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Cyanosilylation of benzaldehyde with TMSCN over perovskite-type oxide catalyst prepared by thermal decomposition of heteronuclear cyano complex precursors

机译:异核氰基配合物前驱体热分解制备的钙钛矿型氧化物催化剂上苯甲醛与TMSCN的氰基硅烷化反应

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摘要

The perovskite-type oxide catalyst, SmFeO3, prepared by decomposition method of heteronuclear cyano complex precursor (CN method) was applied to liquid-phase organic reaction, cyanosilylation of benzaldehyde with TMSCN. The maximum catalytic activity per catalyst weight was achieved at 800 A degrees C of calcination temperature in CN method and it was found that the catalytic activity was strongly related to the crystallinity of SmFeO3 catalyst. The catalytic reaction performed in the presence of pyridine and 2,6-di-tert-butylpyridine suggests that the catalytically active sites are the Bronsted acid sites formed on the SmFeO3 catalyst. The catalytic activity of SmFeO3 catalyst prepared by CN method was much higher than those of acid catalysts: SiO2-Al2O3 and Amberlyst.
机译:通过异核氰基配合物前驱体的分解方法(CN法)制备的钙钛矿型氧化物催化剂SmFeO3被用于液相有机反应,苯甲醛与TMMSCN的氰基化反应。在CN法中,在800℃的煅烧温度下,达到每催化剂重量的最大催化活性,发现该催化活性与SmFeO 3催化剂的结晶度密切相关。在吡啶和2,6-二叔丁基吡啶的存在下进行的催化反应表明,催化活性位是在SmFeO3催化剂上形成的布朗斯台德酸位。 CN法制得的SmFeO3催化剂的催化活性远高于SiO2-Al2O3和Amberlyst等酸性催化剂。

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