光诱导福尔摩斯反应产物在Xerogels中的自发分辨和超卷曲。

Sergey V Stovbun, Anatoly M Zanin, Mikhail V Shashkov, Aleksey A Skoblin, Dmitry V Zlenko, Vsevolod A Tverdislov, Marya G Mikhaleva, Oxana P Taran, Valentin N Parmon
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引用次数: 6

摘要

这项研究探讨了福尔摩斯反应产物在 xerogels 中的超分子自组织。紫外线诱导的甲糖反应是在 70∘C 的过饱和甲醛溶液中进行的,不使用催化剂。将得到的碳水化合物溶液在玻璃载玻片上干燥,得到的异凝胶显示出显著的光学活性,而初始溶液则无光学活性。异凝胶中含有高度拉长的螺旋结构和等距结构的结晶元素。因此,异凝胶的形成伴随着对映体的自发分解和不同形状超分子结构的分离。粗螺旋由细螺旋缠绕而成,而细螺旋则由直径远小于 400 纳米的基本结构缠绕而成。生物大分子(DNA、蛋白质和纤维素)也具有类似的结构层次。在总结所获结果的基础上,我们提出了一种假设机制,用以解释初始对映体过量的放大,以及生命进化开始所必需的物质的手性和化学纯化。
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Spontaneous Resolution and Super-coiling in Xerogels of the Products of Photo-Induced Formose Reaction.

This work addresses the supramolecular self-organization in the xerogels of formose reaction products. The UV-induced formose reaction was held in over-saturated formaldehyde solutions at 70C without a catalyst. The solutions of the obtained carbohydrates were dried on a glass slide, and the obtained xerogels demonstrated a prominent optical activity, while the initial solutions were optically inactive. The xerogels contained highly elongated crystalline elements of a helical structure as well as the isometric ones. Thus xerogel formation was accompanied by a spontaneous resolution of enantiomers and separation of different-shaped supramolecular structures. The thick helices were twisted of thinner ones, while the latter were twisted of elementary structures having a diameter much smaller than 400 nm. Similar structural hierarchy is typical of biological macromolecules (DNA, proteins, and cellulose). Summarizing the obtained results, we proposed a hypothetical mechanism explaining the amplification of the initial enantiomeric excess, as well as chiral and chemical purification of the substances which were essential for the evolution of Life to start.

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