Related Experiment Video
Updated: Sep 16, 2025

Synthesis of Single-Crystalline Core-Shell Metal-Organic Frameworks
Published on: February 10, 2023
Giant Five-Shell Polyoxometalate Cages and the Single-Cluster-Based Nanowire Superstructures
Wen-Zhu Yang1, Ya-Jie Liu2, Ming-Yue Wang1
1Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Institute of Physical Chemistry, College of Chemistry and Materials Science, Zhejiang Normal University, Jinhua 321004, China.
Abstract:
The preparation of polyoxometalate molecular cages has always been a long-term and challenging pursuit. In this work, we have successfully prepared two unprecedented giant heterogeneous POM-based purely inorganic molecular cages with Oh symmetry, which contain the aggregation of M6 (M = Ni, Co)-substituted trilacunary {PW9} and Mn-bridged {W4}. Sodium ions are used as templates to fill the cages. The polyanions of cages can be represented as {Na6(MnO6)12(W4O4)12[MnO4(OH2)]6(PW9Ni6O49H15)8} and {Na6(MnO6)12(W4O4)12[MnO4(OH2)]6(PW9Co6O49H15)8}. The entire structure can also be considered as a five-shell Na6@Mn12@{W4}12@Mn6@{PW9M6}8 arrangement. The electrostatic effects of sodium ions within the cages enhance the stability of the structures, allowing them to maintain a monodisperse and stable state in aqueous solutions. Interestingly, the cages assemble into nanowires through electrostatic contact with the cationic CTA+ ligand, demonstrating its flexible assembly capability at the single-cluster level. This giant POM inorganic molecular cage holds significant potential for application in the preparation of functional nanomaterials.
Related Concept Videos
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Valence Bond Theory
Metallic Solids
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...

