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首页> 外文期刊>Polymer bulletin >Ethylene polymerization by binuclear chromium complex with tetrakis(pyrazolyl-methyl)benzene ligand
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Ethylene polymerization by binuclear chromium complex with tetrakis(pyrazolyl-methyl)benzene ligand

机译:用四核铬配合物与四核(吡唑基 - 甲基)苯配体进行乙烯聚合

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摘要

The reaction of one equivalent of 1,2,4,5-tetrakis(pyrazolyl-methyl)benzene ligand (L) with two equivalents of Cr(THF)(3)Cl-3 in tetrahydrofuran has produced a binuclear neutral complex of general formula [Cr2L(THF)(2)Cl-6] (1). It was characterized by mass spectrometry, Fourier-transformed infrared, X-ray photoelectron spectroscopy, and magnetic susceptibility. Theoretical calculations supported the formation of binuclear complex (1) with each hexacoordinate metal center. This complex was active in ethylene polymerization employing methylaluminoxane as cocatalyst, with moderate activities (5.7-20.8 kg polymer/(mol precat.) (bar) (h)). The reaction parameters such as temperature, monomer pressure, and Al/Cr ratio were studied. An increase of reaction temperature produced a decreasing of catalytic activity. However, an increase in the monomer pressure did not produce a significant increase in catalytic activity. The Al/Cr ratios used to activate this complex are smaller than those reported for the tris(pyrazolyl)borate chromium complex. This system produced high-density polyethylenes with wide molecular weight, M-w, distributions between 42,280 and 74,346 and polydispersity index from 2.3 to 6.6.
机译:1,2,5-四(吡唑基 - 甲基)苯配体(L)具有两当量的Cr(THF)(3)Cl-3中的1,2,4,5-四(吡唑基 - 甲基)苯配体(L)的反应产生了四氢呋喃中的一般式核中性复合物[Cr2L(THF)(2)CL-6](1)。它的特征在于质谱,傅里叶变换的红外,X射线光电子能谱和磁性敏感性。理论计算支持与每个六坐标金属中心形成双核复合物(1)。该复合物在乙烯聚合中活性甲基聚合,其甲基铝氧烷作为助催化剂,具有中等的活性(5.7-20.8kg聚合物/(mol precat。)(bar)(h))。研究了温度,单体压力和Al / Cr比的反应参数。反应温度的增加产生了催化活性的降低。然而,单体压力的增加不会产生催化活性的显着增加。用于激活该复合物的Al / Cr比小于Tris(吡唑基)硼酸铬络合物的那些。该系统产生具有宽分子量,M-W,42,280和74,346之间的分布的高密度聚乙烯,从2.3到6.6的多分散指数。

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