Issue 34, 2013

Synthesis of binuclear phenoxyimino organoaluminum complexes and their use as the catalyst precursors for efficient ring-opening polymerisation of ε-caprolactone

Abstract

A series of novel binuclear phenoxyimino organoaluminum complexes of the type [(RN[double bond, length as m-dash]CH)C6H3OAlMe2]2 [R = C6H5 (2a), 2,6-iPr2C6H3 (2b), 2,6-Ph2C6H3 (2c), adamantyl (2d), tBu (2e)] have been prepared in high yields, and these complexes were identified by 1H, 13C NMR and elemental analysis. Structural analysis for 2a–e revealed that these complexes have a distorted tetrahedral geometry around Al and both the Al–O and the Al–N bond distances were considerably influenced by substituents in the imino groups. The complexes were tested as catalyst precursors for ring-opening polymerisation (ROP) of ε-caprolactone (CL) in the presence of BnOH, and their catalytic activities were strongly affected by the catalyst structures and polymerisation conditions. An efficient living ROP has been achieved using the 2b/BnOH system.

Graphical abstract: Synthesis of binuclear phenoxyimino organoaluminum complexes and their use as the catalyst precursors for efficient ring-opening polymerisation of ε-caprolactone

Supplementary files

Article information

Article type
Paper
Submitted
31 Jan 2013
Accepted
27 Jun 2013
First published
03 Jul 2013

Dalton Trans., 2013,42, 12346-12353

Synthesis of binuclear phenoxyimino organoaluminum complexes and their use as the catalyst precursors for efficient ring-opening polymerisation of ε-caprolactone

H. Han, Y. Liu, J. Liu, K. Nomura and Y. Li, Dalton Trans., 2013, 42, 12346 DOI: 10.1039/C3DT50264C

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