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基于聚己内酯和聚(ε-硫代己内酯)接枝到壳聚糖主链上的原始大分子结构。

Original Macromolecular Architectures Based on poly(ε-caprolactone) and poly(ε-thiocaprolactone) Grafted onto Chitosan Backbone.

机构信息

BioTeam/ICPEES-ECPM, UMR CNRS 7515, Université de Strasbourg, 25 Rue Becquerel, 67087 Strasbourg CEDEX 2, France.

Science & Letters Faculty, Chemistry Department, Istanbul Technical University, Maslak, TR34469 Istanbul, Turkey.

出版信息

Int J Mol Sci. 2018 Nov 29;19(12):3799. doi: 10.3390/ijms19123799.

Abstract

Polyester and/or polythioester grafted chitosan copolymers were synthesized. For that, poly(ε-caprolactone) (PCL), poly(ε-thiocaprolactone) (PTCL), and their copolymers were first synthesized by ring opening polymerization. Copolymers with caprolactone:thiocaprolactone (CL:TCL) molar ratios of 2:1, 1:1, 1:2 were synthesized. All of the synthesized macromolecular architectures were characterized using different spectral (Fourier transform infrared (FTIR), proton nuclear magnetic resonance (¹H-NMR), X-Ray diffraction (XRD)) and thermal (Differential scanning calorimetry (DSC), Thermogravimetric analysis (TGA)) methods. Grafting was then performed according two distinct routes: (i) using a blend of both homopolymers (PCL and PTCL) or (ii) using pre-synthesized copolymers with controlled CL:TCL ratios. Hexamethylene diisocyanate was used as a grafting/coupling agent through urethane bonds with high yield. Grafting preferentially occurred at sulfur sites. The results indicated that PTCL is more reactive and favorable than PCL for grafting onto chitosan. With the homopolymers blend grafting route, the corresponding materials mostly had a higher PTCL portion than expected. To obtain polyester grafted chitosan with a determined CL:TCL ratio, the copolymer grafting route would yield better results.

摘要

聚酯和/或聚硫酯接枝壳聚糖共聚物被合成。为此,首先通过开环聚合合成聚(ε-己内酯)(PCL)、聚(ε-硫代己内酯)(PTCL)及其共聚物。合成了具有己内酯:硫代己内酯(CL:TCL)摩尔比为 2:1、1:1、1:2 的共聚物。使用不同的光谱(傅里叶变换红外(FTIR)、质子核磁共振(¹H-NMR)、X 射线衍射(XRD))和热(差示扫描量热法(DSC)、热重分析(TGA))方法对所有合成的大分子结构进行了表征。接枝是通过两种不同的途径进行的:(i)使用两种均聚物(PCL 和 PTCL)的混合物,或(ii)使用具有受控 CL:TCL 比的预合成共聚物。己二异氰酸酯通过高收率的氨酯键用作接枝/偶联剂。接枝优先发生在硫原子上。结果表明,PTCL 比 PCL 更具反应性和有利于接枝到壳聚糖上。使用均聚物共混物接枝途径,相应的材料大多具有比预期更高的 PTCL 部分。为了获得具有确定 CL:TCL 比的聚酯接枝壳聚糖,共聚物接枝途径将产生更好的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed5/6321519/a3560bdaaca0/ijms-19-03799-g001.jpg

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