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同一周期中三种元素(铟、锡和锑)作为催化剂用于丙交酯开环聚合反应的比较:从无定形聚酯到半结晶聚酯

Comparison of three elements (In, Sn, and Sb) in the same period as catalysts in the ring-opening polymerization of l-lactide: from amorphous to semicrystalline polyesters.

作者信息

González-Belman Oscar F, Jiménez-Halla J Oscar C, González Gerardo, Báez José E

机构信息

Department of Chemistry, University of Guanajuato (UG) Noria Alta S/N 36050 Guanajuato Gto Mexico

出版信息

RSC Adv. 2024 Oct 31;14(47):34733-34745. doi: 10.1039/d4ra06783e. eCollection 2024 Oct 29.

DOI:10.1039/d4ra06783e
PMID:39483385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11526846/
Abstract

The ring-opening polymerization (ROP) of l-lactide (l-LA) is the main method for synthesizing poly(l-lactide) (PLLA), in which choosing the catalyst is one of the most important parameters. In this work, we focused on the systematic study of catalysts based on p-block elements from period 5, such as indium(iii), tin(ii), tin(iv) and antimony(iii) acetates, which displayed contrasting performances influenced by the oxidation state of the metal center. Analysis of the obtained oligomers by different techniques, including nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), polarized optical microscopy (POM) and matrix-assisted laser desorption ionization-time-of-flight (MALDI-TOF), revealed the selectivity of each catalyst toward the ROP of l-LA. Tin(ii) acetate showed the best performance, making it the best catalyst of this series for synthesizing PLLA. Indium(iii) and tin(ii) acetates induced an amorphous and semicrystalline polyester, respectively. The kinetic study evidenced the excellent performance of tin(ii) acetate in the ROP of l-LA. This catalyst reached high conversions in a quarter of the total reaction time, positioning it as the most catalytically active of the selected p-block acetate catalysts. Finally, the coordination-insertion mechanism by the catalyst in the initiation step was corroborated through the development of a mechanistic study applying the density functional theory (DFT).

摘要

左旋丙交酯(l-LA)的开环聚合(ROP)是合成聚左旋丙交酯(PLLA)的主要方法,其中催化剂的选择是最重要的参数之一。在本工作中,我们重点对基于第5周期p区元素的催化剂进行了系统研究,例如铟(III)、锡(II)、锡(IV)和醋酸锑(III),这些催化剂表现出受金属中心氧化态影响的不同性能。通过不同技术对所得低聚物进行分析,包括核磁共振(NMR)、差示扫描量热法(DSC)、偏光显微镜(POM)和基质辅助激光解吸电离飞行时间(MALDI-TOF),揭示了每种催化剂对l-LA的ROP的选择性。醋酸锡(II)表现出最佳性能,使其成为该系列中合成PLLA的最佳催化剂。醋酸铟(III)和醋酸锡(II)分别诱导生成无定形和半结晶聚酯。动力学研究证明了醋酸锡(II)在l-LA的ROP中的优异性能。该催化剂在总反应时间的四分之一内达到了高转化率,使其成为所选p区醋酸盐催化剂中催化活性最高的。最后,通过应用密度泛函理论(DFT)开展机理研究,证实了催化剂在引发步骤中的配位插入机理。

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