Metal Ion Selective Self-Assembly of a Ligand Functionalized Polymer into [1+1] Macrocyclic and Supramolecular Polymer Structures via Metal-Ligand Coordination

Macromol Rapid Commun. 2020 Jan;41(1):e1900305. doi: 10.1002/marc.201900305. Epub 2019 Aug 16.

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.

Keywords: [1+1] metallomacrocycle; metal-ligand coordination; supramolecular polymers.

MeSH terms

  • Coordination Complexes / chemistry*
  • Cyclization
  • Ions / chemistry
  • Ligands*
  • Metals / chemistry*
  • Polyethylene Glycols / chemistry
  • Polymers / chemistry*

Substances

  • Coordination Complexes
  • Ions
  • Ligands
  • Metals
  • Polymers
  • Polyethylene Glycols