4.6 Article

N-Heterocyclic Carbene-Based Zinc Complexes: Same Precursors for Different Lactide Ring-Opening Polymerization Mechanisms.

期刊

CHEMCATCHEM
卷 14, 期 20, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.202200962

关键词

Carbene ligands; Reaction mechanisms; Renewable resources; Ring-opening polymerization; Zinc complexes

资金

  1. Universita degli Studi di Salerno within the CRUI-CARE Agreement

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Two zinc complexes with NHC ligands were synthesized and studied for their behavior in the Ring-Opening Polymerization of lactides, showing efficiency as initiators with molecular weights dependent on cocatalysts. Microstructural analysis revealed enriched heterotactic PLA, with kinetic parameters compared between different conditions and reactions showing pseudo-first-order dependence on monomer concentration. Reactivity studies aimed to uncover the active species in polymerization processes with different catalytic systems, including zinc complexes alone or in combination with neutral or ionic cocatalysts.
Two zinc complexes bearing NHC ligands were synthesized and fully characterized by NMR spectroscopy. Their behavior in the Ring-Opening Polymerization (ROP) of lactides was investigated under several conditions of reaction. They showed to be efficient initiators, producing polylactides with molecular weights depending on the cocatalysts. Microstructural analysis of poly(rac-LA) by H-1 NMR spectroscopy revealed a slightly enriched-heterotactic PLAs with P-r values up to 0.66. Inspection of the kinetic parameters for L-LA and rac-LA allowed to compare the k(obs) of the studied complexes 1 and 2 under different conditions, and showed that propagations present the usual pseudo-first-order dependence on monomer concentration. Hence, some reactivity studies were carried out, addressed to unravel the nature of the active species in the polymerization processes conducted in the presence of different catalytic systems, namely zinc complexes alone and in combination with neutral or ionic cocatalysts.

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