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      Double-Decker Coordination Cages : Double-Decker Coordination Cages

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          Recent Developments in the Preparation and Chemistry of Metallacycles and Metallacages via Coordination.

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            Supramolecular systems chemistry.

            The field of supramolecular chemistry focuses on the non-covalent interactions between molecules that give rise to molecular recognition and self-assembly processes. Since most non-covalent interactions are relatively weak and form and break without significant activation barriers, many supramolecular systems are under thermodynamic control. Hence, traditionally, supramolecular chemistry has focused predominantly on systems at equilibrium. However, more recently, self-assembly processes that are governed by kinetics, where the outcome of the assembly process is dictated by the assembly pathway rather than the free energy of the final assembled state, are becoming topical. Within the kinetic regime it is possible to distinguish between systems that reside in a kinetic trap and systems that are far from equilibrium and require a continuous supply of energy to maintain a stationary state. In particular, the latter systems have vast functional potential, as they allow, in principle, for more elaborate structural and functional diversity of self-assembled systems - indeed, life is a prime example of a far-from-equilibrium system. In this Review, we compare the different thermodynamic regimes using some selected examples and discuss some of the challenges that need to be addressed when developing new functional supramolecular systems.
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              Self-assembled M24L48 polyhedra and their sharp structural switch upon subtle ligand variation.

              Self-assembly is a powerful technique for the bottom-up construction of discrete, well-defined nanoscale structures. Large multicomponent systems (with more than 50 components) offer mechanistic insights into biological assembly but present daunting synthetic challenges. Here we report the self-assembly of giant M24L48 coordination spheres from 24 palladium ions (M) and 48 curved bridging ligands (L). The structure of this multicomponent system is highly sensitive to the geometry of the bent ligands. Even a slight change in the ligand bend angle critically switches the final structure observed across the entire ensemble of building blocks between M24L48 and M12L24 coordination spheres. The amplification of this small initial difference into an incommensurable difference in the resultant structures is a key mark of emergent behavior.
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                Author and article information

                Journal
                European Journal of Inorganic Chemistry
                Eur. J. Inorg. Chem.
                Wiley-Blackwell
                14341948
                June 2016
                June 24 2016
                : 2016
                : 17
                : 2816-2827
                Article
                10.1002/ejic.201600259
                4e998024-c96b-4936-8ac9-f6aadc92eb97
                © 2016

                http://doi.wiley.com/10.1002/tdm_license_1.1

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