Key Laboratory of Engineering Plastics, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Dalton Trans. 2011 Oct 21;40(39):10209-14. doi: 10.1039/c1dt11062d. Epub 2011 Sep 12.
A series of unsymmetrical 2,6-bis(imino)pyridylcobalt(II) complexes, {2-[2,6-(CH(C(6)H(5))(2))(2)-4-Me-C(6)H(2)N==C(CH(3))]-6-(2,6-R(1)(2)-4-R(2)-C(6)H(2)N==CCH(3))-C(5)H(3)NCoCl(2)} where R(1) = Me, Et or (i)Pr, R(2) = H or Me, together with the new symmetrical complex 2,6-2,6-(CH(C(6)H(5))(2))(2)-4-Me-C(6)H(2)N==C(CH(3))-C(5)H(3)NCoCl(2), were synthesized. All of the compounds were fully characterized by (1)H NMR and IR spectroscopy, as well as by elemental analysis. The molecular structures of Co1 (R(1) = Me, R(2) = H) and Co5 (R(1) = Et, R(2) = Me) were further confirmed by single crystal X-ray diffraction, which indicated that the cobalt centres were penta-coordinate with a pseudo square-pyramidal geometry. Upon treatment with MAO or MMAO, these cobalt pre-catalysts exhibited higher activities than any previously reported cobalt pre-catalysts, with values as high as 4.64 × 10(6) g PE mol(-1)(Co) h(-1) for ethylene polymerization at atmospheric pressure. The polyethylenes obtained were of high molecular weight and narrow molecular weight distribution.
一系列不对称的 2,6-双(亚氨基)吡啶钴(II)配合物,{2-[2,6-(CH(C(6)H(5))(2))(2)-4-Me-C(6)H(2)N==C(CH(3))]-6-(2,6-R(1)(2)-4-R(2)-C(6)H(2)N==CCH(3))-C(5)H(3)NCoCl(2)},其中 R(1)= Me、Et 或(i)Pr,R(2)= H 或 Me,以及新的对称配合物 2,6-[2,6-(CH(C(6)H(5))(2))(2)-4-Me-C(6)H(2)N==C(CH(3))](2)-C(5)H(3)NCoCl(2)被合成。所有化合物均通过(1)H NMR 和 IR 光谱以及元素分析进行了充分表征。Co1(R(1)= Me,R(2)= H)和 Co5(R(1)= Et,R(2)= Me)的分子结构进一步通过单晶 X 射线衍射得到证实,这表明钴中心具有五配位的假四方锥几何形状。在 MAO 或 MMAO 处理下,这些钴预催化剂表现出比以前报道的任何钴预催化剂更高的活性,在大气压下进行乙烯聚合时,其值高达 4.64×10(6)g PE mol(-1)(Co)h(-1)。得到的聚乙烯具有高分子量和较窄的分子量分布。