AbstractsChemistry

Studies of single-site zinc, magnesium and calcium catalyst precursors for ring-opening polymerization of lactides

by Khamphee Phomphrai




Institution: The Ohio State University
Department: Chemistry
Degree: PhD
Year: 2003
Keywords: Lactide polymerization; Single-site catalyst; Calcium catalyst; Magnesium catalyst; Heterotactic polylactide; Stereoselective polymerization
Record ID: 1739023
Full text PDF: http://rave.ohiolink.edu/etdc/view?acc_num=osu1061244312


Abstract

Polyesters derived from the ring-opening polymerization (ROP) of lactides formed from inexpensive renewable resources constitute one important class of biodegradable and biocompatible polymers. Herein, the preparation and characterization of a series of closely related magnesium and zinc compounds that are active for ROP of lactides are reported using three ß-diiminate ligands L<sup>1</sup>, L<sup>2</sup> and L<sup>3</sup> where L<sup>1</sup> = CH(CMeNC<sub>6</sub>H<sub>3</sub>-2,6-<sup>i</sup>Pr<sub>2</sub>)<sub>2</sub>, L<sup>2</sup> = CH(CMeNC<sub>6</sub>H<sub>4</sub>-2-<sup>t</sup>Bu)<sub>2</sub> and L<sup>3</sup> = CH(CMeNC<sub>6</sub>H<sub>4</sub>-2-OMe)<sub>2</sub>. For the L<sup>1</sup> ligand, L<sup>1</sup>Mg(N<sup>i</sup>Pr<sub>2</sub>)•(THF), L<sup>1</sup>Zn(N<sup>i</sup>Pr<sub>2</sub>), L<sup>1</sup>Mg(O<sup>t</sup>Bu)•(THF), L<sup>1</sup>Zn(O<sup>t</sup>Bu) and L<sup>1</sup>Zn(OSiPh<sub>3</sub>)•(THF) have been synthesized. All compounds initiate and sustain ROP of lactides. For a related series L<sup>1</sup>MX(THF)<sub>n</sub>, where n = 0 or 1, the reactivity follows the order M = Mg > Zn and X = O<sup>t</sup>Bu > N<sup>i</sup>Pr<sub>2</sub> > N(SiMe<sub>3</sub>)<sub>2</sub> > OSiPh<sub>3</sub>. Heterotactic polylactide (PLA) is produced from ROP of rac-lactide by the zinc catalysts in CH<sub>2</sub>Cl<sub>2</sub>. The magnesium catalysts produce atactic and heterotactic PLA in CH<sub>2</sub>Cl<sub>2</sub> and THF, respectively. The resting states for Zn and Mg are proposed to be L<sup>1</sup>Zn(¿<sup>2</sup>-OCHMeC(O)OP) and L<sup>1</sup>Mg(µ-OP)<sub>2</sub>MgL<sup>1</sup>. For the L<sup>2</sup> ligand, L<sup>2</sup>MgN<sup>i</sup>Pr<sub>2</sub>•(THF) and L<sup>2</sup>ZnN<sup>i</sup>Pr<sub>2</sub> are prepared. In solution, L<sup>2</sup>ZnN<sup>i</sup>Pr<sub>2</sub> exists as a mixture of syn- and anti-rotamers while L<sup>2</sup>MgN<sup>i</sup>Pr<sub>2</sub>•(THF) exists only as a syn-rotamer. In the zinc compound, the syn-conformer is shown to be more reactive than the anti–conformer and is responsible for the polymerization. Heterotactic PLA is obtained in CH<sub>2</sub>Cl<sub>2</sub> for the zinc compound and in THF for the magnesium compound. For the L<sup>3</sup> ligand, L<sup>3</sup>MgN(SiMe<sub>3</sub>)<sub>2</sub>, [L<sup>3</sup>MgO<sup>t</sup>Bu]<sub>2</sub>, L<sup>3</sup>ZnN(SiMe<sub>3</sub>)<sub>2</sub>, L<sup>3</sup>ZnO<sup>i</sup>Pr and L<sup>3</sup>CaN(SiMe<sub>3</sub>)<sub>2</sub>•(THF) are prepared. The OMe groups of ligand L<sup>3</sup> show little affinity toward zinc and in the ROP of rac-lactide give PLA with only moderately enhanced heterotactic tetrads. The OMe groups are shown to bind to Mg reversibly and display significant enhancement of heterotactic PLA. Herein, the first single-site calcium complexes of L<sup>1</sup> and tris(pyrazolyl/indazolyl)borate ligands are reported and shown to initiate and sustain ROP of lactide: L<sup>1</sup>CaNR<sup>1</sup><sub>2</sub>•(THF), Tp<sup>R2</sup>CaNR<sup>1</sup><sub>2</sub>•(THF)<sub>n</sub>,…