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Metal ion selective self-assembly of a ligand functionalized polymer into [1+1] macrocyclic and dupramolecular polymer structures via metal-ligand coordination

Authors
  • Xu, Xiaowen
  • Van Guyse, Joachim
  • Jerca, Valentin-Victor
  • Hoogenboom, Richard
Publication Date
Jan 01, 2020
Identifiers
DOI: 10.1002/marc.201900305
OAI: oai:archive.ugent.be:8638851
Source
Ghent University Institutional Archive
Keywords
Language
English
License
Unknown
External links

Abstract

The design and synthesis of polymer-based metallomacrocycles relying on metal-ligand interactions remain a challenge in the polymer field. Instead of utilizing chemical reactions to synthesize macrocycles, a general approach is proposed to construct metallomacrocyclic structures through supramolecular self-assembly of a specific macroligand with suitable transition metal ions. Therefore, a new ditopic macroligand (L) consisting of PEG end-capped with 2,6-bis(1,2,3-triazol-4-yl)pyridine derivatives is prepared via CuAAC "click" reaction. Four types of metal (Fe2+, Zn2+, Ni2+, and Cu2+) complexes are obtained by simply mixing a solution of metal ions and L in appropriate concentrations. The investigation of the coordination chemistry suggests that coordination of L with Cu2+ results in the formation of a [1+1] metallomacrocycle, while the other metal complexes exclusively lead to the formation of linear metallopolymers and/or larger aggregates. This work provides new insights into designing metallomacrocycles and may have potential application in the synthesis of catenanes and other cyclic or cycle-based topological architectures.

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