靳晓娟.化学通报,2018,81(2):165-169. |
双齿有机膦二茂铁钯(II)配合物的合成和催化活性 |
Synthesis and Catalytic Activity of Palladium Complexes of Organic Bidentate Phosphine Ferrocene |
投稿时间:2017-09-13 修订日期:2017-10-13 |
DOI: |
中文关键词: 双齿有机膦二茂铁钯配合物 合成 催化活性 |
英文关键词:the organic bidentate phosphine ferrocene palladium complexes synthesis catalytic activity |
基金项目:国家科技支撑计划项目“铂族金属催化材料产业化技术开发”(2012BAE06B08);云南省科技人才计划“铂族金属化合物制备技术创新团队建设”(2015HC022) |
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中文摘要: |
以1,1’-双(二苯基膦)二茂铁(dppf)、1,1’-双(二叔丁基膦)二茂铁(dtbpf)为配体,合成了一类双齿有机膦二茂铁钯(II)配合物[(dppf)PdCl2]、[(dtbpf)PdCl2] 、[(dppf)PdBr2]和[(dtbpf)PdBr2],通过核磁共振对配合物进行化学结构表征。评价了它们对Suzuki偶联反应、Sonogashira偶联反应、Heck偶联反应以及2-羟基吡啶与硼酸试剂之间的偶联反应的催化作用。结果表明,配合物化学性质稳定,在非保护气氛下能高效地催化一系列偶联反应。催化剂在单边Sonogashira偶联反应中不但具有较高的催化活性,而且有很好的选择性,显示出很好的应用前景。 |
英文摘要: |
Four palladium(II) complexes of organic bidentate phosphine ferrocene, [(dppf)PdCl2], [(dtbpf)PdCl2], [(dppf)PdBr2], [(dtbpf)PdBr2], were prepared via a direct reaction in an inert atmosphere using Na2PdX4 (X=Cl, Br) as the palladium precursor and the corresponding phosphine ferrocene as the ligand (dppf=1,1’-bis(dipheny-phosphino)ferrocene, dtbpf=1,1’-bis(di-tert-butylphosphino) ferrocene). The complexes were characterized by 1H NMR. The catalytic performance of the complexes was evaluated not only in three well-kunown coupling reactions (Suzuki, Sonogashira and Heck coupling reaction) but also in the coupling reaction between 2-hydroxypyridine and boronic acid reagent. The results showed that the complexes are stable and can efficiently catalyze a series of coupling reactions in a non-protective atmosphere. The catalyst not only has high catalytic activity in unilateral Sonogashira coupling reaction, but also has good selectivity, showing a good application prospect. |
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