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Chemoselective Hydrogenation of Nitroarenes Catalyzed by Molybdenum Sulphide Clusters

机译:硫化钼簇催化的硝基酮的化学选择性氢化

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摘要

Herein, we describe an atom efficient and general protocol for the chemoselective hydrogenation of nitroarenes to anilines catalyzed by well-defined diimino and diamino cubane-type Mo3S4 clusters. The novel diimino [Mo3S4Cl3(dnbpy)(3)](+) ([5](+)) (dnbpy=4,4'-dinonyl-2,2'-dipyridyl, L1) trinuclear complex was synthesized in high yields by simple ligand substitution reactions starting from the thiourea (tu) [Mo3S4(tu)(8)(H2O)]Cl-4 center dot 4H(2)O (3) precursor. This strategy has also been successfully adapted for the isolation of the diamino [Mo3S4Cl3(dmen)(3)](BF4) ([6](BF4)), (dmen=N, N'-dimethylethylenediamine) salt. Applying these catalysts, high selectivity in the hydrogenation of functionalized nitroarenes has been accomplished. Over thirty anilines bearing synthetically functional groups have been synthesized in 70 to 99% yield. Notably, the integrity of the cluster core is preserved during catalysis. Based on kinetic studies on the hydrogenation of nitrobenzene and other potential reaction intermediates, the direct reduction to aniline is the preferential route.
机译:在此,我们描述了用良好定义的二聚氨基和二氨基嵌合型MO3S4簇催化的硝基酮对苯胺的化学选择性氢化的原子有效和一般方案。新的DIIMImino [MO3S4Cl3(DNBPY)(3)(3)](+)([5](+))(DNBPY = 4,4'-二烷基-2,2'-二吡啶基,L1)TININCTCLEC含量通过从硫脲(Tu)开始的简单配体取代反应[Mo3S4(Tu)(8)(8)(H2O)] Cl-4中心点4h(2)O(3)前体。该策略也已成功适用于分离偶数[Mo3S4Cl3(Dmen)(3)](BF4)([6](BF4)),(Dmen = N,N'-二甲基乙基二胺)盐。施加这些催化剂,已经完成了官能化硝基酮的氢化的高选择性。在含有合成官能团的30多个苯胺中已在70%至99%的产率中合成。值得注意的是,在催化期间保留了群集核心的完整性。基于硝基苯的氢化的动力学和其他潜在反应中间体的动力学研究,直接还原对苯胺是优先途径。

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