Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
  • C08L9/06—Copolymers with styrene
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B60—VEHICLES IN GENERAL
  • B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
  • B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
  • B60C1/0016—Compositions of the tread
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
  • C07F7/02—Silicon compounds
  • C07F7/08—Compounds having one or more C—Si linkages
  • C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N 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
  • C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
  • C08F212/02—Monomers containing only one unsaturated aliphatic radical
  • C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
  • C08F212/06—Hydrocarbons
  • C08F212/08—Styrene
• • 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
  • C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
  • C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
  • C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
• • 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
  • C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
  • C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
  • C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
  • C08F236/06—Butadiene
• • 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
  • C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
  • C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
  • C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
  • C08F236/14—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen
• • 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
  • C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
  • C08F297/02—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
  • C08F297/04—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type polymerising vinyl aromatic monomers and conjugated dienes
  • C08F297/044—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type polymerising vinyl aromatic monomers and conjugated dienes using a coupling agent
• • 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
  • C08F4/00—Polymerisation catalysts
  • C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
  • C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
  • C08F4/54—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with other compounds thereof
  • C08F4/545—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with other compounds thereof rare earths being present, e.g. triethylaluminium + neodymium octanoate
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/02—Elements
  • C08K3/04—Carbon
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/34—Silicon-containing compounds
  • C08K3/36—Silica
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L19/00—Compositions of rubbers not provided for in groups C08L7/00 - C08L17/00
  • C08L19/006—Rubber characterised by functional groups, e.g. telechelic diene polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L21/00—Compositions of unspecified rubbers
• • 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
  • C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
  • C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
  • C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
  • C08F236/10—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl-aromatic monomers

Definitions

• the present invention relates to aminosilyl-functionalized conjugated dienes, their preparation and their use in the production of rubbers. Further, the invention relates to rubbers and rubber compositions, and tires produced therefrom.
• conjugated diene monomers A variety of conjugated diene monomers is known that can be used in the production of synthetic rubbers. However, there is a need in the art for further conjugated diene monomers that can be used in advantageous polymerization processes, or that confer advantageous properties to the rubbers produced from such conjugated diene monomers.
• EP 3 159 346 A1 teaches aminosilane-functionalized diene compounds that are useful as modifying monomers in the polymerization of conjugated diene monomers, optionally together with aromatic vinyl monomers, thus producing polymers, specifically elastomeric polymers, which can be used in rubber articles such as tires.
• WO2016/162473 A1 and WO2016/162528 A1 disclose aminosilyl-functionalized styrenes and methods for their preparation, as well as the use of the styrene derivatives in the preparation of copolymers thereof.
• EP 3 064 546 A1 teaches the use of vinylsilanes in the production of rubbers.
• EP 2 857 446 A1 teaches a conjugated diene polymer derived from conjugated diene, a monomer unit V 1 -S 1 , and a monomer unit V 2 -A 2 , where V 1 and V 2 each represent a hydrocarbyl group containing a polymerizable carbon-carbon double bond, S 1 represents a substituted silyl group, and A 2 is an amino group or a nitrogen-containing heterocycle group.
• conjugated diene monomers for the production of synthetic rubbers.
• conjugated diene monomers should be based on easily accessible starting materials, and should be accessible via simple synthetic routes.
• the conjugated diene monomers should be universally applicable, i.e. in a variety of different polymerization processes, and should confer advantageous properties to the rubbers, rubber compositions, and tires produced therefrom.
• the functionalized conjugated dienes of the invention are selected from the group of compounds of formulae (Ilia), (lllb), (lllc)
• R is an organylene group optionally containing one or more heteroatoms selected from an oxygen atom, a sulfur atom, a nitrogen atom, and a silicon atom, and the starting conjugated diene selected from the group of compounds of formula (la), (lb), (lc)
• R 1 is selected from i) a single bond, ii) one or more of an oxygen atom, a sulfur atom, a group NR 6 , and a group SiR 7 R 8 ; and iii) an organylene group optionally containing one or more selected from an oxygen atom, a sulfur atom, a group NR 6 , and a group SiR 7 R 8 ;
• R 2 , R 3 , R 6 , R 7 , R 8 can be the same or different and represent an organyl group optionally containing one or more heteroatoms selected from an oxygen atom, a sulfur atom, a nitrogen atom, and a silicon atom; and i) R 4 and R 5 can be the same or different and each R 4 and R 5 independently represents an organyl group optionally containing one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom; or ii) R 4 and R 5 are bonded to each other to form a heterocyclic ring containing the nitrogen atom and at least one carbon atom and, optionally, one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom.
• the functionalized conjugated dienes of the invention when used e.g. in the production of solution styrene butadiene rubber (S-SBR) and Ziegler-Natta catalyzed (e.g. neodymium) butadiene rubber (Nd-BR), increase the interaction of the polymer with fillers and thus filler dispersion in the polymer matrix, helping to improve the dynamic and mechanical properties of tire tread compounds.
• S-SBR solution styrene butadiene rubber
• Nd-BR Ziegler-Natta catalyzed (e.g. neodymium) butadiene rubber
• the present invention relates to methods for the preparation of a functionalized conjugated diene.
• the invention relates to the functionalized conjugated diene.
• the invention relates to the use of the functionalized conjugated dienes in the production of an elastomeric copolymer.
• the invention relates to a process for the production of copolymer component comprising coupled copolymer and terminally modified copolymer.
• the invention relates to a process for producing an elastomeric copolymer comprising anionic polymerization conditions.
• the invention relates to a process for producing an elastomeric copolymer comprising Ziegler-Natta polymerization conditions.
• the invention relates to an elastomeric copolymer.
• the invention relates to a method for producing a rubber.
• the invention relates to a rubber.
• the invention relates to a rubber composition.
• the invention relates to a tire component.
• the invention relates to a tire.
• the invention relates to a method for the preparation of a functionalized conjugated diene selected from the group of compounds of formula (Ilia), (I I lb), (I I Sc)
• R is an organylene group optionally containing one or more heteroatoms selected from an oxygen atom, a sulfur atom, a nitrogen atom, and a silicon atom, and the starting conjugated diene selected from the group of compounds of formula (la), (lb), (lc)
• R 1 is selected from i) a single bond, ii) one or more of an oxygen atom, a sulfur atom, a group NR 6 , and a group SiR 7 R 8 ; and iii) an organylene group optionally containing one or more selected from an oxygen atom, a sulfur atom, a group NR 6 , and a group SiR 7 R 8 ;
• R 2 , R 3 , R 6 , R 7 , R 8 can be the same or different and represent an organyl group optionally containing one or more heteroatoms selected from an oxygen atom, a sulfur atom, a nitrogen atom, and a silicon atom; and i) R 4 and R 5 can be the same or different and each R 4 and R 5 independently represents an organyl group optionally containing one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom; or ii) R 4 and R 5 are bonded to each other to form
• the invention in a second embodiment, relates to a method for the preparation of a functionalized conjugated diene selected from the group of compounds of formula (Ilia), (Nib), (lllc), the method comprising A) reacting, under Grignard conditions, a conjugated diene halide selected from the group of compounds of formula (lla), (lib), (lie) with a compound of formula (V)
• Y 2 and Y 3 are independently selected from fluorine, chlorine, bromine, and iodine atoms, and preferably Y 2 and Y 3 are each chlorine atoms, to result in a compound of formula (Via), (Vlb), (Vic)
• M wherein M is an alkali metal selected from lithium, sodium and potassium, and M is preferably sodium.
• the preparation of the conjugated diene halide intermediate of formula (lla), (lib), (lie) wherein Y 1 is a chlorine atom may be performed using a chlorinating agent comprising trichloroisocyanuric acid, dichloroisocyanuric acid, an alkali metal salt of dichloroisocy- anuric acid, or a mixture thereof. Further details regarding the synthesis of this conjugated diene chloride intermediate are given in PCT/EP2018/070768.
• the functionalized conjugated diene of the second aspect of the invention is selected from the group of compounds of formula (Ilia), (lllb), (lllc) wherein
• R is an organylene group optionally containing one or more heteroatoms selected from an oxygen atom, a sulfur atom, a nitrogen atom, and a silicon atom, and the starting conjugated diene selected from the group of compounds of formula (la), (lb), (lc)
• R 1 is selected from i) a single bond, ii) one or more of an oxygen atom, a sulfur atom, a group NR 6 , and a group SiR 7 R 8 ; and iii) an organylene group optionally containing one or more selected from an oxygen atom, a sulfur atom, a group NR 6 , and a group SiR 7 R 8 ;
• R 2 , R 3 , R 6 , R 7 , R 8 can be the same or different and represent an organyl group optionally containing one or more heteroatoms selected from an oxygen atom, a sulfur atom, a nitrogen atom, and a silicon atom; and i) R 4 and R 5 can be the same or different and each R 4 and R 5 independently represents an organyl group optionally containing one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom; or ii) R 4 and R 5 are bonded to each other to form a heterocyclic ring containing the nitrogen atom and at least one carbon atom and, optionally, one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom.
• an organyl group is any organic substituent group, regardless of functional type, having one free valence at a carbon atom.
• an organyl group contains from 1 to 10 carbon atoms, and optionally one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom, or an aryl, heteroaryl or aralkyl group containing from 6 to 10 carbon atoms, and optionally one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom.
• an organylene group is any organic substituent group, regardless of functional type, having two free valences at one carbon atom, or one free valence at each of two carbon atoms.
• R 1 of the functionalized conjugated diene of the present invention is i) a single bond.
• R 2 , R 3 , R 6 , R 7 , R 8 may be the same or different and represent an organyl group containing from 1 to 10 carbon atoms, and optionally one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom, or an aryl, heteroaryl or aralkyl group containing from 6 to 10 carbon atoms, and optionally one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom.
• R 2 , R 3 , R 6 , R 7 , and R 8 are the same or different and represent a linear or branched, saturated or unsaturated hydrocarbyl group (preferably containing from 1 to 10 carbon atoms). Further preferably, R 2 , R 3 , R 6 , R 7 , and R 8 are the same or different and represent a linear or branched alkyl, aryl, or alkaryl group; more preferably, R 2 , R 3 , R 6 , R 7 , and R 8 are the same or different and represent Chh or CeHs, in particular R 2 , R 3 , R 6 , R 7 , and R 8 all represent Chta.
• R 4 and R 5 are each a group that at least has a carbon atom bound to the nitrogen atom, i.e. groups R 4 and R 5 are not bound to the nitrogen atom via any heteroatom that may optionally be present in R 4 or R 5 .
• R 4 and R 5 can be the same or different and each R 4 and R 5 independently represents a linear, branched or cyclic hydrocarbyl group containing from 1 to 10 carbon atoms, the hydrocarbyl group optionally containing at least one heteroatom selected from a silicon atom, an oxygen atom, and a nitrogen atom; the hydrocarbyl group is saturated or unsaturated.
• R 4 and R 5 are the same or different and each R 4 and R 5 independently represents a linear, branched or cyclic, saturated or unsaturated alkyl group containing from 1 to 10 carbon atoms, the alkyl group optionally containing one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom; or ii) R 4 and R 5 are the same or different and each R 4 and R 5 independently represents an aryl or aralkyl group containing from 6 to 10 carbon atoms, the alkyl group optionally one or more heteroatoms selected from a silicon atom, an oxygen atom, a sulfur atom, and a nitrogen atom.
• R 4 and R 5 are the same and represent a linear, branched or cyclic, saturated or unsaturated alkyl group. More preferably, R 4 and R 5 are the same and represent -CH(CH 3 )2 or Chta. Most preferably, R 4 and R 5 are the same and represent -CH(CH3)2.
• the conjugated diene selected from the group of compounds of formula (la), (lb), (lc)
• R is a linear or branched, saturated or unsaturated hydrocarbylene, hydrocarbylidene, or hydrocarbylidyne group; more preferably, R is a branched, unsaturated hydrocarbylene group; most preferably, the conjugated diene of formula (I la), (lib), (lie) is selected from terpenes and 4,8-dimethyl-1 ,3,7-nonatriene. Even more preferably, the terpene is selected from myreene and ocimene, most preferably the terpene is myreene selected from omyreene and b-myrcene.
• the functionalized conjugated diene according to the invention is in all aspects most preferably a myreene derivative of formula (VIII), (IX), or (X)
• the myrcene derivative is of formula (Villa), (IXa), or (Xa)
• the present invention relates to the use of one or more functionalized conjugated dienes of the second aspect in the production of an elastomeric copolymer.
• the elastomeric copolymer preferably comprises, in addition to one or more units derived from the one or more functionalized conjugated dienes selected from the group of compounds of formula (Ilia), (lllb), (lllc), units derived from one or more conjugated diene monomers.
• the conjugated diene monomer as used in the production of the elastomeric copolymer according to the third aspect of the invention is preferably selected from 1 ,3-butadiene, isoprene, 1 ,3-pentadiene, 2,3-dimethyl-1 ,3-butadiene, 2-methyl-1 ,3-pentadiene, 2,3-dime- thyl-1 ,3-pentadiene, 2-phenyl-1 ,3-butadiene, and 4,5-diethyl-1 ,3-octadiene. More preferably, the conjugated diene monomer is selected from 1 ,3-butadiene and isoprene, in particular, the conjugated diene monomer is 1 ,3-butadiene.
• the use according to the third aspect is in the production of an elastomeric copolymer by 1 ) anionic polymerization or by 2) coordination polymerization.
• the elastomeric copolymer further comprises units derived from one or more vinyl aromatic monomers.
• the vinyl aromatic monomer is preferably selected from styrene, 1-vinylnaphthalene, 3-methyl styrene, 3,5-diethylstyrene, 4-propylstyrene, 2,4,6- trimethylstyrene, 4-dodecylstyrene, 3-methyl-5-n-hexylstyrene, 4-phenylstyrene, 2-ethyl-4- benzylstyrene, 3,5-diphenylstyrene, 2,3,4,5-tetraethylstyrene, 3-ethyl-1 -vinylnaphthalene, 6-isopropyl-1 -vinylnaphthalene, 6-cyclohexyl-1 -vinylnaphthalene, 7-dodecyl-2-vinylnaph-
• the amount of units derived from the one or more functionalized conjugated dienes selected from of the group of compounds of formula (Ilia), (lllb), (life) is preferably in a range of from 0.05 to 5 wt.%, based on the weight of the elastomeric copolymer, more preferably in a range of from 0.2 to 1.5 wt.%, most preferably in a range of from 0.4 to 1.2 wt.%, e.g. in a range of from 0.6 to 1.0 wt.%, such as about 0.8 wt.%.
• the use according to the third aspect may be of an alkali metal salt derivative of the functionalized conjugated diene selected from the group of compounds of formula (Ilia), (lllb), (lllc), as initiator for the anionic copolymerization of one or more conjugated diene monomers, optionally one or more vinyl aromatic monomers, and optionally one or more functionalized conjugated dienes selected from the group of compounds of formula (Ilia), (lllb), (lllc).
• the invention relates to a process for the production of a copolymer component comprising coupled copolymer and terminally modified copolymer, the process comprising the following steps: (1 ) providing an initiator component, wherein the initiator component preferably comprises one or more alkali metal salt derivatives of a one or more functionalized conjugated dienes selected from the group of compounds of formula (Ilia), (lllb), (lllc),
• step (6) optionally terminally modifying a part of the copolymer of step (3) or the functionalized copolymer of step (4) with one or more terminal modifying agents, to result in terminally modified copolymer.
• the invention relates to a process for producing an elastomeric copolymer comprising subjecting i) one or more functionalized conjugated dienes selected from the group of compounds of formula (Ilia), (lllb), (lllc), ii) one or more conjugated diene monomers, and iii) optionally one or more vinyl aromatic monomers to anionic polymerization conditions.
• the anionic polymerization conditions include initiating the polymerization with an alkali metal salt derivative of the one or more functionalized conjugated dienes of formula (Ilia), (lllb), (lllc), wherein the alkali metal is selected from lithium, sodium, and potassium.
• copolymers having a linear structure or a star structure may be obtained.
• branching may be performed with e.g. divinylbenzene.
• the branching level is difficult to predict since it is difficult to fractionate the specific polymer fractions.
• M w /M n dispersity index
• the invention relates to a process for producing an elastomeric copolymer comprising subjecting i) one or more functionalized conjugated dienes selected from the group of compounds of formula (Ilia), (lllb), (II lc) and ii) one or more conjugated diene monomers to Ziegler-Natta polymerization conditions.
• a Ziegler- Natta catalyst is used in the coordination polymerization of conjugated diene (such as 1 ,3-butadiene).
• Typical catalyst compositions are binary, ternary, or quaternary systems.
• Binary systems comprise catalytic metal chloride (e.g. chloride of Ni, Co, Ti, Nd, V, Ti, Zr, or Fe) and co-catalyst (e.g. aluminum alkyl or a magnesium alkyl compound).
• a halide-free metal precursor such as neodymium phosphate
• co-catalyst such as aluminium or magnesium alkyl
• a halide donor such as aluminium or magnesium alkyl
• Adding halide donors to halide-free catalyst systems significantly increases catalyst activities and c/ ' s- 1 ,4 or trans- 1 ,4 contents.
• a solubilizing agent for either the metal-salt or for the halide donor is used, in addition to the components as used in ternary systems.
• the Ziegler-Natta polymerization conditions consequently preferably include a catalyst system comprising 1 ) metal chloride and 2) co-catalyst. More preferably, the metal chloride 1 ) is selected from chlorides of one or more of Ni, Co, Ti, Nd, V, Ti, Zr, and Fe, and the cocatalyst 2) is selected from one or more of aluminium and magnesium alkyl compounds. Also, the Ziegler-Natta polymerization conditions may include the presence of further monomers.
• the Ziegler-Natta polymerization conditions include a catalyst system comprising 1 ) non-halide metal compound, 2) co-catalyst, and 3) halide donor compound.
• the non-halide metal compound 1 ) is preferably one or more Nd compounds; more preferably the Nd compound is selected from neodymium carboxylates, neodymium alcoholates, neodymium phosphates, neodymium phosphonates, neodymium ally! compounds, neodymium cyclopentadienyl complexes, neodymium amides, and neodymium acetylacetonates.
• neodymium carboxylates e.g. neodymium(lll) versatate (NdV), neodymium(lll) octanoate (NdO), neodymium(lll) iso- octanoate (NdiO), neodymium(lll) naphthenate (NdN); 2) neodymium alcoholates (e.g.
• monocyclopentadienyl neodymium dichloride CpNdCh
• monocyclopentadienyl dialkyl neodymium CpNdR ⁇
• monocyclopentadienyl diallyl neodymium CpNd(/]3-C3H5) 2
• salts of monoclopentadienyl tris allyl neodymium e.g Li[CpNd(rj3-C3H5)3]
• dicyclopentadienyl neodymium monochloride Cp2NdCI
• dicyclopentadienyl monoalkyl neodymium Cp2NdR
• silylene-bridged dicyclopentadienyl neodymium derivatives e.g.
• neodymium amides e.g. Nd(N(SiMe3) 2 )3); or 7) neodymium acetylacetonates are used, in combination with one or more co-catalyst such as: AIMb3 (TMA), AIEt3 (TEA), AI/BU3 (TIBA), AIOct3, methyl alumox- ane (MAO), tetra isobutyl dialumoxane (TIBAO), B(CeFs)3, modified methyl alumoxane (MMAO), hexaisobutylalumoxane (HIBAO), diisobutylaluminum hydride (DIBAH), MgR ⁇ , AIPr3, AIBU3, AIHex3, AlOcte, AIDodec3, AIEts, or AIMb3.
• TMA methyl alumox- ane
• MAO methyl alumox- an
• halide donors are SiCU, ethylaluminium sesquichloride (EASC), diethylalu- minium chloride (DEAC), dimethylaluminium chloride, butyl chloride (BuCI), dibutylalumin- ium chloride, AIBr3, EtAIC , and MesSiCI.
• the copolymer as produced in accordance with the sixth aspect i.e. by coordination polymerization, preferably has linear structure or branched structure.
• the polymer structure is dictated by catalyst composition and is typically as follows (M w /M n ):
• the invention relates to an elastomeric copolymer comprising repeat units that are derived from
• the amount of B) conjugated diene monomer in the elastomeric copolymer of the seventh aspect is preferably 50 to 92 wt.%, by weight of the copolymer, more preferably 60 to 90 wt.%, by weight of the copolymer, in particular 65 to 80 wt.%, by weight of the copolymer.
• the vinyl aromatic monomer when present, is preferably selected from styrene, 1-vi- nylnaphthalene, 3-methylstyrene, 3,5-diethylstyrene, 4-propylstyrene, 2,4,6-trimethylstyrene, 4-dodecylstyrene, 3-methyl-5-n-hexylstyrene, 4-phenylstyrene, 2-ethyl-4-benzylsty- rene, 3,5-diphenylstyrene, 2,3,4,5-tetraethylstyrene, 3-ethyl-1 -vinylnaphthalene, 6-isopro- pyl-1-vinylnaphthalene, 6-cyclohexyl-1 -vinylnaphthalene, 7-dodecyl-2-vinylnaphthalene, and omethylstyrene. More preferably, the vinyl aromatic mono
• the amount of C) vinyl aromatic monomer in the elastomeric copolymer according to the seventh aspect of the present invention is preferably 8 to 45 wt.%, by weight of the copolymer, more preferably 10 to 40 wt.%, by weight of the copolymer, in particular 20 to 35 wt.%, by weight of the copolymer.
• the elastomeric copolymer comprises less than 1 wt.% C) vinyl aromatic monomer (and preferably no C) vinyl aromatic monomer), and the amount of B) conjugated diene monomer is 95 to 99.95 wt.%, by weight of the copolymer, preferably 98 to 99.6 wt.%, by weight of the copolymer, in particular 99.0 to 99.4 wt.%, by weight of the copolymer.
• the conjugated diene monomer in the elastomeric copolymer according to the seventh aspect is preferably selected from 1 ,3-butadiene, isoprene, 1 ,3-pentadiene, 2,3-dimethyl-
• the conjugated diene monomer is selected from 1 ,3-butadiene and isoprene.
• the conjugated diene monomer is in particular
• the elastomeric copolymer according to the invention may comprise units having a linear structure.
• the copolymer may comprise units having a branched structure.
• the elastomeric copolymer may comprise units having a star structure and being produced by the reaction of metal-terminated living linear copolymer with one or more coupling agents in anionic polymerization conditions.
• the coupling agent may be
• a tin halide coupling agent preferably the tin halide coupling agent is tin tetrachloride
• a silicon halide coupling agent preferably the silicon halide coupling agent is selected from silicon tetrachloride, silicon tetrabromide, silicon tetrafluoride, silicon tetraiodide, hexachlorodisilane, hexabromodisilane, hexafluorodisilane, hexaiodo- disilane, octachlorotrisilane, octabromotrisilane, octafluorotrisilane, octaiodo- trisilane, hexachlorodisiloxane, 2,2,4,4,6,6-hexachloro-2,4,6-trisilaheptane- 1 ,2,3,4,5,6-hexakis[2-(methyldichlorosilyl)ethyl]benzene, and alkyl silicon halides of general formula (XI)
• the fraction of units having star structure is preferably between 0 and 75 %, by weight of the copolymer.
• the invention relates to a method for producing a rubber comprising vulcanizing the elastomeric copolymer according to the seventh aspect in the presence of one or more vulcanizing agents.
• the invention relates to a rubber as obtainable according to the method of the eighth aspect.
• the invention relates to a rubber composition
• a rubber composition comprising x) a rubber component comprising the rubber according to the ninth aspect.
• the rubber composition further comprises y) one or more fillers.
• the filler is preferably selected from the group consisting of silica and carbon black.
• the rubber composition comprises y) both silica and carbon black.
• the amount of filler component y) in the rubber composition is 10 to 150 parts by mass relative to 100 parts by mass of the rubber component x) (phr).
• the amount of filler component y) is 20 to 140 phr. More preferably, the amount of filler component y) is 30 to 130 phr.
• the rubber component x) in the rubber composition according to the tenth aspect additionally comprises one or more further rubbery polymers.
• the further rubbery polymer is selected from the group consisting of natural rubber, synthetic isoprene rubber, butadiene rubber, styrene-butadiene rubber, ethylene-a-olefin copolymer rubber, ethylene-a-olefin-diene copolymer rubber, acrylonitrile-butadiene copolymer rubber, chloroprene rubber and halogenated butyl rubber.
• the tire component according to the eleventh aspect of the invention comprises the rubber composition according to the tenth aspect.
• the tire component is a tire tread.
• the tire according to the twelfth aspect of the invention comprises the tire component of the eleventh aspect.
• DIBAH diisobutylalumin- ium hydride
• the reactor temperature was maintained in the range of 40°C for one hour, followed by cooling to room temperature.
• To neutralize a small excess of Grignard reagent 0.6 mL of water were added.
• the solvent was evaporated from the post-reaction mixture under reduced pressure and 1 .0 L of n-hexane were added to the reaction residue.
• the obtained suspension was filtered off and the precipitate was washed with three portions of n-hexane of 200 mL each. Then, the solvent was evaporated from the obtained filtrate under reduced pressure at 40°C until a constant pressure was achieved. 146.30 g of product were obtained, with a yield of 91 %.
• Cyclohexane (1.2 kg) was added to a nitrogen-purged two-liter reactor and treated with 1 gram of 1.6 M n-butyllithium solution in cyclohexane. The solution was heated to 70 C and vigorously stirred for 10 minutes, to perform cleaning and inertization of the reactor. After that, solvent was removed via a drain valve and nitrogen was purged again.
• Cyclohexane (820 g) was added to the inerted two-liter reactor, followed by addition of styrene (31 g) and of 1 ,3-butadiene (1 17 g). Inhibitor from styrene and 1 ,3 butadiene was removed. Next, tetramethylethylenediamine (TMEDA, 2.21 mmol) was added, to provide random incorporation of styrene monomer and to increase the vinyl content, from the butadiene-derived units. The solution inside the reactor was heated to 60°C and continuously stirred during the whole process. When the desired temperature was reached, n-butyllith- ium (0.045 mmol) was added, to perform quenching of residual impurities.
• TEDA tetramethylethylenediamine
• n-butyl- lithium (0.845 mmol) was added to initiate the polymerization process.
• the reaction was carried out as a isothermic process for 60 minutes.
• silicon tetrachloride (5.25 x 10 ⁇ 2 mmol) was added to the polymer solution as a coupling agent. Coupling was performed for 5 minutes.
• the reaction solution was terminated, using nitrogen-purged isopropyl alcohol (1 mmol), and rapidly stabilized by addition of 2-methyl-4,6-bis(octylsulfanylme- thyl)phenol (at 1.0 phr polymer).
• the polymer solution was treated with isopropanol, and precipitation of polymer occurred.
• the final product was dried overnight in a vacuum oven.
• Example 2b (myrcene derivative from example as comonomer)
• Cyclohexane (820 g) was added to the inerted two-liter reactor, followed by addition of styrene (31 g), functionalized myrcene of Example 1a (0.59 g) and 1 ,3-butadiene (1 17 g). Inhibitor from styrene and 1 ,3-butadiene was removed. Next, 2,2-Bis(2-tetrahydrofuryl)pro- pane (DTHFP, 2.52 mmol) was added, to provide random incorporation of styrene monomer and to increase the vinyl content, from the butadiene-derived units. The solution inside the reactor was heated to 60°C and continuously stirred during the whole process.
• DTHFP 2,2-Bis(2-tetrahydrofuryl)pro- pane
• n-butyllithium (0.045 mmol) was added, to perform quenching of residual impurities. Then, n-butyllithium (0.845 mmol) was added to initiate the polymerization process. The reaction was carried out as a isothermic process for 60 minutes. After this time, silicon tetrachloride (6.30 * 10 ⁇ 2 mmol) was added to the polymer solution as a coupling agent. Coupling was performed for 5 minutes. The reaction solution was terminated, using nitrogen-purged isopropyl alcohol (1 mmol), and rapidly stabilized by addition of 2-methyl-4,6-bis(octylsulfanylmethyl)phenol (at 1.0 phr polymer). The polymer solution was treated with isopropanol, and precipitation of polymer occurred. The final product was dried overnight in a vacuum oven.
• Example 3b (myrcene derivative from example 1a as both initiator component and as comonomer)
• Cyclohexane (820 g) was added to the inerted two-liter reactor, followed by addition of styrene (31 g), functionalized myrcene of Example 1a (0.59 g) and 1 ,3-butadiene (1 17 g). Inhibitor from styrene and 1 ,3-butadiene was removed. Next, 2,2-Bis(2-tetrahydrofuryl)pro- pane (DTHFP, 3.69 mmol) was added as a styrene randomizer and to increase the vinyl content, from the butadiene-derived units. The solution inside the reactor was heated to 60°C and continuously stirred during the whole process.
• DTHFP 2,2-Bis(2-tetrahydrofuryl)pro- pane
• n-butyllithium (0.045 mmol) was added to the reactor, to perform quenching of residual impurities.
• n-Butyllithium (1.23 mmol) and functionalized myrcene of Example 1a (0.38 g) were mixed together in a burette, the contact time was about 15 min, and then the mixture was added to initiate the polymerization process. The reaction was carried out over 60 minutes, as an isothermic process. After this time, silicon tetrachloride (6.30 * 10 ⁇ 2 mmol) was added to the polymer solution as a coupling agent. Coupling was performed for 5 minutes.
• the reaction solution was terminated, using nitrogen-purged isopropyl alcohol (1 mmol), and rapidly stabilized by addition of 2-methyl-4,6-bis(octylsulfanylmethyl)phenol (at 1 .0 phr polymer).
• the polymer solution was treated with isopropanol, and precipitation of polymer occurred.
• the final product was dried overnight in a vacuum oven.
• a butadiene-styrene copolymer was prepared in a cascade of three continuous reactors having a volume of 10 L (reactor 1 ), 20 L (reactor 2) and 10 L (reactor 3), respectively, where each reactor was equipped with a paddle stirrer.
• the agitation speed was 150-200 rpm and filling factor at the level of 50 %-60 %.
• Hexane, styrene, 1 ,3-butadiene, 1 ,2-buta- diene (gel formation prevention additive), DTHFP and functionalized myrcene of Example 1a (the last three reactants as solutions in hexane) were dosed into the first reactor, with flow rates of 10752.00 g/h, 398.00 g/h, 1499.00 g/h, 19.00 g/h, 102.00 g/h and 46,03 g/h, respectively.
• n-Butyllithium flow rate (as a solution in hexane) was 107.00 g/h, and functionalized myrcene of Example 1a (as a solution in hexane) flow rate was 153,92 g/h.
• Streams of n-butyllithium and 50/50 by weight of functionalized myrcene of Example 1a were mixed together in the pipe static mixer, before entering the reactor, and the contact time was about 15 min.
• the temperature in the reactors was between 70°C to 85°C.
• To obtain branched rubber silicon tetrachloride was added at the reactor 3 inlet, at the entry of static mixer, in a SiCU/active n-butyllithium ratio of 0.05.
• the polymer solution was subsequently transferred to a stripper.
• Distilled water, in an amount of double of the total mass of polymer solution, as well as pH regulator and soap were added to the polymer solution, and the stripper contents were then treated with steam. Steam-stripping was carried out until the entire amount of solvent had been removed, and rubber crumbs were obtained. Then, the rubber crumbs were removed from the stripper, cooled to room temperature, milled and dried in a stream of hot air.
• a vulcanized rubber compound was prepared using a polymer obtained in each of Examples, and was measured for the following test parameters. i) Tire predictors (tan d at 60°C, tan d at 0°C, tan d at -10°C)
• DMA 450+ MetraviB dynamic mechanical analyzer
• frequency 10 Hz
• Table 1 shows the characterization results for the four samples synthesized for this study.
• the second stage was to further improve the distribution of the silica along with adding of carbon black, then the compound was allowed to sit for 24 hours. In order to be conditioned for the final pass, the rubber compound was allowed to condition for four hours. The final mixing was performed on a two roll mill. The last step was used to add the cure packages. Then, each compound was vulcanized at 170°C, for T95+1.5 minutes (based on RPA results), to obtain vulcanizates. Each vulcanized rubber compound was evaluated and measured for the above-mentioned curing characteristics, tire predictors and rebound resilience. The results are shown in Table 3.
• SSBR 3b according to the invention imparts to the corresponding rubber composition 3c reinforcement properties which are superior to those obtained with the control SSBR 1 b and with the other SSBR 2b according to the invention.
• the data in Table 3 shows that SSBR 4b obtained in continuous polymerization has better reinforcement properties compared to control SSBR 1 b and SSBR 2b.
• tire predictors of rubber composition 3c according to the invention are improved relative to those of the control rubber composition 1 c and of the rubber compositions 2c and 4c (in terms of rolling resistance) according to the invention. Moreover, said tire predictors are improved for rubber composition 2c according to the invention relative to the control rubber composition 1 c. Furthermore, tire predictors are improved for rubber composition 4c according to the invention relative to the control rubber composition 1 c; additionally, ice traction and dry traction properties are improved relative to those of rubber compositions 1 c, 2c, and 3c.
• a twenty litre reactor was filled with dry 1 ,3-butadiene and dry solvent (cyclohexane), and functionalized myrcene of Example 1a, and heated to 60°C.
• catalyst was added in the following sequence: neodymium bis(2-ethylhexyl)phosphate (NdP), diisobutylaluminum hydride (DIBAH) (both 0.1 mol/L solutions in cyclohexane).
• DIBAH diisobutylaluminum hydride
• Polymerization was started by addition of ethylaluminum sesquichloride (EASC) (1.0 mol/L solution in cyclohexane). The solution inside the reactor was heated and continuously stirred during the whole process.
• EASC ethylaluminum sesquichloride
• the temperature of the reaction mixture was kept between 60 and 90°C.
• the reaction solution was terminated, using nitrogen-purged isopropyl alcohol, and was rapidly stabilized by the addition of 2-methyl-4,6-bis(octylsulfanylmethyl)phenol (at 1.0 phr polymer).
• the polymers were recovered by a conventional recovery operation using steam stripping of the solvent and were dried in a stream of hot air.
• the microstructure of butadiene rubber was determined by infrared spectroscopy (Thermo Scientific Nicolet Is10). The following peaks were used for quantitative determination of the poly(butadiene) microstructure:
• a vulcanized rubber compound was produced using a polymer obtained in each of the examples, and was measured for the following test parameters i) Tire predictors (tan d at 60°C, tan d at 0°C, tan d at -10°C, J” at 30° C)
• DMA 450+ MetraviB dynamic mechanical analyzer
• the first stage was used to mix the rubbers with oil, silica, silane coupling agent, 6PPD and activators in several steps.
• the second stage was performed to further improve the distribution of the silica along with adding of carbon black, then the compound was conditioned for 24 hours..
• the final mixing was performed on a two roll mill.
• the last step was used to add the cure packages.
• each compound was vulcanized at 170°C, for T95 +i . s minutes (based on RPA results), to obtain vulcanizates.
• Each vulcanized rubber compound was evaluated and measured for the above-mentioned curing characteristics, Payne effect and tire predictors. The results are shown in Table 6.
• Example 5c was compared with Example 6c, and Example 7c with Example 8c, since they correspond to similar Mooney ranges, namely higher (58, 64) and lower (44, 51 ).
• tire predictors obtained from DMA such as rolling resistance, dry traction, winter traction are improved when comparing functionalized (Ex. 6c, 8c - Table 6) and nonfunctionalized (Ex. 5c, 7c - Table 6) rubber, the same is true with respect to rebound at high temperature.
• the reinforcement index the ratio of modulus 300 % to modulus 100 %, was also found to be increased, as well as much higher silica dispersion (dispeGRADER). This confirmed a much higher interaction between functionalized cis- polybutadiene rubber and filler (silica), as compared to the use of non-functionalized rubber.

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