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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Anisole hydrogenation with well-characterized polyoxoanion- and tetrabutylammonium-stabilized Rh(0) nanoclusters: Effects of added water and acid, plus enhanced catalytic rate, lifetime, and partial hydrogenation selectivity
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Anisole hydrogenation with well-characterized polyoxoanion- and tetrabutylammonium-stabilized Rh(0) nanoclusters: Effects of added water and acid, plus enhanced catalytic rate, lifetime, and partial hydrogenation selectivity

机译:苯甲醚加氢与特性良好的聚氧阴离子和四丁基铵稳定的Rh(0)纳米团簇:添加水和酸的影响,以及提高的催化速率,寿命和部分氢化选择性

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摘要

Following a comprehensive look at the arene hydrogenation literature by soluble nanocluster catalysts, six key, unfulfilled goals in nanocluster arene hydrogenation catalysis are identified. To begin to address those six goals, well-characterized polyoxoanion- and tetrabutylammonium-stabilized Rh(0) nanoclusters have been synthesized by the reduction of the precisely defined precatayst [BU4N](5)Na-3[(1,5-COD)(RhP2W15Nb3O62)-P-.] with H-2 in propylene carbonate solvent. These Rh(0) nanoclusters are characterized by their stoichiometry of formation, transmission electron microscopy, and the two rate constants which characterize their mechanism of formation; previous studies in our laboratories have provided additional characterization of polyoxoanion-stabilized Rh(0) nanoclusters. Propylene carbonate solutions of the Rh(0) nanoclusters catalyze the hydrogenation of anisole (methoxybenzene) under mild conditions (22-78 degreesC, 30-40 psig H-2). Proton donors such as water or (HBF4Et2O)-Et-. are discovered to affect both nanocluster formation and nanocluster arene hydrogenation catalysis. Under identical conditions, the Rh(0) nanoclusters are 10-fold more active than a commercially available, oxide-supported 5% Rh/Al2O3 catalyst of the same average metal-particle size. A series of lifetime experiments shows that the Rh(0) nanoclusters are capable of at least 2600 total turnovers (TTO), a lifetime significantly longer than the similar to 100 TTO often seen for nanocluster arene hydrogenation catalysts, and a lifetime slightly better than the prior record of 2000 TTO for a literature nanocluster system. The present polyoxoanion-stabilized Rh(0) nanoclusters also display a record, albeit modest, 30% selectivity for the partial hydrogenation of anisole to I -methoxycyclohexene with an overall yield of up to 8% at higher temperatures. In comparison to the 5% Rh/Al2O3 catalyst, the polyoxoanion-stabilized nanoclusters yield a 4.7-fold higher maximum yield of I -methoxycyclohexene. Finally, the seven main findings of the present work are summarized, including how they address five of the aforementioned six main goals in nanocluster arene hydrogenation. [References: 81]
机译:在对可溶性纳米簇催化剂对芳烃加氢的文献进行全面研究之后,确定了纳米簇芳烃加氢催化的六个关键的,未实现的目标。为了开始解决这六个目标,已通过还原精确定义的前催化剂[BU4N](5)Na-3 [(1,5-COD)合成了表征充分的聚氧阴离子和四丁基铵稳定的Rh(0)纳米簇。 (RhP2W15Nb3O62)-P-。]在碳酸亚丙酯溶剂中用H-2洗脱。这些Rh(0)纳米团簇的特征是其形成的化学计量,透射电子显微镜以及表征其形成机理的两个速率常数。我们实验室中的先前研究提供了聚氧阴离子稳定的Rh(0)纳米团簇的其他特征。 Rh(0)纳米簇的碳酸丙烯酯溶液在温和的条件下(22-78℃,30-40 psig H-2)催化苯甲醚(甲氧基苯)的氢化。质子供体,例如水或(HBF4Et2O)-Et-。已发现它们既影响纳米团簇的形成又影响纳米团簇的芳烃氢化催化。在相同的条件下,Rh(0)纳米团簇的活性比市售的氧化物负载的5%Rh / Al2O3催化剂具有相同的平均金属粒度大10倍。一系列寿命实验表明,Rh(0)纳米团簇的总周转率(TTO)至少为2600,寿命比纳米簇芳烃加氢催化剂通常所见的100 TTO更长,寿命略长于TTO。先前的2000 TTO用于文献纳米集群系统的记录。本发明的聚氧阴离子稳定的Rh(0)纳米簇也显示出创纪录的选择性,尽管在较高温度下苯甲醚部分氢化为I-甲氧基环己烯的选择性为30%,总收率高达8%。与5%Rh / Al2O3催化剂相比,聚氧阴离子稳定的纳米团簇的I-甲氧基环己烯的最大产率高4.7倍。最后,总结了本工作的七个主要发现,包括它们如何解决纳米簇芳烃氢化中上述六个主要目标中的五个。 [参考:81]

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