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首页> 外文期刊>European journal of inorganic chemistry >Iron and cobalt complexes of tridentate N-donor ligands in ethylene polymerization: Efficient shielding of the active sites by simple phenyl groups
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Iron and cobalt complexes of tridentate N-donor ligands in ethylene polymerization: Efficient shielding of the active sites by simple phenyl groups

机译:乙烯聚合中三齿N供体配体的铁和钴配合物:简单的苯基有效屏蔽活性位

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摘要

Tridentate 2,6-bis[3(5)-pyrazolyl]pyridines and 2,6-bis(4-pyrimidinyl)pyridine were synthesized and characterized spectroscopically and by single-crystal X-ray structure analysis. The derived complexes with FeCl2 and CoCl2 were investigated for their activity in the ethylene polymerization in the presence of methylalumoxane (MAO). Iron and cobalt catalysts bearing the ligand 2,6-bis[5-butyl-1-(4-nitrophenyl)pyrazol-3-yl)pyridine showed moderate catalytic activity and gave PE with high molecular weight, although the aryl substituents are not equipped with additional bulky side chains in the 2,6-positions to shield the metal centre. This can be explained by the geometric parameters of the pyrazole units, which provide efficient shielding of the active site, even with unsubstituted aryl groups. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).
机译:合成了三齿2,6-双[3(5)-吡唑基]吡啶和2,6-双(4-嘧啶基)吡啶,并通过光谱和单晶X射线结构分析对其进行了表征。在甲基铝氧烷(MAO)存在下,研究了衍生的FeCl2和CoCl2配合物在乙烯聚合中的活性。带有配体2,6-双[5-丁基-1-(4-硝基苯基)吡唑-3-基)吡啶的铁和钴催化剂显示适中的催化活性,并具有高分子量的PE,尽管没有配备芳基取代基在2,6位带有额外的笨重侧链,以屏蔽金属中心。这可以通过吡唑单元的几何参数来解释,所述吡唑单元的几何参数即使对于未取代的芳基也可以提供对活性位点的有效屏蔽。 ((C)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,Germany,2008)。

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