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Functionalization of permanently porous coordination cages has been used to tune phase, surface area, stability, and solubility in this promising class of adsorbents. For many cages, however, these properties are intricately tied together, and installation of functional groups, for example, to increase solubility often leads to a decrease in surface area. Calixarene-capped cages offer the advantage in that they are cluster-terminated cages whose solid-state packing, and thus surface area, is typically governed by the nature of the capping ligand rather than the bridging ligand. In this work we investigate the influence of ligand functionalization on two series of isoreticular Ni(II)- and Co(II)-based calixarene-capped cages. The two types of materials described are represented as octahedral and rectangular prismatic coordination cages and can be synthesized in a modular manner, allowing for the substitution of dicarboxylate bridging ligands and the introduction of functional groups in specific locations on the cage. We ultimately show that highly soluble cages can be obtained while still having access to high surface areas for many of the isolated phases.
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http://dx.doi.org/10.1021/acs.inorgchem.0c03554 | DOI Listing |
J Am Chem Soc
September 2025
Department of Chemistry, National Taiwan University, Taipei 106319, Taiwan.
The exclusive formation of artificial multicomponent assemblies remains a significant challenge, in contrast to the well-established organization observed in natural systems, due to intrinsic entropic constraints. To overcome this limitation, recent efforts have been focused on developing precision self-assembly strategies for the rational construction of such architectures. Here, we construct an ideal complementary pair of 2,2':6',2″-terpyridine (tpy)-based ligands by fine-tuning the substituent bulkiness, which enables the quantitative formation of robust nested cages through efficient dynamic heteroleptic complexation with multivalent coordination.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
September 2025
University of the Free State, Chemistry Department, Bloemfontein, South Africa.
The crystal structure of a nitrate anion caged in spherical vanadium and oxygen structure surrounded by sodium hy-droxy and water solvent mol-ecules, systematic name poly[[hepta-deca-aqua-tetra-deca-oxidonona-sodium][penta-cosa-aqua-nitratoundeca-oxido-penta-deca-vanadium]], HNNaOV is reported. The complex crystallizes in the non-centrosymmetric space group and exhibits many inter- and intra-molecular hydrogen-bonding inter-actions. The complex contains V and V centres, which are six-coordinate or octa-hedrally coordinated.
View Article and Find Full Text PDFNatl Sci Rev
September 2025
Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, China.
Precision in controlling the microenvironment of nanospaces is a potent strategy for exploring architecture‒function relationships. Herein, a face-capped tetrahedral cage, featuring Pd‒Pd-bonded vertices, with a tailored nanospace surrounded by 12 ethyl units, was facilitated to adaptively accommodate a library of guests with different sizes and shapes, including C6 cyclic hydrocarbons, adamantane derivatives, S and P. This nanocavity can achieve strong binding with cyclohexane in non-aqueous media in contrast to reported structurally similar non--functionalized cages by an increase of four orders of magnitude.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, G1 1RX, UK.
Porous metal-organic polyhedra (MOPs) have strong covalent and coordinate bonds that define the intrinsic pore of the cage. The intermolecular interactions between cages tend to be weaker, such that they rearrange during the solvent exchange process preceding gas sorption measurements. The reduction in crystal size that this often causes limits the availability of structural data that could enable understanding of observed gas uptake.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
STFC Scientific Computing Department, Daresbury Laboratory, Keckwick Lane, Daresbury, Warrington, WA4 4AD, UK.
Silica polymorphs and zeolites are fundamental to a wide range of mineralogical and industrial applications owing to their diverse structural characteristics and thermodynamic and mechanical stability under varying conditions. Computational modelling has played a crucial role in understanding the relationship between the structure and functionality of silicas and silicates, including zeolites. In this study, we apply the MACE machine learnt interatomic potentials (MACE MP) to model the framework energies of siliceous zeolites and examine the phase transitions of silica and silicalite polymorphs under high-pressure conditions.
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