Ring-opening polymerization of ε-caprolactone with a macrocyclic tetracarbene indium complex

Abstract

The first chiral tetracarbene indium(III) complexes have been synthesized by employing a rigid dianionic macrocyclic tetra-NHC ligand. The macrocyclic indium tetra-NHC bromide and ethoxide complexes are structurally similar to analagous salen complexes. The indium ethoxide complex effectively promotes living ring-opening polymerization of ε-caprolactone at room temperature.

Graphical abstract: Ring-opening polymerization of ε-caprolactone with a macrocyclic tetracarbene indium complex

Supplementary files

Article information

Article type
Communication
Submitted
15 Nov 2024
Accepted
04 Dec 2024
First published
17 Dec 2024

Dalton Trans., 2025, Advance Article

Ring-opening polymerization of ε-caprolactone with a macrocyclic tetracarbene indium complex

H. R. Brothers, R. Chambenahalli, G. S. Nichol, J. A. Garden and D. M. Jenkins, Dalton Trans., 2025, Advance Article , DOI: 10.1039/D4DT03198A

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