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Self‐Assembly of Polyoxometalate‐Based Sub‐1 nm Polyhedral Building Blocks into Rhombic Dodecahedral Superstructures

Self‐assembly of subnanometer (sub‐1 nm) scale polyhedral building blocks can yield some superstructures with novel and interesting morphology as well as potential functionalities. However, achieving the self‐assembly of sub‐1 nm polyhedral building blocks is still a great challenge. Herein, through...

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Published in:Angewandte Chemie 2023-12, Vol.135 (51), p.n/a
Main Authors: Wang, Tian, Chen, Weichao, Liu, Qingda, Wang, Wei, Wang, Yinming, Wu, Biao, Shi, Wenxiong, Zhu, Yunqing, He, Peilei, Wang, Xun
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container_issue 51
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container_title Angewandte Chemie
container_volume 135
creator Wang, Tian
Chen, Weichao
Liu, Qingda
Wang, Wei
Wang, Yinming
Wu, Biao
Shi, Wenxiong
Zhu, Yunqing
He, Peilei
Wang, Xun
description Self‐assembly of subnanometer (sub‐1 nm) scale polyhedral building blocks can yield some superstructures with novel and interesting morphology as well as potential functionalities. However, achieving the self‐assembly of sub‐1 nm polyhedral building blocks is still a great challenge. Herein, through encapsulating the titanium‐substituted polyoxometalate (POM, K7PTi2W10O40) with tetrabutylammonium cations (TBA+), we first synthesized a sub‐1 nm rhombic dodecahedral building block by further tailoring the spatial distribution of TBA+ on the POM. Molecular dynamics (MD) simulations demonstrated the eight TBA+ cations interacted with the POM cluster and formed the sub‐1 nm rhombic dodecahedron. As a result of anisotropy, the sub‐1 nm building blocks have self‐assembled into rhombic dodecahedral POM (RD‐POM) assemblies at the microscale. Benefiting from the regular structure, Br− ions, and abundant active sites, the obtained RD‐POM assemblies exhibit excellent catalytic performance in the cycloaddition of CO2 with epoxides without co‐catalysts. This work provides a promising approach to tailor the symmetry and structure of sub‐1 nm building blocks by tuning the spatial distribution of ligands, which may shed light on the fabrication of superstructures with novel properties by self‐assembly. Tailoring the spatial distribution of ligands on polyoxometalates has led to subnanometer rhombic dodecahedral building blocks being obtained. The anisotropy of these sub‐1 nm building blocks results in them self‐assembling into rhombic dodecahedral assemblies, which exhibit excellent catalytic performance in the cycloaddition of CO2 with epoxides.
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subjects Anisotropy
Assemblies
Carbon dioxide
Catalysts
Cations
Chemistry
Cycloaddition
Epoxides
Fabrication
Ligand Distribution
Molecular dynamics
Polyoxometalates
Polyoxometallates
Rhombic Dodecahedron
Self-Assembly
Spatial distribution
Subnanometer
Superstructures
title Self‐Assembly of Polyoxometalate‐Based Sub‐1 nm Polyhedral Building Blocks into Rhombic Dodecahedral Superstructures
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