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Silylcellulose from silylation/desilylation of cellullose in ammonia

机译:来自氨中纤维素的甲硅烷基化/去甲硅烷基化的甲硅烷基纤维素

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Silylation of cellulose with hexamethyldisilazane (HMDS) in liquid ammonia is described emphasizing mechanistic features. Conditions for complete as well as for stoichiometric partial silylation have been established which proved that the ratio of silylating agent and hydrogen bonding capability of the solvent are crucial for complete silylation. The heterogeneous reaction follows first order kinetics in the presence of saccharine as catalyst indicating that the accessability of hydroxy groups is not the rate determining factor. Stoichiometric desilylation of trimethylsilyl cellulose is also possible in tetrahydrofurane containing ammonia as hydrogen bond donor. Trimethylsilyl celluloses have a solubility window in THF with a DS from 1.6 to 2.6 which is narrower for higher molecular weight of the cellulose. Trimethylsilyl celluloses with DS above 2.7 show thermotropic behaviour. [References: 19]
机译:描述了在液态氨中纤维素与六甲基二硅氮烷(HMDS)的甲硅烷基化,强调了机械特性。建立了完全以及化学计量的部分甲硅烷基化的条件,这证明了甲硅烷基化剂的比例和溶剂的氢键合能力对于完全甲硅烷基化至关重要。在糖精作为催化剂的存在下,异相反应遵循一级动力学,表明羟基的可及性不是决定速率的因素。在含有氨作为氢键供体的四氢呋喃中,三甲基甲硅烷基纤维素的化学计量脱甲硅烷基化也是可能的。三甲基甲硅烷基纤维素在THF中的溶解度窗口具有1.6至2.6的DS,这对于较高的纤维素分子量而言较窄。 DS大于2.7的三甲基硅烷基纤维素表现出热致行为。 [参考:19]

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