Abstract
Using dialkylgallium alkoxides with N-hetrocyclic carbenes (Me(2)GaOR(NHC)) for the ring-opening polymerization of rac-lactide, we have demonstrated the effect of the chelate interaction between the growing PLA chain and gallium on the stereoselectivity of dialkylgallium alkoxide propagating species - Me(2)Ga(OPLA)(NHC). In order to do so, we have conducted the structure-activity studies of both Me(2)Ga(OCH(2)CH(2)OMe)(NHC) (NHC = SIMes (1) and IMes (2)) and Me(2)Ga(OCH(Me)CO(2)Me)(NHC) (NHC = SIMes (3) and IMes (4)), the latter mimicking active species in the ROP of lactide with growing PLA chain. Based on VT NMR and FTIR spectroscopy, the effect of toluene, CH(2)Cl(2) and THF on the structure of 3 and 4 have been demonstrated, especially with regard to the interaction of methyl lactate ligand with gallium. In a combination with the latter, the studies on the activity of 1 and 2 in the ROP of rac-LA, in different solvents, and at temperatures between -40 °C and 40 °C, have shown the extent of the chelation effect on the isoselectivity of Me(2)Ga(OPLA)(NHC) in the ROP of rac-LA, which varied between P (m) of 0.75 and 0.89 depending on the polymerization conditions. Both the latter, and the contribution resulting from the structure of Me(2)Ga(OPLA)(NHC) (P (m) = 0.75) have been decisive for the total isoselectivity observed under specific conditions. Our finding represents the first evidence demonstrating that the chelation effect, resulting from the weak interaction between the growing PLA chain and the metal centre, can be responsible for the enhancement of stereoselectivity in the ROP of rac-LA with metal alkoxide propagating species. It should remain of interest, especially in the case of metal based catalysts, which are able to carry out the stereoselective polymerization of rac-LA at mild conditions, under which the chelation effect can manifest itself.