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Chemically and thermally stable permanently porous coordination cages are appealing candidates for separations, catalysis, and as the porous component of new porous liquids. However, many of these applications have not turned to microporous cages as a result of their poor solubility and thermal or hydrolytic stability. Here we describe the design and modular synthesis of iron and cobalt cages where the carboxylate groups of the bridging ligands of well-known calixarene capped coordination cages have been replaced with more basic triazole units. The resultingly higher M-L bond strengths afford highly stable cages that are amenable to modular synthetic approaches and potential functionalization or modification. Owing to the robust nature of these cages, they are highly processable and are isolable in various physical states with tunable porosity depending on the solvation methods used. As the structural integrity of the cages is maintained upon high activation temperatures, apparent losses in porosity can be mediated by resolvation and crystallization or precipitation.
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http://dx.doi.org/10.1039/d3dt03365a | 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 PDFAdv Mater
September 2025
Instituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico, Universitat de València-Universitat Politècnica de València, Camino de Vera s/n, Valencia, 46022, Spain.
Bioorthogonal chemistry that can be controlled through near-infrared (NIR) light is a promising route to therapeutics. This study proposes a method to intracellularly photoactivate prodrugs using plasmonic gold nanostars (AuNSt) and NIR irradiation. Two strategies are followed.
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 PDFBiomed Eng Lett
September 2025
Department of Mechanical Engineering, Sejong University, 209, Neungdong-Ro, Gwangjin-gu, Seoul, 05006 Republic of Korea.
Cage subsidence is a common complication following transforaminal lumbar interbody fusion (TLIF) that can lead to poor clinical outcomes, including recurrent pain and segmental instability. Conventional TLIF cage designs often fail to distribute stress evenly, increasing the risk of endplate damage and subsequent subsidence. This study aims to evaluate the effect of a modified TLIF cage with upper and lower open windows (lattice structure) in reducing cage subsidence in patients with lumbar degenerative disc disease (LDDD).
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