Chemistry in Self-Assembled Nanoreactors

Jarl Ivar van der Vlugt, Tehila S. Koblenz, Jeroen Wassenaar, and Joost N. H. Reek Supramolecular and Homogeneous Catalysis, Van t Hoff Institute for Molecular Sciences, University of Amsterdam, 1018 WV Amsterdam, The Netherlands 

Molecular Encapsulation Organic Reactions in Constrained Systems 2010 John Wiley Sons, Ltd 

Since the nineties of the last century, research groups around the world have explored the application of nanocapsules as nanoreactors, i.e. reaction vessels for chemical transformations, and the influence of different cavity effects. In this chapter the focus will mainly be on recent developments concerned with synthetic nanoreactors that can be obtained in a selective and controlled manner through the use of self-assembly principles and rational design, and on their application as catalytically active capsules for respective chemical reactions. For the sake of clarity, each specific type of nanoreactor will be discussed in a separate section. Particular types of nanocapsules to be reviewed include assemblies held together by hydrogen bonding, metal-ligand interactions and hydrophobic 

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One particular asset of structured self-assemblies is their ability to create nano- to microsized domains, snch as cavities, that could be exploited for chemical synthesis and catalysis. Many kinds of organized self-assemblies have been proved to act as efficient nanoreactors, and several chapters of this book discnss some of them such as small discrete supramolecular vessels (Chapter Reactivity In Nanoscale Vessels, Supramolecular Reactivity), dendrimers (Chapter Supramolecular Dendrlmer Chemistry, Soft Matter), or protein cages and virus capsids (Chapter Viruses as Self-Assembled Templates, Self-Processes). In this chapter, we focus on larger and softer self-assembled structures such as micelles, vesicles, liquid crystals (LCs), or gels, which are made of surfactants, block copolymers, or amphiphilic peptides. In addition, only the systems that present a high kinetic lability (i.e., dynamic) of their aggregated building blocks are considered more static objects such as most of polymersomes and molecularly imprinted polymers are discussed elsewhere (Chapters Assembly of Block Copolymers and Molecularly Imprinted Polymers, Soft Matter, respectively). Finally, for each of these dynamic systems, we describe their functional properties with respect to their potential for the promotion and catalysis of molecular and biomolecu-lar transformations, polymerization, self-replication, metal colloid formation, and mineralization processes. 

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