Highly selective and immortal magnesium calixarene complexes for the ring-opening polymerization of rac-lactide

Mark J. Walton, Simon J. Lancaster, Carl Redshaw

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57 Citations (Scopus)


The lithiation of 1,3-dipropoxy-p-tert-butylcalix[4]arene (LH2) followed by reaction with nBuMgBr in THF resulted in the formation of the hetero-bimetallic complex [Li(THF)Mg(nBu)L] (1). By contrast, the treatment of tripropoxy-p-tert-butylcalix[4]arene (L′H) with nBu2Mg afforded a mononuclear complex [L′Mg(nBu)] (2). Single-crystal XRD studies revealed that in both structures the calix[4]arene adopts a cone conformation, and a Li cation resides in the cavity for 1. Both 1 and 2 were active for the ring-opening polymerisation of rac-lactide. Compound 2 displayed not only exceptional activity (100 equivalents, 3 min, 92 % conversion, BnOH, room temperature) but also high selectivity (probability to form an r dyad, Pr=0.85) and exhibited an immortal character in THF. Surprisingly, compound 2 also showed isotactic bias (Pr=0.30–0.36) and an immortal character if toluene was employed as the solvent; 2 D J-resolved 1H NMR spectroscopy was employed for the assignment of the stereoselectivity.
Original languageEnglish
Pages (from-to)1892-1898
Number of pages7
Issue number7
Publication statusPublished - 1 Jul 2014


  • calixarenes
  • heterometallic complexes
  • magnesium
  • NMR spectroscopy
  • ring-opening polymerization

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