4.8 Review

Transmetalation of self-assembled, supramolecular complexes

Journal

CHEMICAL SOCIETY REVIEWS
Volume 43, Issue 6, Pages 1825-1834

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cs60349k

Keywords

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Funding

  1. NSF CCI Center for Sustainable Materials Chemistry [CHE-1102637]
  2. University of Oregon
  3. Direct For Mathematical & Physical Scien
  4. Division Of Chemistry [1102637] Funding Source: National Science Foundation

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Substituting one metal for another in inorganic and organometallic systems is a proven strategy for synthesizing complex molecules, and in some cases, provides the only route to a particular system. The multivalent nature of the coordination in metal-ligand assemblies lends itself more readily to some types of transmetalation. For instance, a binding site can open up for exchange without greatly effecting the many other interactions holding the structure together. In addition to exchanging the metal and altering the local binding environment, transmetalation in supramolecular systems can also lead to substantial changes in the nature of the secondary and tertiary structure of a larger assembly. In this tutorial review we will cover discrete supramolecular assemblies in which metals are exchanged. First we will address fully formed structures where direct substitution replaces one type of metal for another without changing the overall supramolecular assembly. We will then address systems where the disruptive exchange of one metal for another leads to a larger change in the supramolecular assembly. When possible we have tried to highlight systems that use supramolecular self-assembly in tandem with transmetalation to synthesize new structures not accessible through a more direct approach. At the end of this review, we highlight the use of transmetalation in self-assembled aqueous inorganic clusters and discuss the consequences for material science applications.

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