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Updated: Jan 12, 2026

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in PolyS-Divinylbenzene
Published on: May 20, 2019
Successive Sulfur Oxidation Directs Topological Transformation From 41 Knot to 6 3 2 $6_3^2$ Link
Yan Zou1, Shu-Jin Bao1, Haitong Tang1
1Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Department of Chemistry, Fudan University, Shanghai, 200433, P. R. China.
Abstract:
Achieving transformation between different types of topologies remains a challenge in supramolecular chemistry. Herein, sulfur oxidation was utilized as the stimuli to trigger topological transformations from knots to links. The process began with a thioether-type precursor, M (41 metallic knot), which was synthesized by self-assembling the sulfur-bridged ligand L with building block B in high yield. Following oxidation reactions, we successfully transformed the octanuclear 41 metallic knot (M) with four crossing points into a sulfoxide-type dodecanuclear metallic link (M-O) with six crossing points as an intermediate product, and then to a sulfone-type dodecanuclear metallic link (M-2O) with six crossing points, which achieves a dual leap in both metal nuclearity and crossing complexity. Remarkably, the key to the transformation lies in using the embedded S-centres of M as molecular triggers and stepwise oxidation (-S-→-S(O)-→-S(O)2-) enabled precise modulation of the geometric configuration of the sp3 S-centres, drastically altering the range of accessible coordination vectors and inducing conformational self-adaptation among components. This strategy establishes a novel oxidation-mediated interconversion paradigm among complex topologies, offering new insights for designing dynamic molecular triggers in intelligent material systems.
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