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通过 27Al{1H} REDOR (3Q) MAS NMR 光谱和 DFT/分子力学确定沸石中骨架铝路易斯位和受扰铝原子的结构。

Structure of framework aluminum Lewis sites and perturbed aluminum atoms in zeolites as determined by 27Al{1H} REDOR (3Q) MAS NMR spectroscopy and DFT/molecular mechanics.

机构信息

Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Heyrovsky sq. 2, 162 06 Prague 6 (Czech Republic).

出版信息

Angew Chem Int Ed Engl. 2015 Jan 7;54(2):541-5. doi: 10.1002/anie.201409635. Epub 2014 Nov 13.

Abstract

Zeolites are highly important heterogeneous catalysts. Besides Brønsted SiOHAl acid sites, also framework AlFR Lewis acid sites are often found in their H-forms. The formation of AlFR Lewis sites in zeolites is a key issue regarding their selectivity in acid-catalyzed reactions. The local structures of AlFR Lewis sites in dehydrated zeolites and their precursors--"perturbed" AlFR atoms in hydrated zeolites--were studied by high-resolution MAS NMR and FTIR spectroscopy and DFT/MM calculations. Perturbed framework Al atoms correspond to (SiO)3AlOH groups and are characterized by a broad (27)Al NMR resonance (δi = 59-62 ppm, CQ = 5 MHz, and η = 0.3-0.4) with a shoulder at 40 ppm in the (27)Al MAS NMR spectrum. Dehydroxylation of (SiO)3AlOH occurs at mild temperatures and leads to the formation of AlFR Lewis sites tricoordinated to the zeolite framework. Al atoms of these (SiO)3Al Lewis sites exhibit an extremely broad (27)Al NMR resonance (δi ≈ 67 ppm, CQ ≈ 20 MHz, and η ≈ 0.1).

摘要

沸石是非常重要的多相催化剂。除了 Brønsted SiOHAl 酸位,沸石的 H 形式中通常还存在骨架 AlFR 路易斯酸位。沸石中 AlFR 路易斯位的形成是其在酸催化反应中选择性的关键问题。通过高分辨率 MAS NMR 和傅里叶变换红外光谱以及 DFT/MM 计算研究了脱水沸石及其前体——水合沸石中的“扰动”AlFR 原子中的 AlFR 路易斯位的局部结构。受扰骨架 Al 原子对应于(SiO)3AlOH 基团,并具有宽的(27)Al NMR 共振(δi = 59-62 ppm,CQ = 5 MHz,η = 0.3-0.4),在(27)Al MAS NMR 谱中在 40 ppm 处有一个肩峰。(SiO)3AlOH 的脱羟基作用在温和的温度下发生,导致 AlFR 路易斯位形成三配位到沸石骨架上。这些(SiO)3Al 路易斯位点的 Al 原子表现出极宽的(27)Al NMR 共振(δi ≈ 67 ppm,CQ ≈ 20 MHz,η ≈ 0.1)。

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