首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Vanadium chlorides supported by BIAN (BIAN = bis(arylimo)-acenaphthene) ligands: Synthesis, characterization, and catalysis on ethylene polymerization
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Vanadium chlorides supported by BIAN (BIAN = bis(arylimo)-acenaphthene) ligands: Synthesis, characterization, and catalysis on ethylene polymerization

机译:Bian(BIAN = BIS(芳基) - 宿萘)配体的钒氯化物:合成,表征和乙烯聚合的催化

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摘要

Several vanadium chlorides bearing bis(arylimino)-acenaphthene (BIAN) ligands, (2,6-Me2C6H3-BIAN)V (THF)Cl-3 (1), (2,6-Et2C6H3-BIAN)V(THF)Cl-3 (2), (2,6-(Pr2C6H3)-Pr-i-BIAN)V(THF)Cl-3 (3), [3,5-(CF3)(2)C6H3-BIAN] V(THF)Cl-3 (4), [4-OMe-C6H4-BIAN]V(THF)Cl-3 (5), and [2,6-(Ph2CH)(2)-4-OMeC6H2-BIAN]V. (THF)Cl-3 (6) were synthesized by direct reaction of VCl3(THF)(3) with corresponding BIAN ligands. All these complexes were characterized by elemental analyses, and FT-IR spectroscopy. The molecular structures of 1, 2, and 4 were identified by X-ray crystallography, in which the six-coordinated vanadium metal centers were in distorted octahedral geometry with the oxygen atom of the coordinated THF, two nitrogen atoms of the diimine ligand and one chlorine atom in the same plane. When activated with AlEt2Cl these vanadium complexes showed high catalytic activities for ethylene polymerization affording linear polyethylene with high molecular weight. However, when MAO was used as co-catalyst, ultra high molecular-weight polymers were obtained albeit with decreased activity. (C) 2019 Elsevier Ltd. All rights reserved.
机译:几种含有双(芳基氨基氨基) - 丙烯骨(Bian)配体的几种钒氯化物,(2,6-Me2C6H3-Bian)V(THF)Cl-3(1),(2,6-Et 2 C6H3-Bian)V(THF)Cl- 3(2),(2,6-(PR2C6H3)-PR-I-Bian)V(THF)Cl-3(3),[3,5-(CF3)(2)C6H3-Bian] V(THF) C1-3(4),[4-OME-C6H4-BIAN] V(THF)CL-3(5),[2,6-(pH2CH)(2)-4-OMEC6H2-BIAN] v。 (THF)通过直接反应VCL3(THF)(3)与相应的Bian配体来合成Cl-3(6)。所有这些配合物都是通过元素分析和FT-IR光谱的特征。通过X射线晶体学鉴定了1,2和4的分子结构,其中六个协调的钒金属中心与配位THF的氧原子变形,二氨基配体的两个氮原子和1个氮原子扭曲的八面体几何形状同一平面中的氯原子。当用Alet2Cl活化时,这些钒络合物显示出高乙烯聚合的高催化活性,得到具有高分子量的线性聚乙烯。然而,当MAO被用作助催化剂时,虽然活性降低,但仍获得超高分子量聚合物。 (c)2019 Elsevier Ltd.保留所有权利。

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