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Dual stimuli-induced formation of a μ-hydroxido bridged [Zn(9)L(5)(μ-OH)(6)](12+) half-pipe

Low-symmetry metal–organic architectures that feature unusual binding motifs are useful for exploring new modes of guest recognition. Such structures remain difficult to create using current rational design principles. One approach to constructing such architectures is to employ ligands with coordin...

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Detalles Bibliográficos
Autores principales: Wood, Christopher S., Ronson, Tanya K., McConnell, Anna J., Roberts, Derrick A., Nitschke, Jonathan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5535065/
https://www.ncbi.nlm.nih.gov/pubmed/28808538
http://dx.doi.org/10.1039/c5sc03926f
Descripción
Sumario:Low-symmetry metal–organic architectures that feature unusual binding motifs are useful for exploring new modes of guest recognition. Such structures remain difficult to create using current rational design principles. One approach to constructing such architectures is to employ ligands with coordination vectors oriented to preclude the formation of simple, low nuclearity molecular assemblies upon complexation to metal ions. Here we report two new supramolecular assemblies generated from such a ligand: a simple metastable [Zn(3)L(3)](6+) assembly, which was observed to convert to a more complex [Zn(9)L(5)(μ-OH)(6)](12+) twisted half-pipe architecture. Two chemically distinct stimuli—an anionic template and a base—must be applied for the conversion to occur. Perchlorate, perrhenate, trifluoromethanesulfonate and 2-naphthalenesulfonate were found to act as competent templates for the [Zn(9)L(5)(μ-OH)(6)](12+) structure.