A new, simple, and efficient strategy for the preparation of active antifungal biodegradable materials via ring-opening polymerization of l-lactide with zinc aryloxides.

Abstract

In this work, zinc aryloxides supported by monodentate hydroxybiphenyls [ArOH: ortho-phenylphenol (o-XenOH), meta-phenylphenol (m-XenOH), or para-phenylphenol (p-XenOH] and N,N,N',N'-tetramethylethylenediamine (TMEDA) were used to develop active polymeric materials for antifungal agents for agricultural use. The direct reaction of ligand precursor ArOH with ZnEt2 (1 : 2) in a toluene/TMEDA mixture (1 : 10) afforded a series of three isostructural monomeric compounds, namely [Zn(o-XenO)2(TMEDA)] (1), [Zn(m-XenO)2(TMEDA)] (2), and [Zn(p-XenO)2(TMEDA)] (3). These were characterized by single-crystal X-ray diffraction, and spectroscopic and other analytical methods. The results show that 1-3 are effective initiators for the ring-opening polymerization (ROP) of l-lactide (l-LA) via bifunctional activation of the monomer with Lewis pairs to give polymers terminated with TMEDA and Zn(OAr)2 as the α- and ω-chain ends, respectively. Combinations of ZnEt2 with two molar equivalents of ArOH proligands were used to synthesize polylactides containing fungicide molecules covalently bonded via ester linkers. The ROP of l-LA initiated by these zinc-based systems could be used for the preparation of polyesters with promising antifungal activities.