Tashiro Shohei, Kuwabara Kyohei, Otsuru Kosei, Shionoya Mitsuhiko
Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba, 278-8510, Japan.
Small. 2024 Dec;20(49):e2405507. doi: 10.1002/smll.202405507. Epub 2024 Jul 30.
Selective separation and conversion of furan-based biomass-derived compounds, which are closely related to biorefineries, is currently an important issue. To improve their performance, it is important to deepen the understanding of non-covalent interactions that act on the molecular recognition of furanic compounds on separation or catalyst matrices. Here, a new method is reported to comprehensively visualize such intermolecular interactions using a porous supramolecular crystalline probe with polar and non-polar binding sites within a low-symmetric nanochannel consisting of four isomeric Pd -macrocycles. Single-crystal X-ray diffraction analysis of the crystals including 5-hydroxymethylfurfural, furfural, furfuryl alcohol, or 2-acetylfuran reveals a variety of interactions involving their furan rings and polar substituents. It is also found that cooperative and competitive effects between guest and solvent molecules significantly change their recognition mode.
与生物炼制密切相关的呋喃基生物质衍生化合物的选择性分离和转化是当前一个重要问题。为提高其性能,深入了解作用于分离或催化剂基质上呋喃类化合物分子识别的非共价相互作用很重要。在此,报道了一种新方法,该方法使用由四个异构钯大环组成的低对称纳米通道内具有极性和非极性结合位点的多孔超分子晶体探针,全面可视化此类分子间相互作用。对包含5-羟甲基糠醛、糠醛、糠醇或2-乙酰呋喃的晶体进行的单晶X射线衍射分析揭示了涉及它们呋喃环和极性取代基的多种相互作用。还发现客体分子和溶剂分子之间的协同和竞争效应显著改变了它们的识别模式。