説明:
(abstract)Ligand-protected gold nanoclusters have attracted attention as building blocks for functional materials. In this study, we have demonstrated the programmed assembly of the icosahedral Ir@Au12 nanoclusters into a dimer, a linear trimer, linear oligomers, or a triangular trimer via the reaction between the IrAu12 with predefined binding sites and bi- or tri-dentate isocyanide linkers. The formation of the intended structures was confirmed by high-angle annular dark-field scanning transmission electron microscopy using a newly developed sampling protocol. Statistical analysis of the inter-particle distances provided quantitative structure models consistent with the theoretically predicted structures. The linear oligomers exhibited a new absorption peak at ~480 nm. Theoretical calculations indicated that the electron transfers from the IrAu12 moiety to the linker ligand or another IrAu12 moiety involve the absorption. This study demonstrates that programmed assemblies of Au nanoclusters will provide an opportunity to elucidate how novel collective properties arise through assembly.
権利情報:
This document is the Accepted Manuscript version of a Published Work that appeared in final form in Nano Letters, copyright © 2025 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.nanolett.5c02770.
キーワード: gold nanoclusters, programmed assembly, transmission electron microscopy, photoinduced intercluster electron transfer
刊行年月日: 2025-08-13
出版者: American Chemical Society (ACS)
掲載誌:
研究助成金:
原稿種別: 著者最終稿 (Accepted manuscript)
MDR DOI: https://doi.org/10.48505/nims.5629
公開URL: https://doi.org/10.1021/acs.nanolett.5c02770
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更新時刻: 2025-08-18 10:45:19 +0900
MDRでの公開時刻: 2026-07-30 08:29:14 +0900
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