Catalyst system for ethylene selective oligomerization and ethylene oligomerization method
A catalyst and selective technology, applied in the field of catalysis, can solve the problem of low total selectivity of 1-hexene and 1-octene, and achieve the effects of low cost, simple synthesis and long catalyst life
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[0080] In one embodiment of the present invention, the preparation method of catalyst system comprises the following steps:
[0081] Components a, b, and c are pre-mixed or directly added to the reaction system for in-situ synthesis. That is to say, the preparation of the catalyst is to pre-mix the ligand a, the transition metal compound b, and the activator c connected by a bridging group containing a heteroatom; Body a, transition metal compound b, and activator c are directly added to the reaction system for in-situ synthesis;
[0082] The reaction mode of the ligand a, the transition metal compound b and the activator c connected by a bridging group containing a heteroatom described in the general formula I can be reacted in a liquid phase, such as reacting under the action of a solvent. Selected solvents such as toluene, benzene and their derivatives, etc.; can also be used for solid phase reactions; and can also be used to generate catalysts through in-situ reactions du...
Embodiment 1
[0091] 1. Preparation of ligand: N, N'-bis(diisopropylphosphino)-1,1-dimethyl-N, N'-diphenylsilanediamine (C 26 h 44 N 2 P 2 Si)
[0092] (1) Preparation of Lithium Anilide
[0093] in the N 2 Add dehydrated THF (200ml) and anilinolithium (9.31g, 0.1mol) into a fully replaced stirred 500ml reactor, stir well and cool to -78°C with liquid nitrogen. Use a 100ml syringe to extract n-butyllithium hexane solution (41.6ml, 2.4mol / L), slowly add it dropwise to the above solution while stirring, keep stirring at -78°C for 1h, then rise to room temperature and continue stirring for 1 hour, then vacuum pump The solvent was removed, n-hexane (100ml) was added, stirred and dispersed, and then filtered. The obtained filtrate was vacuum-extracted at room temperature to obtain 9.97g (0.098mol, 97.8%) of the product.
[0094] (2) prepare 1,1-diisopropyl-N-phenylphosphine amine (C 12 h 20 NP)
[0095] in N 2 In an atmosphere glove box, dissolve lithium anilide (4.95g, 0.050mol) in de...
Embodiment 2
[0104] With embodiment 1. The difference is that R 1 , R 2 Both are phenyl, R 3 For cyclopentyl. Obtain 83.2g of oligomerization product, catalyst activity is 5.04×10 6 g oligomer / mol Cr·h. The distribution of the oligomerization products is shown in Table 1.
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