Högler Marc, Kobayashi Takeshi, Kraus Hamzeh, Atwi Boshra, Buchmeiser Michael R, Fyta Maria, Hansen Niels
Institute of Thermodynamics and Thermal Process Engineering, University of Stuttgart, Pfaffenwaldring 9, D-70569, Stuttgart, Germany.
Department of Chemical Engineering, University College London, Gower Street, London, WC1E 6BT, UK.
Chemistry. 2025 Jan 14;31(3):e202403237. doi: 10.1002/chem.202403237. Epub 2024 Dec 11.
Supported ionic-liquid phase (SILP) technology in a biphasic setting with n-heptane as the transport phase was applied to the Ru-alkylidene-N-heterocyclic carbene (NHC) catalyzed macrocyclization of α,ω-dienes to elucidate the effect of ionic liquid (IL)-film thickness, flow rate as well as substrate and product concentration on macrocyclization efficiency, and Z-selectivity. To understand the molecular-level behavior of the substrates and products at the n-heptane/IL interphase, atomistic molecular dynamics simulations were conducted and correlated with experimental observations. The thickness of the IL layer strongly influences the Z/E ratio of the products in that a thin IL layer favors higher Z/E ratios by confining the catalyst between the pore wall and the liquid-liquid interphase whereas a thick IL layer favors formation of the E-product and Ru-hydride catalyzed isomerization reactions. Also, macrocyclization efficiency, expressed by the ratio of oligomers/macromonocycle (O/MMC), is influenced both by the flow rate and the thickness of the IL layer.
在以正庚烷为传输相的双相体系中,将负载型离子液体相(SILP)技术应用于钌-亚烷基-N-杂环卡宾(NHC)催化的α,ω-二烯大环化反应,以阐明离子液体(IL)膜厚度、流速以及底物和产物浓度对大环化效率和Z选择性的影响。为了理解底物和产物在正庚烷/离子液体界面处的分子水平行为,进行了原子分子动力学模拟,并与实验观察结果相关联。离子液体层的厚度强烈影响产物的Z/E比,即薄的离子液体层通过将催化剂限制在孔壁和液-液界面之间而有利于更高的Z/E比,而厚的离子液体层有利于E-产物的形成和Ru-氢化物催化的异构化反应。此外,以低聚物/大分子单环(O/MMC)的比例表示的大环化效率受流速和离子液体层厚度的影响。