Au(I)Cl-bound N-heterocyclic carbene ligands form MII4(LAuCl)(6) integrally gilded cages

The incorporation of an N-heterocyclic carbene (NHC) moiety into a self-assembled MII4L(6) cage framework required the NHC first to be metallated with gold(i). Bimetallic cages could then be constructed using zinc(ii) and cadmium(ii) templates, showing weak luminescence. The cages were destroyed by...

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Detalles Bibliográficos
Autores principales: Ramsay, William J., Foster, Jonathan A., Moore, Katharine L., Ronson, Tanya K., Mirgalet, Raphaël J., Jefferson, David A., Nitschke, Jonathan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512534/
https://www.ncbi.nlm.nih.gov/pubmed/28757991
http://dx.doi.org/10.1039/c5sc03065j
Descripción
Sumario:The incorporation of an N-heterocyclic carbene (NHC) moiety into a self-assembled MII4L(6) cage framework required the NHC first to be metallated with gold(i). Bimetallic cages could then be constructed using zinc(ii) and cadmium(ii) templates, showing weak luminescence. The cages were destroyed by the addition of further gold(i) in the form of Au(I)(2,4,6-trimethoxybenzonitrile)(2)SbF(6), which caused the reversibly-formed cages to disassemble and controllably release the Au(I)-NHC subcomponent into solution. This release in turn induced the growth of gold nanoparticles. The rate of dianiline release could be tuned by capsule design or through the addition of chemical stimuli, with different release profiles giving rise to different nanoparticle morphologies.

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