CN112745429A - Process for producing olefin-unsaturated carboxylic acid copolymer - Google Patents

Process for producing olefin-unsaturated carboxylic acid copolymer Download PDF

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CN112745429A
CN112745429A CN201911049741.8A CN201911049741A CN112745429A CN 112745429 A CN112745429 A CN 112745429A CN 201911049741 A CN201911049741 A CN 201911049741A CN 112745429 A CN112745429 A CN 112745429A
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substituent
methyl
alkyl
metal complex
formula iii
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CN112745429B (en
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高榕
郭子芳
王洪涛
周俊领
李昕阳
赖菁菁
顾元宁
徐世媛
赵惠
傅捷
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Sinopec Beijing Research Institute of Chemical Industry
China Petroleum and Chemical Corp
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Sinopec Beijing Research Institute of Chemical Industry
China Petroleum and Chemical Corp
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Priority to PCT/CN2020/125433 priority patent/WO2021083358A1/en
Priority to US17/755,542 priority patent/US20220396646A1/en
Priority to KR1020227018606A priority patent/KR20220097939A/en
Priority to JP2022525809A priority patent/JP2023500504A/en
Priority to EP20880543.2A priority patent/EP4053174A4/en
Priority to BR112022008300A priority patent/BR112022008300A2/en
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    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/02—Ethene
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    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/04—Nickel compounds
    • C07F15/045—Nickel compounds without a metal-carbon linkage
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
    • C08F2410/03—Multinuclear procatalyst, i.e. containing two or more metals, being different or not

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Abstract

The present invention relates to a method for preparing an olefin-unsaturated carboxylic acid copolymer and an olefin-unsaturated carboxylic acid copolymer prepared by the method. The catalyst used in the process comprises a diimine metal complex of formula I. The spherical and/or spheroidal polymer prepared by the preparation method has good prospect in industrial application.
Figure DDA0002255027930000011

Description

Process for producing olefin-unsaturated carboxylic acid copolymer
Technical Field
The invention belongs to the field of preparation of high molecular polymers, and particularly relates to a method for preparing an olefin-unsaturated carboxylic acid copolymer.
Background
The polyolefin product has low price, excellent performance and wide application range. Under the condition of keeping the excellent physical and chemical properties of the original polyolefin, polar groups are introduced into polyolefin molecular chains by a chemical synthesis method, so that the chemical inertness, the printing property, the wettability and the compatibility with other materials can be improved, and new characteristics which are not possessed by raw materials are endowed. Although polar monomers can be directly introduced into polyolefin chains by high-pressure radical copolymerization, the method requires high-temperature and high-pressure conditions, and is high in energy consumption and expensive in equipment cost.
As a preparation technology of polymers at normal temperature and normal pressure, coordination catalytic copolymerization has attracted extensive attention due to its remarkable effects in reducing energy consumption, improving reaction efficiency and the like. The catalyst participates in the reaction process, so that the activation energy of the copolymerization reaction of the olefin monomer and the polar monomer is greatly reduced, and the functional polymer with higher molecular weight can be obtained at lower temperature and pressure. Currently, only a few documents report the use of transition metal complexes to catalyze the copolymerization of olefins and unsaturated carboxylic acids. However, in the prior art, no matter which method is adopted for polymerization reaction, the obtained polymer is viscous massive solid, and is easy to scale in polymerization equipment, thereby bringing difficulties to the transportation, solvent removal, granulation and the like of the polymer.
Disclosure of Invention
The invention provides a novel preparation method of olefin-unsaturated carboxylic acid copolymer, spherical and/or spheroidal polymers can be directly obtained through the copolymerization of olefin and unsaturated carboxylic acid, the polymer has good appearance and good industrial application prospect.
In a first aspect, the present invention provides a process for preparing an olefin-unsaturated carboxylic acid copolymer, which comprises polymerizing an olefin and an unsaturated carboxylic acid in the presence of a catalyst and optionally a chain transfer agent to produce the olefin-unsaturated carboxylic acid copolymer,
wherein the catalyst comprises a main catalyst and an optional cocatalyst, and the main catalyst comprises a diimine metal complex shown as a formula I:
Figure BDA0002255027910000021
in the formula I, R1And R2The same or different, independently selected from C1-C30 hydrocarbyl containing or not containing substituent; r5-R8The same or different, each independently selected from hydrogen, halogen, hydroxyl, C1-C20 alkyl with or without substituent; r5-R8Optionally forming a ring with each other; r12Selected from C1-C20 substituted or unsubstituted hydrocarbon groups; y is selected from non-metal atoms of group VIA; m is a group VIII metal; x is selected from halogen, C1-C10 alkyl with or without substituent and C1-C10 alkoxy with or without substituent.
According to some embodiments of the invention, R1And R2Selected from substituted or unsubstituted C1-C20 alkyl and/or substituted or unsubstitutedSubstituted or unsubstituted C6-C20 aryl, preferably, R1And/or R2Is a group of formula II:
Figure BDA0002255027910000022
in the formula II, R1-R5The aryl group is the same or different and is independently selected from hydrogen, halogen, hydroxyl, C1-C20 alkyl with or without substituent, C2-C20 alkenyl with or without substituent, C2-C20 alkynyl with or without substituent, C3-C20 cycloalkyl with or without substituent, C1-C20 alkoxy with or without substituent, C2-C20 alkenyloxy with or without substituent, C2-C20 alkynyloxy with or without substituent, C3-C20 cycloalkoxy with or without substituent, C6-C20 aryl with or without substituent, C7-C20 aralkyl with or without substituent and C7-C20 alkaryl with or without substituent; r1-R5Optionally forming a ring with each other.
According to some embodiments of the invention, R in formula II1-R5The aryl group is selected from hydrogen, halogen, hydroxyl, C1-C10 alkyl with or without substituent, C2-C10 alkenyl with or without substituent, C2-C10 alkynyl with or without substituent, C3-C10 cycloalkyl with or without substituent, C1-C10 alkoxy with or without substituent, C2-C10 alkenyloxy with or without substituent, C2-C10 alkynyloxy with or without substituent, C3-C10 cycloalkoxy with or without substituent, C6-C15 aryl with or without substituent, C7-C15 aralkyl with or without substituent and C7-C15 alkaryl with or without substituent.
According to some embodiments of the invention, M is selected from nickel and palladium.
According to some embodiments of the invention, Y is selected from O and S; x is selected from halogen, C1-C10 alkyl with or without substituent and C1-C10 alkoxy with or without substituent, preferably selected from halogen, C1-C6 alkyl with or without substituent and C1-C6 alkoxy with or without substituent.
According to some embodiments of the invention, R12Is selected from C1-C20 alkyl with or without substituent, preferably C1-C10 alkyl with or without substituent, more preferably C1-C6 alkyl with or without substituent.
According to some embodiments of the invention, the diimine metal complex is represented by formula III:
Figure BDA0002255027910000031
in the formula III, R1-R11The same or different, each is independently selected from hydrogen, halogen, hydroxyl, C1-C20 alkyl with or without substituent, C2-C20 alkenyl with or without substituent, C2-C20 alkynyl with or without substituent, C3-C20 cycloalkyl with or without substituent, C1-C20 alkoxy with or without substituent, C2-C20 alkenyloxy with or without substituent, C2-C20 alkynyloxy with or without substituent, C3-C20 cycloalkoxy with or without substituent, C6-C20 aryl with or without substituent, C7-C20 aralkyl with or without substituent, and C7-C20 alkaryl with or without substituent, M, X, Y, R-C20 alkenyl with or without substituent in formula III12Have the same definition as formula I.
According to some embodiments of the invention, R1-R11The substituents are respectively and independently selected from hydrogen, halogen, hydroxyl, C1-C10 alkyl with or without substituent, C2-C10 alkenyl with or without substituent, C2-C10 alkynyl with or without substituent, C3-C10 cycloalkyl with or without substituent, C1-C10 alkoxy with or without substituent, C2-C10 alkenyloxy with or without substituent, C2-C10 alkynyloxy with or without substituent, C3-C10 cycloalkoxy with or without substituent, and C3-C10 cycloalkoxy with or without substituentA C6-C15 aryl group without substituents, a C7-C15 aralkyl group with or without substituents, and a C7-C15 alkaryl group with or without substituents.
According to some embodiments of the invention, R1-R11Each independently selected from hydrogen, C1-C10 alkyl, halogenated C1-C10 alkyl, C1-C10 alkoxy, halogenated C1-C10 alkoxy and halogen, more preferably from hydrogen, C1-C6 alkyl, halogenated C1-C6 alkyl, C1-C6 alkoxy, halogenated C1-C6 alkoxy and halogen.
According to some embodiments of the invention, the substituent is selected from the group consisting of halogen, hydroxy, C1-C10 alkyl, halogenated C1-C10 alkyl, C1-C10 alkoxy, and halogenated C1-C10 alkoxy; the substituents are preferably selected from halogen, hydroxy, C1-C6 alkyl, halogenated C1-C6 alkyl, C1-C6 alkoxy and halogenated C1-C6 alkoxy.
According to some embodiments of the invention, the C1-C6 alkyl group is selected from methyl, ethyl, n-propyl, isopropyl, n-butyl and isobutyl, n-pentyl, isopentyl, n-hexyl, isohexyl, 3, 3-dimethylbutyl.
According to some embodiments of the invention, the C1-C6 alkoxy group is selected from methoxy, ethoxy, n-propoxy, isopropoxy, n-and isobutoxy, n-pentoxy, isopentoxy, n-hexoxy, isohexoxy, 3, 3-dimethylbutoxy.
According to some embodiments of the invention, the halogen is selected from fluorine, chlorine, bromine and iodine.
According to some embodiments of the invention, the diimine metal complex is selected from one or more of the following complexes:
1) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
2) a diimine metal complex of formula III wherein R1＝R3Ethyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
3) a diimine metal complex of formula III wherein R1＝R3Is isopropyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
4) a diimine metal complex of formula III wherein R1-R3Methyl, R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
5) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝Br，R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
6) a diimine metal complex of formula III wherein R1＝R3＝F，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
7) a diimine metal complex of formula III wherein R1＝R3＝Cl，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
8) a diimine metal complex of formula III wherein R1＝R3＝Br，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
9) a diimine metal complex of formula III wherein R1＝R3(ii) a methyl group,R2＝R4-R7＝R10＝H，R8＝R9＝R11methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
10) a diimine metal complex of formula III wherein R1＝R3Ethyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
11) a diimine metal complex of formula III wherein R1＝R3Is isopropyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
12) a diimine metal complex of formula III wherein R1-R3Methyl, R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
13) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝Br，R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
14) a diimine metal complex of formula III wherein R1＝R3＝F，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
15) a diimine metal complex of formula III wherein R1＝R3＝Cl，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
16)a diimine metal complex of formula III wherein R1＝R3＝Br，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
17) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
18) a diimine metal complex of formula III wherein R1＝R3Ethyl, R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
19) a diimine metal complex of formula III wherein R1＝R3Is isopropyl, R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
20) a diimine metal complex of formula III wherein R1-R3Methyl, R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
21) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝Br，R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
22) a diimine metal complex of formula III wherein R1＝R3＝F，R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
23) a diimine metal complex of formula III wherein R1＝R3＝Cl，R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
24) a diimine metal complex of formula III wherein R1＝R3＝Br，R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, and X ═ Br.
According to some embodiments of the invention, the unsaturated carboxylic acid is selected from one or more of the unsaturated carboxylic acids represented by formula G:
Figure BDA0002255027910000061
in the formula G, L1-L3Each independently selected from H and C with or without substituent1-C30Alkyl radical, L4Is C having a pendant group1-C30An alkylene group.
According to some embodiments of the present invention, the content of the structural unit derived from the unsaturated carboxylic acid represented by the formula G in the copolymer is 0.2 to 15.0 mol%, more preferably 0.7 to 10.0 mol%.
According to some embodiments of the invention, in formula G, L1And L2Is H.
According to some embodiments of the invention, in formula G, L3Is H or C1-C30An alkyl group.
According to some embodiments of the invention, in formula G, L4Is C having a pendant group1-C30An alkylene group.
According to some embodiments of the invention, in formula G, L3Is H or C1-C20An alkyl group.
According to some embodiments of the invention, in formula G, L4Is C having a pendant group1-C20An alkylene group.
According to some embodiments of the invention, in formula G, L3Is H or C1-C10An alkyl group.
According to some embodiments of the invention, in formula G, L4Is C having a pendant group1-C10An alkylene group.
According to some embodiments of the invention, in formula G, L4Is C having a pendant group1-C6An alkylene group.
According to some embodiments of the invention, L1-L3Wherein said substituents are selected from halogen, C1-C10Alkyl radical, C1-C10Alkoxy radical, C6-C10One or more of aryl, cyano and hydroxyl.
According to some embodiments of the invention, L1-L3Wherein the substituent is selected from one or more of C1-C6 alkyl, halogen and C1-C6 alkoxy.
According to some embodiments of the invention, the pendant group in L4 is selected from halogen, C6-C20Aryl radical, C1-C20Alkyl and C1-C20One or more of alkoxy, said C6-C20Aryl radical, C1-C20Alkyl and C1-C20Alkoxy is optionally substituted by a substituent, preferably selected from halogen, C1-C10Alkyl radical, C1-C10Alkoxy radical, C6-C10One or more of aryl and hydroxyl.
According to a preferred embodiment of the invention, said L4The side group in (A) is selected from halogen and C6-C20Aryl radical, C1-C20Alkyl, hydroxy substituted C1-C20Alkyl and alkoxy substituted C1-C20One or more of alkyl; preferably, said pendant groupSelected from halogen, C6-C20Aryl radical, C1-C10Alkyl, hydroxy substituted C1-C10Alkyl and alkoxy substituted C1-10One or more of alkyl; more preferably, the side group is selected from halogen, phenyl, C1-C6Alkyl and hydroxy substituted C1-C6One or more of alkyl, said C1-C6Alkyl groups include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl and hexyl.
According to a preferred embodiment of the invention, in formula G, L1And L2Is H, L3Is H or C1-C30Alkyl radical, L4Is C having a pendant group1-C30An alkylene group; said C is1-C30Alkyl is optionally substituted by a substituent, preferably selected from halogen, C1-C10Alkyl radical, C1-C10Alkoxy radical, C6-C10One or more of aryl, cyano and hydroxyl.
According to a preferred embodiment of the invention, in formula G, L1And L2Is H, L3Is H, C1-C10Alkyl or halogen substituted C1-C10Alkyl, preferably L3Is H or C1-C10An alkyl group; l is4Is C having a pendant group1-C20Alkylene radicals, e.g. L4Is methylene with side group, ethylene with side group, propylene with side group, butylene with side group, C with side group5Alkylene, C having pendant groups6Alkylene, C having pendant groups7Alkylene, C having pendant groups8Alkylene, C having pendant groups9Alkylene, C having pendant groups10Alkylene, C having pendant groups12Alkylene, C having pendant groups14Alkylene, C having pendant groups18Alkylene, C having pendant groups20Alkylene, preferably C, having pendant groups1-C10An alkylene group.
According to a preferred embodiment of the inventionIn the formula G, L1And L2Is H, L3Is H or C1-6An alkyl group; l is4Is C having a pendant group1-C10An alkylene group.
In the present invention, the carbon number n of the Cn alkylene group means the number of C's in the linear chain, excluding the number of C's in the pendant group, and is, for example, isopropylidene (-CH)2-CH(CH3) -) is referred to herein as C with a pendant group (methyl)2An alkylene group.
According to a preferred embodiment of the present invention, specific examples of the unsaturated carboxylic acid represented by the formula G include, but are not limited to: 2-methyl-4-pentenoic acid, 2, 3-dimethyl-4-pentenoic acid, 2-dimethyl-4-pentenoic acid, 2-ethyl-4-pentenoic acid, 2-isopropyl-4-pentenoic acid, 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-diethyl-4-pentenoic acid, 2-methyl-2-ethyl-4-pentenoic acid, 2,3, 3-tetramethyl-4-pentenoic acid, 2-methyl-, 2-methyl-5-hexenoic acid, 2-ethyl-5-hexenoic acid, 2-propyl-5-hexenoic acid, 2, 3-dimethyl-5-hexenoic acid, 2-dimethyl-5-hexenoic acid, 2-isopropyl-5-hexenoic acid, 2-methyl-2-ethyl-5-hexenoic acid, 2- (1-methylpropyl) -5-hexenoic acid, 2, 3-trimethyl-5-hexenoic acid, 2-diethyl-5-hexenoic acid, 2-methyl-6-heptenoic acid, 2-ethyl-6-heptenoic acid, 2-propyl-6-heptenoic acid, 2, 3-dimethyl-6-heptenoic acid, 2-ethyl-5-hexenoic acid, 2-methyl-5-hexenoic acid, 2-ethyl-5-hexenoic, 2, 4-dimethyl-6-heptenoic acid, 2-dimethyl-6-heptenoic acid, 2-isopropyl-5-methyl-6-heptenoic 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, 3-trimethyl-6-heptenoic acid, 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-methyl-6-heptenoic acid, 2-ethyl-7-octenoic acid, 2-propyl-7-octenoic acid, 2, 4-dimethyl-7-octenoic acid, 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, 3-trimethyl-7-octenoic acid, 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-methyl-7-nonenoic acid, 2-ethyl-8-nonenoic acid, 2-propyl, 2, 4-dimethyl-8-nonenoic acid, 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, or 2-methyl-10-undecenoic acid.
According to a preferred embodiment of the invention, the cocatalyst is chosen from organoaluminum compounds and/or organoboron compounds.
According to a preferred embodiment of the invention, the organoaluminium compound is selected from alkylaluminoxanes or compounds of general formula AlRnX1 3-nWith an organoaluminum compound (alkylaluminum or alkylaluminum halide) of the general formula AlRnX1 3-nWherein R is H, C1-C20Saturated or unsaturated hydrocarbon radicals or C1-C20Saturated or unsaturated hydrocarbyloxy radicals, preferably C1-C20Alkyl radical, C1-C20Alkoxy radical, C7-C20Aralkyl or C6-C20An aryl group; x1Is halogen, preferably chlorine or bromine; 0<n is less than or equal to 3. Specific examples of the organoaluminum compound include, but are not limited to: trimethylaluminum, triethylaluminum, triisobutylaluminum, tri-n-hexylaluminum, trioctylaluminum, diethylaluminum monohydrogen, diisobutylaluminum monohydrogen, diethylaluminum monochloride, diisobutylaluminum monochloride, ethylaluminum sesquichloride, ethylaluminum dichloride, Methylaluminoxane (MAO) and Modified Methylaluminoxane (MMAO). Preferably, the organoaluminum compound is Methylaluminoxane (MAO).
According to a preferred embodiment of the invention, the organoboron compound is selected from an aryl boron and/or a borate. The arylborole is preferably a substituted or unsubstituted phenylborone, more preferably tris (pentafluorophenyl) boron. The borate is preferably N, N-dimethylanilinium tetrakis (pentafluorophenyl) borate and/or triphenylmethyl tetrakis (pentafluorophenyl) borate.
According to a preferred embodiment of the present invention, the concentration of the main catalyst in the reaction system is 0.00001 to 100mmol/L, for example, 0.00001mmol/L, 0.00005mmol/L, 0.0001mmol/L, 0.0005mmol/L, 0.001mmol/L, 0.005mmol/L, 0.01mmol/L, 0.05mmol/L, 0.1mmol/L, 0.3mmol/L, 0.5mmol/L, 0.8mmol/L, 1mmol/L, 5mmol/L, 8mmol/L, 10mmol/L, 20mmol/L, 30mmol/L, 50mmol/L, 70mmol/L, 80mmol/L, 100mmol/L and any value therebetween, preferably 0.0001 to 1mmol/L, more preferably 0.001 to 0.5 mmol/L.
According to a preferred embodiment of the present invention, when the cocatalyst is an organoaluminum compound, the molar ratio of aluminum in the cocatalyst to M in the procatalyst is (10-10000000):1, for example, 10:1, 20:1, 50:1, 100:1, 200:1, 300:1, 500:1, 700:1, 800:1, 1000:1, 2000:1, 3000:1, 5000:1, 10000:1, 100000:1, 1000000:1, 10000000:1 and any value therebetween, preferably (10-100000):1, more preferably (100-10000): 1; when the cocatalyst is an organoboron compound, the molar ratio of boron in the cocatalyst to M in the procatalyst is (0.1-1000):1, e.g., 0.1:1, 0.2:1, 0.5:1, 0.8:1, 1:1, 1.2:1, 1.4:1, 1.6:1, 1.8:1, 2:1, 2.5:1, 3:1, 4:1, 5:1, 8:1, 10:1, 20:1, 50:1, 100:1, 200:1, 300:1, 500:1, 700:1, 800:1, 1000:1, and any value therebetween, preferably (0.1-500): 1.
According to a preferred embodiment of the invention, the olefin comprises an olefin having 2 to 16 carbon atoms, and in some embodiments of the invention, the olefin comprises ethylene or an alpha-olefin having 3 to 16 carbon atoms. In other embodiments of the present invention, the olefin is C3-C16A cyclic olefin, preferably a 5-or 6-membered ring. Preferably, the olefin is ethylene or an alpha-olefin having 3 to 16 carbon atoms, more preferably ethylene or C2-C10Alpha-olefins, such as ethylene, propylene, butene, pentene, hexene, heptene and octene.
According to a preferred embodiment of the present invention, the concentration of the unsaturated carboxylic acid monomer represented by the formula G in the reaction system is 0.01 to 6000mmol/L, preferably 0.1 to 1000mmol/L, more preferably 1 to 500mmol/L, and may be, for example, 1mmol/L, 10mmol/L, 20mmol/L, 30mmol/L, 50mmol/L, 70mmol/L, 90mmol/L, 100mmol/L, 200mmol/L, 300mmol/L, 400mmol/L, 500mmol/L and any value therebetween.
According to a preferred embodiment of the present invention, the chain transfer agent is selected from one or more of aluminum alkyls, magnesium alkyls and zinc alkyls.
According to a preferred embodiment of the invention, the chain transfer agent is a trialkylaluminum and/or a dialkylzinc, preferably one or more selected from the group consisting of trimethylaluminum, triethylaluminum, triisopropylaluminum, triisobutylaluminum, tri-n-hexylaluminum, tri-n-octylaluminum, dimethylzinc and diethylzinc.
According to a preferred embodiment of the invention, the molar ratio of the chain transfer agent to M in the procatalyst is (0.1-2000: 1, e.g. 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, 500:1, 600:1, 800:1, 1000:1, 2000:1 and any value in between, preferably (10-600: 1).
According to a preferred embodiment of the invention, the polymerization is carried out in an alkane solvent selected from C3-C20One or more alkanes, preferably selected from C3-C10The alkane, for example, may be selected from one or more of butane, isobutane, pentane, hexane, heptane, octane and cyclohexane, preferably one or more of hexane, heptane and cyclohexane.
According to a preferred embodiment of the present invention, the unsaturated carboxylic acid is pre-treated with a dehydroactive hydrogen, preferably, the unsaturated carboxylic acid is pre-treated with a co-catalyst or a chain transfer agent as described above to remove the hydroxyl active hydrogen in the unsaturated carboxylic acid. Preferably, the molar ratio of hydroxyl groups in the unsaturated carboxylic acid to co-catalyst or chain transfer agent during pretreatment is from 10:1 to 1: 10.
According to a preferred embodiment of the invention, the reaction is carried out in the absence of water and oxygen.
According to a preferred embodiment of the invention, the conditions of the reaction include: the temperature of the reaction is-50 ℃ to 50 ℃, preferably-20 ℃ to 50 ℃, more preferably 0 ℃ to 50 ℃, and can be, for example, 0 ℃, 10 ℃, 20 ℃, 30 ℃, 40 ℃,50 ℃ and any value therebetween; and/or the reaction time is 10-200min, preferably 20-60 min. In the present invention, the reaction pressure is not particularly limited as long as the monomer can be subjected to coordination copolymerization. When the olefin is ethylene, the pressure of ethylene in the reactor is preferably 1 to 1000atm, more preferably 1 to 200atm, and still more preferably 1 to 50atm, from the viewpoint of cost reduction and simplification of the polymerization process.
In the present invention, the "reaction system" refers to the whole formed by the solvent, the olefin, the unsaturated carboxylic acid monomer, the catalyst and the optional chain transfer agent.
The present invention also provides an olefin-unsaturated carboxylic acid copolymer comprising a spherical and/or spheroidal polymer, which is produced by the above production method.
According to a preferred embodiment of the invention, the copolymer has at least partially spherical and/or spheroidal polymers inside.
According to a preferred embodiment of the invention, the spherical and/or spheroidal polymers have an average particle size of 0.1 to 50.0mm, for example 0.1mm, 0.5mm, 1.0mm, 2.0mm, 3.0mm, 5.0mm, 8.0mm, 10.0mm, 15.0mm, 20.0mm, 25.0mm, 30.0mm, 35.0mm, 40.0mm, 45.0mm, 50.0mm and any value in between, preferably 0.5 to 20.0 mm.
According to a preferred embodiment of the present invention, in the olefin-unsaturated carboxylic acid copolymer, the content of the structural unit derived from the unsaturated carboxylic acid represented by the formula G is 0.4 to 30.0 mol%, for example, may be 0.4 mol%, 0.5 mol%, 0.7 mol%, 0.8 mol%, 1.0 mol%, 1.5 mol%, 2.0 mol%, 5.0 mol%, 8.0 mol%, 10.0 mol%, 15.0 mol%, 20.0 mol%, 25.0 mol%, 30.0 mol% and any value therebetween, preferably 0.7 to 10.0 mol%.
According to a preferred embodiment of the present invention, the weight average molecular weight of the olefin-unsaturated carboxylic acid copolymer is 30000-500000, preferably 50000-400000.
According to a preferred embodiment of the present invention, the olefin-unsaturated carboxylic acid copolymer has a molecular weight distribution of 4.0 or less, and for example, may be 0.1, 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0 and any value therebetween, and preferably, the molecular weight distribution is 1.0 to 4.0.
In the present invention, the particle size of a spherical or spheroidal polymer is herein considered to be equal to the diameter of a sphere having a volume equal to the volume of the particle.
According to still another aspect of the present invention, there is provided a use of the olefin-unsaturated carboxylic acid copolymer as a polyolefin material.
The process for preparing an olefin-unsaturated carboxylic acid copolymer provided by the present invention uses a novel trinuclear metal complex-containing catalyst. The catalyst is not reported, therefore, the technical problem solved by the invention is to provide a novel preparation method of olefin-unsaturated carboxylic acid copolymer.
Furthermore, in the preparation method of the olefin-unsaturated carboxylic acid copolymer provided by the invention, the spherical and/or spheroidal polymers with good shapes are directly prepared by selecting the reacted unsaturated carboxylic acid monomer, the catalyst and a proper polymerization process without subsequent processing steps such as granulation and the like, and the obtained polymerization product is not easy to scale in a reactor and is convenient to transport.
Further, compared with the existing industrial process for preparing the olefin-unsaturated carboxylic acid copolymer, the method for preparing the olefin-unsaturated carboxylic acid copolymer provided by the invention omits the step of saponification reaction, and has simpler preparation process.
Drawings
FIG. 1 is a photograph of an olefin-unsaturated carboxylic acid copolymer obtained in example 2 of the present invention.
Detailed Description
The present invention is described in detail below with reference to the following embodiments and the attached drawings, but it should be understood that the embodiments and the attached drawings are only used for the illustrative description of the present invention and do not limit the protection scope of the present invention in any way. All reasonable variations and combinations that fall within the spirit of the invention are intended to be within the scope of the invention.
The analytical characterization instrument used in the present invention was as follows:
before measurement, the polymer is washed by acid solution, and the content of metal in the polymer is less than or equal to 50 ppm.
Comonomer content of the copolymer (derived fromStructural units of unsaturated carboxylic acids represented by formula G): by using13C NMR spectroscopy was performed on a 400MHz Bruker Avance 400 NMR spectrometer using a 10mm PASEX 13 probe to dissolve a polymer sample with deuterated tetrachloroethane at 130 ℃ for analytical testing.
Molecular weight of copolymer: measured at 150 ℃ using PL-GPC220 in trichlorobenzene (standard: PS, flow rate: 1.0mL/min, column: 3 XPlgel 10um M1 XED-B300X 7.5 nm).
1HNMR nuclear magnetic resonance apparatus: bruker DMX 300(300MHz), Tetramethylsilicon (TMS) as an internal standard, was used to determine the structure of the ligands at 25 ℃.
The activity measurement method comprises the following steps: weight of polymer (g)/nickel (mol). times.2.
Figure BDA0002255027910000121
For the purpose of conciseness and clarity in the examples, the ligands and complexes are illustrated below:
example 1
1) Ligand L1The preparation of (1):
preparation of the Complex (R in formula III)1、R3Is ethyl, R2、R4-R7、R10Is hydrogen, R8、R9And R11Is methyl, R12Is ethyl, M is nickel, Y is O, X is Br)
Under the protection of nitrogen, 2, 6-diethylaniline (2.0ml,12mmol) is dissolved in 20ml toluene, 12ml (1.0M,12mmol) of trimethylaluminum is dropped at normal temperature, the reaction is refluxed for 2 hours, the system is cooled to room temperature, camphorquinone (0.831g,5mmol) is added, and the reflux reaction of the system is carried out for 6 hours. Neutralizing the reaction product with sodium hydroxide water solution, extracting with dichloromethane, drying, and performing column chromatography to obtain yellow ligand L1The yield was 69.2%.1H-NMR(CDCl3):δ6.94-6.92(m,6H,CAr-CH3),2.56-2.51(m,4H,CAr-CH3),2.36-2.31(m,4H,CAr-CH3),1.82-1.78(m,4H,CH2),1.54(m,1H),1.24-1.18(m,12H),1.09(s,3H,CH3),0.94(m,6H,CH3)。
2) Complex Ni1The preparation of (1):
will contain 0.277g (0.9mmol) of (DME) NiBr2Was slowly added dropwise to a solution containing 0.258g (0.6mmol) of ligand L1In dichloromethane (10 mL). The color of the solution immediately turned deep red and a large amount of precipitate formed. Stirring at room temperature for 6h, and precipitating with anhydrous diethyl ether. Filtering to obtain a filter cake, washing the filter cake with anhydrous ether, and vacuum drying to obtain brownish red powdery solid Ni1. Yield: 78.2 percent. Elemental analysis (C)64H90Br6N4Ni3O2): c, 47.96; h, 5.66; n, 3.50; experimental values (%): c, 47.48; h, 6.00; and N, 3.26.
3) Polymerization:
continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.0mg (5. mu. mol) of complex Ni was added115mmol (2.55g)2, 2-dimethyl-7-octenoic acid, 15mL AlEt3(1.0mol/L hexane solution), 6.5mL of MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 2
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.0mg (5. mu. mol) of complex Ni was added130mmol (5.10g)2, 2-dimethyl-7-octenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 6.5mL of MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 3
Will be provided with a machineA stirred 1L stainless steel polymerizer was continuously dried at 130 ℃ for 6 hours, evacuated while hot and charged with N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.0mg (5. mu. mol) of complex Ni was added130mmol (5.10g)2, 2-dimethyl-7-octenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 6.5mL MAO (1.53mol/L toluene solution), and the reaction was stirred at 60 ℃ under 10atm of ethylene pressure for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 4
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.0mg (5. mu. mol) of complex Ni was added130mmol (5.10g)2, 2-dimethyl-7-octenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 0.5mL diethyl zinc (1mol/L hexane solution), 6.5mL MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under 10atm of ethylene pressure for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 5
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.0mg (5. mu. mol) of complex Ni was added130mmol (5.10g)2, 2-dimethyl-7-octenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 1.0mL diethyl zinc (1mol/L hexane solution), 6.5mL MAO (1.53mol/L toluene solution), and the reaction was stirred at 30 ℃ for 30min while maintaining an ethylene pressure of 10 atm. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 6
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of a polymer solution was injected into the polymerization systemHexane with addition of 8.0mg (5. mu. mol) of complex Ni150mmol (8.51g)2, 2-dimethyl-7-octenoic acid, 50mL AlEt3(1.0mol/L hexane solution), 6.5mL of MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 7
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.0mg (5. mu. mol) of complex Ni was added1100mmol (17.02g)2, 2-dimethyl-7-octenoic acid, 100mL AlEt3(1.0mol/L hexane solution), 6.5mL of MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 8
1) Ligand L2The preparation of (1):
preparation of the Complex (R in formula III)1、R3Is isopropyl, R2、R4-R7、R10Is hydrogen, R8、R9And R11Is methyl, R12Is ethyl, M is nickel, Y is O, X is Br)
Under the protection of nitrogen, 2, 6-diisopropylaniline (2.4ml,12mmol) is dissolved in 20ml toluene, 12ml trimethylaluminum (1.0M,12mmol) is dropped at normal temperature, the reaction is refluxed for 2 hours, the system is cooled to room temperature, camphorquinone (0.831g,5mmol) is added, and the system is refluxed and reacted for 6 hours. Neutralizing the reaction product with sodium hydroxide water solution, extracting with dichloromethane, drying, and performing column chromatography to obtain yellow ligand L2The yield was 41.3%.1H NMR(300MHz,CDCl3),δ(ppm):7.06-6.81(m,6H,Ar-H),2.88(m,4H,CH(CH3)2),2.36(m,1H,),1.86(m,4H,CH2),1.24(d,24H,CH(CH3)2),0.96(s,6H,CH3),0.77(s,3H,CH3)。
2) Complex Ni2The preparation of (1): will contain 0.277g (0.9mmol) of (DME) NiBr2Was slowly added dropwise to a solution containing 0.291g (0.6mmol) of ligand L2In dichloromethane (10 mL). The color of the solution immediately turned deep red and a large amount of precipitate formed. Stirring at room temperature for 6h, and precipitating with anhydrous diethyl ether. Filtering to obtain a filter cake, washing the filter cake with anhydrous ether, and vacuum drying to obtain brownish red powdery solid Ni2. The yield was 74.0%. Elemental analysis (C)72H106Br6N4Ni3O2): c, 50.42; h, 6.23; n, 3.27; experimental values (%): c, 50.28; h, 6.42; and N, 3.18.
3) Polymerization: continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.6mg (5. mu. mol) of complex Ni was added230mmol (5.10g)2, 2-dimethyl-7-octenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 6.5mL of MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 9
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.6mg (5. mu. mol) of complex Ni was added250mmol (8.51g)2, 2-dimethyl-7-octenoic acid, 50mL AlEt3(1.0mol/L hexane solution), 6.5mL MAO (1.53mol/L toluene solution), and the reaction was stirred at 60 ℃ under 10atm of ethylene pressure for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 10
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was injected into the polymerization systemWhile adding 8.6mg (5. mu. mol) of complex Ni230mmol (4.69g)2, 2-dimethyl-6-heptenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 6.5mL MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under 10atm of ethylene pressure for 60 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 11
1) Complex Ni3Preparation of (R in the formula III)1、R3Is isopropyl, R2、R4-R7、R10Is hydrogen, R8、R9And R11Is methyl, R12Is isobutyl, M is nickel, Y is O, X is Br):
will contain 0.277g (0.9mmol) of (DME) NiBr2To a solution of 2-methyl-1-propanol (10mL) containing 0.291g (0.6mmol) of ligand L2In dichloromethane (10 mL). The color of the solution immediately turned deep red and a large amount of precipitate formed. Stirring at room temperature for 6h, and precipitating with anhydrous diethyl ether. Filtering to obtain a filter cake, washing the filter cake with anhydrous ether, and vacuum drying to obtain brownish red powdery solid Ni3. The yield was 74.0%. Elemental analysis (C)76H114Br6N4Ni3O2): c, 51.54; h, 6.49; n, 3.16; experimental values (%): c, 51.28; h, 6.82; n, 3.19.
2) Polymerization: continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.9mg (5. mu. mol) of complex Ni was added330mmol (5.10g)2, 2-dimethyl-7-octenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 6.5mL of MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 12
Complex Ni4Preparation (structure)In the formula III, R1-R3Is methyl, R4-R7、R10Is hydrogen, R8、R9And R11Is methyl, R12Is ethyl, M is nickel, Y is O, X is Br):
1) ligand L3The preparation of (1):
under the protection of nitrogen, 2, 4, 6-trimethylaniline (1.7ml,12mmol) is dissolved in 20ml of toluene, 12ml of trimethylaluminum (1.0M,12mmol) is dropped at normal temperature, the reaction is refluxed for 2 hours, the system is cooled to room temperature, camphorquinone (0.831g,5mmol) is added, and the reflux reaction of the system is carried out for 6 hours. Neutralizing the reaction product with sodium hydroxide water solution, extracting with dichloromethane, drying, and performing column chromatography to obtain yellow ligand L3The yield is 62.5 percent.1HNMR(300MHz,CDCl3),δ(ppm)[an isomer ratio of 1.2:1]:major isomer:6.72(s,4H,Ar-H),2.26-2.13(m,12H,CAr-CH3),1.87(s,6H,CAr-CH3),1.79(m,4H,CH2),1.42(m,1H),1.26(s,3H,CH3),1.07(s,6H,CH3)。Minor isomer:6.67(s,4H,Ar-H),2.09-2.01(m,12H,CAr-CH3),1.85(s,6H,CAr-CH3),1.79(m,4H,CH2),1.40(m,1H),1.26(s,3H,CH3),0.94(s,6H,CH3)。
2) Complex Ni4The preparation of (1):
will contain 0.277g (0.9mmol) of (DME) NiBr2Was slowly added dropwise to a solution containing 0.240g (0.6mmol) of ligand L3In dichloromethane (10 mL). The color of the solution immediately turned deep red and a large amount of precipitate formed. Stirring at room temperature for 6h, and precipitating with anhydrous diethyl ether. Filtering to obtain a filter cake, washing the filter cake with anhydrous ether, and vacuum drying to obtain brownish red powdery solid Ni4. The yield was 78.6%. Elemental analysis (C)60H82Br6N4Ni3O2): c, 46.59; h, 5.34; n, 3.62; experimental values (%): c, 46.24; h, 5.67; and N, 3.21.
3) Polymerization:
continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6hrs, vacuumizing while it is hot, and adding N2Air replacement for 3 times. 7.7mg (5. mu. mol) of complex Ni are added4Then, vacuum was applied and ethylene was substituted 3 times. 500mL of hexane, 30mmol (5.10g) of 2, 2-dimethyl-7-octenoic acid, 30mL of AlEt3(1.0mol/L hexane solution), 6.5ml of Methylaluminoxane (MAO) (1.53mol/L toluene solution) was added. The reaction was vigorously stirred at 30min with keeping the ethylene pressure at 10atm at 30 ℃. The polymer was obtained by neutralizing with a 10 wt% hydrochloric acid acidified ethanol solution, and the results are shown in Table 1.
Example 13
Complex Ni5Preparation of (R in the formula III)1、R3Is methyl, R2Is bromine, R4-R7、R10Is hydrogen, R8、R9And R11Is methyl, R12Is ethyl, M is nickel, Y is O, X is Br):
1) ligand L4The preparation of (1):
under the protection of nitrogen, 2, 6-dimethyl-4-bromo-aniline (2.45g,12mmol) is dissolved in 20ml of toluene, 12ml of trimethylaluminum (1.0M,12mmol) is dropped at normal temperature, the reaction is refluxed for 2 hours, the system is cooled to room temperature, camphorquinone (0.831g,5mmol) is added, and the system is refluxed for 6 hours. Neutralizing the reaction product with sodium hydroxide water solution, extracting with dichloromethane, drying, and performing column chromatography to obtain yellow ligand L4The yield is 60.7%.1HNMR(300MHz,CDCl3),δ(ppm)[an isomer ratio of 1.1:1]:major isomer:7.05(s,4H,Ar-H),2.18(m,12H,CAr-CH3),1.85(m,4H,CH2),1.37(m,1H),1.26(s,3H,CH3),1.06(s,6H,CH3).Minor isomer:7.02(s,4H,Ar-H),2.04(m,12H,CAr-CH3),1.85(m,4H,CH2),1.37(m,1H),1.26(s,3H,CH3),0.96(s,6H,CH3)。
2) Complex Ni5The preparation of (1):
will contain 0.277g (0.9mmol) of (DME) NiBr2Was slowly added dropwise to a solution containing 0.318g (0.6mmol) of ligand L4In dichloromethane (10 mL). The color of the solution immediately turned deep red and a large amount of precipitate formed. Stirring at room temperature for 6h, and precipitating with anhydrous diethyl ether. Filtering to obtain filter cakeWashing the filter cake with water and ethyl ether, and vacuum drying to obtain brownish red powdery solid Ni5. The yield was 74.1%. Elemental analysis (C)56H70Br10N4Ni3O2): c, 37.24; h, 3.91; n, 3.10; experimental values (%): c, 37.38; h, 4.30; and N, 3.03.
3) Polymerization:
continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6hrs, vacuumizing while it is hot, and adding N2Replace qi for 3 times. 9.0mg (5. mu. mol) of complex Ni are added5Then, vacuum was applied and ethylene was substituted 3 times. 500mL of hexane, 30mmol (5.10g) of 2, 2-dimethyl-7-octenoic acid, 30mL of AlEt3(1.0mol/L hexane solution), 6.5ml of Methylaluminoxane (MAO) (1.53mol/L toluene solution) was added. The reaction was vigorously stirred at 20 ℃ for 30min while maintaining an ethylene pressure of 10 atm. The polymer was obtained by neutralizing with a 10 wt% hydrochloric acid acidified ethanol solution, and the results are shown in Table 1.
Example 14
Complex Ni6Preparation of (R in the formula III)1、R3Is isopropyl, R2、R4-R7、R10Is hydrogen, R8、R9Is methyl, R11Is CH2Br，R12Is ethyl, M is nickel, Y is O, X is Br):
1) ligand L5The preparation of (1):
under the protection of nitrogen, 2, 6-diisopropyl-aniline (2.30ml,12mmol) is dissolved in 20ml toluene, 12ml trimethylaluminum (1.0M,12mmol) is dropped at normal temperature, the reaction is refluxed for 2 hours, the system is cooled to room temperature, diketone (1.225g,5mmol) is added, and the system is refluxed for 6 hours. Neutralizing the reaction product with sodium hydroxide water solution, extracting with dichloromethane, drying, and performing column chromatography to obtain yellow ligand L5The yield is 62.7 percent.1H NMR(300MHz,CDCl3),δ(ppm):7.05-6.83(m,6H,Ar-H),3.30(m,2H,CH2),2.80(m,4H,CH(CH3)2),1.55(m,1H),1.83(m,4H,CH2),1.26(d,24H,CH(CH3)2),0.99(s,6H,CH3)。
2) Complex Ni6System of (1)Preparing:
will contain 0.277g (0.9mmol) of (DME) NiBr2Was slowly added dropwise to a solution containing 0.338g (0.6mmol) of ligand L5In dichloromethane (10 mL). The color of the solution immediately turned deep red and a large amount of precipitate formed. Stirring at room temperature for 6h, and precipitating with anhydrous diethyl ether. Filtering to obtain a filter cake, washing the filter cake with anhydrous ether, and vacuum drying to obtain brownish red powdery solid Ni6. The yield was 80.2%. Elemental analysis (C)72H104Br8N4Ni3O2): c, 46.17; h, 5.60; n, 2.99; experimental values (%): c, 46.24; h, 5.80; and N, 3.13.
3) Polymerization:
continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6hrs, vacuumizing while it is hot, and adding N2Replace qi for 3 times. 9.4mg (5. mu. mol) of complex Ni are added6Then, vacuum was applied and ethylene was substituted 3 times. 500mL of hexane, 30mmol (5.10g) of 2, 2-dimethyl-7-octenoic acid, 30mL of AlEt3(1.0mol/L in hexane), 6.5Ml of Methylaluminoxane (MMAO) (1.53mol/L in toluene) was further added. The reaction was vigorously stirred at 50 ℃ for 30min while maintaining an ethylene pressure of 10 atm. The polymer was obtained by neutralizing with a 10 wt% hydrochloric acid acidified ethanol solution, and the results are shown in Table 1.
Example 15
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.0mg (5. mu. mol) of complex Ni was added130mmol (5.10g)2, 2-dimethyl-7-octenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 15mL of a toluene solution of N, N-dimethylanilinium tetrakis (pentafluorophenyl) borate (1mmol/L toluene solution) was added, and the reaction was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 16
Continuously heating a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.CDrying for 6h, vacuumizing while hot and adding N2Replace qi for 3 times. 500mL of hexane was poured into the polymerization system, and 8.0mg (5. mu. mol) of complex Ni was added130mmol (5.53g 10-undecenoic acid), 30mL AlEt3(1.0mol/L hexane solution), 6.5mL of MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
Example 17
Continuously drying a 1L stainless steel polymerization kettle equipped with mechanical stirring at 130 deg.C for 6h, vacuumizing while hot, and adding N2Replace qi for 3 times. 500mL of toluene was injected into the polymerization system while adding 8.0mg (5. mu. mol) of complex Ni130mmol (5.10g)2, 2-dimethyl-7-octenoic acid, 30mL AlEt3(1.0mol/L hexane solution), 6.5mL of MAO (1.53mol/L toluene solution), and the reaction mixture was stirred at 30 ℃ under an ethylene pressure of 10atm for 30 min. Finally, the polymer was obtained by neutralizing the mixture with a 10 wt% ethanol solution acidified with hydrochloric acid. The polymerization activity and the polymer performance parameters are shown in Table 1.
TABLE 1
Figure BDA0002255027910000191
Figure BDA0002255027910000201
As can be seen from Table 1, the catalyst of the present invention exhibits high polymerization activity when it catalyzes the copolymerization of ethylene and an unsaturated carboxylic acid, and the resulting polymer has a high molecular weight. The copolymerization activity of the catalyst can reach 21.7 multiplied by 10 to the maximum6g·mol-1(Ni)·h-1. The molecular weight of the polymer can be controlled within a wide range according to the addition of the chain transfer agent. In addition, by regulating and controlling the polymerization conditions, a copolymerization product with good particle morphology can be prepared.
It should be noted that the above-mentioned embodiments are only for explaining the present invention, and do not set any limit to the present invention. The present invention has been described with reference to exemplary embodiments, but the words which have been used herein are words of description and illustration, rather than words of limitation. The invention can be modified, as prescribed, within the scope of the claims and without departing from the scope and spirit of the invention. Although the invention has been described herein with reference to particular means, materials and embodiments, the invention is not intended to be limited to the particulars disclosed herein, but rather extends to all other methods and applications having the same functionality.

Claims (11)

1. A process for producing an olefin-unsaturated carboxylic acid copolymer, which comprises polymerizing an olefin and an unsaturated carboxylic acid in the presence of a catalyst and optionally a chain transfer agent to produce the olefin-unsaturated carboxylic acid copolymer,
wherein the catalyst comprises a main catalyst and an optional cocatalyst, and the main catalyst comprises a diimine metal complex shown as a formula I:
Figure FDA0002255027900000011
in the formula I, R1And R2The same or different, independently selected from C1-C30 hydrocarbyl containing or not containing substituent; r5-R8The same or different, each independently selected from hydrogen, halogen, hydroxyl, C1-C20 alkyl with or without substituent; r5-R8Optionally forming a ring with each other; r12Selected from C1-C20 substituted or unsubstituted hydrocarbon groups; y is selected from non-metal atoms of group VIA; m is a group VIII metal; x is selected from halogen, C1-C10 alkyl with or without substituent and C1-C10 alkoxy with or without substituent.
2. The method of claim 1, wherein R is1And R2Selected from containing or not containing substituentsC1-C20 alkyl and/or substituted or unsubstituted C6-C20 aryl, preferably R1And/or R2Is a group of formula II:
Figure FDA0002255027900000012
in the formula II, R1-R5The aryl group is the same or different and is independently selected from hydrogen, halogen, hydroxyl, C1-C20 alkyl with or without substituent, C2-C20 alkenyl with or without substituent, C2-C20 alkynyl with or without substituent, C3-C20 cycloalkyl with or without substituent, C1-C20 alkoxy with or without substituent, C2-C20 alkenyloxy with or without substituent, C2-C20 alkynyloxy with or without substituent, C3-C20 cycloalkoxy with or without substituent, C6-C20 aryl with or without substituent, C7-C20 aralkyl with or without substituent and C7-C20 alkaryl with or without substituent; r1-R5Optionally forming a ring with each other;
preferably, in formula II, R1-R5The aryl group is the same or different and is independently selected from hydrogen, halogen, hydroxyl, C1-C10 alkyl with or without substituent, C2-C10 alkenyl with or without substituent, C2-C10 alkynyl with or without substituent, C3-C10 cycloalkyl with or without substituent, C1-C10 alkoxy with or without substituent, C2-C10 alkenyloxy with or without substituent, C2-C10 alkynyloxy with or without substituent, C3-C10 cycloalkoxy with or without substituent, C6-C15 aryl with or without substituent, C7-C15 aralkyl with or without substituent and C7-C15 alkaryl with or without substituent;
m is selected from nickel and palladium; y is selected from O and S; x is selected from halogen, C1-C10 alkyl with or without substituent and C1-C10 alkoxy with or without substituent, preferably selected from halogen, C1-C6 alkyl with or without substituent and C with or without substituentA substituted or unsubstituted C1-C6 alkoxy group; r12Is selected from C1-C20 alkyl with or without substituent, preferably C1-C10 alkyl with or without substituent, more preferably C1-C6 alkyl with or without substituent.
3. A process according to claim 1 or 2, wherein the diimine metal complex is of formula III:
Figure FDA0002255027900000021
in the formula III, R1-R11The same or different, each is independently selected from hydrogen, halogen, hydroxyl, C1-C20 alkyl with or without substituent, C2-C20 alkenyl with or without substituent, C2-C20 alkynyl with or without substituent, C3-C20 cycloalkyl with or without substituent, C1-C20 alkoxy with or without substituent, C2-C20 alkenyloxy with or without substituent, C2-C20 alkynyloxy with or without substituent, C3-C20 cycloalkoxy with or without substituent, C6-C20 aryl with or without substituent, C7-C20 aralkyl with or without substituent, and C7-C20 alkaryl with or without substituent,
m, X, Y, R in formula III12Have the same definition as formula I.
4. The method of any one of claims 1-3, wherein R is1-R11The substituents are respectively and independently selected from hydrogen, halogen, hydroxyl, C1-C10 alkyl with or without substituent, C2-C10 alkenyl with or without substituent, C2-C10 alkynyl with or without substituent, C3-C10 cycloalkyl with or without substituent, C1-C10 alkoxy with or without substituent, C2-C10 alkenyloxy with or without substituent, C2-C10 alkynyloxy with or without substituent, C3-C3583-C10 alkynyloxy with or without substituent10 cycloalkoxy, substituted or unsubstituted C6-C15 aryl, substituted or unsubstituted C7-C15 aralkyl, and substituted or unsubstituted C7-C15 alkaryl;
preferably, R1-R11Each independently selected from hydrogen, C1-C10 alkyl, halogenated C1-C10 alkyl, C1-C10 alkoxy, halogenated C1-C10 alkoxy and halogen, more preferably from hydrogen, C1-C6 alkyl, halogenated C1-C6 alkyl, C1-C6 alkoxy, halogenated C1-C6 alkoxy and halogen.
5. A process according to any one of claims 1 to 4, characterised in that the substituents are selected from halogen, hydroxy, C1-C10 alkyl, halogenated C1-C10 alkyl, C1-C10 alkoxy and halogenated C1-C10 alkoxy; the substituents are preferably selected from halogen, hydroxy, C1-C6 alkyl, halogenated C1-C6 alkyl, C1-C6 alkoxy and halogenated C1-C6 alkoxy;
preferably, the C1-C6 alkyl group is selected from methyl, ethyl, n-propyl, isopropyl, n-butyl and isobutyl, n-pentyl, isopentyl, n-hexyl, isohexyl, 3, 3-dimethylbutyl;
preferably, the C1-C6 alkoxy group is selected from methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy and isobutoxy, n-pentoxy, isopentoxy, n-hexoxy, isohexoxy, 3, 3-dimethylbutoxy;
preferably, the halogen is selected from fluorine, chlorine, bromine and iodine.
6. A process according to any one of claims 1 to 5, characterised in that the diimine metal complex is selected from one or more of the following complexes:
1) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
2) a diimine metal complex of formula III wherein R1＝R3Ethyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
3) a diimine metal complex of formula III wherein R1＝R3Is isopropyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
4) a diimine metal complex of formula III wherein R1-R3Methyl, R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
5) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝Br，R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
6) a diimine metal complex of formula III wherein R1＝R3＝F，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
7) a diimine metal complex of formula III wherein R1＝R3＝Cl，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
8) a diimine metal complex of formula III wherein R1＝R3＝Br，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
9) diimines of the formula IIIA metal complex in which R1＝R3Methyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
10) a diimine metal complex of formula III wherein R1＝R3Ethyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
11) a diimine metal complex of formula III wherein R1＝R3Is isopropyl, R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
12) a diimine metal complex of formula III wherein R1-R3Methyl, R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
13) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝Br，R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
14) a diimine metal complex of formula III wherein R1＝R3＝F，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
15) a diimine metal complex of formula III wherein R1＝R3＝Cl，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M Ni, YO，X＝Br；
16) A diimine metal complex of formula III wherein R1＝R3＝Br，R2＝R4-R7＝R10＝H，R8＝R9＝R11Methyl, R12Isobutyl, M ═ Ni, Y ═ O, X ═ Br;
17) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
18) a diimine metal complex of formula III wherein R1＝R3Ethyl, R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
19) a diimine metal complex of formula III wherein R1＝R3Is isopropyl, R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
20) a diimine metal complex of formula III wherein R1-R3Methyl, R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
21) a diimine metal complex of formula III wherein R1＝R3Methyl, R2＝Br，R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
22) a diimine metal complex of formula III wherein R1＝R3＝F，R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
23) a diimine metal complex of formula III wherein R1＝R3＝Cl，R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, X ═ Br;
24) a diimine metal complex of formula III wherein R1＝R3＝Br，R2＝R4-R7＝R10＝H，R8＝R9Methyl, R11Bromomethyl, R12Ethyl, M ═ Ni, Y ═ O, and X ═ Br.
7. The process according to any one of claims 1 to 6, wherein the olefin comprises an olefin having 2 to 16 carbon atoms, preferably the olefin comprises ethylene or an alpha-olefin having 3 to 16 carbon atoms, and/or the unsaturated carboxylic acid is selected from one or more unsaturated carboxylic acids of formula G:
Figure FDA0002255027900000061
in the formula G, L1-L3Each independently selected from H and C with or without substituent1-C30Alkyl radical, L4Is C having a pendant group1-C30An alkylene group;
preferably, the content of the structural unit derived from the unsaturated carboxylic acid represented by the formula G in the copolymer is 0.2 to 15.0 mol%, more preferably 0.7 to 10.0 mol%;
preferably, L1And L2Is H, L3Is H or C1-C30Alkyl radical, L4Is C having a pendant group1-C30An alkylene group;
more preferably, L1And L2Is H, L3Is H or C1-C20Alkyl radical, L4Is C having a pendant group1-C20An alkylene group;
still more preferably, L1And L2Is H, L3Is H or C1-C10Alkyl radical, L4Is C having a pendant group1-C10An alkylene group;
further preferably, L1And L2Is H, L3Is H or C1-C10Alkyl radical, L4Is C having a pendant group1-C6An alkylene group.
8. The method of claim 7, wherein L is1-L3Wherein said substituents are selected from halogen, C1-C10Alkyl radical, C1-C10Alkoxy radical, C6-C10One or more of aryl, cyano and hydroxy; more preferably L1-L3Wherein the substituent is selected from one or more of C1-C6 alkyl, halogen and C1-C6 alkoxy;
the side group in L4 is selected from halogen and C6-C20Aryl radical, C1-C20Alkyl and C1-C20One or more of alkoxy, said C6-C20Aryl radical, C1-C20Alkyl and C1-C20Alkoxy is optionally substituted by a substituent, preferably selected from halogen, C1-C10Alkyl radical, C1-C10Alkoxy radical, C6-C10One or more of aryl and hydroxyl.
9. A process according to any one of claims 1 to 8, characterised in that the cocatalyst is selected from organoaluminium compounds and/or organoboron compounds; the organic aluminum compound is selected from one or more of alkyl aluminoxane, alkyl aluminum and alkyl aluminum halide; the organoboron compound is selected from an aryl boron and/or a borate; the chain transfer agent is selected from one or more of alkyl aluminum, alkyl magnesium and alkyl zinc;
preferably, when the cocatalyst is an organoaluminum compound, the molar ratio of aluminum in the cocatalyst to M in the diimine metal complex is (10-10)7):1, preferably (10-100000) 1, more preferably (100-; when the cocatalyst is an organic boron compound, the molar ratio of boron in the cocatalyst to M in the diimine metal complex is (0.1-1000):1, preferably (0.1-500): 1; the molar ratio of the chain transfer agent to M in the diimine metal complex is (0.1-5000):1, preferably (1.0-1000): 1.
10. The olefin-unsaturated carboxylic acid copolymer prepared according to the method of any one of claims 1 to 9, which is spherical and/or spheroidal, and/or has a particle diameter of 0.1 to 50 mm.
11. Use of an olefin-unsaturated carboxylic acid copolymer prepared according to the process of any one of claims 1 to 9 as a polyolefin material or of an olefin-unsaturated carboxylic acid copolymer according to claim 10 as a polyolefin material.
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