Isolated and Paired Metal Sites in Zeolites Using Solid-State Ion Exchange

Rio G. Moore, James M. Crawford
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引用次数: 0

Abstract

Isolated and paired extraframework transition metal cations in zeolites are emerging as top candidates for numerous applications, including, but not limited to, selective methane oxidation to methanol, selective catalytic reduction of nitrogen oxides, propane dehydrogenation, propylene epoxidation, and direct air capture of carbon dioxide. Importantly, these well-defined heterogeneous catalysts offer parallels with molecular and metalloenzyme catalytic active sites. Aqueous-phase ion exchange (APIE) is the most common synthesis technique to obtain these catalysts. Solid-state ion exchange (SSIE) is an often overlooked technique that offers synthetic advantages compared to APIE. Thus, recent advances in solid-state synthesis strategies merit contemporary contextualization. In this minireview, we describe the basic principles, methods, mechanisms, challenges, and advances in solid-state ion exchange in the context of well-defined transition metal cation active sites located in extraframework positions of the zeolite.

固体离子交换在沸石中的分离和配对金属位
沸石中分离的和成对的框架外过渡金属阳离子正在成为许多应用的首选,包括但不限于,选择性甲烷氧化为甲醇,选择性催化还原氮氧化物,丙烷脱氢,丙烯环氧化和二氧化碳的直接空气捕获。重要的是,这些定义良好的多相催化剂与分子和金属酶的催化活性位点相似。水相离子交换法(APIE)是制备这些催化剂最常用的方法。固态离子交换(SSIE)是一种经常被忽视的技术,与APIE相比,它具有综合优势。因此,固态合成策略的最新进展值得当代语境化。在这篇综述中,我们描述了固态离子交换的基本原理、方法、机制、挑战和进展,以及在沸石框架外位置明确定义的过渡金属阳离子活性位点的背景下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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1 months
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