P,O-Phosphinophenolate zinc(ii) species: Synthesis, structure and use in the ring-opening polymerization (ROP) of lactide, ε-caprolactone and trimethylene carbonate

Christophe Fliedel, Vitor Rosa, Filipa M. Alves, Ana M. Martins, Maria Teresa Avilés, Samuel Dagorne

Research output: Contribution to journalArticlepeer-review

44 Citations (Scopus)

Abstract

The P,O-type phosphinophenol proligands (1·H, 2-PPh2-4-Me-6-Me-C6H2OH; 2·H, 2-PPh2-4-Me-6-tBu-C6H2OH) readily react with one equiv. of ZnEt2 to afford in high yields the corresponding Zn(ii)-ethyl dimers of the type [(κ2-P,O)Zn-Et]2 (3 and 4) with two μ-OPh bridging oxygens connecting the two Zn(ii) centers, as determined by X-ray diffraction (XRD) studies in the case of 3. Based on diffusion-ordered NMR spectroscopy (DOSY), both species 3 and 4 retain their dimeric structures in solution. The alcoholysis reaction of Zn(ii) alkyls 3 and 4 with BnOH led to the high yield formation of the corresponding Zn(ii) benzyloxide species [(κ2-P,O)Zn-OBn]2 (5 and 6), isolated in a pure form as colorless solids. The centrosymmetric and dimeric nature of Zn(ii) alkoxides 5 and 6 in solution was deduced from DOSY NMR experiments and multinuclear NMR data. Though the heteroleptic species 5 is stable in solution, its analogue 6 is instable in CH2Cl2 solution at room temperature to slowly decompose to the corresponding homoleptic species 8 via the transient formation of (κ2-P,O)2Zn2(μ-OBn)(μ-κ11-P,O) (6′). Crystallization of compound 6 led to crystals of 6′, as established by XRD analysis. The reaction of ZnEt2 with two equiv. of 1·H and 2·H allowed access to the corresponding homoleptic species of the type [Zn(P,O)2] (7 and 8). All gathered data are consistent with compound 7 being a dinuclear species in the solid state and in solution. Data for species 8, which bears a sterically demanding P,O-ligand, are consistent with a mononuclear species in solution. The Zn(ii) alkoxide species 5 and the [Zn(P,O)2]-type compounds 7 and 8 were evaluated as initiators of the ring-opening polymerization (ROP) of lactide (LA), ε-caprolactone (ε-CL) and trimethylene carbonate (TMC). Species 5 is a well-behaved ROP initiator for the homo-, co- and ter-polymerization of all three monomers with the production of narrow disperse materials under living and immortal conditions. Though species 7 and 8 are ROP inactive on their own, they readily polymerize LA in the presence of a nucleophile such as BnOH to produce narrow disperse PLA, presumably via an activated-monomer ROP mechanism.

Original languageEnglish
Pages (from-to)12376-12387
Number of pages12
JournalDalton Transactions
Volume44
Issue number27
DOIs
Publication statusPublished - 21 Jul 2015

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