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作 者:范瑞清[1] 朱东升[1] 母瀛[1] 李光华[2] 冯守华[2]
机构地区:[1]吉林大学超分子化学与材料教育部重点实验室 [2]吉林大学无机合成与制备化学国家重点实验室,长春130012
出 处:《高等学校化学学报》2005年第7期1215-1219,M004,共6页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:20374023)资助.
摘 要:由三齿配体2,6-二[1-(2-甲基苯基亚胺)乙基]吡啶(L1)和2,6-二[(1-苯基亚胺)乙基]吡啶(L2)分别与N iC l2.6H2O在乙腈中反应,合成了两个吡啶二亚胺基氯化镍配合物L1N i(Ⅱ)C l2.CH3CN(1)和L2N i(Ⅱ)C l2(2).通过元素分析、IR和1H NM R对配体和配合物进行了结构表征,并测定了配合物1和2的晶体结构.X射线衍射分析结果表明,两个配合物均为五配位扭曲三角双锥构型,属单斜晶系,Cc空间群.配合物1的晶胞参数a=2.578 3(5)nm,b=1.484 3(3)nm,c=1.586 6(3)nm;β=122.82(3),°V=5.102 4(18)nm3,Z=4,R1=0.070 8,配合物2的晶胞参数a=1.577 2(1)nm,b=0.859 4(1)nm,c=1.545 9(1)nm;β=103.27(1),°V=2.039(2)nm3,Z=4,R1=0.037 5.配合物1和2经M AO活化后对乙烯聚合表现出较低的催化活性.Reactions of equimolar ratios of NiCl_2·6H_2O to the tridentate ligands 2,6-bis[1-(2-methyl-phenylimino)ethyl]pyridine(L^1) or 2,6-bis[(1-phenylimino)ethyl]pyridine(L^2) in acetonitrile afford the five-coordinated complexes NiCl_2L^1·CH_3CN(1) and [NiCl_2L^2·CH_3CN](2), respectively. All ligands and complexes were characterized by using elemental analysis, IR and ()~1H NMR spectroscopy. The structures of complexes 1 and 2 were determined by single-crystal X-ray diffraction. Crystallographic studies on complexes 1 and 2 reveal both complexes to be pentacoordinated with geometries that can be best described as distorted trigonal bipyramidal. Complex 1 crystallizes in the monoclinic system, space group Cc, with -{a=-}2.578 3(5) nm, b=1.484 3(3) nm, c=1.586 6(3) nm; β=122.82(3)°, V=5.102 4(18) nm^3, -{Z=4-}, R_1=0.070 8. Complex 2 belongs to monoclinic system with space group Cc, a=1.577 2(1) nm, -{b=-}0.859 4(1) nm, c=1.545 9(1) nm; β=103.27(1)°, (V=2.039 4(2) nm^3,) Z=4, R_1=0.037 5. Complexes 1 and 2 exhibit lower catalytic activities for ethylene polymerization upon activation with MAO.
关 键 词:吡啶二亚胺基镍配合物 晶体结构 乙烯聚合
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