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Zinc complexes supported by maltolato ligands : synthesis, structure, solution behavior, and application in ring-opening polymerization of lactides.
Autorzy
Rok wydania
2012
Czasopismo
Numer woluminu
31
Strony
4755-4762
DOI
10.1021/om300321h
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
A series of novel zinc alkoxides supported by chelating maltolato (MalO; MalOH = maltol) ligands were successfully synthesized and characterized. Reaction of MalOH with ZnEt2 (3:4) gives a trinuclear cluster [Zn3(Et)2(MalO)4] (1), which spontaneously disproportionates in solution to mononuclear species [Zn(MalO)2] (1a) and [Zn(Et)(MalO)] (1b); (1a) and (1b) form [Zn(MalO)2(py)] (2), [Zn(Et)(MalO)(py)] (3), [Zn(MalO)2]2 ((1a)2), [Zn(MalO)(OBn)]2 ((1c)2), and [Zn4(Et)2(OEt)2(MalO)4] (4) on addition of pyridine, benzyl alcohol (BnOH), or dry O2, respectively. Compounds 1, 2, (1a)2, and 4 were characterized by elemental analysis, NMR, ESI-MS, and single-crystal X-ray structural analysis. Variable-temperature NMR experiments showed that (1a)2 and (1c)2 are in equilibrium with the monomeric form in solution. The addition of l-lactide (l-LA) to a combination of 1 and 2 equiv of BnOH in dichloromethane at room temperature in different molar ratios leads to rapid and efficient generation of poly(l-LA) with end-capped BnO groups. According to kinetic studies, propagation by [Zn(OBn)(MalO)] (1c) is first-order with respect to both the monomer and 1c concentrations; 1a in ring-opening polymerization of l-LA shows no activity. These results suggest a single-site active species in the ring-opening polymerization of l-LA.
Adres publiczny
https://doi.org/10.1021/om300321h
Strona internetowa wydawcy
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