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Rapid homogeneous lauroylation of wheat straw hemicelluloses under mild conditions

机译:温和条件下小麦秸秆半纤维素的快速均相月桂酰化

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Hemicellulose-based hydrophobic biomaterials with degrees of substitution ranging from 0.46 to 1.54 were synthesized under mild conditions in homogeneous media (N,N-dimethylformamide-lithium chloride) by reacting the native wheat straw hemicellulosic polymers with lauroyl chloride using 4-dimethylaminopyricline as a catalyst. Other catalysts such as N-bromosuccinimide, N-methyl pyrrolidine, N-methyl pyrrolidinone. and pyridine were also investigated. Under optimum reaction conditions (2 equiv of lauroyl chloride and triethylamine per hydroxyl group, 5% 4-dimethylaminopyridine, 40 degrees C, 35 min), a high DS value of 1.54 was obtained. The biomaterials were characterized by FT-IR spectroscopy and C-13 NMR spectroscopy as well as by thermal analysis. The results showed that the lauroylation occurred preferably at the C-3 hydroxyl group of beta-D-Xylp units in the hemicelluloses, and the thermal stability of the hydrophobic polymers increased by esterification. (C) 2008 Elsevier Ltd. All rights reserved.
机译:以4-二甲基氨基吡啶为催化剂,使天然小麦秸秆半纤维素聚合物与月桂酰氯反应,在均质介质(N,N-二甲基甲酰胺-氯化锂)中于温和条件下合成取代度为0.46至1.54的半纤维素疏水生物材料。 。其他催化剂,例如N-溴琥珀酰亚胺,N-甲基吡咯烷,N-甲基吡咯烷酮。还研究了吡啶和吡啶。在最佳反应条件下(每个羟基2当量的月桂酰氯和三乙胺,5%的4-二甲基氨基吡啶,40°C,35分钟),获得的高DS值为1.54。通过FT-IR光谱和C-13 NMR光谱以及通过热分析来表征生物材料。结果表明,月桂酰化优选发生在半纤维素的β-D-Xylp单元的C-3羟基处,并且疏水性聚合物的热稳定性通过酯化而增加。 (C)2008 Elsevier Ltd.保留所有权利。

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