posted on 2020-03-30, 17:08authored byShazia Soobrattee, Xiaofang Zhai, Kudzanai Nyamayaro, Carlos Diaz, Paul Kelley, Tannaz Ebrahimi, Parisa Mehrkhodavandi
We report imine-
and amine-based dinucleating ligands bearing a
bisphenol backbone and explore their coordination chemistry with zinc
to form zinc alkyl, alkoxide, acetate, and amide complexes. Full characterization
of the complexes shows that this ligand framework can support dinuclear
and trinuclear complexes. We explore the reactivity of the zinc alkyl
and alkoxide complexes as catalysts for the ring opening polymerization
of lactide and compared this reactivity to analogous mononuclear complexes.
We show that 1) The amine-based complexes are more reactive than the
imine-based analogues; 2) The trinuclear zinc alkyl species show unusual
control and reproducibility for lactide polymerization; and 3) The
extent of bimetallic cooperation is hampered by the ability of the
ligand framework to form trinuclear clusters.