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SG1 氮氧自由基对未保护的糖和锂盐的稳定性:氮氧自由基介导的接枝聚合改性纤维素的前言。

Stability of SG1 nitroxide towards unprotected sugar and lithium salts: a preamble to cellulose modification by nitroxide-mediated graft polymerization.

机构信息

Aix-Marseille Université, CNRS, ICR UMR 7273, 13397 Marseille, France.

出版信息

Beilstein J Org Chem. 2013 Aug 6;9:1589-600. doi: 10.3762/bjoc.9.181. eCollection 2013.

Abstract

The range of applications of cellulose, a glucose-based polysaccharide, is limited by its inherently poor mechanical properties. The grafting of synthetic polymer chains by, for example, a "grafting from" process may provide the means to broaden the range of applications. The nitroxide-mediated polymerization (NMP) method is a technique of choice to control the length, the composition and the architecture of the grafted copolymers. Nevertheless, cellulose is difficult to solubilize in organic media because of inter- and intramolecular hydrogen bonds. One possibility to circumvent this limitation is to solubilize cellulose in N,N-dimethylformamide (DMF) or N,N-dimethylacetamide (DMA) with 5 to 10 wt % of lithium salts (LiCl or LiBr), and carry out grafted polymerization in this medium. The stability of nitroxides such as SG1 has not been studied under these conditions yet, even though these parameters are of crucial importance to perform the graft modification of polysaccharide by NMP. The aim of this work is to offer a model study of the stability of the SG1 nitroxide in organic media in the presence of unprotected glucose or cellobiose (used as a model of cellulose) and in the presence of lithium salts (LiBr or LiCl) in DMF or DMA. Contrary to TEMPO, SG1 proved to be stable in the presence of unprotected sugar, even with an excess of 100 molar equivalents of glucose. On the other hand, lithium salts in DMF or DMA clearly degrade SG1 nitroxide as proven by electron-spin resonance measurements. The instability of SG1 in these lithium-containing solvents may be explained by the acidification of the medium by the hydrolysis of DMA in the presence of LiCl. This, in turn, enables the disproportionation of the SG1 nitroxide into an unstable hydroxylamine and an oxoammonium ion. Once the conditions to perform an SG1-based nitroxide-mediated graft polymerization from cellobiose have been established, the next stage of this work will be the modification of cellulose and cellulose derivatives by NMP.

摘要

纤维素是一种基于葡萄糖的多糖,其应用范围受到其固有机械性能差的限制。例如,通过“接枝到”过程接枝合成聚合物链,可以提供拓宽应用范围的手段。氮氧自由基介导的聚合(NMP)方法是控制接枝共聚物的长度、组成和结构的首选技术。然而,由于纤维素分子内和分子间存在氢键,因此很难在有机溶剂中溶解。一种克服此限制的可能性是将纤维素溶解在 N,N-二甲基甲酰胺(DMF)或 N,N-二甲基乙酰胺(DMA)中,其中含有 5 至 10wt%的锂盐(LiCl 或 LiBr),并在此介质中进行接枝聚合。尽管这些参数对于通过 NMP 对多糖进行接枝改性至关重要,但迄今为止,尚未研究过 SG1 等氮氧自由基在这些条件下的稳定性。这项工作的目的是提供一个模型研究,即在 DMF 或 DMA 中存在未保护的葡萄糖或纤维二糖(用作纤维素的模型)以及存在锂盐(LiBr 或 LiCl)的情况下,SG1 氮氧自由基在有机介质中的稳定性。与 TEMPO 不同,SG1 即使在有 100 摩尔当量以上的葡萄糖过量的情况下,在存在未保护的糖的情况下也表现出稳定性。另一方面,通过电子自旋共振测量证明,DMF 或 DMA 中的锂盐明显降解了 SG1 氮氧自由基。在含有这些锂的溶剂中,SG1 的不稳定性可能是由于 LiCl 存在下 DMA 的水解导致介质酸化所致。反过来,这使得 SG1 氮氧自由基歧化为不稳定的羟胺和氧铵离子。一旦建立了基于 SG1 的氮氧自由基介导的从纤维二糖接枝聚合的条件,这项工作的下一阶段将是通过 NMP 对纤维素及其衍生物进行改性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d09d/3740501/527948616d5f/Beilstein_J_Org_Chem-09-1589-g002.jpg

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