Self-assembly of high-nuclear core-shell polyoxovanadates with Lindqvsit templates

被引:0
|
作者
Wu, Shuangxue [1 ]
Fu, Yaomei [2 ]
Gan, Hongmei [1 ]
Zhao, Liang [1 ]
Wang, Xinlong [1 ]
Qin, Chao [1 ]
Su, Zhongmin [3 ]
机构
[1] Northeast Normal Univ, Key Lab Polyoxometalate & Reticular Mat Chem, Minist Educ, Changchun 130024, Jilin, Peoples R China
[2] Weifang Univ Sci & Technol, Shandong Peninsula Engn Res Ctr Comprehens Brine U, Shouguang 262700, Peoples R China
[3] Hainan Univ, Key Lab Adv Mat Trop Isl Resources, Haikou 570228, Peoples R China
来源
INORGANIC CHEMISTRY FRONTIERS | 2025年 / 12卷 / 03期
基金
中国国家自然科学基金;
关键词
CLUSTER; POLYOXOMETALATE;
D O I
10.1039/d4qi02884h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Only rarely have polyoxometalates been recorded to form core-shell clusters, which presumably relates to the scarcity of appropriate building blocks. Herein, two high-nuclear core-shell polyoxophosphovanadates [M6O19]2-subset of[Na8VV6VIV12O18(PhPO3)24]2+ (M = W 1, Mo 2) are synthesized utilizing Lindqvist polyoxometalates as templates. Both clusters exhibit a nested three-shell architecture characterized by an octahedron@cube@octahedron configuration. The outer shell [VV6VIV12O18(PhPO3)24]6- consists of two simple {VO5} and {PhPO3} building blocks connected alternately and exhibits the same octahedral geometry as the inner core [M6O19]2- due to anionic template effects. To the best of our knowledge, compounds 1 and 2 represent the first core-shell polyoxovanadates templated by Lindqvist polyoxometalates. Furthermore, compound 1 demonstrates efficacy and stability as a catalyst for the oxidation of sulfide. This work provides a new perspective on the construction of novel core-shell polyoxometalates.
引用
收藏
页码:1021 / 1027
页数:7
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