Coordination precipitation polymerization method for olefin polymerization and polyolefin

Abstract

The present invention relates to the technical field of polyolefin, and discloses a coordination precipitation polymerization method for olefin polymerization and polyolefin, the method comprises: mixing an olefin monomer, a catalyst and an auxiliary agent, and carrying out a polymerization reaction, the olefin monomer contains a non-polar monomer and a polar monomer, the non-polar monomer is selected from one or more than two of ethylene, alpha-olefin and internal olefin, and the polar monomer is selected from one or more than two of enol, unsaturated carboxylic acid and unsaturated carboxylic ester; the catalyst is selected from late transition metal complexes as shown in a formula (I). According to the invention, the loading process flow of the catalyst can be omitted, polymerization self-forming of the olefin homogeneous catalyst is realized, and polyolefin with good particle morphology is prepared. # imgabs0 #

Description

Technical Field

[0001] The invention relates to the technical field of polyolefins, and in particular to a coordination precipitation polymerization method for olefin polymerization and polyolefins. Background Art

[0002] Polyolefin products are inexpensive, have excellent performance and a wide range of applications. Olefin polymerization catalysts and polymerization processes are the core of polyolefin technology. From the perspective of the development of olefin polymerization catalysts, there are two main aspects: (1) Developing catalysts that can prepare polyolefin resins with special properties or better performance, such as metallocene catalysts and non-metallocene late transition metal catalysts; (2) On the basis of further improving catalyst performance, simplifying catalyst preparation processes, reducing catalyst costs, and developing environmentally friendly technologies to improve efficiency and enhance competitiveness. Before the 1980s, the focus of polyethylene catalyst research was on pursuing catalyst efficiency. After nearly 30 years of efforts, the catalytic efficiency of polyethylene catalysts has increased by orders of magnitude, thereby simplifying the production process of polyolefins and reducing energy and material consumption. Ziegler-Natta catalysts have been around for nearly 60 years. Although polyolefin catalysts such as metallocenes and non-metallocenes have emerged during this period, there are many problems in their industrialization, such as expensive co-catalysts and difficulties in loading the main catalyst. In recent years, olefin polymerization catalyst products have emerged in an endless stream at home and abroad, and catalyst stability and polymerization catalytic activity have also been continuously improved. However, there are still deficiencies in hydrogen sensitivity, control of catalyst particle regularity and particle size distribution. Current research is still focused on developing spherical or quasi-spherical supported catalysts with simple process, good hydrogen sensitivity and uniform particle size distribution.

[0003] Common polymerization processes in the polyolefin industry include slurry, gas phase, and bulk polymerization, and the catalysts used are mostly supported catalysts. The polymerized monomers are inserted and complex-grown on the supported catalyst to prepare granular polymer particles. The stability of the catalyst in the device and the morphology of the polymer depend to a large extent on the particle morphology, particle strength, and particle size distribution of the catalyst. Therefore, the catalyst loading technology plays a vital role in the olefin polymerization effect.

[0004] In his book Principles of Polymerization, Odian pointed out that precipitation polymerization is a polymerization process in which the polymerization reaction starts from a homogeneous system but can be quickly converted into a heterogeneous system. Usually, precipitation polymerization occurs in a solution of monomers or monomers and solvents, and the formed polymer precipitates out because it is insoluble in the reaction medium. In recent years, precipitation polymerization has aroused widespread research interest because it can obtain polymer microsphere particles with pure surfaces. However, precipitation polymerization is mostly used in free radical polymerization reactions. If precipitation polymerization can be combined with co-coordination polymerization, in a commonly used solvent for coordination polymerization, by controlling the polymerization reaction process, it is possible to directly prepare polymer particles with good particle morphology from non-loaded transition metal complexes through precipitation polymerization, which has good application prospects. Summary of the invention

[0005] The purpose of the present invention is to overcome the problems of complicated catalyst loading process and polymer deashing and granulation post-treatment procedures in the prior art, and to provide a coordination precipitation polymerization method and polyolefin for olefin polymerization. The method controls the polymerization reaction process to realize the direct preparation of polyolefin with good particle morphology by precipitation polymerization of olefin monomers under the action of late transition metal complexes, thereby eliminating the complicated catalyst loading process, greatly simplifying the preparation process of the main catalyst, having low equipment requirements, low energy consumption and low environmental pollution.

[0006] In order to achieve the above object, the present invention provides a coordination precipitation polymerization method for olefin polymerization, which comprises mixing olefin monomers, a catalyst and an auxiliary agent to carry out a polymerization reaction; the olefin monomers contain non-polar monomers and polar monomers, the non-polar monomers are selected from one or more of ethylene, α-olefins and internal olefins, and the polar monomers are selected from one or more of ene alcohols, unsaturated carboxylic acids and unsaturated carboxylic acid esters; the catalyst is selected from a late transition metal complex represented by formula (I),

[0007]

[0008] Wherein, M is selected from Group VIII metals, R1 is selected from substituted or unsubstituted C6-C20 aromatic groups, R3 and R4 are each independently selected from halogen, C1-C10 hydrocarbon groups, P(R5)3, NR6R7 and OR8R9, or R3 and R4 are interconnected to form an eight-membered ring, wherein R5 is selected from substituted or unsubstituted C1-C10 alkyl groups and substituted or unsubstituted C6-C10 aromatic groups, R6, R7, R8 and R9 are each independently selected from C1-C10 hydrocarbon groups, or R6, R7 and N are interconnected to form a five-membered ring or a six-membered ring, or R8, R9 and O are interconnected to form a five-membered ring or a six-membered ring.

[0009] Preferably, the structural formula of the late transition metal complex is as shown in formula (II),

[0010]

[0011] Among them, R 11 -R 15 Each is independently selected from hydrogen, halogen, hydroxyl, and substituted or unsubstituted C1-C20 hydrocarbon groups.

[0012] Preferably, the late transition metal complex is selected from the following complexes,

[0013] Complex 1: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 2: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is F, R3 is methyl, and R4 is pyridine;

[0014] Complex 3: Complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0015] Complex 4: Complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0016] Complex 5: Complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0017] Complex 6: Complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0018] Complex 7: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0019] Complex 8: Complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0020] Complex 9: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is methyl, and R4 is pyridine;

[0021] Complex 10: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0022] Complex 11: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0023] Complex 12: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0024] Complex 13: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0025] Complex 14: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is pyridine;

[0026] Complex 15: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0027] Complex 16: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 17: a complex represented by formula (II), wherein M is Ni, R 11 and R 15 is F, R3 is phenyl, and R4 is PMe3; Complex 18: a complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3;

[0028] Complex 19: A complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3;

[0029] Complex 20: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0030] Complex 21: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0031] Complex 22: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0032] Complex 23: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R15 is H, R3 is phenyl, and R4 is PMe3;

[0033] Complex 24: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is phenyl, and R4 is PMe3;

[0034] Complex 25: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0035] Complex 26: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0036] Complex 27: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0037] Complex 28: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0038] Complex 29: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is phenyl, and R4 is PMe3;

[0039] Complex 30: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3;

[0040] Complex 31: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0041] Complex 32: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0042] Complex 33: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0043] Complex 34: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0044] Complex 35: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0045] Complex 36: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 and R4 are connected to each other to form cyclooctene;

[0046] Complex 37: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0047] Complex 38: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 39: a complex represented by formula (II), wherein M is Ni, R 11 -R15 is F, R3 is Cl, and R4 is tetrahydrofuran; Complex 40: a complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0048] Complex 41: A complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0049] Complex 42: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0050] Complex 43: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0051] Complex 44: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0052] Complex 45: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0053] Complex 46: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0054] Complex 47: A complex represented by formula (II), wherein M is Ni, R13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0055] Complex 48: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0056] Complex 49: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0057] Complex 50: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0058] Complex 51: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0059] Complex 52: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran;

[0060] Complex 53: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 54: a complex represented by formula (II), wherein M is Ni, R 11 -R 15 is F, R3 is Br, and R4 is tetrahydrofuran; Complex 55: a complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0061] Complex 56: A complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0062] Complex 57: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0063] Complex 58: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0064] Complex 59: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0065] Complex 60: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0066] Complex 61: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is Br, and R4 is tetrahydrofuran;

[0067] Complex 62: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0068] Complex 63: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0069] Complex 64: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0070] Complex 65: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0071] Complex 66: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is Br, and R4 is tetrahydrofuran;

[0072] Complex 67: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0073] Complex 68: A complex represented by formula (II), wherein M is Pd, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 69: a complex represented by formula (II), wherein M is Pd, R 11 -R 15 is F, R3 is methyl, and R4 is pyridine; Complex 70: a complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0074] Complex 71: A complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12-R 15 is H, R3 is methyl, and R4 is pyridine;

[0075] Complex 72: A complex represented by formula (II), wherein M is Pd, R 11 is methyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0076] Complex 73: A complex represented by formula (II), wherein M is Pd, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0077] Complex 74: A complex represented by formula (II), wherein M is Pd, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0078] Complex 75: A complex represented by formula (II), wherein M is Pd, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0079] Complex 76: A complex represented by formula (II), wherein M is Pd, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0080] Complex 77: A complex represented by formula (II), wherein M is Pd, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is methyl, and R4 is pyridine;

[0081] Complex 78: A complex represented by formula (II), wherein M is Pd, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0082] Complex 79: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0083] Complex 80: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0084] Complex 81: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0085] Complex 82: A complex represented by formula (II), wherein M is Pd, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is pyridine;

[0086] Complex 83: A complex represented by formula (II), wherein M is Pd, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0087] Complex 84: A complex represented by formula (II), wherein M is Pd, R 11 -R 15 is H, R3 is methyl, and R4 is Cl;

[0088] Complex 85: A complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is Cl;

[0089] Complex 86: A complex represented by formula (II), wherein M is Pd, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is Cl;

[0090] Complex 87: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is Cl;

[0091] Complex 88: A complex represented by formula (II), wherein M is Pd, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is Cl;

[0092] Complex 89: A complex represented by formula (II), wherein M is Pd, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is Cl.

[0093] Preferably, the enol is selected from the monomers represented by formula (G1),

[0094]

[0095] Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, and L4 is selected from C1-C30 alkylene having a side group.

[0096] Preferably, the unsaturated carboxylic acid is selected from the monomers represented by formula (G2),

[0097]

[0098] Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, and L4 is selected from C1-C30 alkylene having a side group.

[0099] Preferably, the unsaturated carboxylic acid ester is selected from the monomers represented by formula (G3),

[0100]

[0101] Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, L4 is selected from C1-C30 alkylene having a side group, and L5 is selected from C1-C30 alkyl.

[0102] Preferably, the auxiliary agent is selected from one or more of an organoaluminum compound, an organoboron compound and an organosilicon compound.

[0103] Preferably, the organoaluminum compound is AlY n X1 3-n ; wherein Y is selected from H, C1-C20 saturated or unsaturated hydrocarbon group and C1-C20 saturated or unsaturated hydrocarbonoxy group, preferably C1-C20 alkyl group, C1-C20 alkoxy group, C7-C20 aralkyl group or C6-C20 aryl group; X 1 is selected from halogen, preferably chlorine or bromine; <n≤3。

[0104] Preferably, the organic boron compound is an aromatic boron and / or a borate.

[0105] Preferably, the aromatic hydrocarbon boron is selected from substituted or unsubstituted phenyl boron, preferably tris(pentafluorophenyl)boron.

[0106] Preferably, the borate is selected from N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate and / or triphenylmethyl tetrakis(pentafluorophenyl)borate.

[0107] Preferably, the organosilicon compound is an alkyl silicon compound.

[0108] Preferably, the general formula of the alkyl silicon compound is SiH1H2H3H4, wherein H1 is selected from C1-C10 alkyl, and H2, H3 and H4 are each independently selected from C1-C10 alkyl or halogen.

[0109] Preferably, when the auxiliary agent contains an organic aluminum compound, the molar ratio of the amount of aluminum element in the organic aluminum compound to the amount of M element in the catalyst is (10-10000000):1.

[0110] Preferably, when the auxiliary agent contains an organic boron compound, the molar ratio of the amount of the boron element in the organic boron compound to the amount of the M element in the catalyst is (0.1-1000):1.

[0111] Preferably, when the auxiliary agent contains an organosilicon compound, the molar ratio of the amount of silicon element in the organosilicon compound to the amount of M element in the catalyst is (10-10000000):1.

[0112] Preferably, when the auxiliary agent is a combination of an organic aluminum compound, an organic boron compound and an organic silicon compound, the molar ratio of the total amount of aluminum, boron and silicon in the auxiliary agent to the amount of M element in the catalyst is (10-11000000):1.

[0113] Preferably, the polymerization reaction is carried out in the presence of a solvent.

[0114] Preferably, the solvent is selected from one or more of alkanes, halogenated alkanes and aromatic hydrocarbons.

[0115] Preferably, the alkane is selected from one or more of C3-C20 alkanes.

[0116] Preferably, the general formula of the halogenated alkane is R 1 X 2 n2 R 2 X 3 m2 , where X 2 and X 3 Each is independently selected from halogen, m2+n2≥1, R 1 is selected from C1-C10 alkyl or alkenyl, R 2 Selected from C1-C10 alkylene or alkenylene.

[0117] Preferably, the general formula of the aromatic hydrocarbon is R 4 -Ph-R 3 , where R 3 and R 4 Each is independently selected from hydrogen, phenyl and C1-C10 alkane.

[0118] Preferably, the polymerization reaction conditions include: temperature of -50 to 180° C. and time of 10 to 200 min.

[0119] The second aspect of the present invention provides a polyolefin prepared by the above-mentioned coordination precipitation polymerization method for olefin polymerization, wherein the shape of the polyolefin is spherical or quasi-spherical.

[0120] Preferably, the average particle size of the polyolefin is 0.02-50 mm.

[0121] Preferably, the weight average molecular weight of the polyolefin is 10,000-800,000.

[0122] Preferably, the molecular weight distribution index of the polyolefin is ≤10.

[0123] Preferably, the melting point of the polyolefin is 90-140°C.

[0124] Compared with the prior art, the present invention has the following beneficial effects:

[0125] (1) In the coordination precipitation polymerization method for olefin polymerization described in the present invention, before the olefin monomer is polymerized, the system is a uniform reaction solution, and the late transition metal complex does not need to be loaded on an inorganic or organic carrier. By controlling the polymerization process, the polyolefin is precipitated from the system, and the polyolefin is self-formed to prepare spherical or quasi-spherical polyolefins. Therefore, the present invention can avoid the catalyst loading process flow, realize the self-formation of olefin homogeneous catalyst polymerization, and prepare olefin polymers with good particle morphology;

[0126] (2) The coordination precipitation polymerization method for olefin polymerization described in the present invention can prepare spherical or quasi-spherical polar polyolefins with polar groups and a relatively high melting point, that is, polar groups can be introduced into the polyolefin chain, thereby improving the interfacial compatibility of the polyolefin while retaining its crystallization properties;

[0127] (3) The coordination precipitation polymerization method for olefin polymerization described in the present invention does not require subsequent processing such as granulation, and can directly obtain spherical or quasi-spherical polyolefins, which greatly simplifies the preparation process of the main catalyst, has low equipment requirements, low energy consumption, and low environmental pollution. Therefore, the present invention has good industrial application prospects;

[0128] (4) The coordination precipitation polymerization method for olefin polymerization of the present invention directly prepares spherical or quasi-spherical polyolefins with good morphology by selecting the late transition metal complex, olefin monomer and appropriate reaction conditions. The obtained polyolefin is not easy to scale in the reactor and is convenient for transportation.

[0129] (5) The coordination precipitation polymerization method for olefin polymerization described in the present invention can catalyze the polymerization reaction of olefin monomers with high activity, greatly simplify the process flow, and reduce production costs. DETAILED DESCRIPTION

[0130] The specific embodiments of the present invention are described in detail below. It should be understood that the specific embodiments described herein are only used to illustrate and explain the present invention, and are not used to limit the present invention.

[0131] The endpoints and any values ​​of the ranges disclosed in this article are not limited to the precise ranges or values, and these ranges or values ​​should be understood to include values ​​close to these ranges or values. For numerical ranges, the endpoint values ​​of each range, the endpoint values ​​of each range and the individual point values, and the individual point values ​​can be combined with each other to obtain one or more new numerical ranges, which should be considered as specifically disclosed in this article.

[0132] The present invention provides a coordination precipitation polymerization method for olefin polymerization, which comprises mixing olefin monomers, a catalyst and an auxiliary agent to carry out a polymerization reaction; the olefin monomers contain non-polar monomers and polar monomers; the non-polar monomers are selected from one or more of ethylene, α-olefins and internal olefins; the polar monomers are selected from one or more of enols, unsaturated carboxylic acids and unsaturated carboxylic acid esters; the catalyst is selected from a late transition metal complex represented by formula (I),

[0133]

[0134] Wherein, M is selected from Group VIII metals, R1 is selected from substituted or unsubstituted C6-C20 aromatic groups, R3 and R4 are each independently selected from halogen, C1-C10 hydrocarbon groups, P(R5)3, NR6R7 and OR8R9, or R3 and R4 are interconnected to form an eight-membered ring, wherein R5 is selected from substituted or unsubstituted C1-C10 alkyl groups and substituted or unsubstituted C6-C10 aromatic groups, R6, R7, R8 and R9 are each independently selected from C1-C10 hydrocarbon groups, or R6, R7 and N are interconnected to form a five-membered ring or a six-membered ring, or R8, R9 and O are interconnected to form a five-membered ring or a six-membered ring.

[0135] In a preferred embodiment, the late transition metal complex has a structural formula as shown in formula (II),

[0136]

[0137] Among them, R 11 -R 15 Each is independently selected from hydrogen, halogen, hydroxyl, substituted or unsubstituted C1-C20 hydrocarbon group. 11 -R 15 Each is independently selected from hydrogen, halogen, hydroxy, substituted or unsubstituted C1-C10 alkyl and substituted or unsubstituted C6-C15 aryl.

[0138] In formula (I) and formula (II), preferably, M is selected from nickel and palladium.

[0139] In formula (I) and formula (II), preferably, at least one of R3 and R4 is selected from halogen and C1-C8 hydrocarbon group, or R3 and R4 are interconnected to form an eight-membered ring. In one embodiment, R3 and R4 are independently selected from halogen and C1-C8 hydrocarbon group (such as C1-C8 alkyl or aryl). In another embodiment, R3 is selected from halogen and C1-C8 hydrocarbon group (such as C1-C8 alkyl or aryl), R4 is selected from P(R5)3, NR6R7 and OR8R9, wherein R5 is selected from substituted or unsubstituted C1-C10 alkyl and substituted or unsubstituted C6-C10 aryl, R6, R7, R8 and R9 are each selected from C1-C6 hydrocarbon group, and R6, R7 and N are interconnected to form a five-membered ring or a six-membered ring, and R8, R9 and O are interconnected to form a five-membered ring or a six-membered ring. In another embodiment, R3 and R4 are interconnected to form an eight-membered ring.

[0140] In the present invention, when R3 and R4 are connected to form an eight-membered ring, R3 and R4 can be connected to form cyclooctene, etc. When R3 and / or R4 are independently selected from P(R5)3, for example, PMe3, PPh 3、PEt3, etc. When R3 and / or R4 are each independently selected from NR6R7, for example, pyridine (C5H5N), 2-methylpyridine, 3-methylpyridine, 4-methylpyridine, etc. When R3 and / or R4 are each independently selected from OR8R9, for example, tetrahydrofuran (C4H8O), 2-methyltetrahydrofuran, 3-methyltetrahydrofuran, 2,5-dimethyltetrahydrofuran, 2,2-dimethyltetrahydrofuran, etc. In this article, "Me" refers to methyl, "Ph" refers to phenyl, and "Et" refers to ethyl.

[0141] In the present invention, the "substituted" in "substituted or unsubstituted" refers to containing substituents, and the substituents here can be selected from halogen, hydroxyl, C1-C6 alkyl, halogenated C1-C6 alkyl, C1-C6 alkoxy or halogenated C1-C6 alkoxy.

[0142] In the present invention, the alkyl group (such as C1-C6 alkyl, C1-C8 alkyl or C1-C10 alkyl) can be selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, n-pentyl, isopentyl, n-hexyl, isohexyl or 3,3-dimethylbutyl.

[0143] In the present invention, the alkoxy group (such as C1-C6 alkoxy group) can be selected from methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, n-pentoxy, isopentoxy, n-hexoxy, isohexoxy or 3,3-dimethylbutoxy.

[0144] In the present invention, the aryl group (such as a C6-C10 aryl group or a C6-C15 aryl group) may be selected from a phenyl group, a 4-methylphenyl group, a 4-ethylphenyl group, a dimethylphenyl group or a vinylphenyl group.

[0145] In the present invention, the halogen is selected from fluorine, chlorine, bromine or iodine.

[0146] In a further preferred embodiment, the late transition metal complex is selected from the following complexes,

[0147] Complex 1: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5) (in this case, the N on pyridine forms a coordination with the metal Ni);

[0148] Complex 2: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is F, R3 is methyl, and R4 is pyridine (-NC5H5); Complex 3: Complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0149] Complex 4: Complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0150] Complex 5: Complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0151] Complex 6: Complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0152] Complex 7: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0153] Complex 8: Complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0154] Complex 9: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0155] Complex 10: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0156] Complex 11: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0157] Complex 12: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0158] Complex 13: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0159] Complex 14: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0160] Complex 15: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0161] Complex 16: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 17: a complex represented by formula (II), wherein M is Ni, R 11 and R 15 is F, R3 is phenyl, and R4 is PMe3; Complex 18: a complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3;

[0162] Complex 19: A complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3;

[0163] Complex 20: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0164] Complex 21: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0165] Complex 22: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0166] Complex 23: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0167] Complex 24: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is phenyl, and R4 is PMe3;

[0168] Complex 25: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0169] Complex 26: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0170] Complex 27: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0171] Complex 28: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is phenyl, and R4 is PMe3;

[0172] Complex 29: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is phenyl, and R4 is PMe3;

[0173] Complex 30: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3;

[0174] Complex 31: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0175] Complex 32: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0176] Complex 33: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0177] Complex 34: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0178] Complex 35: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0179] Complex 36: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 and R4 are connected to each other to form cyclooctene;

[0180] Complex 37: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene;

[0181] Complex 38: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8) (at this time, the O on tetrahydrofuran forms a coordination with the metal Ni);

[0182] Complex 39: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is F, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0183] Complex 40: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0184] Complex 41: A complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0185] Complex 42: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0186] Complex 43: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0187] Complex 44: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0188] Complex 45: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0189] Complex 46: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0190] Complex 47: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0191] Complex 48: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R13 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0192] Complex 49: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0193] Complex 50: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0194] Complex 51: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0195] Complex 52: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran (-OC4H8);

[0196] Complex 53: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0197] Complex 54: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is F, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0198] Complex 55: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0199] Complex 56: A complex represented by formula (II), wherein M is Ni, R11 is methyl, R 12 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0200] Complex 57: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0201] Complex 58: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0202] Complex 59: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0203] Complex 60: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0204] Complex 61: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0205] Complex 62: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0206] Complex 63: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0207] Complex 64: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0208] Complex 65: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0209] Complex 66: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0210] Complex 67: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran (-OC4H8);

[0211] Complex 68: A complex represented by formula (II), wherein M is Pd, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5); Complex 69: The complex represented by formula (II), wherein M is Pd, R 11 -R 15 is F, R3 is methyl, and R4 is pyridine (-NC5H5); Complex 70: a complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0212] Complex 71: A complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0213] Complex 72: A complex represented by formula (II), wherein M is Pd, R 11 is methyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0214] Complex 73: A complex represented by formula (II), wherein M is Pd, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0215] Complex 74: A complex represented by formula (II), wherein M is Pd, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0216] Complex 75: A complex represented by formula (II), wherein M is Pd, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0217] Complex 76: A complex represented by formula (II), wherein M is Pd, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0218] Complex 77: A complex represented by formula (II), wherein M is Pd, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0219] Complex 78: A complex represented by formula (II), wherein M is Pd, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine;

[0220] Complex 79: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0221] Complex 80: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0222] Complex 81: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0223] Complex 82: A complex represented by formula (II), wherein M is Pd, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is pyridine;

[0224] Complex 83: A complex represented by formula (II), wherein M is Pd, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0225] Complex 84: A complex represented by formula (II), wherein M is Pd, R 11 -R 15 is H, R3 is methyl, and R4 is Cl;

[0226] Complex 85: A complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12 -R15 is H, R3 is methyl, and R4 is Cl;

[0227] Complex 86: A complex represented by formula (II), wherein M is Pd, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is Cl;

[0228] Complex 87: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is Cl;

[0229] Complex 88: A complex represented by formula (II), wherein M is Pd, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is Cl;

[0230] Complex 89: A complex represented by formula (II), wherein M is Pd, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is Cl.

[0231] In the present invention, the method for preparing the above-mentioned late transition metal complex comprises the following steps:

[0232] (1) reacting the compound represented by formula (III) with the compound represented by formula (IV) to generate a ligand;

[0233] (2) reacting the ligand with an M metal compound;

[0234]

[0235] Wherein, the M metal is selected from Group VIII metals, preferably nickel and / or palladium; the definition of R1 is the same as described above.

[0236] In the method of the present invention, the M metal compound can be selected from nickel dimethyldipyridine (Py2NiMe2), bis(1,5-cyclooctadiene) nickel (Ni(COD)2), nickel dichlorotetrapyridine (Ni2Cl2Py4), ethylene glycol dimethyl ether nickel bromide ((DME)NiBr2), ethylene glycol dimethyl ether nickel chloride ((DME)NiCl2), dichlorobis(trimethylphosphine) nickel (NiCl2(PMe3)2), di(pyridine)bis[(trimethylsilyl)methyl]nickel (Ni(Py)2(CH2SiMe3)2), chloro(phenyl)(N,N,N',N'-tetramethyl-1,2-ethylenediamine) nickel (NiArBr(TMEDA)), dibenzyldipyridine nickel (Ni(CH2 Ph)2Py2), phenyl(trimethylphosphine)nickel bromide (NiPhBr(PMe3)2, phenyl(triethylphosphine)nickel chloride (NiPhCl(PEt3)2), diphenylbis(trimethylphosphine)nickel (NiPh2(PMe3)2), dichlorobis(trimethylphosphine)nickel (NiCl2(PMe3)2), dimethyldipyridine palladium (Pd(Me)2Py2), dichlorodipyridine palladium (PdCl2Py2), di(pyridine)bis[(trimethylsilyl)methyl]palladium (Pd(Py)2(CH2SiMe3)2), dibenzyldipyridine palladium (Pd(CH2Ph)2Py2) and methyl-1,5-cyclooctadiene-palladium chloride (Pd(COD)ClMe).

[0237] In the method of the present invention, the reaction of step (2) is carried out in the presence of a reaction solvent. In a specific embodiment, the reaction solvent can be selected from toluene and tetrahydrofuran. In a preferred embodiment, the reaction solvent is tetrahydrofuran.

[0238] In a more preferred case, the reaction process of step (1) and step (2) is as shown in the following reaction formula.

[0239]

[0240] Among them, M, R3, R4, R 11 -R 15 The definition of is the same as described above.

[0241] In a specific embodiment, the preparation process of step (1) comprises: in a protective gas (such as nitrogen) atmosphere, dissolving the compound represented by formula (III) in anhydrous ether, adding a hydrogen extraction agent (such as n-butyl lithium) at room temperature, stirring at room temperature, adding tetrahydrofuran, and further stirring the obtained black solution containing the precipitate; then adding the compound represented by formula (V), stirring at room temperature, and adding NH4Cl aqueous solution to quench; then extracting the organic phase with ethyl acetate, drying the obtained organic phase with anhydrous sodium sulfate, and recrystallizing with dichloromethane / hexane to obtain a yellow crystalline compound; then adding methanol and concentrated hydrochloric acid, reflux reaction, removing the organic solvent after the reaction is completed, dissolving the product in ethyl acetate, adding NaHCO3 aqueous solution to neutralize, extracting the organic phase, and then drying, filtering, concentrating, and column chromatography in sequence to obtain a ligand.

[0242] In a specific embodiment, the preparation process of step (2) comprises: in a protective gas (such as nitrogen) atmosphere, dissolving the ligand obtained in step (1) and the M metal compound in an organic solvent (such as toluene, tetrahydrofuran, etc.), respectively, and then stirring and mixing the ligand solution and the M metal compound solution and reacting at room temperature, filtering, concentrating the filtrate, adding heptane for recrystallization, and obtaining the late transition metal complex described in the present invention.

[0243] In the present invention, the α-olefin is selected from one or more of propylene, butene, pentene, hexene, octene and 4-methyl-1-pentene.

[0244] In the present invention, the internal olefin refers to an olefin whose double bond is not at the terminal position. The internal olefin of an olefin can be a mixture of multiple isomers or a single internal olefin. For example, butene can be 1-C4, cis-2-C4, trans-2-C4 and isobutylene, or a mixture of one or more isomers. The catalyst structure and the composition of the mixed olefins have a certain influence on the structure and properties of the polymer product.

[0245] In the present invention, the enol is selected from the monomers represented by formula (G1),

[0246]

[0247] Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, and L4 is selected from C1-C30 alkylene having a side group.

[0248] In a preferred case, in formula (G1), L1 and L2 are H; L3 is H, C1-C10 alkyl or halogen-substituted C1-C10 alkyl, preferably H or C1-C10 alkyl; L4 is C1-C20 alkylene with a side group, preferably C1-C10 alkylene with a side group, and more preferably C1-C6 alkylene with a side group. The carbon number of the C1-C30 alkylene with a side group refers to the number of C on the straight chain, and does not include the number of C on the side group. For example, isopropylidene (-CH2-CH(CH3)-) is referred to herein as C2 alkylene with a side group (methyl).

[0249] In the present invention, in formula (G1), the side group is selected from one or more of halogen, substituted or unsubstituted C6-C20 aryl, substituted or unsubstituted C1-C20 alkyl, hydroxyl-substituted C1-C20 alkyl and alkoxy-substituted C1-C20 alkyl.

[0250] Preferably, in formula (G1), the side group is selected from halogen, phenyl and substituted or unsubstituted C1-C6 alkyl.

[0251] Further preferably, in formula (G1), the substituted or unsubstituted C1-C6 alkyl group is selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl or hexyl.

[0252] In the present invention, the enol is selected from at least one of the following compounds: 2-methyl-3-butene-1-ol, 2-ethyl-3-butene-1-ol, 1,1-diphenyl-3-butene-1-ol, 2-methyl-3-butene-2-ol, 2,2-dimethyl-3-butene-1-ol, 3-methyl-1-pentene-3-ol, 2,4-dimethyl-4-pentene-2-ol, 4-alkenyl-2-pentanol, 4-methyl-4-pentene-2-ol, 2-methyl-4-pentene-2-ol, 2-phenyl-4-pentene-2-ol, 2-allylhexafluoroisopropanol, 2-hydroxy-5-hexene, 3-butene-1-ol, 2-hydroxy-5-hexene, 3-butene-2-ol, 2-methyl-4-pentene-2-ol, 2-phenyl-4-pentene-2-ol, 2-allylhexafluoroisopropan ...1-ol, 2-methyl-3-butene-2-ol, 2-methyl-3-butene-1-ol, 3-methyl-1-pentene-3-ol, 2,4-dimethyl-4-pentene-2-ol, 4-alkenyl-2-pentanol, 4-methyl-4-pentene-2-ol, 2-methyl-4-pentene-2-ol, 2-phenyl-4-pentene-2-ol, 2-allylhexafluoroisopropanol, 2-hydroxy-5-hexene, 3-butene-1-ol, 3- 2-Methyl-2-hydroxy-5-hexene, 3-methyl-5-hexen-3-ol, 2-methyl-2-hydroxy-5-hexene, 1-allylcyclohexanol, 2,3-dimethyl-2-hydroxy-5-hexene, 1-heptene-4-ol, 4-methyl-1-heptene-4-ol, 4-n-propyl-1-heptene-4-ol, 6-heptene-3-ol, 2-methyl-2-hydroxy-6-heptene, 5-methyl-2-hydroxy-6-heptene, 2-hydroxy-3-methyl-6-heptene, 2-hydroxy-3-ethyl-6-heptene, 2-hydroxy-4-methyl-6-heptene, 2-hydroxy-5-methyl-6-heptene, 2,5-dimethyl -1-heptene-4-ol, 2,6-dimethyl-7-octen-2-ol, 2-hydroxy-2,4,5-trimethyl-6-heptene, 2-methyl-3-hydroxy-7-octene, 3-methyl-3-hydroxy-6-heptene, 2-methyl-2-hydroxy-7-octene, 3-methyl-3-hydroxy-7-octene, 4-methyl-2-hydroxy-7-octene, 4-methyl-3-hydroxy-7-octene, 5-methyl-3-hydroxy-7-octene, 6-methyl-3-hydroxy-7-octene, 3-ethyl-3-hydroxy-7-octene, 1,2-dihydroxy-7-octene, 2,6-dimethyl-2,6 -dihydroxy-7-octene, 2,6-dimethyl-2,3-dihydroxy-7-octene, 2-methyl-2-hydroxy-3-chloro-7-octene, 2-methyl-2-hydroxy-3,5-dichloro-7-octene, 3,4-dimethyl-4-hydroxy-8-nonene, 4-methyl-4-hydroxy-8-nonene, 4-ethyl-4-hydroxy-8-nonene, 4-propyl-4-hydroxy-8-nonene, 7-octen-2-ol, 3,5-dichloro-2-methyl-7-octen-2-ol, 3-chloro-2-methyl-7-octen-2,3-diol, 2,6-dimethyl-7-octen-2,6-diol.

[0253] In the present invention, the unsaturated carboxylic acid is selected from the monomers represented by formula (G2),

[0254]

[0255] Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, and L4 is selected from C1-C30 alkylene having a side group.

[0256] In a preferred embodiment, in formula (G2), L1 and L2 are H; L3 is H, C1-C10 alkyl or halogen-substituted C1-C10 alkyl, preferably H or C1-C10 alkyl; L4 is C1-C20 alkylene with a side group, preferably C1-C10 alkylene with a side group, and more preferably C1-C6 alkylene with a side group. The carbon number of the C1-C30 alkylene with a side group refers to the number of C on the straight chain, and does not include the number of C on the side group. For example, isopropylidene (-CH2-CH(CH3)-) is referred to herein as C2 alkylene with a side group (methyl).

[0257] In the present invention, in formula (G2), the side group is selected from one or more of halogen, substituted or unsubstituted C6-C20 aryl, substituted or unsubstituted C1-C20 alkyl, hydroxyl-substituted C1-C20 alkyl and alkoxy-substituted C1-C20 alkyl.

[0258] Preferably, in formula (G2), the side group is selected from halogen, phenyl and substituted or unsubstituted C1-C6 alkyl.

[0259] Further preferably, in formula (G2), the substituted or unsubstituted C1-C6 alkyl group is selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl or hexyl.

[0260] In the present invention, the unsaturated carboxylic acid is selected from at least one of the following compounds: 2-methyl-4-pentenoic acid, 2,3-dimethyl-4-pentenoic acid, 2,2-dimethyl-4-pentenoic acid, 2-ethyl-4-pentenoic acid, 2-isopropyl-4-pentenoic acid, 2,2,3-trimethyl-4-pentenoic acid, 2,3,3-trimethyl-4-pentenoic acid, 2-ethyl-3-methyl-4-pentenoic acid, 2-(2-methylpropyl)-4-pentenoic acid, 2,2-diethyl-4-pentenoic acid, 2-methyl-2-ethyl-4-pentenoic acid, 2,2,3,3-tetramethyl-4-pentenoic acid, 2-methyl-5-hexenoic acid, 2- ethyl-5-hexenoic acid, 2-propyl-5-hexenoic acid, 2,3-dimethyl-5-hexenoic acid, 2,2-dimethyl-5-hexenoic acid, 2-isopropyl-5-hexenoic acid, 2-methyl-2-ethyl-5-hexenoic acid, 2-(1-methylpropyl)-5-hexenoic acid, 2,2,3-trimethyl-5-hexenoic acid, 2,2-diethyl-5-hexenoic acid, 2-methyl-6-hexenoic acid, 2-ethyl-6-hexenoic acid, 2-propyl-6-hexenoic acid, 2,3-dimethyl-6-hexenoic acid, 2,4-dimethyl-6-hexenoic acid, 2,2-dimethyl-6-hexenoic acid, 2-isopropyl-5-methyl-6-hexenoic acid, 2 -isopropyl-6-heptenoic acid, 2,3,4-trimethyl-6-heptenoic acid, 2-methyl-2-ethyl-6-heptenoic acid, 2-(1-methylpropyl)-6-heptenoic acid, 2,2,3-trimethyl-6-heptenoic acid, 2,2-diethyl-6-heptenoic acid, 2-methyl-7-octenoic acid, 2-ethyl-7-octenoic acid, 2-propyl-7-octenoic acid, 2,3-dimethyl-7-octenoic acid, 2,4-dimethyl-7-octenoic acid, 2,2-dimethyl-7-octenoic acid, 2-isopropyl-5-methyl-7-octenoic acid, 2-isopropyl-7-octenoic acid, 2,3,4-trimethyl-7-octenoic acid, 2-methyl- 2-ethyl-7-octenoic acid, 2-(1-methylpropyl)-7-octenoic acid, 2,2,3-trimethyl-7-octenoic acid, 2,2-diethyl-7-octenoic acid, 2-methyl-8-nonenoic acid, 2-ethyl-8-nonenoic acid, 2-propyl-8-nonenoic acid, 2,3-dimethyl-8-nonenoic acid, 2,4-dimethyl-8-nonenoic acid, 2,2-dimethyl-8-nonenoic acid, 2,2-diethyl-8-nonenoic acid, 2-isopropyl-5-methyl-8-nonenoic acid, 2-methyl-9-decenoic acid, 2,3-dimethyl-9-decenoic acid, 2,4-dimethyl-9-decenoic acid, 2-methyl-10-undecenoic acid.

[0261] In the present invention, the unsaturated carboxylic acid ester is selected from the monomers represented by formula (G3),

[0262]

[0263] Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, L4 is selected from C1-C30 alkylene with a side group, and L5 is selected from C1-C30 alkyl. In a preferred case, L5 is C1-C20 alkyl, more preferably C1-C10 alkyl, and more preferably C1-C6 alkyl.

[0264] In a preferred case, in formula (G3), L1 and L2 are H; L3 is H, C1-C10 alkyl or halogen-substituted C1-C10 alkyl, preferably H or C1-C10 alkyl; L4 is C1-C20 alkylene with a side group, preferably C1-C10 alkylene with a side group, and more preferably C1-C6 alkylene with a side group. The carbon number of the C1-C30 alkylene with a side group refers to the number of C on the straight chain, and does not include the number of C on the side group. For example, isopropylidene (-CH2-CH(CH3)-) is referred to herein as C2 alkylene with a side group (methyl).

[0265] In the present invention, in formula (G3), the side group is selected from one or more of halogen, substituted or unsubstituted C6-C20 aryl, substituted or unsubstituted C1-C20 alkyl, hydroxyl-substituted C1-C20 alkyl and alkoxy-substituted C1-C20 alkyl.

[0266] Preferably, in formula (G3), the side group is selected from halogen, phenyl and substituted or unsubstituted C1-C6 alkyl.

[0267] Further preferably, in formula (G3), the substituted or unsubstituted C1-C6 alkyl group is selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl or hexyl.

[0268] In the present invention, the unsaturated carboxylic acid ester is selected from at least one of the following compounds: methyl 2-methyl-3-butenoate, methyl 2-methyl-4-pentenoate, ethyl 2-methyl-4-pentenoate, methyl 2,3-dimethyl-4-pentenoate, ethyl 2-methyl-3-butenoate, methyl 2,3-dimethylbutenoate, methyl 2-ethyl-3-butenoate, methyl 2,2-dimethyl-3-butenoate, methyl 2-methyl-3-methylenepentenoate, ethyl 2,3-dimethyl-3-butenoate, methyl 2-vinylhexanoate, ethyl 2-ethyl-3-butenoate, methyl 2-vinyl-3-pentanoate, methyl 2-vinyl-4-methyl-4-pentenoate, methyl 2,2-dimethyl-3-butenoate 2-Hydroxy-2-methyl-3-butenoic acid methyl ester, 2-methyl-3-butenoic acid isobutyl ester, 2-(1-methylethyl)-3-butenoic acid ethyl ester, 2,2,3-trimethyl-3-butenoic acid methyl ester, 2-vinylhexanoic acid ethyl ester, 2-ethyl-2-methyl-3-butenoic acid methyl ester, 3-methyl-5-hexenoic acid methyl ester, 4-methyl-5-hexenoic acid methyl ester, 4-methyl-5-hexenoic acid ethyl ester, 2-methyl-6-heptenoic acid methyl ester, 2,4-dimethyl-5-hexenoic acid methyl ester, 2-ethyl-5-hexenoic acid methyl ester, 3-methyl-5-hexenoic acid methyl ester, 4-methyl-5-hexenoic acid methyl ester, 2-ethyl-4-pentenoic acid methyl ester, 2-propyl-4-pentenoic acid methyl ester, 2 -propyl-5-hexenoic acid methyl ester, 2-propyl-4-pentenoic acid methyl ester, 2-butyl-5-hexenoic acid methyl ester, 3-vinyl hexanoic acid methyl ester, 2-(2-propen-1-yl)-4-pentanoic acid methyl ester, 2-(3-buten-1-yl)-5-hexenoic acid methyl ester, 3,3-dimethyl-5-hexenoic acid methyl ester, 3-propyl-5-hexenoic acid ethyl ester, 3,3-dimethyl-5-hexenoic acid ethyl ester, 3,4,4-trimethyl-5-hexenoic acid methyl ester, 3-(1,1-dimethylethyl)-5-hexenoic acid ethyl ester, 3-methyl-2-oxo-5-hexenoic acid ethyl ester, 2-vinyl-3,3-dimethyl-5-hexanoic acid methyl ester, methyl-β-vinylbenzopropionic acid ester, 3-methyl-5-hexenoic acid Benzyl ester, 2-propyl-6-heptenoic acid methyl ester, 2-methyl-6-heptenoic acid methyl ester, 2-methyl-6-heptenoic acid ethyl ester, 2,2-dimethyl-6-heptenoic acid methyl ester, 2,4-dimethyl-6-heptenoic acid ethyl ester, 2-propyl-6-heptenoic acid ethyl ester, 2,2-dimethyl-6-heptenoic acid ethyl ester, 2-(4-penten-1-yl)malonic acid 1,3-dimethyl ester, 6-heptenoic acid-2-methyl-1,1-dimethylethyl ester, 2-methyl-3-butenoic acid tert-butyl ester, 2-isopropyl-3-butenoic acid ethyl ester, 2-isobutyl-4-pentenoic acid methyl ester, 2,2-dimethyl-4-pentenoic acid methyl ester, 3,3-dimethyl-4-pentenoic acid methyl ester, 3,3-dimethyl-4-pentenoic acid ethyl ester, 2,2-dimethyl-4-pentenoic acid ethyl ester, 2-n-propyl-4-pentenoic acid methyl ester, 2-isopropyl-4-pentenoic acid methyl ester, 2-methyl-4-pentenoic acid isobutyl ester, allylmalonate diethyl ester, allylmalonate dimethyl ester, allylsuccinic anhydride, 2-methyl-4-pentenoic acid ethyl ester, 2-methyl-4-pentenoic acid methyl ester, 3-methyl-4-pentenoic acid methyl ester, 3-ethyl-4-pentenoic acid methyl ester, 3-methyl-4-pentenoic acid isobutyl ester, 2-(tert- butyl)-4-pentenoic acid ethyl ester, 3-allyldihydrofuran-2(3H)-one, 2-(dimethylamino)-2-methylpent-4-enoic acid methyl ester, 3-methyl-4-pentenoic acid methyl ester, 2-methyl-5-hexenoic acid methyl ester, 2,2-dimethyl-5-hexenoic acid methyl ester, 2,2-dimethyl-5-hexenoic acid ethyl ester, 2-methyl-5-hexenoic acid benzyl ester, 4,4-dimethyl-6-heptenoic acid methyl ester, 2,4-dimethyl-9-decenoic acid methyl ester.

[0269] In the present invention, the auxiliary agent is selected from one or more of an organoaluminum compound, an organoboron compound and an organosilicon compound.

[0270] In the present invention, when the auxiliary agent contains an organic aluminum compound, the organic aluminum compound is AlY n X 1 3-n ; wherein Y is selected from H, C1-C20 saturated or unsaturated hydrocarbon group and C1-C20 saturated or unsaturated hydrocarbonoxy group, preferably C1-C20 alkyl group, C1-C20 alkoxy group, C7-C20 aralkyl group or C6-C20 aryl group; X 1 is halogen, preferably chlorine or bromine; <n≤3。

[0271] In the present invention, the C1-C20 alkyl group may be methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, tert-pentyl, neopentyl, n-hexyl, n-heptyl, n-octyl, n-decyl, cyclopropyl, cyclopentyl, cyclohexyl, 4-methylcyclohexyl, 4-ethylcyclohexyl, 4-n-propylcyclohexyl or 4-n-butylcyclohexyl; the C1-C20 alkoxy group may be methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert-butoxy, n-pentyloxy, isopentyloxy or tert-pentyloxy; the C7-C20 aralkyl group may be phenylmethyl, phenylethyl, phenyl n-propyl, phenyl isopropyl, phenyl n-butyl or phenyl tert-butyl; the C6-C20 aryl group may be phenyl, 4-methylphenyl, 4-ethylphenyl, dimethylphenyl or vinylphenyl.

[0272] Preferably, the organoaluminum compound is selected from one or more of trimethylaluminum, triethylaluminum, triisobutylaluminum (AliBu3), tri-n-hexylaluminum, trioctylaluminum, diethylaluminum monohydrogenate, diisobutylaluminum monohydrogenate, diethylaluminum monochloride (AlEt2Cl), diisobutylaluminum monochloride, sesquiethylaluminum chloride, ethylaluminum dichloride, methylaluminoxane (MAO) and modified methylaluminoxane (MMAO).

[0273] In a further preferred embodiment, the organoaluminum compound is methylaluminoxane (MAO).

[0274] In the present invention, when the auxiliary agent contains an organic boron compound, the organic boron compound is an aromatic boron and / or a borate.

[0275] In the present invention, when the organic boron compound is an aromatic boron, the aromatic boron is a substituted or unsubstituted phenyl boron, preferably tris(pentafluorophenyl)boron.

[0276] In the present invention, when the organic boron compound is a borate, the borate is N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate and / or triphenylmethyl tetrakis(pentafluorophenyl)borate.

[0277] In the present invention, when the auxiliary agent contains an organic silicon compound, the organic silicon compound is an alkyl silicon compound.

[0278] In the present invention, the general formula of the alkyl silicon compound is SiH1H2H3H4, wherein H1 is selected from C1-C10 alkyl, and H2, H3 and H4 are each independently selected from C1-C10 alkyl or halogen.

[0279] In a preferred embodiment, the alkyl silicon compound is selected from one or more of trimethylchlorosilane, dichlorodimethylsilane, propyldimethylchlorosilane, dichloroethylmethylsilane, tert-butyldimethylchlorosilane, diisopropylchlorosilane, trichloroethylsilane, chloromethyldimethylchlorosilane, di-tert-butylchlorosilane, dichloro(methyl)propylsilane, methyltrichlorosilane and trichloroethylsilane.

[0280] In the present invention, when the auxiliary agent contains an organoaluminum compound, the molar ratio of the amount of aluminum element in the organoaluminum compound to the amount of M element in the catalyst is (10-10000000): 1, preferably (10-100000): 1, and more preferably (100-10000): 1. Specifically, the molar ratio of the amount of aluminum element in the organoaluminum compound to the amount of M element in the catalyst can be 100: 1, 200: 1, 300: 1, 500: 1, 700: 1, 800: 1, 1000: 1, 2000: 1, 3000: 1, 5000: 1 or 10000: 1.

[0281] In the present invention, when the auxiliary agent contains an organic boron compound, the molar ratio of the amount of the boron element in the organic boron compound to the amount of the M element in the catalyst is (0.1-1000): 1, preferably (0.1-500): 1. Specifically, the molar ratio of the amount of the boron element in the organic boron compound to the amount of the M element in the catalyst can be 0.1:1, 0.2:1, 0.5:1, 1:1, 2:1, 3:1, 5:1, 8:1, 10:1, 20:1, 50:1, 100:1, 200:1, 300:1 or 500:1.

[0282] In the present invention, when the auxiliary agent contains an organosilicon compound, the molar ratio of the amount of silicon element in the organosilicon compound to the amount of M element in the catalyst is (10-10000000): 1, preferably (10-200000): 1. Specifically, the molar ratio of the amount of silicon element in the organosilicon compound to the amount of M element in the catalyst can be 10: 1, 20: 1, 50: 1, 100: 1, 500: 1, 1000: 1, 1500: 1, 2000: 1, 5000: 1, 10000: 1, 100000: 1, 200000: 1.

[0283] In the present invention, in order to achieve better polymerization effect, when the auxiliary agent is a combination of an organic aluminum compound, an organic boron compound and an organic silicon compound, the molar ratio of the total amount of aluminum, boron and silicon in the auxiliary agent to the amount of M element in the catalyst is (10-11000000): 1, preferably (10-200000): 1. Specifically, the molar ratio of the total amount of aluminum, boron and silicon in the auxiliary agent to the amount of M element in the catalyst can be 10: 1, 20: 1, 50: 1, 100: 1, 500: 1, 1000: 1, 1500: 1, 2000: 1, 5000: 1, 10000: 1, 100000: 1, 150000: 1 or 200000: 1.

[0284] In the present invention, in order to make the polymerization reaction more complete, the polymerization reaction is carried out in the presence of a solvent.

[0285] In a preferred embodiment, the solvent is selected from one or more of alkanes, halogenated alkanes and aromatic hydrocarbons.

[0286] In the present invention, the alkane is selected from one or more of C3-C20 alkanes, preferably one or more of C3-C10 alkanes, further preferably one or more of butane, isobutane, pentane, hexane, heptane, octane and cyclohexane, and further preferably one or more of hexane, heptane and cyclohexane.

[0287] In the present invention, the general formula of the halogenated alkane is R 1 X 2 n2 R 2 X 3 m2 , where X 2 and X 3 Each is independently selected from halogen, m2+n2≥1, R 1 is selected from C1-C10 alkyl or alkenyl, R 2 is selected from C1-C10 alkylene or alkenylene. The alkenyl refers to a straight chain alkenyl, a branched chain alkenyl or a cycloalkenyl, and specifically, the alkenyl is vinyl, allyl or butenyl.

[0288] In a preferred embodiment, the halogenated alkane is selected from one or more of chloroform, dichloromethane, dichloroethane, dichloropropane and trichloroethylene.

[0289] In the present invention, the general formula of the aromatic hydrocarbon is R 4 -Ph-R 3 , where R 3 and R 4 Each is independently selected from hydrogen, phenyl and C1-C10 alkane, Ph represents a benzene ring, and in a preferred case, the aromatic hydrocarbon is selected from one or more of pentylbenzene, ethylbenzene, xylene, toluene and benzene.

[0290] Preferably, the polymerization reaction is carried out under anhydrous and oxygen-free conditions.

[0291] In the present invention, the non-polar monomer having a carbon number of ≤3 is generally a gas, and its amount is adjusted by controlling the pressure of the reaction system. In some specific embodiments, the amount of the non-polar monomer is such that the pressure of the reaction system is 1-20 atm, preferably 5-15 atm. Specifically, when the non-polar monomer is ethylene, the ethylene pressure in the reaction system is 1-20 atm, preferably 5-15 atm, and specifically can be 5 atm, 8 atm, 10 atm, 11 atm, 12 atm, 13 atm, 14 atm or 15 atm.

[0292] In the present invention, the pressure refers to absolute pressure.

[0293] In the present invention, the polar monomer is generally a liquid, and its amount is regulated by controlling the concentration of the polar monomer in the liquid raw material. In some specific embodiments, the concentration of the polar monomer in the liquid raw material (usually including polar monomer, catalyst, auxiliary agent and solvent) is 0.01-6000mmol / L, preferably 0.1-1000mmol / L, more preferably 1-500mmol / L, and further preferably 30-500mmol / L. Specifically, the concentration of the polar monomer in the polymerization raw material can be 30mmol / L, 50mmol / L, 100mmol / L, 150mmol / L, 200mmol / L, 250mmol / L, 300mmol / L, 350mmol / L, 400mmol / L, 450mmol / L or 500mmol / L.

[0294] In the present invention, the concentration of the catalyst in the liquid raw material is 0.00001-100mmol / L, preferably 0.0001-1mmol / L, more preferably 0.001-0.5mmol / L. More preferably, it is 0.002-0.1mmol / L. Specifically, the concentration of the catalyst in the liquid raw material can be 0.002mmol / L, 0.004mmol / L, 0.006mmol / L, 0.008mmol / L, 0.01mmol / L, 0.02mmol / L, 0.04mmol / L, 0.06mmol / L, 0.08mmol / L or 0.1mmol / L.

[0295] In the present invention, the conditions of the polymerization reaction include: a temperature of -50 to 180°C and a time of 10 to 200 min. Preferably, the temperature of the polymerization reaction is -20 to 100°C, more preferably 20 to 100°C, specifically, the temperature of the polymerization reaction may be 20°C, 30°C, 40°C, 50°C, 60°C, 70°C, 80°C, 90°C or 100°C; the time of the polymerization reaction is 20 to 60 min, specifically, the time of the polymerization reaction may be 20 min, 25 min, 30 min, 35 min, 40 min, 45 min, 50 min, 55 min or 60 min.

[0296] The second aspect of the present invention provides a polyolefin prepared by the above-mentioned coordination precipitation polymerization method for olefin polymerization, wherein the shape of the polyolefin is spherical or quasi-spherical; the average particle size of the polyolefin is 0.02-50 mm, preferably 0.05-50 mm, and further preferably 0.2-20 mm. Specifically, the average particle size of the spherical or quasi-spherical polymer can be 0.2 mm, 0.5 mm, 1 mm, 1.5 mm, 2 mm, 3 mm, 5 mm, 8 mm, 10 mm, 15 mm or 20 mm.

[0297] In the present invention, the weight average molecular weight of the polyolefin is 10,000-800,000, preferably 10,000-500,000. Specifically, the molecular weight of the polyolefin may be 10,000, 20,000, 30,000, 40,000 or 50,000.

[0298] In the present invention, the molecular weight distribution index of the polyolefin is ≤10, preferably 1.5-10. Specifically, the molecular weight distribution index of the polyolefin may be 1.5, 2, 2.5, 3, 3.5, 4, 6, 8 or 10.

[0299] In the present invention, the molecular weight distribution index represents M w / M n .

[0300] In the present invention, the melting point of the polyolefin is 90-140°C. Specifically, the melting point of the polyolefin may be 90°C, 100°C, 110°C, 120°C, 125°C, 130°C, 135°C or 140°C.

[0301] In the present invention, the density of the polyolefin is 0.3-0.85 g / cm 3 , preferably 0.4-0.75g / cm 3 Specifically, the density of the spherical or quasi-spherical polymer may be 0.4 g / cm 3 , 0.45g / cm 3 , 0.5g / cm 3 , 0.55g / cm 3 , 0.6g / cm 3 , 0.65g / cm 3 , 0.7g / cm 3 , 0.75g / cm 3 .

[0302] In the present invention, the density is measured using the method in GB / T6343-2009.

[0303] In the present invention, according to the coordination precipitation polymerization method, non-polar monomers and polar monomers undergo polymerization reaction in the presence of a non-loaded catalyst to prepare spherical or spherical polymer particles. This method not only eliminates the complicated catalyst loading process, but also greatly simplifies the polymer deashing and granulation post-treatment procedures, which can inject new blood into olefin polymerization technology.

[0304] The coordination precipitation polymerization method for olefin polymerization and polyolefin of the present invention are further described by examples. The examples are implemented on the premise of the technical solution of the present invention, and detailed implementation methods and specific operation processes are given, but the protection scope of the present invention is not limited to the following examples.

[0305] The experimental methods in the following examples, unless otherwise specified, are all conventional methods in the art. The experimental materials used in the following examples, unless otherwise specified, are all commercially available.

[0306] The polymer was washed with a dilute acid solution before measurement to ensure that the metal content in the polymer was ≤50 ppm.

[0307] The analytical characterization instruments used in the present invention are as follows:

[0308] 1. Nuclear magnetic resonance instrument: Bruker DMX 300 (300 MHz), tetramethylsilane (TMS) as internal standard, used to test the structure of complex ligands at 25°C.

[0309] 2. Comonomer content of copolymer: 13 C NMR spectra were measured on a 400 MHz Bruker Avance 400 NMR spectrometer using a 10 mm PASEX 13 probe and the polymer samples were dissolved in deuterated tetrachloroethane at 130°C for analysis.

[0310] 3. Molecular weight and molecular weight distribution index PDI (PDI = M w / M n ): PL-GPC220 was used with trichlorobenzene as solvent and the measurement was performed at 150°C (standard sample: PS, flow rate: 1.0 mL / min, column: 3×Plgel 10um M1×ED-B300×7.5 nm).

[0311] 4. Activity measurement method: gravimetric analysis. The calculation method of polymerization activity is: polymerization activity = polymerization

[0312] Weight of metal complex (g) / metal complex (mol) × 60 / polymerization time (min).

[0313] 5. Polymer density test method: refer to GBT 6343-2009 method test.

[0314] Example 1

[0315] Complex 1: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine (-NC5H5);

[0316] In a nitrogen atmosphere, the compound represented by formula (III) (11.23 g, 30 mmol, S type) was dissolved in anhydrous ether (150 mL), and n-butyl lithium solution (2.7 M, 33.3 mL, 90 mmol) was added dropwise at room temperature, and stirred at room temperature for 4 h. Tetrahydrofuran (150 mL) was added, and the obtained black solution containing the precipitate was further stirred for 1 h; diphenylphosphine chloride (PPh2Cl) (90 mmol, 16.7 mL) was added at 0°C, and after stirring at room temperature for 1 h, NH4Cl aqueous solution ( 5mL) quenching; extracting the organic phase with ethyl acetate, drying the obtained organic phase with anhydrous sodium sulfate, and recrystallizing with dichloromethane / hexane to obtain a yellow crystalline compound (15.54g); adding methanol (100mL) and 5mL concentrated hydrochloric acid, reflux reaction for 16h, tracking the reaction with TLC, removing the organic solvent, dissolving the product in ethyl acetate, adding NaHCO3 aqueous solution to neutralize, extracting the organic phase, drying with anhydrous MgSO4, filtering, concentrating, and column chromatography (dichloromethane as solvent) to obtain ligand I1 with a yield of 67%; 1 H NMR (400MHz, CDCl3): δ=5.41 (s, 2H), 7.13-7.15 (m, 2H), 7.24-7.29 (m, 4H), 7.38-7.45 (m, 22H), 7.62-7.64 (m, 2H); 31 P NMR (162MHz, CDCl3): δ = -17.19 (s); High-resolution mass spectrometry test: Theoretical calculated value: 654.19, measured value: 655.20;

[0317] In a nitrogen atmosphere, ligand I1 (0.654 g, 1 mmol) and metal nickel source (Py2NiMe2) (0.49 g, 2 mmol) were dissolved in toluene (10 mL) respectively; the ligand solution was then dripped into the metal nickel source solution dropwise, stirred vigorously, reacted at room temperature for 10 h, filtered to obtain a brown-yellow solution, the solvent was concentrated, and frozen at -30 ° C for crystallization to obtain complex 1 with a yield of 76%; 1 H NMR (400MHz, CDCl3): δ = 7.92 (m, 8H), 7.58-7.63 (m, 2H), 7.32-7.50 (m, 22H), 7.22-7.34 (m, 4H), 7.10-7.15 (m, 2H), 6.60 (m, 2H), -0.41 (d, 6H);31 P NMR (162MHz, CDCl3): δ = 30.98; Elemental analysis test C 56 H 46 N2Ni2O2P2: Theoretical calculated values ​​are: C, 70.19; H, 4.84; N, 2.92; Test values ​​are: C, 69.94; H, 4.92; N, 2.84;

[0318] A 1L stainless steel polymerization kettle equipped with mechanical stirring was dried continuously at 130°C for 6h, evacuated while hot and replaced with N2 gas three times; 500mL heptane, 30mmol (6.0mL) 2,6-dimethyl-7-octen-2-ol, 36mL AliBu3 (1.0mol / L n-pentane solution), 3.5mL MAO (1.53mol / L toluene solution) were injected into the polymerization kettle, and 2.4mg (2.5μmol) of complex 1 was added at the same time, and the ethylene pressure was maintained at 10atm at 30°C, and the reaction was stirred for 30min; finally, the reaction was neutralized with 10wt% hydrochloric acid acidified ethanol solution to obtain polyolefin A1; the polymerization activity of polyolefin A1 was 5.2×10 5 g·mol -1 ·h -1 The weight average molecular weight of polyolefin A1 is 0.92×10 5 The molecular weight distribution index of polyolefin A1 is 2.1, the molar content of hydroxyl groups in polyolefin A1 is 0.93%, the melting point of polyolefin A1 is 121.4°C, the average particle size of the spherical polymer in polyolefin A1 is 2.00 mm, and the density of polyolefin A1 is 0.524 g / cm 3 , the yield of spherical polymer in polyolefin A1 was 62%.

[0319] Example 2

[0320] Complex 1: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0321] The preparation method and preparation process of complex 1 in this embodiment are the same as those of complex 1 in Example 1;

[0322] A 1L stainless steel polymerization kettle equipped with mechanical stirring was dried continuously at 130°C for 6h, evacuated while hot and replaced with N2 gas three times; 500mL hexane, 30mmol (4.0mL) 3,3-dimethyl-4-pentenoic acid, 36mL AliBu3 (1.0mol / L hexane solution), 4.8mg (6.0μmol) N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate were injected into the polymerization kettle, and 2.4mg (2.5μmol) complex 1 was added at 30°C, maintaining an ethylene pressure of 10atm, and stirring for 30min; finally, the mixture was neutralized with an ethanol solution acidified with 10wt% hydrochloric acid to obtain polyolefin A2; the polymerization activity of polyolefin A2 was 6.62×10 5 g·mol -1 ·h -1 The weight average molecular weight of polyolefin A2 is 1.24×10 5 The molecular weight distribution index of polyolefin A2 is 3.48, the molar content of carboxyl groups in polyolefin A2 is 1.21%, the melting point of polyolefin A2 is 127.4°C, the average particle size of the spherical polymer in polyolefin A2 is 2.10 mm, and the density of polyolefin A2 is 0.712 g / cm 3 , the yield of spherical polymer in polyolefin A2 was 64%.

[0323] Example 3

[0324] Complex 1: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0325] The preparation method and preparation process of complex 1 in this embodiment are the same as those of complex 1 in Example 1;

[0326] A 7 mL stainless steel glass-lined polymerization kettle equipped with mechanical stirring was dried continuously at 130°C for 2 h, evacuated while hot and replaced with N2 gas three times; 3.0 mL pentane, 0.5 mL (3.1 mmol) 3,3-dimethyl-4-pentenoic acid methyl ester, 1.1 mL AlEt2Cl (3.0 mol / L hexane solution), 1.0 mL tetrakis(pentafluorophenyl)borate triphenylmethyl salt (2.0 mmol / L dichloromethane solution) were injected into the polymerization kettle, and 0.1 mL complex 1 (3.0 mmol / L dichloromethane solution) was added, and the ethylene pressure was maintained at 10 atm at 20°C, and the reaction was stirred for 20 min; finally, the reaction was neutralized with an ethanol solution acidified with 10 wt% hydrochloric acid to obtain polyolefin A3; the polymerization activity of polyolefin A3 was 8.22×10 5 g·mol -1 ·h -1 The weight average molecular weight of polyolefin A3 is 0.62×10 5The molecular weight distribution index of polyolefin A3 is 3.31, the molar content of ester groups in polyolefin A3 is 2.14%, the average particle size of the spherical polymer in polyolefin A3 is 0.52 mm, and the yield of the spherical polymer in polyolefin A3 is 63%.

[0327] Example 4

[0328] Complex 1: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine;

[0329] The preparation method and preparation process of complex 1 in this embodiment are the same as those of complex 1 in Example 1;

[0330] A 7 mL stainless steel glass-lined polymerization kettle equipped with mechanical stirring was dried continuously at 130° C. for 2 h, evacuated while hot and replaced with N2 gas three times; 4.0 mL heptane, 600 μL (3.86 mmol) 2-octene, 100 μL AliBu3 (0.1 mol / L heptane solution), 60.0 μL triphenylmethyl tetrakis(pentafluorophenyl)borate (1.0 mmol / L dichloromethane solution) were injected into the polymerization kettle, and 50 μL complex 1 (1.0 mmol / L dichloromethane solution) was added, and the ethylene pressure was maintained at 10 atm at 60° C. and the reaction was stirred for 30 min; finally, the reaction was neutralized with an ethanol solution acidified with 10 wt% hydrochloric acid to obtain polyolefin A4; the polymerization activity of polyolefin A4 was 8.22×10 5 g·mol -1 ·h -1 The weight average molecular weight of polyolefin A4 is 0.82×10 5 The molecular weight distribution index of polyolefin A4 is 3.2, the melting point of polyolefin A4 is 119.7°C, the average particle size of the spherical polymer in polyolefin A4 is 0.57 mm, and the yield of the spherical polymer in polyolefin A4 is 55%.

[0331] Example 5

[0332] Complex 53: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0333] The preparation method and preparation process of ligand I1 in this embodiment are the same as those of ligand I1 in embodiment 1;

[0334] In a nitrogen atmosphere, ligand I1 (0.654 g, 1 mmol) was dissolved in tetrahydrofuran, excess NaH (0.072 g, 3 mmol) was added, and the mixture was stirred at room temperature for 10 h. NaH was filtered out. (DME) NiBr2 (0.617 g, 2 mmol) tetrahydrofuran solution was added dropwise, and the mixture was reacted at room temperature overnight. The solvent was drained, and dichloromethane (40 mL) was added to dissolve the mixture. The filter cake was removed by filtration, and the filtrate was concentrated. Heptane was added for recrystallization to obtain complex 53 with a yield of 79%. Elemental analysis test: C 52 H 46 Br2Ni2O4P2: Theoretical calculated values ​​are: C, 58.15; H, 4.32; Test values ​​are: C, 58.01; H, 4.53;

[0335] A 50 mL stainless steel polymerization kettle equipped with mechanical stirring was dried continuously at 130°C for 6 h, evacuated while hot and replaced with N2 gas three times; 20 mL hexane, 0.5 mL (3.1 mmol) 3,3-dimethyl-4-pentenoic acid methyl ester, 1.60 mL AlEt2Cl (2.0 mol / L hexane solution) were injected into the polymerization kettle, and 0.5 mL complex 53 (1.0 mmol / L toluene solution) was added, and the reaction was stirred vigorously at 30°C while maintaining an ethylene pressure of 10 atm for 30 min; the reaction was neutralized with an ethanol solution acidified with 10 wt% hydrochloric acid to obtain polyolefin A5; the polymerization activity of polyolefin A5 was 9.21×10 5 g·mol -1 ·h -1 The weight average molecular weight of polyolefin A5 is 1.26×10 5 The molecular weight distribution index of polyolefin A5 is 2.3, the molar content of ester groups in polyolefin A5 is 0.98%, the melting point of polyolefin A5 is 121.1°C, the average particle size of the spherical polymer in polyolefin A5 is 0.88 mm, and the yield of the spherical polymer in polyolefin A5 is 61%.

[0336] Example 6

[0337] Complex 53: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0338] The preparation method and preparation process of complex 53 in this embodiment are the same as those of complex 53 in Example 5;

[0339] A 7 mL stainless steel glass-lined polymerization kettle equipped with mechanical stirring was dried continuously at 130°C for 2 h, evacuated while hot and replaced with N2 gas three times; 4.0 mL heptane, 0.5 mL (2.66 mmol) 2,6-dimethyl-7-octen-2-ol, 1.0 mL AliBu3 (95%), 60.0 μL tetrakis(pentafluorophenyl)borate triphenylmethyl salt (1.0 mmol / L toluene solution) were injected into the polymerization system, and 50 μL complex 53 (1.0 mmol / L toluene solution) was added; at 30°C, the ethylene pressure was maintained at 10 atm, and the reaction was stirred for 30 min; finally, the reaction was neutralized with an ethanol solution acidified with 10 wt% hydrochloric acid to obtain polyolefin A6; the polymerization activity of polyolefin A6 was 6.64×10 5 g·mol -1 ·h -1 The weight average molecular weight of polyolefin A6 is 1.07×10 5 The molecular weight distribution index of polyolefin A6 is 3.4, the melting point of polyolefin A6 is 118.3°C, the molar content of hydroxyl monomer in polyolefin A6 is 1.07%, the average particle size of spherical polymers in polyolefin A6 is 0.62 mm, and the yield of spherical polymers in polyolefin A6 is 60%.

[0340] Example 7

[0341] Complex 65: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran;

[0342] In a nitrogen atmosphere, compound III (3.74 g, 10 mmol, R type) was dissolved in anhydrous ether (120 mL), and n-BuLi (2.7 M, 11.1 mL, 30 mmol) solution was added dropwise at room temperature, and stirred at room temperature for 4 h. Tetrahydrofuran (120 mL) was added, and the black solution containing the precipitate was further stirred for 1 h. Bis(3,5-di(trifluoromethyl)phenyl)chlorophosphine (30 mmol, 14.78 g) was added at 0 ° C. After stirring at room temperature for 1 h, NH4Cl aqueous solution was added. The organic phase was extracted with ethyl acetate, and the obtained organic phase was dried over anhydrous sodium sulfate, and then recrystallized from dichloromethane / hexane to obtain a white crystalline compound; methanol (100 mL) and 5 mL of concentrated hydrochloric acid were added, and the reaction was refluxed for 16 h. After the reaction was completed, the organic solvent was removed, the compound was dissolved in ethyl acetate, and a NaHCO3 aqueous solution was added to neutralize it. The organic phase was extracted, dried over anhydrous MgSO4, filtered, concentrated, and column chromatography (dichloromethane as solvent) was performed to obtain 4.78 g of ligand I2, with a yield of 40%;1 H NMR (400MHz, DMSO): δ=9.10 (s, 2H), 8.17 (s, 2H), 8.13 (s, 2H), 8.08 (dd, J=13.3, 6.5Hz, 8H), 7.81 (d, J=7.6Hz, 2H), 7.56 (d, J=8.4Hz, 2H), 7.27 (dd, 4H), 6.90 (d, J=8.2Hz, 2H); 31 P NMR (162 MHz, DMSO): δ = -8.37 (s); high-resolution mass spectrometry test: theoretical calculated value: 1198.09, tested value: 1198.95.

[0343] In a nitrogen atmosphere, ligand I2 (1.20 g, 1 mmol) was dissolved in tetrahydrofuran, excess NaH (0.072 g, 3 mmol) was added, and the mixture was stirred at room temperature for 10 h. NaH was filtered out. (DME) NiBr2 (0.617 g, 2 mmol) tetrahydrofuran solution was added dropwise, and the reaction was carried out at room temperature overnight. The solvent was drained, and dichloromethane (40 mL) was added to dissolve the mixture. The filter cake was removed by filtration, and the filtrate was concentrated and recrystallized by adding heptane to obtain complex 65 (C 60 H 38 Bf 24 Ni2O4P2), yield 76%; elemental analysis test C 60 H 38 Bf 24 Ni2O4P2: Theoretical calculated values ​​are: C, 44.54; H, 2.37; tested values ​​are: C, 44.31; H, 2.51.

[0344] A 50 mL stainless steel polymerization kettle equipped with mechanical stirring was dried continuously at 130° C. for 6 h, evacuated while hot and replaced with N2 gas three times; 20 mL heptane, 0.5 mL (3.1 mmol) 3,3-dimethyl-4-pentenoic acid methyl ester, 3.4 mL AliBu3 (1.0 mol / L hexane solution), 60.0 μL triphenylmethyl tetrakis(pentafluorophenyl)borate (1.0 mmol / L dichloromethane solution) were injected into the polymerization kettle, and 0.5 mL complex 65 (1.0 mmol / L toluene solution) was added; at 20° C., the ethylene pressure was maintained at 13 atm, and the reaction was stirred vigorously for 30 min; and the reaction was neutralized with an ethanol solution acidified with 10 wt% hydrochloric acid to obtain polyolefin A7, and the polymerization activity of polyolefin A7 was 1.2×10 6 g·mol -1 ·h -1 The weight average molecular weight of polyolefin A7 is 1.54×10 5The molecular weight distribution index of polyolefin A7 is 2.2, the molar content of ester groups in polyolefin A7 is 1.02%, the melting point of polyolefin A7 is 120.4°C, the average particle size of the spherical polymer in polyolefin A7 is 0.58 mm, and the yield of the spherical polymer in polyolefin A7 is 66%.

[0345] Comparative Example 1

[0346] A 1L stainless steel polymerization kettle equipped with mechanical stirring was dried continuously at 130°C for 6h, evacuated while hot and replaced with N2 gas three times; 500mL hexane, 30mmol (4.0mL) 3,3-dimethyl-4-pentenoic acid, 36mL AliBu3 (1.0mol / L hexane solution), 4.8mg (6.0μmol) N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate were injected into the polymerization system, and 2.5mg (5.0μmol) complex F (the synthesis process of complex F refers to Acta Agron.Sin.2012, 29, 1381; ACS Catalysis 2021, 11, 5, 2902-2911) was added at the same time; at 30°C, the ethylene pressure was maintained at 10atm and the reaction was stirred for 30min; finally, it was neutralized with 10wt% hydrochloric acid acidified ethanol solution to obtain polyolefin D1; the polymerization activity of polyolefin D1 was 1.42×10 5 g·mol -1 ·h -1 The weight average molecular weight of polyolefin D1 is 0.1×10 5 The molecular weight distribution index of polyolefin D1 is 3.72, the molar content of carboxyl groups in polyolefin D1 is 0.91%, and no quasi-spherical polymer is generated.

[0347]

[0348] In the present invention, compared with the use of the complex in Comparative Example 1, when the late transition metal metal complex of the present invention is used as the main catalyst, the obtained polyolefin has higher polymerization activity, the molecular weight of the obtained polyolefin is significantly higher than the molecular weight of the polyolefin obtained in Comparative Example 1, and the coordination precipitation polymerization method for olefin polymerization of the present invention can prepare polar polyolefins with good particle morphology and polar groups.

[0349] The preferred embodiments of the present invention are described in detail above, but the present invention is not limited thereto. Within the technical concept of the present invention, the technical solution of the present invention can be subjected to a variety of simple modifications, including the combination of various technical features in any other suitable manner, and these simple modifications and combinations should also be regarded as the contents disclosed by the present invention and belong to the protection scope of the present invention.

Claims

1. A coordination precipitation polymerization method for olefin polymerization, characterized in that: The method comprises mixing olefin monomers, a catalyst and an auxiliary agent to carry out a polymerization reaction; The olefin monomers contain non-polar monomers and polar monomers; The non-polar monomer is selected from one or more of ethylene, α-olefins and internal olefins; The polar monomer is selected from one or more of enol, unsaturated carboxylic acid and unsaturated carboxylic acid ester; The catalyst is selected from the late transition metal complex represented by formula (I), Wherein, M is selected from Group VIII metals, R1 is selected from substituted or unsubstituted C6-C20 aromatic groups, R3 and R4 are each independently selected from halogen, C1-C10 hydrocarbon groups, P(R5)3, NR6R7 and OR8R9, or R3 and R4 are interconnected to form an eight-membered ring, wherein R5 is selected from substituted or unsubstituted C1-C10 alkyl groups and substituted or unsubstituted C6-C10 aromatic groups, R6, R7, R8 and R9 are each independently selected from C1-C10 hydrocarbon groups, or R6, R7 and N are interconnected to form a five-membered ring or a six-membered ring, or R8, R9 and O are interconnected to form a five-membered ring or a six-membered ring.

2. The coordination precipitation polymerization method for olefin polymerization according to claim 1, characterized in that: The structural formula of the late transition metal complex is shown in formula (II), Among them, R 11 -R 15 Each is independently selected from hydrogen, halogen, hydroxyl, and substituted or unsubstituted C1-C20 hydrocarbon groups.

3. The coordination precipitation polymerization method for olefin polymerization according to claim 2, characterized in that: The late transition metal complex is selected from the following complexes, Complex 1: Complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 2: Complex represented by formula (II), where M is Ni, R 11 -R 15 is F, R3 is methyl, and R4 is pyridine; Complex 3: Complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 4: Complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 5: Complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 6: Complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 7: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 8: Complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 9: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is methyl, and R4 is pyridine; Complex 10: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 11: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 12: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 13: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 14: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is pyridine; Complex 15: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 16: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 17: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is F, R3 is phenyl, and R4 is PMe3; Complex 18: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 19: A complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 20: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 21: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 22: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 23: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 24: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is phenyl, and R4 is PMe3; Complex 25: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 26: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 27: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 28: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 29: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is phenyl, and R4 is PMe3; Complex 30: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is phenyl, and R4 is PMe3; Complex 31: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene; Complex 32: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene; Complex 33: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene; Complex 34: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 and R4 are connected to each other to form cyclooctene; Complex 35: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 and R4 are connected to each other to form cyclooctene; Complex 36: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 and R4 are connected to each other to form cyclooctene; Complex 37: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 and R4 are connected to each other to form cyclooctene; Complex 38: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 39: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is F, R3 is Cl, and R4 is tetrahydrofuran; Complex 40: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 41: A complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 42: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 43: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 44: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 45: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 46: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 47: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 48: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 49: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 50: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 51: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 52: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is Cl, and R4 is tetrahydrofuran; Complex 53: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 54: A complex represented by formula (II), wherein M is Ni, R 11 -R 15 is F, R3 is Br, and R4 is tetrahydrofuran; Complex 55: A complex represented by formula (II), wherein M is Ni, R 11 is phenyl, R 12 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 56: A complex represented by formula (II), wherein M is Ni, R 11 is methyl, R 12 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 57: A complex represented by formula (II), wherein M is Ni, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 58: A complex represented by formula (II), wherein M is Ni, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 59: A complex represented by formula (II), wherein M is Ni, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 60: A complex represented by formula (II), wherein M is Ni, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 61: A complex represented by formula (II), wherein M is Ni, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 62: A complex represented by formula (II), wherein M is Ni, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 63: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 64: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 65: A complex represented by formula (II), wherein M is Ni, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 66: A complex represented by formula (II), wherein M is Ni, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 67: A complex represented by formula (II), wherein M is Ni, R 11 is methoxy, R 12 -R 15 is H, R3 is Br, and R4 is tetrahydrofuran; Complex 68: A complex represented by formula (II), wherein M is Pd, R 11 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 69: A complex represented by formula (II), wherein M is Pd, R 11 -R 15 is F, R3 is methyl, and R4 is pyridine; Complex 70: A complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 71: A complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 72: A complex represented by formula (II), wherein M is Pd, R 11 is methyl, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 73: A complex represented by formula (II), wherein M is Pd, R 13 is methyl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 74: A complex represented by formula (II), wherein M is Pd, R 13 For -CF3, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 75: A complex represented by formula (II), wherein M is Pd, R 13 For F, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 76: A complex represented by formula (II), wherein M is Pd, R 13 Cl, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 77: A complex represented by formula (II), wherein M is Pd, R 11 , R 13 and R 15 is methyl, R 12 and R 14 is H, R3 is methyl, and R4 is pyridine; Complex 78: A complex represented by formula (II), wherein M is Pd, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 79: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 is methyl, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 80: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 is methyl, R 13 is methoxy, R 11 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 81: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is pyridine; Complex 82: A complex represented by formula (II), wherein M is Pd, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is pyridine; Complex 83: A complex represented by formula (II), wherein M is Pd, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is pyridine; Complex 84: A complex represented by formula (II), wherein M is Pd, R 11 -R 15 is H, R3 is methyl, and R4 is Cl; Complex 85: A complex represented by formula (II), wherein M is Pd, R 11 is phenyl, R 12 -R 15 is H, R3 is methyl, and R4 is Cl; Complex 86: A complex represented by formula (II), wherein M is Pd, R 13 is methoxy, R 11 , R 12 , R 14 and R 15 is H, R3 is methyl, and R4 is Cl; Complex 87: A complex represented by formula (II), wherein M is Pd, R 12 and R 14 For -CF3, R 11 , R 13 and R 15 is H, R3 is methyl, and R4 is Cl; Complex 88: A complex represented by formula (II), wherein M is Pd, R 11 and R 15 is methoxy, R 12 -R 14 is H, R3 is methyl, and R4 is Cl; Complex 89: A complex represented by formula (II), wherein M is Pd, R 11 is methoxy, R 12 -R 15 is H, R3 is methyl, and R4 is Cl.

4. The coordination precipitation polymerization method for olefin polymerization according to claim 1 or 2, characterized in that: The enol is selected from the monomers represented by formula (G1), Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, and L4 is selected from C1-C30 alkylene having a side group.

5. The coordination precipitation polymerization method for olefin polymerization according to claim 1 or 2, characterized in that: The unsaturated carboxylic acid is selected from the monomers represented by formula (G2), Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, and L4 is selected from C1-C30 alkylene having a side group.

6. The coordination precipitation polymerization method for olefin polymerization according to claim 1 or 2, characterized in that: The unsaturated carboxylic acid ester is selected from the monomers represented by formula (G3), Wherein, L1-L3 are each independently selected from H or C1-C30 alkyl, L4 is selected from C1-C30 alkylene having a side group, and L5 is selected from C1-C30 alkyl.

7. The coordination precipitation polymerization method for olefin polymerization according to claim 1 or 2, characterized in that: The auxiliary agent is selected from one or more of an organoaluminum compound, an organoboron compound and an organosilicon compound; Preferably, the organoaluminum compound is AlY n X 1 3-n ; wherein Y is selected from H, C1-C20 saturated or unsaturated hydrocarbon group and C1-C20 saturated or unsaturated hydrocarbonoxy group, preferably C1-C20 alkyl group, C1-C20 alkoxy group, C7-C20 aralkyl group or C6-C20 aryl group; X 1 is selected from halogen, preferably chlorine or bromine; <n≤3; Preferably, the organic boron compound is an aromatic boron and / or a borate; Preferably, the aromatic hydrocarbon boron is selected from substituted or unsubstituted phenyl boron, preferably tris(pentafluorophenyl)boron; Preferably, the borate is selected from N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate and / or triphenylmethyl tetrakis(pentafluorophenyl)borate; Preferably, the organosilicon compound is an alkyl silicon compound; Preferably, the general formula of the alkyl silicon compound is SiH1H2H3H4, wherein H1 is selected from C1-C10 alkyl, and H2, H3 and H4 are each independently selected from C1-C10 alkyl or halogen.

8. The coordination precipitation polymerization method for olefin polymerization according to claim 7, characterized in that: When the auxiliary agent contains an organic aluminum compound, the molar ratio of the amount of aluminum element in the organic aluminum compound to the amount of M element in the catalyst is (10-10000000):1; Preferably, when the auxiliary agent contains an organic boron compound, the molar ratio of the amount of the boron element in the organic boron compound to the amount of the M element in the catalyst is (0.1-1000):1; Preferably, when the auxiliary agent contains an organosilicon compound, the molar ratio of the amount of silicon element in the organosilicon compound to the amount of M element in the catalyst is (10-10000000):1; Preferably, when the auxiliary agent is a combination of an organic aluminum compound, an organic boron compound and an organic silicon compound, the molar ratio of the total amount of aluminum, boron and silicon in the auxiliary agent to the amount of M element in the catalyst is (10-11000000):

1.

9. The coordination precipitation polymerization method for olefin polymerization according to claim 1 or 2, characterized in that: The polymerization reaction is carried out in the presence of a solvent; Preferably, the solvent is selected from one or more of alkanes, halogenated alkanes and aromatic hydrocarbons; Preferably, the alkane is selected from one or more of C3-C20 alkanes; Preferably, the general formula of the halogenated alkane is R 1 X 2 n2 R 2 X 3 m2 , where X 2 and X 3 Each is independently selected from halogen, m2+n2≥1, R 1 is selected from C1-C10 alkyl or alkenyl, R 2 Selected from C1-C10 alkylene or alkenylene; Preferably, the general formula of the aromatic hydrocarbon is R 4 -Ph-R 3 , where R 3 and R 4 Each is independently selected from hydrogen, phenyl and C1-C10 alkane.

10. The coordination precipitation polymerization method for olefin polymerization according to claim 1 or 2, characterized in that: The polymerization reaction conditions include: temperature of -50 to 180° C. and time of 10 to 200 min.

11. The polyolefin prepared by the coordination precipitation polymerization method for olefin polymerization according to any one of claims 1 to 10, characterized in that: The polyolefin is spherical or quasi-spherical in shape; Preferably, the average particle size of the polyolefin is 0.02-50 mm.

12. The polyolefin according to claim 11, characterized in that The weight average molecular weight of the polyolefin is 10000-800000; Preferably, the molecular weight distribution index of the polyolefin is ≤10; Preferably, the melting point of the polyolefin is 90-140°C.

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