Metallophilicity-Driven Dynamic Aggregation of a Phosphorescent Gold(I)-Silver(I) Cluster Prepared by Solution-Based and Mechanochemical Approaches

被引:117
作者
Ni, Wen-Xiu [1 ,2 ]
Qiu, Yu-Min [1 ,2 ]
Li, Mian [1 ,2 ]
Zheng, Ji [1 ,2 ]
Sun, Raymond Wai-Yin [1 ,2 ]
Zhan, Shun-Ze [1 ,2 ]
Ng, Seik Weng [3 ,4 ]
Li, Dan [1 ,2 ]
机构
[1] Shantou Univ, Dept Chem, Shantou 515063, Guangdong, Peoples R China
[2] Shantou Univ, Key Lab Preparat & Applicat Ordered Struct Mat Gu, Shantou 515063, Guangdong, Peoples R China
[3] Univ Malaya, Dept Chem, Kuala Lumpur 50603, Malaysia
[4] King Abdulaziz Univ, Dept Chem, Fac Sci, Jeddah 21589, Saudi Arabia
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
METAL-METAL INTERACTIONS; TRINUCLEAR COMPLEXES; GOLD; LUMINESCENCE; PHOTOPHYSICS; CHEMISTRY; AG; MODULATION; EMISSION; DESIGN;
D O I
10.1021/ja5025113
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We observed an unusual reversible aggregation process showing stimuli-responsive structural dynamics and optical changes attributed to the formation of a sandwich-like Au-3-Ag-Au-3 cluster, which can be synthesized through both solution and mechanochemical methods. Unlike many other heteronudear gold-silver clusters, the affinity of two cyclic Au-3 complexes and a Ag-I ion is solely bound by ligand unsupported Au-Ag bonding. The assembly/disassembly behavior, further forming nanoaggregates, is controllable by adjusting the concentration of the solution. In the solid state, the insertion of Ag-I ion can be implemented through a mechanochemical approach, accompanied by visual color changes and reversible luminochromism. Furthermore, an uncommon solid-liquid extraction is demonstrated, showing the uniqueness of this labile Au-Ag metallophilicity and hinting at the possibility of manipulating a bonding process through a heterogeneous route.
引用
收藏
页码:9532 / 9535
页数:4
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