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Self-Assembly of Cellulose Oligomers into Nanoribbon Network Structures Based on Kinetic Control of Enzymatic Oligomerization

机译:基于酶寡聚化动力学控制的纤维素寡聚体的自组装成纳米卷网结构

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The ability to chemically synthesize desired molecules followed by their in situ self-assembly in reaction solution has attracted much attention as a simple and environmentally friendly method to produce self-assembled nanostructures. In this study, alpha-D-glucose 1-phosphate monomers and cellobiose primers were subjected to cellodextrin phosphorylase-catalyzed reverse phosphorolysis reactions in aqueous solution in order to synthesize cellulose oligomers, which were then in situ self-assembled into crystalline nanoribbon network structures. The average degree-of-polymerization (DP) values of the cellulose oligomers were estimated to be approximately 7-8 with a certain degree of DP distribution. The cellulose oligomers crystallized with the cellulose II allomorph appeared to align perpendicularly to the base plane of the nanoribbons in an antiparallel manner. Detailed analyses of reaction time dependence suggested that the production of nanoribbon network structures was kinetically controlled by the amount of water-insoluble cellulose oligomers produced.
机译:在反应溶液中化学合成所需分子的能力,然后在反应溶液中的原位自组装被吸引了许多关注,以产生自组装纳米结构的简单和环保的方法。在该研究中,对水溶液中的α-D-葡萄糖1-磷酸三种磷酸纤维素催化的反向磷光解反应进行纤维素,然后以原位自组装成结晶纳米纳米网络结构,以合成纤维素寡聚体。纤维素低聚物的平均聚合(DP)值估计为约7-8,具有一定程度的DP分布。用纤维素II Allomorph结晶的纤维素低聚物似乎以反平行的方式垂直于纳米波纹的基面向对准。反应时间依赖性的详细分析表明,纳米骨网络结构的产生是通过产生的水不溶性纤维素低聚物的量控制。

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