Parisa Mehrkhodavandi is a
Canadian chemist and Professor of Chemistry at the University of British Columbia (UBC).[1] Her research focuses on the design of new catalysts that can effect polymerization of sustainably sourced or biodegradable polymers.
Mehrkhodavandi pursued graduate studies at the
Massachusetts Institute of Technology under the supervision of
Richard R. Schrock. Her work at MIT focused on the synthesis of cationic
zirconium and
hafnium complexes bearing arylated diamidopyridine ligands,[5] and the polymerization of 1-hexene with these catalysts.[6][7][8] Mehrkhodavandi graduated with her Ph.D. in 2002.
Mehrkhodavandi’s research focuses on catalysis, where her group is pursuing new ligand design strategies. Her work has contributed to new synthetic routes for
biodegradable polymers,[11] and fundamental insights into polymerization mechanisms. Her group has a specific interest in the formation of catalysts, such as
chiraldinuclear indium complexes, that allow for
enantioselective organic reactions.[12][13][14][15] Mehrkhodavandi is also working on the development of
biodegradable polyesters using these ligands using cyclic
ester monomers. This is being done in three main ways: the first of which is the use of
Lewis acid metal centers with
chiral ligand supports to open cyclic
lactones via
ring-opening polymerizations.[16][17] The second is the use of a chiral indium salen catalyst that allows for more precise iso-selectivity similar to chiral aluminum salen catalysts, but with higher activity than aluminum catalysts. The final method utilizes an
ethoxy-bridged dinuclear indium catalyst[14] that allows for the creation of
diblock copolymers due to its high activity and selective control.
Mehrkhodavandi has patented salen indium catalysts for the ring-opening polymerization of cyclic ester monomers like lactides.[18][19][20]
Publications
Mehrkhodavandi has published a significant amount of publications over her career. In recent works, Mehrkhodavandi writes about the role of the first
alkoxide-bridged indium complex and the zinc analogues as important catalysts in the ring opening polymerization of lactides into
polylactic acid.[12] The article pertains to how the indium complex bearing either the chiral or achiral ligand allows for the polymerization of
racemic lactide into a highly
heterotactic polylactic acid and how the indium complex along with the chiral ligand polymerizes meso-
lactide into virtually atactic polylactic acid. Mehrkhodavandi discusses the mechanisms of these reactions in detail, along with the synthesis of the catalysts and activity of the resulting polymers. In another paper, Mehrkhodavandi writes about the use of an indium catalyst as a catalyst for lactide polymerization that has both high activity and high enantioselectivity - other lactide polymerizations feature either high activity or high enantioselectivity.[13] The results demonstrate site control as the primary factor behind the selectivity of the catalyst.
^US 9777023, Mehrkhodavandi, Parisa; Yu, Insun & Acosta-Ramirez, J. Alberto, "Dinuclear indium catalysts and their use for (Co)polymerization of cyclic esters", published 2017-10-03, assigned to
University of British Columbia
^US 10280185, Mehrkhodavandi, Parisa & Aluthge, Dinesh C., "Mononuclear salen indium catalysts and methods of manufacture and use thereof", published 2019-05-07, assigned to
University of British Columbia