Montmorillonite-based heterogeneous catalysts for efficient organic reactions

被引:22
作者
Takabatake, Moe [1 ,2 ]
Motokura, Ken [1 ,2 ]
机构
[1] Tokyo Inst Technol, Dept Chem Sci & Engn, Yokohama 2268502, Japan
[2] Yokohama Natl Univ, Dept Chem & Life Sci, Yokohama 2408501, Japan
来源
NANO EXPRESS | 2022年 / 3卷 / 01期
基金
日本科学技术振兴机构;
关键词
montmorillonites; heterogeneous catalyst; acid catalysis; organic reaction; metal catalysis; PROTON-EXCHANGED MONTMORILLONITE; RING-OPENING POLYMERIZATION; SOLID ACID; CARBONYL-COMPOUNDS; CARBOXYLIC-ACIDS; SHEET SILICATES; ALCOHOLS; TITANIUM; ALKENES; CLAY;
D O I
10.1088/2632-959X/ac5ac3
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this review, we give a brief overview of recently developed montmorillonite-based heterogeneous catalysts used for efficient organic reactions. Cation-exchanged montmorillonite catalysts, metal catalysts supported on montmorillonite, and an interlayer design used for selective catalysis are introduced and discussed. In traditional syntheses, homogeneous acids and metal salts were used as catalysts, but the difficulty in separation of catalysts from products was a bottleneck when considering industrialization. The use of solid heterogeneous catalysts is one of the major solutions to overcome this problem. Montmorillonite can be used as a heterogeneous catalyst and/or catalyst support. This clay material exhibits strong acidity and a stabilizing effect on active species, such as metal nanoparticles, due to its unique layered structure. These advantages have led to the development of montmorillonite-based heterogeneous catalysts. Acidic montmorillonite, such as proton-exchanged montmorillonite, exhibits a high catalytic activity for the activation of electrophiles, such as alcohols, alkenes, and even alkanes. The montmorillonite interlayer/surface also functions as a good support for various metal species used for oxidation and carbon-carbon bond forming reactions. The use of an interlayer structure enables selective reactions and the stabilization of catalytically active species.
引用
收藏
页数:11
相关论文
共 68 条
[11]   Ring-opening polymerization of lactones catalyzed by ion-exchanged clay montmorillonite and the application to well-defined block copolymer synthesis with seven-membered cyclic carbonate [J].
Hachemaoui, A ;
Belbachir, M .
MATERIALS LETTERS, 2005, 59 (29-30) :3904-3908
[12]   Kinetics of the ring opening polymerization of ε-caprolactone catalysed by a proton exchanged montmorillonite clay [J].
Harrane, Amine ;
Meghabar, Rachid ;
Belbachir, Mohamed .
REACTIVE & FUNCTIONAL POLYMERS, 2006, 66 (12) :1696-1702
[13]   From Conventional Lewis Acids to Heterogeneous Montmorillonite K10: Eco-Friendly Plant-Based Catalysts Used as Green Lewis Acids [J].
Hechelski, Marie ;
Ghinet, Alina ;
Louvel, Brice ;
Dufrenoy, Pierrick ;
Rigo, Benoit ;
Daich, Adam ;
Waterlot, Christophe .
CHEMSUSCHEM, 2018, 11 (08) :1249-1277
[14]   SOLID ACID AND BASE-CATALYZED CYANOSILYLATION OF CARBONYL-COMPOUNDS WITH CYANOTRIMETHYLSILANE [J].
HIGUCHI, K ;
ONAKA, M ;
IZUMI, Y .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1993, 66 (07) :2016-2032
[15]   Advances in liquid-phase organic reactions using heteropolyacid and clay [J].
Izumi, Y ;
Urabe, K ;
Onaka, M .
MICROPOROUS AND MESOPOROUS MATERIALS, 1998, 21 (4-6) :227-233
[16]  
Izumi Y., 1997, CATAL SURV JPN, V1, P17023, DOI [10.1023/A:1019056425569, DOI 10.1023/A:1019056425569]
[17]   Cation-exchanged montmorillonites as solid acid catalysts for organic synthesis [J].
Kaneda, Kiyotomi .
SYNLETT, 2007, (07) :999-1015
[18]   Design of high-performance heterogeneous metal catalysts for green and sustainable chemistry [J].
Kaneda, Kiyotomi ;
Ebitani, Kohki ;
Mizugaki, Tomoo ;
Mori, Kohsuke .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2006, 79 (07) :981-1016
[19]  
Kaur N., 2012, Journal of Chemical and Pharmaceutical Research, V4, P991
[20]   Monomeric metal aqua complexes in the interlayer space of montmorillonites as strong Lewis acid catalysts for heterogeneous carbon-carbon bond-forming reactions [J].
Kawabata, T ;
Kato, M ;
Mizugaki, T ;
Ebitani, K ;
Kaneda, K .
CHEMISTRY-A EUROPEAN JOURNAL, 2005, 11 (01) :288-297