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  4. TMPMgnBu(L), where L = THF, 2-MeTHF, pyridine and dimethylaminopyridine and TMP = 1,5,9-trimesityldipyrromethene: Reaction with lactide and ε-caprolactone
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TMPMgnBu(L), where L = THF, 2-MeTHF, pyridine and dimethylaminopyridine and TMP = 1,5,9-trimesityldipyrromethene: Reaction with lactide and ε-caprolactone

Author(s)
Balasanthiran, Vagulejan
Chisholm, Malcolm H.
Choojun, Kittisak
Durr, Christopher B.
Jing, Stanley
Wambua, Pasco M.
Date Issued
January 1, 2017
Type
Article
DOI
10.1016/j.jorganchem.2017.05.016
Abstract
The compounds TMPMgnBu(L), where L = THF, 2-MeTHF, pyridine (py) and dimethylaminopyridine (DMAP) and TMP = 1,5,9-trimesityldipyrromethene, have been synthesized and allowed to initiate polymerization with rac-lactide (rac-LA) and ε-caprolactone (ε – CL). Both the rate of rac-LA polymerization and the tacticity were found to be solvent dependent, with CH2Cl2 being faster than THF and yielding heterotactic polylactic acid with Pr ∼70% and 95%, respectively. For ε-CL, rates of polymerization were in the inverse order with THF being faster than CH2Cl2. In CH2Cl2 the reactions showed a dependence on the coordinating ligand with rates, 2-MeTHF > THF > py > DMAP in the polymerization of rac-LA and ε-CL. The molecular structure of TMPMgnBu(2-MeTHF) was shown to contain a trigonally distorted tetrahedron of TMPMg(nBu) with a weak axial Mg—-2-MeTHF bond.
Citation
Journal of Organometallic Chemistry, 842, 74-81, 2017
Subjects

Caprolactone

Polylactide

Ring opening polymeri...

Solvent effect

Tacticity

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