Heterodinuclear complexes featuring Zn(ii) and M = Al(iii), Ga(iii) or In(iii) for cyclohexene oxide and CO2 copolymerisation

The ring opening copolymerisation of CO2 and epoxides is a useful means to valorise waste emissions and to reduce pollution in polymer manufacturing. Heterodinuclear catalysts, particularly those of Zn(ii)/Mg(ii), have shown better performances than homodinuclear analogues in this reaction. As part...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2020-01, Vol.49 (1), p.223-231
Hauptverfasser: Deacy, Arron C, Durr, Christopher B, Williams, Charlotte K
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Sprache:eng
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Zusammenfassung:The ring opening copolymerisation of CO2 and epoxides is a useful means to valorise waste emissions and to reduce pollution in polymer manufacturing. Heterodinuclear catalysts, particularly those of Zn(ii)/Mg(ii), have shown better performances than homodinuclear analogues in this reaction. As part of on-going efforts to better understand the catalytic synergy, this work describes a series of heterodinuclear complexes, combining Zn(ii) with a metal from Group 13 (M = Al(iii), Ga(iii) or In(iii)). The complexes are synthesised from a symmetrical macrocyclic ligand in high yields via sequential metalation steps and are the thermodynamic reaction products. The Zn(ii)/Group 13 complexes are effective homogeneous catalysts for the ring opening copolymerisation (ROCOP) of cyclohexene oxide at 1 bar pressure of carbon dioxide, but all show inferior performances compared to the di-zinc analogue. The CO2 uptake into the polymer increases in the order Al(iii) < Ga(iii) < In(iii) which is attributed to lower Lewis acidity heavier Group 13 homologues showing a reduced tendency to form ether linkages. Concurrently, polycarbonate activity increases down the Group 13 series consistent with weaker metal–oxygen bonds which show enhanced lability to insertion reactions.
ISSN:1477-9226
1477-9234
DOI:10.1039/c9dt02918d