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富含胺的镍(II)-干凝胶作为用于水相Knoevenagel缩合和无溶剂CO环加成反应的高活性双功能金属有机催化剂。

Amine-rich Nickel(II)-Xerogel as a Highly Active Bifunctional Metallo-organo Catalyst for Aqueous Knoevenagel Condensation and Solvent-free CO Cycloaddition.

作者信息

Saha Ekata, Jungi Hiren, Dabas Shilpa, Mathew Abra, Kuniyil Rositha, Subramanian Saravanan, Mitra Joyee

机构信息

Inorganic Materials & Catalysis (IMC) Division, CSIR-Central Salt & Marine Chemicals Research Institute, Gijubhai Badheka Marg, Bhavnagar 364002, Gujarat, India.

Academy of Scientific and Innovative Research (AcSIR), AcSIR Headquarters, CSIR-HRDC Campus, Sector-19, Kamla Nehru Nagar, Ghaziabad 201002, India.

出版信息

Inorg Chem. 2023 Sep 18;62(37):14959-14970. doi: 10.1021/acs.inorgchem.3c01669. Epub 2023 Sep 6.

Abstract

Metallogels formed from supramolecular interactions of low-molecular-weight gelators (LMWGs) combine the qualities of heterogeneous catalysts and offer the advantages of multifunctionality owing to the facile installation of desired task-specific moieties on the surface and along the channels of the gels. We discuss the applications of a triazole-based Ni(II) gel-derived xerogel () having a high density of Ni(II)-nodes and appended primary amines as a recyclable heterogeneous catalyst for Knoevenagel condensation of aldehyde and malononitrile in water and the solvent-free cycloaddition of CO to form a series of cyclic carbonates with near-quantitative conversion of the respective epoxides, with low catalyst loading (0.59 mol %), high catalyst stability, and recyclability. The structural advantages of , due to the concurrent presence of bifunctional Lewis acid-base sites on the channels, open Ni(II) nodes, N, pendant -NH and its chemical stability, are conducive to the cooperative heterogeneous catalytic activity under mild conditions. This work emphasizes the effective amalgamation of metals with purpose-built ligand systems for the construction of metallogels and their utility as heterogeneous catalysts for desired organic transformations.

摘要

由低分子量凝胶剂(LMWGs)的超分子相互作用形成的金属凝胶结合了多相催化剂的特性,并且由于能够在凝胶表面和通道上轻松引入所需的特定任务部分而具有多功能性的优势。我们讨论了一种基于三唑的镍(II)凝胶衍生干凝胶()的应用,该干凝胶具有高密度的镍(II)节点和连接的伯胺,可作为可回收的多相催化剂,用于醛与丙二腈在水中的Knoevenagel缩合反应以及无溶剂条件下CO的环加成反应,以形成一系列环状碳酸酯,相应环氧化物的转化率接近定量,催化剂负载量低(0.59 mol%),具有高催化剂稳定性和可回收性。由于通道上同时存在双功能路易斯酸碱位点、开放的镍(II)节点、N、侧链 -NH及其化学稳定性,的结构优势有利于在温和条件下产生协同多相催化活性。这项工作强调了将金属与专门构建的配体系统有效结合以构建金属凝胶及其作为所需有机转化的多相催化剂的实用性。

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