Heterometallic Titanium-Organic Frameworks as Dual Metal Catalysts for Synergistic Non-Buffered Hydrolysis of Nerve Agent Simulants

J. Castells‐Gil, Natalia M. Padial, Neyvis Almora‐Barrios, R. Gil-San-Millan, María Romero-Angel, V. Torres, I. da Silva, J. Waerenborgh, Jaciek Jagiello, J. Navarro, S. Tatay, C. Martí‐Gastaldo
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引用次数: 32

Abstract

Summary Mixed-metal or heterometallic metal-organic frameworks (MOFs) are gaining importance as a route to produce materials with increasing chemical and functional complexities. We report a family of heterometallic titanium frameworks, MUV-101(M), and use them to exemplify the advantages of controlling metal distribution across the framework in heterogeneous catalysis by exploring their activity toward the degradation of a nerve agent simulant of Sarin gas. MUV-101(Fe) is the only pristine MOF capable of catalytic degradation of diisopropyl-fluorophosphate (DIFP) in non-buffered aqueous media. This activity cannot be explained only by the association of two metals, but to their synergistic cooperation, to create a whole that is more efficient than the simple sum of its parts. Our simulations suggest a dual-metal mechanism reminiscent of bimetallic enzymes, where the combination of Ti(IV) Lewis acid and Fe(III)–OH Bronsted base sites leads to a lower energy barrier for more efficient degradation of DIFP in absence of a base.
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异质金属钛-有机骨架作为双金属催化剂在神经毒剂模拟物协同非缓冲水解中的应用
混合金属或异金属金属有机骨架(MOFs)作为一种生产化学和功能日益复杂的材料的途径正变得越来越重要。我们报道了一个异质金属钛框架家族,MUV-101(M),并通过探索它们对沙林毒气神经毒剂模拟物降解的活性,用它们来举例说明控制金属分布在异质催化框架中的优势。MUV-101(Fe)是唯一能够在非缓冲水介质中催化降解二异丙基氟磷酸(DIFP)的原始MOF。这种活动不能仅仅用两种金属的结合来解释,而是用它们的协同合作来解释,以创造一个比各部分简单相加更有效的整体。我们的模拟表明了一种双金属机制,让人想起双金属酶,其中Ti(IV) Lewis酸和Fe(III) -OH Bronsted碱基位点的结合导致了更低的能垒,从而在没有碱基的情况下更有效地降解DIFP。
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