H 型聚乳酸的制备与表征。

IF 5.1 Q1 POLYMER SCIENCE
Aristotelis Zografos, Erin M. Maines, Joseph F. Hassler, Frank S. Bates* and Marc A. Hillmyer*, 
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引用次数: 0

摘要

H 型聚合物的结构由对称连接在聚合物骨架两端的四个分支组成,形状类似于字母 "H"。本文展示了一种仅使用开环酯交换反应就能高效合成的可再生 H 型聚合物。该策略依赖于一种四官能团聚(±-内酯)大引发剂,从该引发剂中同时生长出四个聚(±-内酯)分支。利用 1H NMR 光谱、尺寸排阻色谱法 (SEC) 和基质辅助激光解吸/电离 (MALDI) 光谱法来验证大引发剂的纯度。利用 1H NMR 光谱和 SEC 对枝条生长进行了探测,以揭示独特的酯交换现象,这种现象可加以控制,以获得结构纯净或更复杂的材料。H 型聚乳酸的制备达到了多克级,平均摩尔质量 Mw > 100 kg/mol,低分散度 Đ < 1.15。纯化过程包括常规沉淀步骤,得到的产品在结构上相对纯净(∼93%)。小振幅振荡剪切和拉伸流变测量结果表明,H 型结构具有独特的粘弹性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Preparation and Characterization of H-Shaped Polylactide

Preparation and Characterization of H-Shaped Polylactide

Preparation and Characterization of H-Shaped Polylactide

An H-polymer has an architecture that consists of four branches symmetrically attached to the ends of a polymer backbone, similar in shape to the letter “H”. Here, a renewable H-polymer efficiently synthesized using only ring-opening transesterification is demonstrated. The strategy relies on a tetrafunctional poly(±-lactide) macroinitiator, from which four poly(±-lactide) branches are grown simultaneously. 1H NMR spectroscopy, size exclusion chromatography (SEC), and matrix-assisted laser desorption/ionization (MALDI) spectrometry were used to verify the macroinitiator purity. Branch growth was probed using 1H NMR spectroscopy and SEC to reveal unique transesterification phenomena that can be controlled to yield architecturally pure or more complex materials. H-shaped PLA was prepared at the multigram scale with a weight-average molar mass Mw > 100 kg/mol and low dispersity Đ < 1.15. Purification involved routine precipitations steps, which yielded products that were architecturally relatively pure (∼93%). Small-amplitude oscillatory shear and extensional rheology measurements demonstrate the unique viscoelastic behavior associated with the H-shaped architecture.

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来源期刊
CiteScore
10.40
自引率
3.40%
发文量
209
审稿时长
1 months
期刊介绍: ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science. With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.
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