镍络合物催化乙烯均匀寡聚反应的螯合控制

Q4 Chemical Engineering 分子催化 Pub Date : 1994-08-12 DOI:10.1016/0304-5102(94)00050-6
Wilhelm Keim, Rolf P. Schulz
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引用次数: 81

摘要

研究了不同的k2-P O螯合配体对镍催化乙烯低聚反应的影响。配体4-8和14,15与双(π-甲基)镍反应,得到了7个新的配合物9-13和16,17,改变了k2-P O螯合物的环大小,并在k2-P O螯合物中引入了甲基取代基。这些配合物作为前驱配合物,导致活性乙烯低聚催化剂。将螯合环的大小从五元增加到六元或七元,会显著降低催化活性。然而,通过在六元镍杂环中引入双键或芳香环,产生了非常活跃的乙烯低聚体系。在Ph2PCH(CH3)COOH(14)和Ph2PC(CH3)2COOH(15)中引入甲基也能显著提高活性。
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Chelate control in the nickel-complex catalysed homogeneous oligomerization of ethylene

The impact of various k2-P⌢O chelate ligands on nickel catalysed ethylene oligomerization has been investigated. The ligands 4-8 and 14, 15 were reacted with bis(π-methallyl)nickel yielding seven new complexes, 9-13 and 16, 17 in which the k2-P⌢O chelate ring size was altered and in which methyl substituents were introduced into the k2-P⌢O chelate. These complexes served as precursor complexes leading to active ethylene oligomerization catalysts. Increasing the chelate ring size from a five-membered to a six or seven-membered ring diminishes catalytic activity dramatically. However, by introducing double bonds or an aromatic ring into the six-membered nickelaheterocycle yielded very active ethylene oligomerization systems. Introducing methyl groups into Ph2PCH(CH3)COOH (14) and Ph2PC(CH3)2COOH (15) also leads to a significant increase in activity.

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来源期刊
分子催化
分子催化 Chemical Engineering-Catalysis
CiteScore
1.50
自引率
0.00%
发文量
2959
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Author index Subject index Hydrolysis of sucrose by dealuminated Y-zeolites Synthesis and application of organophilic polystyrene-montmorillonite supported onium salts in organic reactions Effect of the reduction temperature on the selectivity of the high temperature reaction of acetone and hydrogen over alumina and titania supported nickel and cobalt catalysts
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