Inorganic Chemistry· 2026Q1
Beyond Structural Analogy: Electronic and Functional Divergence in Isostructural Zr, Hf, and Th Metal–Organic Frameworks
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- 2026year
Short summary
Th6-ADC metal–organic frameworks exhibit distinct optical, electronic, and functional properties compared to their isostructural Zr and Hf analogues, despite nearly identical structures.
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Key points
- Isostructural M6-ADC frameworks (M=Zr, Hf, Th) were synthesized and compared.
- Th6-ADC exhibits unique red coloration and extended visible-to-near-infrared absorption compared to Zr and Hf analogues.
- A pronounced ligand-centered radical signature was observed in Th6-ADC.
- Th6-ADC shows enhanced photothermal conversion under near-infrared irradiation.
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract Zr(IV), Hf(IV), and Th(IV) exhibit closely related coordination chemistry and can form structurally analogous materials, underpinning the widespread use of Zr as a nonradioactive surrogate for Th(IV). Here we demonstrate that such structural analogy does not necessarily extend to electronic and functional properties through a comparative study of three isostructural M6-ADC (M = Zr, Hf, and Th;ADC = 9,10-anthracenedicarboxylate) metal–organic frameworks. Despite their nearly identical framework structures, Th6-ADC exhibits optical and electronic characteristics distinct from its Zr and Hf analogues, including distinctive red coloration, extended visible-to-near-infrared absorption, and a pronounced ligand-centered radical signature. These electronic differences are further manifested in their functional behavior, with Th6-ADC displaying substantially enhanced photothermal conversion under near-infrared irradiation. These results reveal a clear divergence between structural and electronic similarity among Zr-, Hf-, and Th-based frameworks.
The authors' abstract, as published at the source. Inorganic Chemistry, 2026 · DOI ↗
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Field: Inorganic Chemistry
Inorganic ChemistryChemistry