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沸石咪唑酯骨架结构的酸碱催化的结构-性能-活性关系研究进展。

Insights into the Structure-Property-Activity Relationship of Zeolitic Imidazolate Frameworks for Acid-Base Catalysis.

机构信息

Boreskov Institute of Catalysis SB RAS, Prospekt Akad. Lavrentieva 5, 630090 Novosibirsk, Russia.

Department of Chemistry and Green-Nano Materials Research Center, Kyungpook National University, Daegu 41566, Republic of Korea.

出版信息

Int J Mol Sci. 2023 Feb 22;24(5):4370. doi: 10.3390/ijms24054370.

Abstract

Zeolitic imidazolate frameworks (ZIFs) have been extensively examined for their potential in acid-base catalysis. Many studies have demonstrated that ZIFs possess unique structural and physicochemical properties that allow them to demonstrate high activity and yield products with high selectivity. Herein, we highlight the nature of ZIFs in terms of their chemical formulation and the textural, acid-base, and morphological properties that strongly affect their catalytic performance. Our primary focus is the application of spectroscopic methods as instruments for analyzing the nature of active sites because these methods can allow an understanding of unusual catalytic behavior from the perspective of the structure-property-activity relationship. We examine several reactions, such as condensation reactions (the Knoevenagel condensation and Friedländer reactions), the cycloaddition of CO to epoxides, the synthesis of propylene glycol methyl ether from propylene oxide and methanol, and the cascade redox condensation of 2-nitroanilines with benzylamines. These examples illustrate the broad range of potentially promising applications of Zn-ZIFs as heterogeneous catalysts.

摘要

沸石咪唑酯骨架(ZIFs)因其在酸碱催化中的潜在应用而受到广泛研究。许多研究表明,ZIFs 具有独特的结构和物理化学性质,使它们能够表现出高活性和高选择性的产物。在此,我们重点介绍 ZIFs 的化学组成以及强烈影响其催化性能的结构、酸碱和形态特性。我们主要关注的是光谱方法作为分析活性位性质的仪器,因为这些方法可以从结构-性质-活性关系的角度来理解异常催化行为。我们研究了几种反应,如缩合反应(Knoevenagel 缩合和 Friedländer 反应)、CO 与环氧化物的环加成、环氧丙烷和甲醇合成丙二醇甲醚,以及 2-硝基苯胺与苄胺的级联氧化还原缩合。这些例子说明了 Zn-ZIFs 作为多相催化剂的潜在广泛应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bcf/10002606/242741cc5e41/ijms-24-04370-g001.jpg

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