201140-86-5Relevant academic research and scientific papers
Cationic para-benzhydryl substituted α-diimine nickel catalyzed ethylene and 1-decene polymerizations via controllable chain-walking
Tian, Susu,Zhang, Yang,Li, Ruiping,Wang, Fuzhou,Li, Weimin
, p. 492 - 498 (2019)
A series of α-diimine nickel complexes bearing para-benzhydryl groups, {[(2,6-R2-4-CHPh2C6H2N = C)2Nap]NiBr2, Nap: 1,8-naphthdiyl, R = Me (C1); R = Et (C2); R = iPr (C3)}, were s
Binuclear transition metal complexes
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Page/Page column 62, (2010/02/14)
Dinuclear transition metal complexes (I) are new. Dinuclear transition metal complexes (I) are new. M 1, M 2group 3-11 transition metals, A1 or B1; L1-L4 : N, P, S, O, C, Si, Se, As or Sb; A1, A2 : groups and/or atoms that centers L1 with L2 and L3 with L
The formation and polymerization behavior of Ni(II) α-diimine complexes using various aluminum activators
Maldanis, Richard J,Wood, John S,Chandrasekaran,Rausch, Marvin D,Chien, James C.W
, p. 158 - 167 (2007/10/03)
Several Ni(II) α-diimine complexes have been synthesized and examined for ethylene and propylene polymerization in combination with different aluminum co-catalysts. The precatalysts used in the study were [ArN=C(Nap)-C(Nap)-C(Nap)=NAr]NiBr2 (Nap = 1,8-naphthdiyl) (1, Ar = 2,4,6-trimethylphenyl; 2, Ar = 2-tBu phenyl; 3, Ar = 2-iPr phenyl). These complexes were synthesized via a one-pot reaction where the ligand is formed via an acid catalyzed condensation followed by direct addition of nickel(II) bromide. The complexes were also prepared by a two-step procedure where the ligand was first formed by condensation between the appropriate aniline and acenapthoquinone, and the resulting ligand was then allowed to react with (1,2-dimethoxyethane) nickel(II) dibromide. X-ray structural studies of complexes 1 and 2 have been carried out. Diethylaluminum chloride (DEAC), and 1,3-dichloro-1,3-diisobutyldialuminoxane (DCDAO) show higher activities for ethylene and propylene polymerizations in combination with these Ni(II) α-diimine complexes than does polymethylaluminoxane (MAO). The molecular weight of the resulting polymers as well as their respective polydispersities and Tms are also presented. The polypropylenes obtained with 1/DEAC and 2/DEAC at 0 °C show similar rr triad percentage as previously reported for polypropylenes generated by MAO activated Ni(II) α-diimine complexes.
