二甲醚在Ag/ Cs1.5H1.5PW12O40上羰基化:Ag羰基的原位FTIR光谱研究

G. G. Volkova, E. A. Paukshtis
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引用次数: 2

摘要

摘要:二甲醚(DME)在非均相催化剂上无卤化物羰基化制乙酸甲酯为重要工业化学品的生产提供了一条潜在的绿色途径。之前我们已经证明,在Cs1.5H1.5PW12O40中加入1%的银会导致活性增加两倍。用原位红外光谱法证实了银羰基团簇在催化剂表面的形成。在2188 cm-1处观察到羰基银的v(CO),这可能是由于12钨磷酸酸性铯盐表面形成了阳离子羰基银Ag(CO)+。鉴于效率的提高,新型双功能催化剂Ag/ Cs1.5H1.5PW12O40有望在基础有机化学新工艺中具有重要的实际应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carbonylation of Dimethyl Ether on Ag/ Cs1.5H1.5PW12O40: In-Situ FTIR Spectroscopy Study of the Ag-Carbonyls
Abstract Halide-free carbonylation of dimethyl ether (DME) to methyl acetate over heterogeneous catalysts offers a potentially green route to the production of important industrial chemicals. Previously we have shown that the addition of 1% of silver to Cs1.5H1.5PW12O40 led to an increase in activity by a factor of two. Formation of silver carbonyl clusters on the surface of the catalyst was demonstrated by in situ FTIR spectroscopy. The v(CO) of silver carbonyl was observed at 2188 cm-1 and may be explained by the formation of cationic silver carbonyl Ag(CO)+ on the surface of the acidic cesium salt of 12-tungstophosphoric acid. In view of the increased efficiency, the novel bifunctional catalyst Ag/ Cs1.5H1.5PW12O40 is expected to hold significant promise for practical use in new processes of basic organic chemistry.
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