State Key Laboratory for Supramolecular Structure and Materials, Jilin University, 2699 Qianjin Street, Changchun 130012, People's Republic of China.
Dalton Trans. 2012 Aug 28;41(32):9639-45. doi: 10.1039/c2dt30778b. Epub 2012 Jul 5.
Bis(imino)aryl NCN pincer Ni(II) complexes 2,6-(ArN=CH)(2)C(6)H(3)NiBr (1: Ar = 2,6-Me(2)C(6)H(3); 2: Ar = 2,6-Et(2)C(6)H(3); 3: Ar = 2,6-(i)Pr(2)C(6)H(3)) were prepared via the oxidative-addition of Ni(0)(Ph(3)P)(4) with bis(N-aryl)-2-bromoisophthalaldimine. These nickel complexes were characterized by NMR and elemental analyses. Their solid molecular structures were established by X-ray diffraction analyses. The nickel metal centers adopt distorted square planar geometries with the bromine atoms acting as one coordinate ligands. The NCN pincer Fe(II) complexes 2,6-(ArN=CH)(2)C(6)H(3)Fe(μ-Cl)(2)Li(THF)(2) (4: Ar = 2,6-Me(2)C(6)H(3); 5: Ar = 2,6-Et(2)C(6)H(3); 6: Ar = 2,6-(i)Pr(2)C(6)H(3)) were synthesized by lithium salt metathesis reactions of the ligand lithium salts with FeCl(2). X-ray structure analyses of 4 and 5 revealed that the Fe(II) complexes are hetero-dinuclear with the iron atoms in trigonal bipyramidal environments. When activated with MAO, the nickel complexes are active for norbornene vinyl polymerization but are inert for butadiene polymerization. The Fe(II) complexes show moderate activities in butadiene polymerization when activated with alkylaluminium, affording the cis-1,4 enriched polymer.
双(亚胺基)芳基 NCN 钳镍(II)配合物 2,6-(ArN=CH)(2)C(6)H(3)NiBr(1:Ar = 2,6-Me(2)C(6)H(3);2:Ar = 2,6-Et(2)C(6)H(3);3:Ar = 2,6-(i)Pr(2)C(6)H(3))通过 Ni(0)(Ph(3)P)(4)与双(N-芳基)-2-溴异酞亚胺的氧化加成制备。这些镍配合物通过 NMR 和元素分析进行了表征。其固体分子结构通过 X 射线衍射分析确定。镍金属中心采用扭曲的正方形平面几何形状,溴原子作为一个配位配体。NCN 钳铁(II)配合物 2,6-(ArN=CH)(2)C(6)H(3)Fe(μ-Cl)(2)Li(THF)(2)(4:Ar = 2,6-Me(2)C(6)H(3);5:Ar = 2,6-Et(2)C(6)H(3);6:Ar = 2,6-(i)Pr(2)C(6)H(3))通过配体锂盐与 FeCl(2)的锂盐交换反应合成。4 和 5 的 X 射线结构分析表明,铁(II)配合物是异双核的,铁原子处于三角双锥环境中。当用 MAO 激活时,镍配合物对降冰片烯的乙烯聚合具有活性,但对丁二烯聚合不具有活性。当用烷基铝激活时,Fe(II)配合物在丁二烯聚合中表现出中等活性,得到顺 1,4 富集聚合物。