Supramolecular Chemistry and Self-Organization: A Veritable Playground for Catalysis

被引:24
作者
Leclercq, Loic [1 ]
Douyere, Gregory [1 ]
Nardello-Rataj, Veronique [1 ]
机构
[1] Univ Lille, CNRS, Cent Lille, ENSCL,Univ Artois,UMR 8181,UCCS, F-59000 Lille, France
关键词
supramolecular architectures; adaptive chemistry; host-guest complexes; colloidal tectonics; homogeneous catalysis; heterogeneous catalysis; chemzymes; ionic liquids; nanoparticles; SURFACTANT-COMBINED CATALYST; METAL-ORGANIC FRAMEWORKS; INTRAMOLECULAR ALDOL CONDENSATION; PICKERING INTERFACIAL CATALYSIS; P-DODECYLBENZENESULFONIC ACID; IMIDAZOLIUM IONIC LIQUIDS; PHASE-BOUNDARY CATALYSIS; NANO-DROPLET FORMATION; MANNICH-TYPE REACTIONS; DIELS-ALDER REACTION;
D O I
10.3390/catal9020163
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 directed assembly of molecular building blocks into discrete supermolecules or extended supramolecular networks through noncovalent intermolecular interactions is an ongoing challenge in chemistry. This challenge may be overcome by establishing a hierarchy of intermolecular interactions that, in turn, may facilitate the edification of supramolecular assemblies. As noncovalent interactions can be used to accelerate the reaction rates and/or to increase their selectivity, the development of efficient and practical catalytic systems, using supramolecular chemistry, has been achieved during the last few decades. However, between discrete and extended supramolecular assemblies, the newly developed colloidal tectonics concept allows us to link the molecular and macroscopic scales through the structured engineering of colloidal structures that can be applied to the design of predictable, versatile, and switchable catalytic systems. The main cutting-edge strategies involving supramolecular chemistry and self-organization in catalysis will be discussed and compared in this review.
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页数:62
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