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Mn-PNP催化碳酸亚乙酯氢化制甲醇的机理研究
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作者 李婧婧 阳园 王金昭 《分子科学学报》 CAS 北大核心 2023年第1期49-59,共11页
催化氢化CO_(2)及其衍生物转化为高值化学品甲醇符合“绿色化学”的理念,是CO_(2)资源利用中最具应用前景的方法之一.本文基于密度泛函理论系统阐明了PNP配位的金属Mn配合物催化CO_(2)衍生物——碳酸亚乙酯氢化的反应机制.计算结果表明,... 催化氢化CO_(2)及其衍生物转化为高值化学品甲醇符合“绿色化学”的理念,是CO_(2)资源利用中最具应用前景的方法之一.本文基于密度泛函理论系统阐明了PNP配位的金属Mn配合物催化CO_(2)衍生物——碳酸亚乙酯氢化的反应机制.计算结果表明,Mn-PNP首先与氢气反应生成活性催化剂,接着碳酸亚乙酯在Mn—H和N—H物种的协助下经历3次氢化过程得到产物甲醇和副产物乙二醇,其中可能涉及outer-sphere和inner-sphere 2种反应机理,后者的总反应势垒为107.9 kJ·mol^(-1),比前者低了27.0 kJ·mol^(-1).催化氢化反应沿着inner-sphere路径进行更有利,这可能归因于inner-sphere路径有稳定中间体CH3O—Mn配合物的形成.进一步探究了配体的取代基效应对金属Mn配合物催化活性的影响,证实强供电子能力的咪唑基团能够增加金属Mn中心的电子密度,一方面不利于Mn—H成键,另一方面可以提高Mn—H物种的亲核性.研究结果为筛选有效催化CO_(2)衍生物氢化的有机金属催化剂提供一定的理论指导. 展开更多
关键词 金属锰配合物 碳酸亚乙酯氢化 反应机理 密度泛函理论
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Catalytic synthesis of diethyl carbonate with supported Pd-Cu bimetallic nanoparticle catalysts:Cu(Ⅰ) as the active species 被引量:2
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作者 张萍波 周燕 +1 位作者 范明明 蒋平平 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2015年第11期2036-2043,共8页
Cupric oxide (CuO) and copper-cuprous oxide (Cu-Cu2O) nanoparticles were prepared by a simple hydrothermal method for the synthesis of diethyi carbonate (DEC) from ethanol. During these syntheses, varying NaOH a... Cupric oxide (CuO) and copper-cuprous oxide (Cu-Cu2O) nanoparticles were prepared by a simple hydrothermal method for the synthesis of diethyi carbonate (DEC) from ethanol. During these syntheses, varying NaOH and glucose concentrations were applied to explore and pinpoint the active species. It was found that PdCl2/CuO and PdCI2/Cu-Cu2O both catalysts exhibited good thermal stability and morphology. The results of catalytic tests showed that the catalysts prepared with 5 mol/L NaOH show superior catalytic performances because of their lower extent of agglomeration. It is noteworthy that the PdC12/Cu-Cu2O catalysts were the most active, especially the PdCl2/Cu-Cu2O catalyst prepared with 10 mmol glucose and having a higher Cu2O concentration. In Pd(ll)-Cu(II) (PdCl2/CuO) catalysts, there is an induction period, during which Pd(II) is reduced to Pd(0), that must occur prior to electron transfer between Pd and Cu, and this can slow the catalytic reaction. To further pinpoint the active species, PdCl2/Cu-Cu2O catalysts with different Cu2O contents were prepared by controlling the dosages of glucose. The maximum DEC yield obtained with these catalysts was 151.9 mg.g-1.h-1, corresponding to an ethanol conversion of 7.2% and 97.9% DEC selectivity on an ethanol basis. Therefore, it was concluded that Cu+ was the active species in this catalytic system, possibly because a higher proportion of Cu+ reduces the Pd2+ concentration and limits the CO oxidation side reaction, thus increasing DEC selectivity. In addition, Cu+ promotes electron transfer between Pd and Cu without an induction period, which could also promote the catalytic activity. 展开更多
关键词 Cupric oxide Copper-cuprous oxide Diethyl carbonateb Sodium hydroxide concentration Dosages of glucose Active species
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