Issue 23, 2022

Use of heterometallic alkali metal–magnesium aryloxides in ring-opening polymerization of cyclic esters

Abstract

In this work, alkali metal–magnesium aryloxides [Mg2Li2(MesalO)6] (1), [Mg2Na2(MesalO)6(THF)x] for x = 2 or 4 (2), and [Mg2K2(MesalO)6(THF)4] (3) derived from the reaction of MgnBu2 and nBuLi, metallic Na or K with methyl salicylate (MesalOH) were used as molecular platforms for the synthesis of new heterometallic compounds [Mg2Li2(EtsalO)6] (4), [MgK(EtsalO)3]n (5), [Mg6Na4Al(MesalO)13(OH)6(MesalOH)(THF)0.5(H2O)0.5] (6), and [Mg4Na2(MesalO)6(SalO)2(THF)4] (7) (EtsalOH = ethyl salicylate and SalOH2 = salicylic acid) by the reaction with EtOH, exposure to atmospheric moisture or addition of stoichiometric quantities of water. Compounds 4 and 5 were synthesized by transesterification of 1 and 3. Cluster 6 was formed haphazardly by exposing a THF solution of 2 derived using MgnBu2 stabilized with 1 wt% AlEt3 to atmospheric moisture. Compound 7 was synthesized by partial hydrolysis of 2. Homometallic magnesium aryloxide [Mg4(MesalO)4(OMe)4(HOMe)4] (8) was obtained by reaction of MgnBu2 and MesalOH in a methanol solution. The catalytic activity of 1–3 and 6–8 was investigated in the ring-opening polymerization (ROP) of L-lactide (L-LA) or benzaldehyde Tishchenko reaction.

Graphical abstract: Use of heterometallic alkali metal–magnesium aryloxides in ring-opening polymerization of cyclic esters

Supplementary files

Article information

Article type
Paper
Submitted
07 Mar 2022
Accepted
30 May 2022
First published
30 May 2022
This article is Open Access
Creative Commons BY license

Dalton Trans., 2022,51, 9144-9158

Use of heterometallic alkali metal–magnesium aryloxides in ring-opening polymerization of cyclic esters

R. Petrus, T. Lis and A. Kowaliński, Dalton Trans., 2022, 51, 9144 DOI: 10.1039/D2DT00731B

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