WenJuan Zhang

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Name: 张文娟
Organization: Institute of Chemistry , China
Department:
Title: Associate Researcher/Associate Professor(PhD)
Co-reporter:Shengdong Wang;Shizhen Du;Dr. Wenjuan Zhang;Dr. Sin Asuha;Dr. Wen-Hua Sun
ChemistryOpen 2015 Volume 4( Issue 3) pp:328-334
Publication Date(Web):
DOI:10.1002/open.201402113

Abstract

Nickel(II) complexes have attracted much attention as a new generation of olefin catalysts since the α-diiminonickel complex was discovered as a highly efficient procatalyst for ethylene polymerization. A series of novel 4-arylimino-1,2,3-trihydroacridylnickel(II) dihalide complexes was synthesized in a one-pot reaction of 2,3-dihydroacridine-4-one and different anilines with nickel(II) chloride or nickel(II) bromide 1,2-dimethoxyethane complex. The complexes were characterized by infrared spectroscopy and elemental analysis. The molecular structures of the representative complexes 4-(2,6-diisopropylphenylimino)-1,2,3-trihydroacridylnickel(II) dichloride (C3), 4-(2,4,6-trimethylphenylimino)-1,2,3-trihydroacridylnickel dichloride(II) (C4), and 4-(2,4,6-trimethylphenylimino)-1,2,3-trihydroacridylnickel(II) dibromide (C9) were confirmed by single-crystal X-ray crystallography, revealing a distorted tetrahedral geometry around the nickel(II) of C3 and distorted trigonal bipyramidal geometry for C4 and C9. With the activation of trimethylaluminium (TMA), all nickel(II) complexes exhibited good activity for ethylene oligomerization, and oligomer products ranged from butene (C4) to hexadecene (C16).

Co-reporter:Wenjuan Zhang;Shaoli Wang;Shizhen Du;Cun-Yue Guo;Xiang Hao;Wen-Hua Sun
Macromolecular Chemistry and Physics 2014 Volume 215( Issue 18) pp:1797-1809
Publication Date(Web):
DOI:10.1002/macp.201400140
Co-reporter:Youhong Wang, Wenjuan Zhang, Wei Huang, Lin Wang, Carl Redshaw, Wen-Hua Sun
Polymer 2011 Volume 52(Issue 17) pp:3732-3737
Publication Date(Web):3 August 2011
DOI:10.1016/j.polymer.2011.06.036
The series of trichlorotitanium 2-(2-pyridinyliminomethyl)phenolates, [4,6-tBu2C6H2O-2–CHNC5R1–4N]TiCl3 (R1–4 = H (1); R1,3,4 = H, R2 = Me (2); R1,2,4 = H, R3 = Me (3); R2,4 = H, R1,3 = Me (4); R1,3 = H, R2 = CF3, R4 = Cl (5)), were synthesized and characterized by elemental analysis and 1H/13C NMR spectroscopy. The molecular structures of the representative complexes 2 and 4 were confirmed by single-crystal X-ray diffraction, and revealed distorted octahedral geometry at titanium. In the presence of MAO, all titanium pro-catalysts showed good activities for ethylene polymerization with good thermal stability at the optimum temperature of 50 °C. In comparison with the ethylene polymerization results, the activity observed for the co-polymerization of ethylene/1-hexene was far lower, but the polymers produced were of high molecular weight. For the co-polymerization of ethylene/1-octene, enhanced catalytic activity was observed, with 1-octene incorporation of up to 3.83 mol%.
2-PROPIONYL[1,10]PHENANTHROLINE
1H-BENZIMIDAZOLE, 2,2'-(2,6-PYRIDINEDIYL)BIS[1-ETHYL-5,6-DIMETHYL-
1H-BENZIMIDAZOLE, 2,2'-(2,6-PYRIDINEDIYL)BIS[1,6-DIMETHYL-
Phenol, 2,4-bis(1,1-dimethylethyl)-6-(4,5-diphenyl-1H-imidazol-2-yl)-
PHENOL, 2-[[[2,6-BIS(1-METHYLETHYL)PHENYL]IMINO]METHYL]-4,6-DIIODO-