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Cyclization of Pseudoionone into α-Ionone Over Heteropolyacid Supported on Mesoporous Silica SBA-15

机译:介孔二氧化硅SBA-15负载的杂多酸将假紫酮酮环化为α-紫罗兰酮

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摘要

Cyclization of pseudoionone into α-ionone was performed over the series heteropolyacid supported on SBA-15 in liquid-phase at 363 and 373 K using a batch reactor. It has been demonstrated that the liquid-phase synthesis of α-ionone by pseudoionone cyclization can be efficiently achieved on heteropolyacid/SBA-15 materials. The high catalytic performance of PW_(12)/SBA-15 materials is due to their strong Bronsted acidity, high dispersion of active phase and also to absence of steric constraints for pseudoionone cyclization. PW_(12)/SBA-15 catalysts are specially active and selective for this reaction giving predominantly a-ionone, as the main product, with high yield (about 60% at 373 K after 2 h) close to that obtained via the homogeneous synthesis. This catalytic system is more active and efficient in comparison with heteropolyacid supported on commercial silica. In order to achieve comparable amount of a-ionone, as is got for PW_(12)/SBA-15, belongs to apply five times more of the catalyst based on classical SiO2.
机译:使用间歇反应器,在363和373 K下,在液相上负载在SBA-15上的系列杂多酸上,将假紫酮环化为α-紫酮。已经证明在杂多酸/ SBA-15材料上可以有效地实现通过假紫酮环化液相合成α-紫酮。 PW_(12)/ SBA-15材料的高催化性能归因于它们强的布朗斯台德酸度,活性相的高分散性以及缺乏对假紫罗酮环化的空间限制。 PW_(12)/ SBA-15催化剂对该反应特别有活性和选择性,主要产生主要成分为α-紫罗兰酮,接近于均相合成获得的高收率(2小时后在373 K下约为60%)。 。与负载在商业二氧化硅上的杂多酸相比,该催化体系更具活性和效率。如PW_(12)/ SBA-15所获得的,为了获得可比的α-紫罗兰酮,属于应用基于传统SiO2的催化剂的五倍以上。

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