Copper and manganese diazacalix[4]arene complexes: structural and cytotoxicity studies and use in ring opening polymerization of ε-caprolactone and δ-valerolactone

Abstract

From reactions of M(OAc)2•nH2O (M = Cu, Mn) or Cu(NO3)2•3H2O with p-methyl-N,N'-dimethyldiazacalix[4]areneH4 (p-MeLH4) under aerobic conditions, rare examples of azacalixarene-3d-metal complexes were isolated. These, thermally stable non-toxic compounds (≤ µM IC50 values) were screened as catalysts for the ring opening polymerization of the cyclic esters ε-caprolactone (ε-CL) and δ-valerolactone (δ-VL) affording low molecular weight cyclic or linear (H/OH end group) polymers. The Mn-based system exhibited the higher activity.

Supplementary files

Article information

Article type
Communication
Submitted
10 Feb 2026
Accepted
08 Apr 2026
First published
14 Apr 2026
This article is Open Access
Creative Commons BY license

Chem. Commun., 2026, Accepted Manuscript

Copper and manganese diazacalix[4]arene complexes: structural and cytotoxicity studies and use in ring opening polymerization of ε-caprolactone and δ-valerolactone

A. C. Razieh, C. Redshaw, H. C. Sample, E. B. Hobson, T. J. Prior and A. Mueller, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC00888G

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