Issue 75, 2019

Turning on ROP activity in a bimetallic Co/Zn complex supported by a [2+2] Schiff-base macrocycle

Abstract

Homo-dinuclear Co and Zn complexes derived from the macrocycle LH2, {[2-(OH)-5-(R)-C6H2-1,3-(CH)2][CH2CH2(2-C6H4N)2]}2 (R = Me, tBu), revealed near inactivity for the ring opening polymerization (ROP) of the cyclic esters δ-valerolactone (δ-VL) and ε-caprolactone (ε-CL). By contrast, the hetero-bimetallic complexes [LCo(NCMe)(μ-Br)ZnBr]·nMeCN (n = 3 or 3.25) were found to be efficient catalysts for the ROP of ε-CL and δ-VL.

Graphical abstract: Turning on ROP activity in a bimetallic Co/Zn complex supported by a [2+2] Schiff-base macrocycle

Supplementary files

Article information

Article type
Communication
Submitted
11 Jun 2019
Accepted
16 Aug 2019
First published
16 Aug 2019
This article is Open Access
Creative Commons BY license

Chem. Commun., 2019,55, 11279-11282

Turning on ROP activity in a bimetallic Co/Zn complex supported by a [2+2] Schiff-base macrocycle

K. Wang, T. J. Prior and C. Redshaw, Chem. Commun., 2019, 55, 11279 DOI: 10.1039/C9CC04494A

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