, BNLMS, Beijing 100190, Peoples R China
关键词
METAL-ORGANIC FRAMEWORK; HETEROGENEOUS ASYMMETRIC HYDROGENATION; POSTSYNTHETIC COVALENT MODIFICATION; PROPYLENE CARBONATE; IONIC LIQUID; DIMETHYL CARBONATE; CHEMICAL FIXATION; COORDINATION POLYMERS; HOMOGENEOUS CATALYST; GAS-ADSORPTION;
D O I
10.1039/b902550b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of efficient heterogeneous catalysts for the cycloaddition of CO2 with epoxides to produce five-membered cyclic carbonates under mild reaction conditions is of great importance. In this work, the coupling reaction of CO2 with propylene oxide (PO) to produce propylene carbonate (PC) catalyzed by MOF-5 (metal-organic frameworks) in the presence of quaternary ammonium salts (Me4NCl, Me4NBr, Et4NBr, n-Pr4NBr, n-Bu4NBr) was studied in different conditions. It was discovered that MOF-5 and quaternary ammonium salts had excellent synergetic effect in promoting the reaction, and the MOF-5/n-Bu4NBr catalytic system was the most efficient among them. The optimal temperature for the reaction was around 50 degrees C. The reaction could be completed in 6 h at low CO2 pressure with very high selectivity. A decrease of the yield of PC was not noticeable after MOF-5 was reused three times, indicating that the MOF-5 was stable. The MOF-5/n-Bu4NBr catalytic system was also very active and selective for the cycloaddition of CO2 with other epoxides, such as glycidyl phenyl ether, epichlorohydrin and styrene oxide. The mechanism for the coupling reaction is also discussed.
引用
收藏
页码:1031 / 1036
页数:6
相关论文
共 78 条
[51]   Solution infiltration of palladium into MOF-5: synthesis, physisorption and catalytic properties [J].
Sabo, Michal ;
Henschel, Antje ;
Froede, Heidrun ;
Klemm, Elias ;
Kaskel, Stefan .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (36) :3827-3832
[52]  
Sakai T, 2008, GREEN CHEM, V10, P337, DOI 10.1039/b718321f
[53]   Selective conversion of carbon dioxide to dimethyl carbonate by molecular catalysis [J].
Sakakura, T ;
Saito, Y ;
Okano, M ;
Choi, JC ;
Sako, T .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (20) :7095-7096
[54]   Transformation of carbon dioxide [J].
Sakakura, Toshiyasu ;
Choi, Jun-Chul ;
Yasuda, Hiroyuki .
CHEMICAL REVIEWS, 2007, 107 (06) :2365-2387
[55]   The synthesis of organic carbonates from carbon dioxide [J].
Sakakura, Toshiyasu ;
Kohno, Kazufumi .
CHEMICAL COMMUNICATIONS, 2009, (11) :1312-1330
[56]   Efficient carbamate synthesis via a three-component coupling of an amine, CO2, and alkyl halides in the presence of Cs2CO3 and tetrabutylammonium iodide [J].
Salvatore, RN ;
Shin, SI ;
Nagle, AS ;
Jung, KW .
JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (03) :1035-1037
[57]   A homochiral metal-organic porous material for enantioselective separation and catalysis [J].
Seo, JS ;
Whang, D ;
Lee, H ;
Jun, SI ;
Oh, J ;
Jeon, YJ ;
Kim, K .
NATURE, 2000, 404 (6781) :982-986
[58]  
Shen YM, 2004, EUR J ORG CHEM, V2004, P3080
[59]   From CO oxidation to CO2 activation:: An unexpected catalytic activity of polymer-supported nanogold [J].
Shi, F ;
Zhang, QH ;
Ma, YB ;
He, YD ;
Deng, YQ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (12) :4182-4183
[60]   Alternatives to phosgene and carbon monoxide: Synthesis of symmetric urea derivatives with carbon dioxide in ionic liquids [J].
Shi, F ;
Deng, YQ ;
SiMa, TL ;
Peng, JJ ;
Gu, YL ;
Qiao, BT .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (28) :3257-3260