Atom-Precise Modification of Silver(I) Thiolate Cluster by Shell Ligand Substitution: A New Approach to Generation of Cluster Functionality and Chirality

被引:226
作者
Li, Si [1 ]
Du, Xiang-Sha [1 ]
Li, Bing [1 ]
Wang, Jia-Yin [1 ]
Li, Guo-Ping [1 ]
Gao, Guang-Gang [2 ]
Zang, Shuang-Quan [1 ]
机构
[1] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Henan, Peoples R China
[2] Univ Jinan, Sch Mat Sci & Engn, Jinan 250022, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL NANOCLUSTERS; CHALCOGENIDE CLUSTERS; GOLD CLUSTERS; CORE; NANOPARTICLES; MONOLAYER; EMERGENCE; EMISSION; COPPER; SIZE;
D O I
10.1021/jacs.7b12136
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To realize the molecular design of new functional silver(I) clusters, a new synthetic approach has been proposed, by which the weakly coordinating ligands NO3- in a Ag-20 thiolate cluster precursor can be substituted by carboxylic ligands while keeping its inner core intact. By rational: design, novel atom-precise carboxylic or amino acid protected 20-core Ag(I)-thiolate clusters have been demonstrated for the first time. The fluorescence and electrochemical activity of the postmodified Ag-20 clusters can be modulated by alrestatin or ferrocenecarboxylic acid substitution. More strikingly, when chiral amino acids were used as postmodified ligands, CD-ctivity was observed for the Ag-20 clusters, unveiling an efficient way to obtain atom-precise chiral silver(I) clusters.
引用
收藏
页码:594 / 597
页数:4
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