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首页> 外文期刊>Journal of Organometallic Chemistry >Nickel(II) complexes bearing phosphinooxazoline ligands: Synthesis, structures and their ethylene oligomerization behaviors
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Nickel(II) complexes bearing phosphinooxazoline ligands: Synthesis, structures and their ethylene oligomerization behaviors

机译:含膦基恶唑啉配体的镍(II)配合物:合成,结构及其乙烯低聚行为

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摘要

A series of Ni(II) complexes 4a-f ligated by the unsymmetrical phosphino-oxazolines (PHOX) were synthesized and characterized by elemental analysis and IR spectroscopy, and the structures of complexes 4c-4e were confirmed by the X-ray crystallographic analysis. All derivatives showed distorted tetrahedron geometry by the nickel center and coordinative atoms. Upon activation with methylaluminoxane (MAO) or Et2AlCl, these complexes exhibited considerable to high activity of ethylene oligomerization. The ligands environments and reaction conditions significantly affect their catalytic activities, while the highest oligomerization activity (Up to 1. 18 X 10(6) g center dot mol(-1) (Ni) - h(-1)) was observed for 4d at 20 atm of ethylene. Incorporation of 2-4 equivalents of PPh3 as auxiliary ligands in the 4a-f/MAO catalytic systems led to higher activity and longer catalytic lifetime. (c) 2005 Elsevier B.V. All rights reserved.
机译:合成了一系列由不对称膦-恶唑啉(PHOX)连接的Ni(II)配合物4a-f,并通过元素分析和红外光谱对其进行了表征,并通过X射线晶体学分析证实了配合物4c-4e的结构。所有衍生物均显示出镍中心和配位原子扭曲的四面体几何形状。在用甲基铝氧烷(MAO)或Et2AlCl活化后,这些络合物表现出相当高的乙烯低聚活性。配体的环境和反应条件显着影响其催化活性,而最高的低聚活性(高达1. 18 X 10(6)g中心点mol(-1)(Ni)-h(-1)观察到4d在乙烯的20大气压下在4a-f / MAO催化体系中引入2-4当量的PPh3作为辅助配体可导致更高的活性和更长的催化寿命。 (c)2005 Elsevier B.V.保留所有权利。

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