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Trapping an octahedral Ag(6) kernel in a seven-fold symmetric Ag(56) nanowheel

High-nuclearity silver clusters are appealing synthetic targets for their remarkable structures, but most are isolated serendipitously. We report here six giant silver-thiolate clusters mediated by solvents, which not only dictate the formation of an octahedral Ag(6)(4+) kernel, but also influence t...

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Detalles Bibliográficos
Autores principales: Wang, Zhi, Su, Hai-Feng, Kurmoo, Mohamedally, Tung, Chen-Ho, Sun, Di, Zheng, Lan-Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974400/
https://www.ncbi.nlm.nih.gov/pubmed/29844401
http://dx.doi.org/10.1038/s41467-018-04499-9
Descripción
Sumario:High-nuclearity silver clusters are appealing synthetic targets for their remarkable structures, but most are isolated serendipitously. We report here six giant silver-thiolate clusters mediated by solvents, which not only dictate the formation of an octahedral Ag(6)(4+) kernel, but also influence the in situ-generated Mo-based anion templates. The typical sevenfold symmetric silver nanowheels show a hierarchical cluster-in-cluster structure that comprises an outermost Ag(56) shell and an inner Ag(6)(4+) kernel in the centre with seven MoO(4)(2−) anion templates around it. Electrospray ionization mass spectrometry analyses reveal the underlying rule for the formation of such unique silver nanowheels. This work establishes a solvent–intervention approach to construct high-nuclearity silver clusters in which both the formation of octahedral Ag(6)(4+) kernel and in situ generation of various Mo-based anion templates can be simultaneously controlled.