过渡金属
盔甲
化学
纳米技术
材料科学
有机化学
催化作用
图层(电子)
作者
Yeqin Feng,Mengyun Zhao,Jiaxin Yang,Zhimin Wang,Ping Bai,Yongkang Liu,Hongjin Lv,Guo‐Yu Yang
标识
DOI:10.1002/ange.202505511
摘要
Comparing to versatile polyoxometalate (POM)‐templated Ag clusters, the construction of closed Ag clusters using transition‐metal‐containing polyoxometalates (TMCPOMs) as anionic templates have, to our knowledge, never been reported. In this work, we have synthesized three TMCPOM‐templated gigantic closed Ag clusters, [{(Co0.58W0.42)3(OH)3(Ag0.5O3)(SiW9O34)}4@Ag114Br4(tBuC≡C)72]· [SiW12O40]2·10CH3CN (1), [{(Cu0.58W0.42)3(OH)3(Ag0.5O3)(SiW9O34)}4@Ag114Br4 (tBuC≡C)72]·[SiW12O40]2 (2), and [{(Co0.58W0.42)3(OH)3 (Ag0.5O3)(GeW9O34)}4@Ag114Br4(tBuC≡C)72]·[GeW12O40]2 (3), using a universal one‐pot solvothermal synthetic approach. Single‐crystal X‐ray diffraction analyses demonstrate that the high‐nuclearity transition metal‐containing (M=Co/Cu) POMs with idealized Td symmetry are closely covered by gigantic Ag armors, representing the largest TMCPOM‐templated closed Ag clusters to date. Moreover, compounds 1−3 can form interesting supertetrahedral intercluster packing structures through Columbic and hydrogen bonding interactions between the cationic TMCPOM‐templated gigantic {Ag114} clusters and the counter [XW12O40]4− (X=Si/Ge) anions. Upon light irradiation, all three compounds exhibited decent photocatalytic CO2 reduction activity which is dependent on their different electronic structures.
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