説明:
(abstract)One or two phenylacetylide (PA) ligand(s) were successfully removed from the IrAu12 superatomic core of [IrAu12(dppe)5(PA)2]+ (dppe = 1,2-bis(diphenylphosphino)ethane) by reaction with controlled amounts of tetrafluoroboric acid. Optical and nuclear magnetic resonance spectroscopies and density functional theory calculations revealed the formation of open Au site(s) on the IrAu12 core of [IrAu12(dppe)5(PA)1]2+ and [IrAu12(dppe)5]3+ with the remaining structure intact. Isocyanide was efficiently trapped at the open electrophilic site on [IrAu12(dppe)5(PA)1]2+, whereas a dimer or trimer of the IrAu12 superatoms was formed using diisocyanide as a linker. These results open the door to designed assembly of chemically modified metal superatoms.
権利情報:
キーワード: ligand desorption reaction, superatoms, gold clusters, nanoclusters
刊行年月日: 2024-04-24
出版者: Wiley
掲載誌:
研究助成金:
原稿種別: 出版者版 (Version of record)
MDR DOI:
公開URL: https://doi.org/10.1002/anie.202402025
関連資料:
その他の識別子:
連絡先:
更新時刻: 2024-08-20 12:30:21 +0900
MDRでの公開時刻: 2024-08-20 12:30:21 +0900
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Angew Chem Int Ed - 2024 - Fukumoto - Diphosphine‐Protected IrAu12 Superatom with Open Site s Synthesis and Programmed.pdf
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サイズ | 2.54MB | 詳細 |