Synthesis, structure and ROP capability of a tetra(amidine)bis(zirconium) calix[8]arene complex

The tetra(amidine)bis(zirconium) calix[8]arene complex {Zr[NHC(Me)NMe 2 ] 2 } 2 , formed via acetonitrile insertion into Zr–N bonds, is an active catalyst for the ring opening polymerization (ROP) of the cyclic esters ε-caprolactone and δ-valerolactone.

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Publication Details

Journal
New Journal of Chemistry
Published
2025-12-22
DOI
https://doi.org/10.1039/d5nj04144a
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
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article

Synthesis, structure and ROP capability of a tetra(amidine)bis(zirconium) calix[8]arene complex

Mark Robert James Elsegood, Carl Redshaw, William Clegg
New Journal of Chemistry
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
article

Synthesis, structure and ROP capability of a tetra(amidine)bis(zirconium) calix[8]arene complex

Mark Robert James Elsegood, Carl Redshaw, William Clegg
article en

Abstract

The tetra(amidine)bis(zirconium) calix[8]arene complex {Zr[NHC(Me)NMe 2 ] 2 } 2 , formed via acetonitrile insertion into Zr–N bonds, is an active catalyst for the ring opening polymerization (ROP) of the cyclic esters ε-caprolactone and δ-valerolactone.

New Journal of ChemistryVol. 50(3)
Loughborough University (GB), Tokyo Metropolitan University (JP), Newcastle University (GB)
Openalex Percentile: Top 34%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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