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Separation of Linear and Branched Alkanes Using Host-Guest Complexation of Cyclic and Branched Alkane Vapors by Crystal State Pillar[6]arene

机译:用晶体状态柱的宿主 - 客气络络络络络络络络络络合分离晶体状态柱[6]芳烃

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摘要

Activated crystals of pillar[6] arene produced by removing the solvent upon heating were able to take up branched and cyclic alkane vapors as a consequence of their gate-opening behavior. The uptake of branched and cyclic alkane vapors by the activated crystals of pillar[6] arene induced a crystal transformation to form one-dimensional channel structures. However, the activated crystals of pillar[6] arene hardly took up linear alkane vapors because the cavity size of pillar[6] arene is too large to form stable complexes with linear alkanes. This shape-selective uptake behavior of pillar[6] arene was further utilized for improving the research octane number of an alkane mixture of isooctane and n-heptane: interestingly, the research octane number was dramatically improved from a low research octane number (17%) to a high research octane number ( 99%) using the activated crystals of pillar[6] arene.
机译:通过在加热时除去溶剂而产生的柱[6]芳烃的活性晶体能够作为其浇口开放行为而占用分支和环状烷烃蒸气。 通过柱[6]芳烃的活性晶体的分支和环状烷烃的吸收诱导晶体变换以形成一维沟道结构。 然而,柱[6]芳烃的活性晶体几乎没有接受直线烷烃蒸气,因为柱的腔体尺寸太大,不能与线性烷烃形成稳定的配合物。 柱[6]芳烃的这种形状选择性摄取行为进一步用于改善异辛烷和正庚烷的烷烃混合物的研究辛烷值:有趣的是,从低研究辛烷值数(17%)显着改善了研究辛烷值(17%) )使用柱子[6]芳烃的活性晶体,至高研究辛烷值(& 99%)。

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