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Updated: May 19, 2026

Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers
Published on: May 12, 2023
Discrete and extended supersandwich structures based on weak interactions between phosphorus and mercury
Martin Fleischmann1, Claudia Heindl, Michael Seidl
1Institut für Anorganische Chemie, Universität Regensburg, 93040 Regensburg, Germany.
New research shows supersized mercury adducts form complex polymeric or discrete supersandwich structures. These structures arise from specific interactions between mercury and phosphorus-containing molecules in the solid state.
Area of Science:
- Organometallic Chemistry
- Solid-State Chemistry
- Supramolecular Chemistry
Background:
- Mercury complexes are known for diverse structural motifs.
- Triple-decker complexes offer unique coordination environments.
- Understanding intermolecular interactions is key to designing novel materials.
Purpose of the Study:
- To investigate the solid-state adduct formation between a trinuclear mercury complex and a triple-decker complex.
- To characterize the resulting polymeric and discrete supersandwich structures.
- To elucidate the role of intermolecular interactions in adduct assembly.
Main Methods:
- Solid-state reaction of [(o-C(6)F(4)Hg)(3)] and [(CpMo)(2)(μ-η(6):η(6)-P(6))].
- Single-crystal X-ray diffraction analysis to determine the structures of the adducts.
- Analysis of intermolecular P···Hg interactions.
Main Results:
- Formation of "supersized" mercury adducts in the solid state.
- Observation of both polymeric and discrete supersandwich structural arrangements.
- Identification of significant P···Hg interactions driving the assembly.
Conclusions:
- The reaction between the trinuclear mercury complex and the triple-decker complex yields novel supramolecular architectures.
- Intermolecular P···Hg interactions are crucial for the formation of these "supersized" adducts.
- This study highlights the potential for designing complex solid-state structures through directed intermolecular forces.
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