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Polymer Networks Synthesized from Poly(Sorbitol Adipate) and Functionalized Poly(Ethylene Glycol)

机译:聚合物网络由聚(山梨糖醇己二酸酯)合成官能化聚(乙二醇)

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摘要

Polymer networks were prepared by Steglich esterification using poly(sorbitol adipate) (PSA) and poly(sorbitol adipate)-graft-poly(ethylene glycol) mono methyl ether (PSA-g-mPEG12) copolymer. Utilizing multi-hydroxyl functionalities of PSA, poly(ethylene glycol) (PEG) was first grafted onto a PSA backbone. Then the cross-linking of PSA or PSA-g-mPEG12 was carried out with disuccinyl PEG of different molar masses (Suc-PEGn-Suc). Polymers were characterized through nuclear magnetic resonance (NMR) spectroscopy, gel permeation chromatography (GPC), and differential scanning calorimetry (DSC). The degree of swelling of networks was investigated through water (D2O) uptake studies, while for detailed examination of their structural dynamics, networks were studied using 13C magic angle spinning NMR (13C MAS NMR) spectroscopy, 1H double quantum NMR (1H DQ NMR) spectroscopy, and 1H pulsed field gradient NMR (1H PFG NMR) spectroscopy. These solid state NMR results revealed that the networks were composed of a two component structure, having different dipolar coupling constants. The diffusion of solvent molecules depended on the degree of swelling that was imparted to the network by the varying chain length of the PEG based cross-linking agent.
机译:使用聚(山梨糖醇己二酸酯)(PSA)和聚(山梨糖醇己二酸酯) - 聚乙二醇 - 聚(乙二醇)单甲基醚(PSA-G-MPEG12)共聚物制备聚合物网络。利用PSA的多羟基官能团,首先将聚(乙二醇)(PEG)接枝到PSA主链上。然后用不同摩尔质量的二琥珀橡胶(Suc-PENT-SUC)进行PSA或PSA-G-MPEG12的交联。通过核磁共振(NMR)光谱,凝胶渗透色谱(GPC)和差示扫描量热法(DSC)表征聚合物。通过水(D2O)摄取研究研究了网络的肿胀程度,同时详细检查了它们的结构动力学,使用13C魔法角旋转NMR(13C MAS NMR)光谱,1H双量子NMR(1H DQ NMR)进行了网络。光谱学和1H脉冲场梯度NMR(1H pFG NMR)光谱。这些固态NMR结果表明,网络由具有不同双极耦合常数的两个分量结构组成。溶剂分子的扩散依赖于通过基于PEG的交联剂的不同链长赋予网络的溶胀度。

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