4.7 Article

Ligand-Free Magnesium Catalyst System: Immortal Polymerization of L-Lactide with High Catalyst Efficiency and Structure of Active Intermediates

Journal

MACROMOLECULES
Volume 45, Issue 17, Pages 6957-6965

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma3007625

Keywords

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Funding

  1. National Natural Science Foundation of China [20904051, 51021003]
  2. U.S. National Science Foundation [NSF-1012326]
  3. State Key Lab of Rare-Earth Sources Utilization

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A simple, inexpensive, and convenient catalyst system consisting of supporting ligand-free (MgBu2)-Bu-n in combination with an alcohol, isopropanol ((PrOH)-Pr-i), 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 (MgBu2)-Bu-n/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 (MgBu2)-Bu-n and Ph2CHOH and structurally characterized as a tetranuclear complex, Mg-4(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.

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