作者：Wang, Y,Zhao, W,Liu, XL,Cui, DM,Chen, EYX
关键字：ring-opening polymerization; n,o multidentate ligands; group-3 metal-complexes; cyclic esters; epsilon-caprolactone; rac-lactide; aluminum complexes; bulk-polymerization; racemic lactide; trimethylene carbonate
论文来源：期刊
具体来源：http://pubs.acs.org/doi/abs/10.1021/ma3007625
发表时间：2012年

A simple, inexpensive, and convenient catalyst system consisting of supporting ligand-free MgnBu2 in combination with an alcohol, isopropanol (iPrOH), benzyl methanol (PhCH2OH), diphenylmethanol (Ph2CHOH), or triphenylmethanol (Ph3COH), generates a convenient catalyst system to promote the polymerization of l-LA. In particular, the binary system MgnBu2/Ph2CHOH demonstrates an unprecedentedly high activity in the presence of a large excess amount of Ph2CHOH with the [OH]0/[Mg]0 ratio varying from 2 to 500, producing up to 500 polylactide (PLA) chains per Mg center and thus showing a typical nature of immortal polymerization. The molecular weights of the obtained PLAs with a broad range of monomer-to-metal ratios ([l-LA]0/[Mg]0 = 200–5000) are rather accurately controlled by the Ph2CHOH loading, relative to [Mg]0, while the molecular weight distributions remain nearly constant with polydispersity index (PDI) = 1.08–1.18. Moreover, the active polymerization intermediate has been isolated from the stoichiometric reaction between MgnBu2 and Ph2CHOH and structurally characterized as a tetranuclear complex, Mg4(Ph2CHO)8(THF)2 (1). Complex 1 remains the tetranuclear structure in solution or in the presence of excess Ph2CHOH as determined by 2D DOSY. On the basis of structural information about the active intermediates and polymerization kinetics, a coordination–insertion polymerization mechanism is proposed.