Iron complexes and methods for polymerization
US-2016272742-A1 · Sep 22, 2016 · US
US10793653B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10793653-B2 |
| Application number | US-201716343716-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 20, 2017 |
| Priority date | Oct 20, 2016 |
| Publication date | Oct 6, 2020 |
| Grant date | Oct 6, 2020 |
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A process for preparing conjugated diene (co)polymers comprising polymerizing at least one conjugated diene in the presence of a catalytic system comprising: (a) at least one pyridyl iron (III) complex having general formula (I) or (II): wherein: —R 1 , R 2 , R 3 and R 4 , identical or different, represent a hydrogen atom; or are selected from linear or branched, optionally halogenated C 1 -C 20 , preferably C 1 -C 15 , alkyl groups, optionally substituted cycloalkyl groups, optionally substituted aryl groups; —R 5 represents a hydrogen atom, or is selected from linear or branched, optionally halogenated C 1 -C 20 , preferably C 1 -C 15 , alkyl groups, optionally substituted cycloalkyl groups, optionally substituted aryl groups; —X, identical or different, represent a halogen atom such as, for example, chlorine, bromine, iodine; or are selected from linear or branched C 1 -C 20 , preferably C 1 -C 15 , alkyl groups, —OCOR 6 groups or —OR 6 groups wherein R 6 is selected from linear or branched C 1 -C 20 , preferably C 1 -C 15 , alkyl groups. —n is 3; (b) at least one co-catalyst selected from organo-aluminum derivatives, preferably from: (b 1 ) aluminum compounds having general formula (III): Al(R 7 )(R 8 )(R 9 ) (IIl) wherein R 7 represents a hydrogen atom, or is selected from linear or branched C 1 -C 20 alkyl groups, cycloalkyl groups, aryl groups, alkylaryl groups, arylalkyl groups, alkoxy groups; R 8 and R 9 , identical or different, are selected from linear or branched C 1 -C 20 alkyl groups, cycloalkyl groups, aryl groups, alkylaryl groups, arylalkyl groups; (b 2 ) aluminoxanes having general formula (IV): (R 10 ) 2 —Al—O—[-AI(R 11 )—O-] m -AI-(R 12 ) 2 (IV), wherein R 10 , R 11 and R 12 , identical or different, represent a hydrogen atom, or a halogen atom such as chlorine, bromine, iodine, fluorine; or are selected from linear or branched C 1 -C 20 alkyl groups, cycloalkyl groups, aryl groups, said groups being optionally substituted with one or more silicon or germanium atoms; and m is an integer ranging from 0 to 1000; (b 3 ) partially hydrolyzed organo-aluminum derivatives; (b 4 ) haloaluminum alkyls having general formula (V) or (VI): AI(R 13 ) p (X′) 3-p (V) AI 2 (R 13 ) q (X′) 3-q (VI) wherein p is 1 or 2; q is an integer ranging from 1 to 5; R 13 , identical or different, are selected from linear or branched C 1 -C 20 alkyl groups; X′ represents a chlorine or bromine atom, preferably chlorine; provided that said co-catalyst (b) is not selected from organo-boron derivatives.
Opening claim text (preview).
The invention claimed is: 1. Process for preparing conjugated diene (co)polymers comprising polybutadiene comprising (co)polymerizing at least one conjugated diene in the presence of a catalytic system comprising: (a) at least one pyridyl iron (III) complex having general formula (I) or (II): wherein: R 1 , R 2 , R 3 and R 4 , identical or different, represent a hydrogen atom; or are selected from a linear or branched, optionally halogenated C 1 -C 20 alkyl group, an optionally substituted cycloalkyl group, or an optionally substituted aryl group; R 5 represents a hydrogen atom, or is selected from a linear or branched, optionally halogenated C 1 -C 20 alkyl group, an optionally substituted cycloalkyl group or an optionally substituted aryl group; X, identical or different, represent a halogen atom; or are selected from a linear or branched C 1 -C 20 alkyl group, an —OCOR 6 group or an —OR 6 group wherein R 6 is selected from a linear or branched C 1 -C 20 alkyl group; n is 3 ; (b) at least one co-catalyst selected from the following organo-aluminum derivatives: (b 1 ) aluminum compounds having general formula (III): Al(R 7 )(R 8 )(R 9 ) (III) wherein R 7 represents a hydrogen atom, or is selected from a linear or branched C 1 -C 20 alkyl group, a cycloalkyl group, an aryl group, an alkylaryl group, an arylalkyl group or an alkoxy group; Rs and R 9 , identical or different, are selected from a linear or branched C 1 -C 20 alkyl group, a cycloalkyl group, an aryl group, an alkylaryl group or an arylalkyl group; (b 2 ) aluminoxanes having general formula (IV): (R 10 ) 2 —Al—O—[—Al(R 11 )—O-] m -Al—(R 12 ) 2 (IV) wherein R 10 , R 11 and R 12 , identical or different, represent a hydrogen atom, or a halogen atom, or are selected from a linear or branched C 1 -C 20 alkyl group, a cycloalkyl group or an aryl group, said groups being optionally substituted with one or more silicon or germanium atoms; and m is an integer ranging from 0 to 1000; (b 3 ) partially hydrolyzed organo-aluminum derivatives; (b 4 ) haloaluminum alkyls having general formula (V) or (VI): Al(R 13 ) p (X′) 3-p (V) Al 2 (R 13 ) q (X′) 3-q (VI) wherein p is 1 or 2; q is an integer ranging from 1 to 5; R 13 , identical or different, are selected from a linear or branched C 1 -C 20 alkyl group; X′ represents a chlorine or bromine atom; wherein polybutadiene obtained has a higher content of 1,2 unit than 1,4 cis unit. 2. Process for preparing conjugated diene (co)polymers including polybutadiene according to claim 1 , wherein in said pyridyl iron (III) complex having general formula (I) or (II): R 1 , R 2 , R 3 and R 4 , identical or different, represent a hydrogen atom; or are selected from a linear or branched C 1 -C 20 alkyl group; R 5 is selected from an aryl group optionally substituted with one or more of a methyl, ethyl, Cert-butyl or iso-propyl group; is selected from a phenyl group, a 2-methylphenyl group, a 2-ethylphenyl group, a 2-tert-butylphenyl group, a 2-iso-propylphenyl group, a 2,6-diethylphenyl group, a 2,6-di-iso-propylphenyl group, or a 2,4,6-trimethylphenyl group; or is an optionally substituted cyclohexyl group; X, mutually identical, represent a halogen atom; n is 3. 3. Process for preparing conjugated diene (co)polymers comprising polybutadiene according to claim 1 , wherein said aluminum compounds having general formula (III) (b 1 ) are selected from: diethylaluminum hydride, di-n-propylaluminum hydride, di-n-butylaluminum hydride, di-iso-butyl-aluminum hydride (DIBAH), diphenylaluminum hydride, di-p-tolylaluminum hydride, dibenzylaluminum hydride, phenyl-n-propylaluminum hydride, p-tolylethylaluminum hydride, p-tolyl-n-propylaluminum hydride, p-tolyl-iso-propylaluminum hydride, benzylethylaluminum hydride, benzyl-n-propylaluminum hydride, benzyl-iso-propylaluminum hydride, diethylaluminum ethoxide, di-iso-butylaluminum ethoxide, dipropylaluminum ethoxide, trimethylaluminum, triethylaluminum (TEA), tri-n-propylaluminum, tri-iso-butylaluminum (TIBA), tri-n-butylaluminum, tripentylaluminum, trihexylaluminum, triciclohexylaluminum, trioctylalurninurn, trip henylaluminum, tri-p-tolylaluminum, tribenzylalurninurn, ethyldiphenylaluminum, ethyl-di-p- tolylaluminum, ethyldibenzylaluminum, diethylphenylaluminum, diethyl-p-tolylaluminum or diethylbenzylaluminum, or mixtures thereof. 4. Process for preparing conjugated diene (co)polymers comprising polybutadiene according to claim 1 , wherein said aluminoxanes having general formula (IV), (b 2 ) are selected from: methylaluminoxane (MAO), ethylaluminoxane, n-butylaluminoxane , tetra-iso-butylaluminoxane (TTMPAO), Cert-butylaluminoxane, tetra-(2,4,4-trimethylpentyl)aluminooxane (TIOAO), tetra-(2,3-dimethylbutyl)aluminoxane (TDMBAO) or tetra-(2,3,3-trimethylbutyl)aluminoxane (TTMBAO), or mixtures thereof. 5. Process for preparing conjugated diene (co)polymers comprising polybutadiene according to claim 1 , wherein said partially hydrolyzed organo-aluminum-derivatives (b 3 ) are selected from aluminum compounds having general formula (III) added with at least one protonating compound, the aluminum compound having general formula (III) and the protonating compound being used in a molar ratio ranging from 0.001:1 to 0.2:1; said protonating compound is selected from: water; alcohols; alcohols with higher molecular weight; carboxylic acids; or mixtures thereof. 6. Process for preparing conjugated diene (co)polymers comprising polybutadiene according to claim 1 , wherein said haloaluminum alkyls having general formula (V) or (VI) are selected from: diethylchloroaluminum (AlEt 2 Cl), dimethylaluminumchloride (AlMe 2 Cl), ethylaluminumdichloride (AlEtCl 2 ), di-iso-butylaluminumchloride [Al(i-Bu) 2 Cl), ethylaluminumsesquichloride (Al 2 Et 3 Cl 3 ) or methylaluminumsesquichloride (Al 2 Me 3 Cl 3 ). 7. Process for preparing conjugated diene (co)polymers comprising polybutadiene according to claim 1 wherein said conjugated diener are selected from at least one of: 1,3-butadiene, 2-methyl-1,3-butadiene (isoprene), or 2,3-dimethyl-1,3-butadiene. 8. Process for preparing conjugated diene (co)polymers including polybutadiene according to claim 1 wherein: said (co)polymerization is carried out in the presence of at least one inert organic solvent selected from: saturated aliphatic hydrocarbons selected from butane, pentane, hexane or heptane, or mixtures thereof; saturated cycloaliphatic hydrocarbons selected from cyclopentane or cyclohexane, or mixtures thereof; mono-olefins selected from 1-butene or 2-butene, or mixtures thereof; aromatic hydrocarbons selected from benzene, toluene or xylene, or mixtures thereof; halogenated hydrocarbons selected from methylene chloride, chloroform, carbon tetrachloride, trichloroethylene, perchloroethylene, 1,2-dichloroethane, chlorobenzene, bromobenzene or chlorotoluene, or mixtures thereof; or selected from said at least one conjugated diene to be (co)polymerized; and/or the concentration of said at least one conjugated diene to be (co)polymerized in said at least one inert organic solvent ranges from 5% by weight to 50% by weight with respect to the total weight of the mixture of said at least one conjugated diene to be (co)polymerized and said at least one inert organic solvent; and / or said process is carried out at a temperature ranging from −70° C. to +100° C. 9. The process for preparing conjugated diene (co)polymers comprising polybutadiene of claim 1 wherein R 5 is substituted with at least one linear or branched C 2 -C 12 alkyl group or linear or branched C 2 -C 12 alkoxyl group at one or
Isoprene · CPC title
Butadiene · CPC title
NN · CPC title
Isoprene · CPC title
Compositions of homopolymers or copolymers of conjugated diene hydrocarbons · CPC title
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