Patent Application
20240376241
The present invention is directed to a diene-norbornene copolymer comprising 1,4 diene repeat units and norbornene repeat units, wherein at least 95% of the 1,4 diene repeat units in the copolymer are cis 1,4 diene repeat units. Furthermore, the invention is directed to methods of making such copolymers and rubber compositions comprising them. Articles of manufacture, such as tires, comprising the diene-norbornene copolymer, are also within the scope of the present invention.
Various copolymers of dienes (such as butadiene and isoprene) and norbornene are known in the art. In most cases, such copolymers are prepared by catalytic polymerization in solution. Norbornene contents are typically relatively high in the prior art such as about 50 to about 75 weight percent. Furthermore, the obtained molecular weights are typically relatively low such as below a number average molecular weight of about 50,000 g/mol. Moreover, such copolymers have typically a significant content of non-cis 1,4 repeat units which can be undesirable for compounding such polymers together with other diene-based elastomers, as for instance in rubber compositions for tires. While progress has been made in the development and availability of different diene-norbornene copolymers, still room for improvement remains.
One object of the present invention may be to provide a new diene-norbornene copolymer, preferably having different chemical and/or physical properties or structures than existing copolymers based on such monomers.
Another object of the present invention may be to provide a diene-norbornene copolymer having a high cis 1,4 diene content.
Yet another object of the present invention may be to provide a diene-norbornene copolymer having a relatively high glass transition temperature and/or which is compatible with other diene-based rubbers, in particular natural rubber and/or synthetic cis 1,4 polyisoprene.
Still another object of the present invention may be to provide a new, preferably efficient method and/or cost-effective method, to synthesize such copolymers.
Still another object of the present invention may be to provide a diene-norbornene copolymer with improved compatibility/miscibility with other diene-based rubbers, in particular polyisoprenes, e.g., high-cis-polyisoprenes, for example compared to styrene butadiene rubbers.
The present invention is defined by the appended independent claim(s). Further preferred embodiments are provided in the dependent claims and in the summary of the invention herein below.
Thus, in a first aspect, the present invention is directed to a diene-norbornene copolymer comprising 1,4 diene repeat units and norbornene repeat units, wherein at least 95% of all 1,4 diene repeat units in the copolymer are cis 1,4 diene repeat units.
Thus, the inventors provide a copolymer which has a new unique structure. Furthermore, the new polymer provides new properties including amongst others an improved miscibility in rubber compositions comprising other diene-based elastomers such as 1,4 polybutadiene or 1,4 polyisoprene. Moreover, due to the incorporation of a high monomeric friction coefficient monomer (i.e., norbornene) such copolymers can support an improved wet/wear balance in rubber compounds.
In one embodiment, the diene-norbornene copolymer has a number average molecular weight Mn of at least 80,000 g/mol, preferably of at least 100,000 g/mol, more preferably of at least 150,000 g/mol, or even more preferably of at least 200,000 g/mol.
In another embodiment, the diene-norbornene copolymer has a number average molecular weight Mn within a range of 80,000 g/mol (preferably 100,000 g/mol, more preferably of at least 150,000 g/mol, or of at least 200,000 g/mol) to 1,500,000 g/mol (preferably at most 1,000,000 g/mol or at most 900,000 g/mol, or even only at most 500.000 g/mol).
In still another embodiment, the diene-norbornene copolymer has a norbornene content of less than 30 percent by weight, preferably of less than 25 percent by weight, or even more preferably of less than 20 percent by weight. Such relatively low norbornene contents have not been suggested before in the described copolymers. Moreover, low norbornene contents help to obtain copolymers with different glass transition temperatures than available before, which can for instance be useful for providing new rubber compositions. Moreover, low norbornene contents can improve the compatibility with natural rubber or synthetic polyisoprene if the diene is isoprene, or with polybutadiene rubber, if the diene is butadiene.
In yet another embodiment, the diene-norbornene copolymer has a norbornene content within a range of 1 percent (preferably 2 percent, or 5 percent) to 45 percent (preferably 30 percent, 25 percent, or 20 percent), all by weight.
In still another embodiment, the diene-norbornene copolymer has a glass transition temperature within a range of 0° to −50° C., or −20° C. to −50° C., preferably within a range of −25° C. to −50° C., or within a range of −25° C. to −45° C., or even within a range of −25° C. to −40° C. Such relatively high glass transition temperatures can be of interest to allow new rubber compositions involving other diene-based elastomers, especially natural rubber or synthetic polyisoprene. In particular, these ranges are preferred for isoprene-norbornene copolymers.
In still another embodiment, the diene-norbornene copolymer has a glass transition temperature within a range of −40° to −90° C., preferably within a range of −51° C. to −85° C. Such glass transition temperatures can be of interest to allow new rubber compositions involving other diene-based elastomers, especially polybutadiene rubber. These ranges are particularly preferred for butadiene-norbornene copolymers.
In still another embodiment, the copolymer is a random diene-norbornene copolymer. In particular, the copolymer is preferably not a di-block copolymer or block copolymer.
In still another embodiment, the copolymer has only one glass transition temperature.
In yet another embodiment, the (random) diene-norbornene copolymer has at most 5 (preferably at most 3, or at most 2) directly neighboring norbornene repeat units.
In yet another embodiment, the 1,4 diene repeat units are one or more of 1,4 isoprene repeat units and 1,4 butadiene repeat units. Preferably the (or in other words all) 1,4 diene repeat units are only 1,4 isoprene repeat units.
In still another embodiment, the diene-norbornene copolymer is an isoprene-norbornene copolymer, wherein the 1,4 diene repeat units are 1,4 isoprene repeat units.
In still another embodiment, the copolymer further comprises 3,4 isoprene repeat units.
In yet another embodiment the copolymer comprises one or more of at least 2 (preferably 5) weight percent norbornene; at least 20 (preferably 30) weight percent 1,4 isoprene; at most 30 (preferably 20) weight percent norbornene; at most 93 (preferably 85) weight percent 1,4 isoprene; at most 30 (preferably at most 20) weight percent 3,4 isoprene; at most 1 (preferably 0.5, or even 0) weight percent 1,2 isoprene; at most 1 (preferably 0.5, or even 0) weight percent trans 1.4 isoprene; a molar ratio of 3,4 isoprene to 1,4 isoprene within a range of 1:1.5 to 1:10 (preferably of 1:2 to 1:9); a percentage of at least 96%, preferably 97%, or 98%, or 99.1%, or even at least 99.9% of all 1,4 diene repeat units (preferably 1,4 isoprene repeat units) in the copolymer being cis 1,4 repeat units; a ratio of weight average molecular weight and number average molecular weight within a range of 1.5 to 5 (preferably 1.9 to 5); and predominantly 1,4 isoprene by weight, based on the total weight of the diene-norbornene (or isoprene-norbornene) copolymer.
In a second aspect, the present invention is directed to a method of synthesizing a copolymer, the method comprising at least the steps of (A) Providing norbornene monomers and diene monomers (preferably selected from one or more of butadiene and isoprene); (B) Providing a catalyst comprising an organometallic compound according to one of formulas (Ia) and (Ib): LALBMX2 (Ia), (LA)2LBM2X (Ib), wherein M is a metal selected from Titanium, Zirconium and Hafnium; X is a ligand independently selected from one or more of a hydrocarbyl and a halogenide; and wherein LA is an independently substituted ligand according to formula (II): C6H4-m(OH)RmCH═NC6H4-nRn (II); LB is an independently substituted ligand according to formula (II) or formula (III): C6H4-m(OH)Rm—CH═NC6H4-nRn—Y—RnC6H4-nN═CH—C6H4-m(OH)Rm (III) wherein R is independently selected from hydrogen, a hydrocarbyl substituent, a substituted hydrocarbyl substituent, and a heteroatom substituent, Y is independently selected from alkylene, arylene, cycloalkylene, hydrocarbyl, a heteroatom and combined radicals thereof, n is selected from 0, 1, 2, 3, and 4, and wherein m is selected from 0, 1, 2, 3, and 4; (C) Activating the catalyst to obtain an activated catalyst; and (D) Polymerizing the monomers with said activated catalyst.
It is also possible herein to mention the catalyst, such as mentioned in step (B) as a “precatalyst” which becomes a “catalyst” or activated catalyst upon activation, e.g., by an activator.
In one embodiment, the catalyst has one of the structures (IIIa) and (IIIb),
wherein R1 and R2 are independently selected from hydrogen, alkyl, aryl, cycloalkyl, hydrocarbyl, ether, an amine group and combined radicals thereof; R3, R5, R6, R8 are independently selected from alkyl, aryl, cycloalkyl groups, and combined radicals thereof; and wherein R4, R7 are independently selected from hydrogen, alkyl, aryl, cycloalkyl, amine groups and combined radicals thereof (preferably with each of R1 to R8 containing at most 12 carbon atoms) and Y is independently selected from alkylene, arylene, cycloalkylene, hydrocarbyl, a heteroatom and combined radicals thereof.
It is noted that structures of molecules and/or complexes are shown two-dimensionally in the present description, but they may have deviating three-dimensional arrangements or shapes which cannot be fully depicted in the two-dimensional representations as depicted herein.
In another embodiment, the method comprises one or more steps of: Providing a co-catalyst selected from one or more of: triethyl aluminum (TEA), (preferably) triisobutyl aluminum (TIBA), methyl aluminoxane (MAO), and modified methyl aluminoxane (MMAO); Providing an activator selected from one or more of: Li[B(C6F5)4], Ph3C[B(C6F5)4], PhNMe2H[B(C6F5)4], Ag[B(C6F5)4], ammonium tetrakis (pentafluorophenyl) borates, B(C6F5)3, and AgSbF6; and Providing a solvent selected from one or more of (preferably) cyclohexane, (preferably) methyl cyclohexane, pentane, hexane, heptane, toluene (less preferable), and (individual) xylenes or mixtures thereof (less preferable). Dichlorobenzene, for instance, would not be desirable.
In still another embodiment, the method comprises one or more of the following steps: Mixing the catalyst, the co-catalyst and optionally the solvent, optionally at a temperature within a range of 1° C. to 50° C., preferably 10° C. to 40° C., to obtain a first mixture; Mixing the first mixture with an/the activator, and optionally the solvent, to obtain an/the activated catalyst, optionally at a temperature within a range of 1° C. to 50° C., preferably 10° C. to 40° C., so as to obtain a second mixture; and Mixing the second mixture with diene (e.g. isoprene and/or butadiene) monomers and norbornene monomers, optionally with the solvent, and optionally at a temperature within a range of 1° C. to 50° C., preferably 10° C. to 40° C.; Polymerizing the monomers at a temperature within a range of 20° C. to 125° C., preferably to 120° C., or to 70° C., preferably at a temperature from 30° C. to 60° C., or even more preferably at a temperature from 35° C. to 50° C.
In a third aspect, the present invention is directed to a method of synthesizing (or in other words manufacturing or making) a (synthetic) diene-norbornene copolymer, the method comprising one or more steps of: (A) Providing diene monomers (such as isoprene and/or butadiene) and norbornene monomers; (B) Providing a catalyst having the structure (IIIa) or (IIIb),
wherein R1 and R2 are independently selected from hydrogen, alkyl, aryl, cycloalkyl, hydrocarbyl, ether, an amine group and combined radicals thereof; R3, R5, R6, R8 are independently selected from alkyl, aryl, cycloalkyl groups, and combined radicals thereof; and wherein R4, R7 are independently selected from hydrogen, alkyl, aryl, cycloalkyl, amine groups and combined radicals thereof, containing each at most 12 carbon atoms (preferably with each of R1 to R8 containing at most 12 carbon atoms) and Y is independently selected from alkylene, arylene, cycloalkylene, hydrocarbyl, a heteroatom and combined radicals thereof; (C) Activating the catalyst, e.g. by an activator, to obtain an activated catalyst; and (D) Polymerizing the diene monomers and norbornene monomers with said catalyst or activated catalyst.
It is emphasized that embodiments of the second aspect of the invention can also be preferred embodiments of the third aspect of the present invention. Moreover, features of the aspects may be combined with one another.
In a fourth aspect of the present invention, the invention is directed to a diene-norbornene copolymer (such as a butadiene-norbornene or isoprene-norbornene copolymer) obtained by the method according to the second aspect or the third aspect of the invention.
In one embodiment, at least 95% of all 1,4 diene repeat units in the copolymer are cis 1,4 repeat units, such as cis 1,4 isoprene units or cis 1,4 butadiene units.
In another embodiment, said diene is isoprene and at least 5% of all isoprene units, by number, in the copolymer are 3,4 isoprene units.
In particular, the embodiments of the first aspect of the invention can also be preferred embodiments of the present fourth aspect of the present invention.
In a fifth aspect of the present invention, the invention is directed to a rubber composition comprising at least 5 phr of the diene-norbornene copolymer and at least 20 phr of filler. The diene-norbornene copolymer may be in accordance with one or more of the above-mentioned aspects and/or embodiments.
In one embodiment, the rubber composition comprises one or more of: 5 phr to 95 phr (preferably 10 phr to 45 phr) of the diene-norbornene copolymer; 5 phr to 95 phr (preferably 55 phr to 90 phr) of at least one polymer selected from the group of natural rubber, synthetic 1,4 polyisoprene, synthetic 3,4 polyisoprene, polybutadiene rubber, styrene-butadiene rubber; and 25 phr to 200 phr (preferably from 40 phr to 180 phr, or 40 phr to 80 phr, or 105 phr to 160 phr) of filler, optionally comprising one or more of carbon black, metal hydroxide, such as aluminum hydroxide, and silica.
In another embodiment, the diene-norbornene copolymer is an isoprene-norbornene copolymer and said at least one polymer includes at least one or more of natural rubber, synthetic 1,4 polyisoprene, and 3,4 polyisoprene. In such an embodiment, the copolymer is combined in a rubber composition with a polyisoprene which particularly allows for advanced miscibility and/or an improvement and/or adjustment of the rubber/polyisoprene matrix glass transition temperature. This can for instance help to improve the balance of tire tread wear and traction properties, and/or the hysteresis, tear or abrasion balance.
In another embodiment, the diene-norbornene copolymer is a butadiene-norbornene copolymer and said at least one polymer includes at least polybutadiene rubber. In such an embodiment, the copolymer is combined in a rubber composition with a polybutadiene rubber, which particularly allows for advanced miscibility and/or an improvement and/or adjustment of the rubber matrix glass transition temperature.
In an embodiment, the rubber composition may include at least one and/or one additional diene-based rubber. Representative synthetic polymers may be the homopolymerization products of butadiene and its homologues and derivatives, for example, methylbutadiene, dimethylbutadiene and pentadiene as well as copolymers such as those formed from butadiene or its homologues or derivatives with other unsaturated monomers. Among the latter may be acetylenes, for example, vinyl acetylene; olefins, for example, isobutylene, which copolymerizes with isoprene to form butyl rubber; vinyl compounds, for example, acrylic acid, acrylonitrile (which polymerize with butadiene to form NBR), methacrylic acid and styrene, the latter compound polymerizing with butadiene to form SBR, as well as vinyl esters and various unsaturated aldehydes, ketones and ethers, e.g. acrolein, methyl isopropenyl ketone and vinylethyl ether. Specific examples of synthetic rubbers include neoprene (polychloroprene), polybutadiene (including cis 1,4-polybutadiene), polyisoprene (including cis 1,4-polyisoprene), butyl rubber, halobutyl rubber such as chlorobutyl rubber or bromobutyl rubber, styrene/isoprene/butadiene rubber, copolymers of 1,3-butadiene or isoprene with monomers such as styrene, acrylonitrile and methyl methacrylate, as well as ethylene/propylene terpolymers, also known as ethylene/propylene/diene monomer (EPDM), and in particular, ethylene/propylene/dicyclopentadiene terpolymers. Additional examples of rubbers which may be used include alkoxy-silyl end functionalized solution polymerized polymers (SBR, PBR, IBR and SIBR), silicon-coupled and tin-coupled star-branched polymers. Preferred rubber or elastomers may be in general natural rubber, synthetic polyisoprene, polybutadiene and SBR including SSBR or ESBR. The rubbers such as the SBR or SSBR may be functionalized for the coupling to silica.
In one embodiment, a synthetic or natural polyisoprene rubber may be used. Synthetic cis-1,4-polyisoprene and natural rubber are as such well known to those having skill in the rubber art. In particular, the cis 1,4-microstructure content may be at least 90% and is typically at least 95% or even higher. For the sake of clarity it is noted that such rubber does usually not have a significant 3,4 isoprene content and in particular not such a content in combination with a full or almost full cis-1,4 isoprene content.
In one embodiment, cis-1,4-polybutadiene rubber (BR or PBD) is used. Suitable polybutadiene rubbers may be prepared, for example, by organic solution polymerization of 1,3-butadiene. The BR may be conveniently characterized, for example, by having at least a 90 percent cis-1,4-microstructure content (“high cis” content) and a glass transition temperature (Tg) in a range of from −95° C. to −110° C. Suitable polybutadiene rubbers are available commercially, such as Budene® 1207, Budene® 1208, Budene® 1223, or Budene® 1280 from The Goodyear Tire & Rubber Company. These high cis-1,4-polybutadiene rubbers can for instance be synthesized utilizing nickel catalyst systems which include a mixture of (1) an organonickel compound, (2) an organoaluminum compound, and (3) a fluorine containing compound as described in U.S. Pat. Nos. 5,698,643 and 5,451,646, which are incorporated herein by reference.
A glass transition temperature, or Tg, of an elastomer represents the glass transition temperature of the respective elastomer in its uncured state. A glass transition temperature of an clastomer composition represents the glass transition temperature of the elastomer composition in its cured state. A Tg is determined by a differential scanning calorimeter (DSC). Prior to measurements, the calorimeter is calibrated using the indium calibration standard. DSC of elastomer sample or clastomer composition is performed with a heating rate of 5° C. min−1 (1st cycle) and 10° C. min−1 (2nd cycle) in the range of −95° C. (preferably −80° C.) to 80° C. A Tg is determined as a transition midpoint (as the midpoint of the transition region) during the second heating cycle at a temperature rate of increase of 10° C. per minute, according to ASTM D3418 or equivalent.
The microstructure of an elastomer (the ratio of number of isoprene units, butadiene units and number of norbornene units) is determined by Nuclear Magnetic Resonance (NMR) spectroscopy in CDCl3 solvent, or equivalent, at 25° C., according to ASTM F2259 or equivalent.
The term “phr” as used herein, and according to conventional practice, refers to “parts by weight of a respective material per 100 parts by weight of rubber, or elastomer”. In general, using this convention, a rubber composition is comprised of 100 parts by weight of rubber/elastomer. The claimed composition may comprise other rubbers/elastomers than explicitly mentioned in the claims, provided that the phr value of the claimed rubbers/elastomers is in accordance with claimed phr ranges and the amount of all rubbers/elastomers in the composition results in total in 100 parts of rubber. In an example, the composition may further comprise from 1 phr to 10 phr, optionally from 1 phr to 5 phr, of one or more additional diene-based rubbers, such as SBR, SSBR, ESBR, PBD/BR, NR and/or synthetic polyisoprene. In another example, the composition may include less than 5 phr, preferably less than 3, phr of an additional diene-based rubber or be also essentially free of such an additional diene-based rubber. The terms “compound” and “composition” and “formulation” may be used herein interchangeably, unless indicated otherwise. The terms “rubber” and “elastomer” may also be used herein interchangeably.
Molecular weights of elastomers/rubbers, such as Mn (number average molecular weight), Mw (weight average molecular weight) and Mz (z average molecular weight), are determined herein using gel permeation chromatography (GPC) in THF at 40° C. according to ASTM 5296-11 using an integrated refractive index (RI) detector and polystyrene calibration standards, or equivalent.
In another embodiment, the rubber composition includes from 1 phr to 80 phr, or from 5 phr to 80 phr, of a resin, preferably having a glass transition temperature Tg greater than 20° C. A Tg for resins is determined as a transition midpoint (as the midpoint of the transition region) by a differential scanning calorimeter (DSC) at a temperature rate of increase of 10° C. per minute, according to ASTM D6604 or equivalent. Preferably, the resin has a softening point above 70° C. as determined by ASTM E28 which might sometimes be referred to as a ring and ball softening point. In one embodiment, the rubber composition includes from 10 phr to 60 phr or from 20 phr to 60 phr or from 30 phr to 60 phr of resin.
In another embodiment, the resin is selected from the group consisting of coumarone-indene resin, petroleum hydrocarbon resin, terpene polymers/resins, styrene/alphamethylstyrene resins, terpene phenol resin, rosin derived resins and copolymers and/or mixtures thereof.
A coumarone-indene resin preferably contains coumarone and indene as monomer components making up the resin skeleton (main chain). Monomer ingredients other than coumarone and indene which may be incorporated into the skeleton are, for example, methyl coumarone, styrene, alphamethylstyrene, methylindene, vinyltoluene, dicyclopentadiene, cyclopentadiene, and diolefins such as isoprene and piperlyene. Coumarone-indene resins have preferably softening points ranging from 10° C. to 160° C. (as measured by the ball-and-ring method). Even more preferably, the softening point ranges from 30° C. to 100° C.
Suitable petroleum resins include both aromatic and nonaromatic types. Several types of petroleum resins are available. Some resins have a low degree of unsaturation and high aromatic content, whereas some are highly unsaturated and yet some contain no aromatic structure at all. Differences in the resins are largely due to the olefins in the feedstock from which the resins are derived. Conventional derivatives in such resins include any C5 species (olefins and diolefines containing an average of five carbon atoms) such as cyclopentadiene, dicyclopentadiene, diolefins such as isoprene and piperylene, and any C9 species (olefins and diolefins containing an average of 9 carbon atoms) such as vinyltoluene, alphamethylstyrene and indene. Such resins are made by any mixture formed from C5 and C9 species mentioned above, and are known as C5/C9 copolymer resins. Petroleum resins are typically available with softening points ranging from 10° C. to 120° C. Preferably, the softening point ranges from 30 to 100° C.
In an embodiment, C5 resins are aliphatic resins made from one or more of the following monomers: 1,3-pentadiene (e.g., cis or trans), 2-methyl-2-butene, cyclopentene, cyclopentadiene, and dicyclopentadiene.
In another embodiment, a C9 resin is a resin made from one or more aromatic monomers, preferably chosen from the group of indene, methylindene, vinyl toluene, styrene and methylstyrene (such as alpha-methylstyrene).
In still another embodiment, a C9 modified resin is a resin (such as a C5 resin) which has been modified or functionalized with one or more aromatic monomers, preferably chosen from the group of indene, methylindene, vinyl toluene, styrene and methylstyrene (such as alpha methylstyrene).
Terpene resins are preferably comprised of polymers of at least one of limonene, alpha pinene, beta pinene and delta-3-carene. Such resins are available with softening points ranging from 10° C. to 135° C.
Terpene-phenol resins may be derived by copolymerization of phenolic monomers with terpenes such as limonenes, pinenes and delta-3-carene.
Representative for resins derived from rosins and derivatives thereof are, for example, gum rosin, wood rosin and tall oil rosin. Gum rosin, wood rosin and tall oil rosin have similar compositions, although the amount of components of the rosins may vary. Such resins may be dimerized, polymerized or disproportionated. Such resins may be in the form of esters of rosin acids and polyols such as pentaerythritol or glycol.
A styrene/alphamethylstyrene resin is considered herein to be a (preferably relatively short chain) copolymer of styrene and alphamethylstyrene with a styrene/alphamethylstyrene molar ratio in a range of about 0.05 to about 1.50. In one aspect, such a resin can be suitably prepared, for example, by cationic copolymerization of styrene and alphamethylstyrene in a hydrocarbon solvent. Thus, the contemplated styrene/alphamethylstyrene resin can be characterized, for example, by its chemical structure, namely its styrene and alphamethylstyrene contents and by its glass transition temperature, molecular weight and molecular weight distribution.
In one embodiment, said resin is partially or fully hydrogenated.
In an embodiment, the rubber composition comprises oil, such as processing oil. Oil may be included in the rubber composition as extending oil typically used to extend elastomers. Oil may also be included in the rubber composition by addition of the oil directly during rubber compounding. Oil used may include both extending oil present in the elastomers, and (process) oil added during compounding. Suitable oils may include various oils as are known in the art, including aromatic, paraffinic, naphthenic, vegetable oils, and low PCA oils, such as MES, TDAE, SRAE and heavy naphthenic oils. Suitable low PCA oils may include those having a polycyclic aromatic content of less than 3 percent by weight as determined by the IP346 method. Procedures for the IP346 method may be found in Standard Methods for Analysis & Testing of Petroleum and Related Products and British Standard 2000 Parts, 2003, 62nd edition, published by the Institute of Petroleum, United Kingdom. Some representative examples of vegetable oils that can be used include soybean oil, sunflower oil, canola (rapeseed) oil, corn oil, coconut oil, cottonseed oil, olive oil, palm oil, peanut oil, and safflower oil. Soybean oil and corn oil are typically preferred vegetable oils. If used, the rubber composition may also include up to 70 phr of processing oil, preferably between 5 phr and 25 phr. Or can be, alternatively less than 10 phr oil, preferably less than 5 phr.
Glass transition temperatures Tg for oils are determined as a transition midpoint (as the midpoint of the transition region) by a differential scanning calorimeter (DSC) at a temperature rate of increase of 10° C. per minute, according to ASTM E1356, or equivalent.
In an embodiment, the rubber composition comprises silica. Silica may be for instance pyrogenic/fumed or precipitated silica. In preferred embodiments, precipitated silica is used. Silicas might be characterized, for example, by having a BET surface area, as measured using nitrogen gas. In one embodiment, the BET surface area may be in the range of 40 to 600 square meters per gram. In another embodiment, the BET surface area may be in a range of 50 to 300 square meters per gram. The BET surface area is determined according to ASTM D6556 or equivalent and is described in the Journal of the American Chemical Society, Volume 60, Page 304 (1930). Silica may also be characterized by having a dibutylphthalate (DBP) absorption value in a range of 100 cm3/100 g to 400 cm3/100 g, alternatively 150 cm3/100 g to 300 cm3/100 g which is determined according to ASTM D 2414 or equivalent. Silica may have an average ultimate particle size, for example, in the range of 0.01 to 0.05 micron as determined by the electron microscope, although the silica particles may be even smaller, or possibly larger, in size. Ranges of silica use could be for instance between 5 and 200 phr. Various commercially available silicas may be used, such as, only for example herein, and without limitation, silicas commercially available from PPG Industries under the Hi-Sil trademark with designations 210, 315G, EZ160G, etc; silicas available from Solvay, with, for example, designations of Z1165MP and Premium200MP, etc.; and silicas available from Evonik AG with, for example, designations VN2 and Ultrasil 6000GR, 9100GR, etc.
In still another embodiment, the rubber composition may comprise pre-silanized and/or hydrophobated silica which may for instance have a CTAB adsorption surface area of between 130 m2/g and 210 m2/g, optionally between 130 m2/g and 150 m2/g and/or between 190 m2/g and 210 m2/g, or even between 195 m2/g and 205 m2/g. The CTAB (cetyl trimethyl ammonium bromide) method for determination of the silica surface area (ASTM D6845) is known to the person skilled in the art. In another embodiment, pre-silanized silica utilized is hydrophobated prior to its addition to the rubber composition by treatment with at least one silane. Suitable silanes include but are not limited to alkylsilanes, alkoxysilanes, organoalkoxysilyl polysulfides and organomercaptoalkoxysilanes.
Some non-limiting examples of pre-treated silicas (i.e., silicas that have been pre-surface treated with a silane) which are suitable for use in the practice of this invention include, but are not limited to, Ciptane® 255 LD and Ciptane® LP (PPG Industries) silicas that have been pre-treated with a mercaptosilane, and Coupsil® 8113 (Degussa) that is the product of the reaction between organosilane Bis(tricthoxysilylpropyl) polysulfide (Si69) and Ultrasil® VN3 silica, and Coupsil® 6508, Agilon® 400 silica from PPG Industries, Agilon® 454 silica from PPG Industries, and Agilon® 458 silica from PPG Industries.
In one embodiment, where the rubber composition contains conventional/no-pre-silanized silica (in addition to said pre-silanized silica), said rubber composition contains added silica coupler (silica coupler added (separately) to said rubber composition), where said silica coupler has a moiety reactive with hydroxyl groups (e.g. silanol groups) on said silica and said pre-silanized silica and another different moiety interactive with the elastomers of the rubber composition. In one embodiment, said silica coupler added to said rubber composition is comprised of bis(3-triethoxysilylpropyl) polysulfide having an average of from about 2 to about 4 connecting sulfur atoms in its polysulfidic bridge.
Representative of the aforesaid silica coupler (or in other words, silica coupling agent) having a moiety reactive with hydroxyl groups on pre-silanized silica and on silica and another moiety interactive with said elastomers, may be comprised of, for example:
(A) bis(3-trialkoxysilylalkyl) polysulfide containing an average in range of from about 2 to about 4, alternatively from about 2 to about 2.6 or from about 3.2 to about 3.8, sulfur atoms in its connecting bridge, or (B) an alkoxyorganomercaptosilane, or (C) their combination. Representative of such bis(3-trialkoxysilylalkyl) polysulfide is comprised of bis(3-triethoxysilylpropyl) polysulfide. As indicated, for the pre-silanized silica, the silica coupler may be desirably an alkoxyorganomercaptosilane. For the non-pre-silanized silica, the silica coupler may be desirably comprised of the bis(3-triethoxysilylpropyl) polysulfide.
In an embodiment, the rubber composition may include carbon black. Representative examples of such carbon blacks include N110, N121, N134, N220, N231, N234, N242, N293, N299, N315, N326, N330, N332, N339, N343, N347, N351, N358, N375, N539, N550, N582, N630, N642, N650, N683, N754, N762, N765, N774, N787, N907, N908, N990 and N991 grades. These carbon blacks have iodine absorptions ranging from 9 g/kg to 145 g/kg and a DBP number ranging from 34 cm3/100 g to 150 cm3/100 g. Iodine absorption values are determined according to ASTM D1510 or equivalent. Commonly employed carbon blacks can be used as a conventional filler in an amount ranging from 1 phr to 150 phr. In another embodiment, from 1 phr to 50 phr of carbon black may be used. For race tires such content may be significantly higher.
In other embodiments, the content of carbon black is at most 10 phr, preferably less than 8 phr or less than 4 phr.
Typically, the carbon black content is at least 0.1 phr.
In one embodiment, the rubber composition may contain sulfur containing organosilicon compounds or {circumflex over ( )}1silanes. Examples of suitable sulfur containing organosilicon compounds are of the formula:
Z—Alk—Sn—Alk—Z I
in which Z is selected from the group consisting of
where R1 is an alkyl group of 1 to 4 carbon atoms, cyclohexyl or phenyl; R2 is an alkoxy of 1 to 8 carbon atoms, or cycloalkoxy of 5 to 8 carbon atoms; Alk is a divalent hydrocarbon of 1 to 18 carbon atoms and n is an integer of 2 to 8. In one embodiment, the sulfur containing organosilicon compounds are the 3,3′-bis(trimethoxy or triethoxy silylpropyl) polysulfides. In one embodiment, the sulfur containing organosilicon compounds are 3,3′-bis(triethoxysilylpropyl) disulfide and/or 3,3′-bis(triethoxysilylpropyl) tetrasulfide. Therefore, as to formula I, Z may be
where R2 is an alkoxy of 2 to 4 carbon atoms, alternatively 2 carbon atoms; Alk is a divalent hydrocarbon of 2 to 4 carbon atoms, alternatively with 3 carbon atoms; and n is an integer of from 2 to 5, alternatively 2 or 4. In another embodiment, suitable sulfur containing organosilicon compounds include compounds disclosed in U.S. Pat. No. 6,608,125. In one embodiment, the sulfur containing organosilicon compounds includes 3-(octanoylthio)-1-propyltriethoxysilane, CH3(CH2)6C(═O)—S—CH2CH2CH2Si(OCH2CH3)3, which is available commercially as NXT™ from Momentive Performance Materials. In another embodiment, suitable sulfur containing organosilicon compounds include those disclosed in United States Patent Application Publication No. 2003/0130535. In one embodiment, the sulfur containing organosilicon compound is Si-363 from Degussa. The amount of the sulfur containing organosilicon compound in a rubber composition may vary depending on the level of other additives that are used. Generally speaking, the amount of the compound may range from 0.5 phr to 20 phr. In one embodiment, the amount will range from 1 phr to 10 phr.
It is readily understood by those having skill in the art that the rubber composition may be compounded by methods generally known in the rubber compounding art, such as mixing the various sulfur-vulcanizable constituent rubbers with various commonly used additive materials such as, for example, sulfur donors, curing aids, such as activators and retarders and processing additives, such as oils, resins including tackifying resins and plasticizers, fillers, pigments, fatty acid, zinc oxide, waxes, antioxidants and antiozonants and peptizing agents. As known to those skilled in the art, depending on the intended use of the sulfur vulcanizable and sulfur-vulcanized material (rubbers), the additives mentioned above are selected and commonly used in conventional amounts. Some representative examples of sulfur donors include elemental sulfur (free sulfur), an amine disulfide, polymeric polysulfide and sulfur olefin adducts. In one embodiment, the sulfur-vulcanizing agent is elemental sulfur. The sulfur-vulcanizing agent may for instance be used in an amount ranging from 0.5 phr to 8 phr, alternatively within a range of 1.5 phr to 6 phr. Typical amounts of tackifier resins, if used, comprise for example 0.5 phr to 10 phr, usually 1 phr to 5 phr. Typical amounts of processing aids, if used, comprise for example 1 phr to 50 phr (this may comprise in particular oil). Typical amounts of antioxidants, if used, may for example comprise 1 phr to 5 phr. Representative antioxidants may be, for example, diphenyl-p-phenylenediamine and others, such as, for example, those disclosed in The Vanderbilt Rubber Handbook (1978), Pages 344 through 346. Typical amounts of antiozonants, if used, may for instance comprise 1 phr to 5 phr. Typical amounts of fatty acids, if used, which can include stearic acid, may for instance comprise 0.5 phr to 3 phr. Typical amounts of waxes, if used, may for example comprise 1 phr to 5 phr. Often microcrystalline waxes are used. Typical amounts of peptizers, if used, may for instance comprise 0.1 phr to 1 phr. Typical peptizers may be, for example, pentachlorothiophenol and dibenzamidodiphenyl disulfide.
Accelerators may be preferably but not necessarily used to control the time and/or temperature required for vulcanization and to improve the properties of the vulcanizate. In one embodiment, a single accelerator system may be used, i.e., primary accelerator. The primary accelerator(s) may be used in total amounts ranging from 0.5 phr to 4 phr, alternatively 0.8 phr to 1.5 phr. In another embodiment, combinations of a primary and a secondary accelerator might be used with the secondary accelerator being used in smaller amounts, such as from 0.05 phr to 3 phr, in order to activate and to improve the properties of the vulcanizate. Combinations of these accelerators might be expected to produce a synergistic effect on the final properties and are somewhat better than those produced by use of either accelerator alone. In addition, delayed action accelerators may be used which are not affected by normal processing temperatures but produce a satisfactory cure at ordinary vulcanization temperatures. Vulcanization retarders might also be used. Suitable types of accelerators that may be used in the present invention are for instance amines, disulfides, guanidines, thiourcas, thiazoles, thiurams, sulfenamides, dithiocarbamates and xanthates. In one embodiment, the primary accelerator is a sulfonamide. If a second accelerator is used, the secondary accelerator may be for instance a guanidine, dithiocarbamate or thiuram compound. Suitable guanidines include dipheynylguanidine and the like. Suitable thiurams include tetramethylthiuram disulfide, tetraethylthiuram disulfide, and tetrabenzylthiuram disulfide.
The mixing of the rubber composition can be accomplished by methods known to those having skill in the rubber mixing art. For example, the ingredients may be typically mixed in at least two stages, namely, at least one nonproductive stage followed by a productive mix stage. The final curatives including sulfur-vulcanizing agents may be typically mixed in the final stage which is conventionally called the “productive” mix stage in which the mixing typically occurs at a temperature, or ultimate temperature, lower than the mix temperature(s) of the preceding nonproductive mix stage(s). The terms “nonproductive” and “productive” mix stages are well known to those having skill in the rubber mixing art. In an embodiment, the rubber composition may be subjected to a thermomechanical mixing step. The thermomechanical mixing step generally comprises a mechanical working in a mixer or extruder for a period of time, for example suitable to produce a rubber temperature between 140° C. and 190° C. The appropriate duration of the thermomechanical working varies as a function of the operating conditions, and the volume and nature of the components. For example, the thermomechanical working may be from 1 to 20 minutes.
In a sixth aspect, the invention is directed to an article of manufacture comprising a rubber composition and/or copolymer in accordance with one or more of the afore-mentioned aspects.
In one embodiment, the article of manufacture is selected from a tire, a power transmission belt, a hose, a track, an air sleeve, and a conveyor belt. Preferably it is a tire.
The rubber composition may be incorporated in a variety of rubber components of a tire (or in other words tire components). For example, the rubber component may be a tread (including tread cap and/or tread base), sidewall, apex, chafer, sidewall insert, wirecoat or innerliner.
The tire may for example be a pneumatic tire or nonpneumatic tire, a race tire, a passenger tire, an aircraft tire, an agricultural tire, an earthmover tire, an off-the-road (OTR) tire, a truck tire, or a motorcycle tire. The tire may also be a radial tire or bias tire.
Vulcanization of the pneumatic tire of the present invention may for instance be carried out at conventional temperatures ranging from 100° C. to 200° C. In one embodiment, the vulcanization is conducted at temperatures which are within a range of 110° C. to 180° C. Any of the usual vulcanization processes may be used such as heating in a press or mold, heating with superheated steam or hot air. Such tires can be built, shaped, molded and cured by various methods which are known and will be readily apparent to those having skill in such art.
While preferred aspects and embodiments are described herein, the features of all aspects and embodiments may be combined with one another.
The inventors have prepared multiple diene-norbornene copolymers in accordance with embodiments of the present invention.
For making such copolymers, the inventors have identified examples of catalysts for polymerizing diene monomers and norbornene monomers to obtain the desired copolymers. In one preferred embodiment, said catalysts have the following structure (IIIa):
wherein R1 and R2 are independently selected from hydrogen, alkyl, aryl, cycloalkyl, hydrocarbyl, ether, an amine group and combined radicals thereof, wherein each of R1 and R2 contains at most 12 carbon atoms. R3, R5, R6, R8 are independently selected from alkyl, aryl, cycloalkyl groups, and combined radicals thereof, with each of R3, R5, R6, R8 containing at most 12 carbon atoms. R4 and R7 are independently selected from hydrogen, alkyl, aryl, cycloalkyl, amine groups and combined radicals thereof, and each contains at most 12 carbon atoms either.
In particular, said catalysts having the structure LALBMX2 (I), may comprise homoligand (LA=LB) catalysts or heteroligand (LA≠LB) catalysts. Respective examples in accordance with embodiments of the present invention are listed herein below.
In a first non-limiting embodiment, the catalyst has the below structure Cat1, which corresponds to a homoligand catalyst herein.
In a second non-limiting embodiment, the catalyst has the below structure Cat2, which corresponds to another homoligand catalyst.
In a third non-limiting embodiment, the catalyst has the below structure Cat3, which corresponds to a heteroligand catalyst.
In a fourth non-limiting embodiment. the catalyst has the below structure Cat4, which corresponds to another heteroligand catalyst.
In a fifth non-limiting embodiment. the catalyst has the below structure Cat5, which corresponds to another heteroligand catalyst.
In a sixth non-limiting embodiment, the catalyst has the below structure Cat6, which corresponds to another heteroligand catalyst.
Moreover, the inventors have identified dinuclear catalysts according to structure (IIIb):
Thus, in a seventh non-limiting embodiment, the catalyst has the below structure Cat7, which corresponds to a dinuclear catalyst, and which is an example of a catalyst in accordance with above formula (IIIb).
In an eighth non-limiting embodiment. the catalyst has the below structure Cat8, which corresponds to another dinuclear catalyst.
In a nineth non-limiting embodiment. the catalyst has the below structure Cat9, which corresponds to still another dinuclear catalyst.
In the aforementioned embodiments, all catalysts are Titanium based. However, the present invention is not limited to such a metal only. In particular, other group IV transition metals are also preferred metals.
Catalysts Cat1 to Cat9 have been used to prepare copolymers as listed in Table 1 below. As shown in Table 1, the obtained copolymers have a norbornene (NB) content ranging from 5 to 18 weight percent. The content of isoprene (IP) is 82 to 95 weight percent. Remarkable is that the content of 1,2 isoprene and trans-1,4 isoprene is almost zero or zero. The only isoprenes in the copolymer are 3,4 isoprene and cis 1,4 isoprene. Obtained glass transition temperatures are relatively high, which allows for instance new applications in rubber compounding. In particular, the glass transition temperatures are within a range of −34.3° C. to −40.7° C. in the non-limiting examples shown herein. Also, the obtained 3,4 isoprene contents in combination with the full cis-1,4 isoprene content (with regard to the absence of trans-1,4 isoprene) provide a good miscibility with other diene-based rubbers, in particular natural rubber or synthetic high-cis 1,4 polyisoprene.
Steps for polymerizing a copolymer with the help of a catalyst in accordance with an embodiment of the present invention is shown in below Reaction Scheme A.
In accordance with Reaction Scheme A, the catalyst is first mixed with a co-catalyst in a solvent (step i)). In the present example, the co-catalyst is TIBA (triisobutylaluminum), but could also be an alternative material, e.g., as mentioned herein above. Preferably, this first step is carried out at room temperature although other temperatures may be possible as also listed herein above. As solvent, cyclohexane is used in the present non-limiting embodiment.
In a next step (step ii)), the mixture of the catalyst, co-catalyst and solvent is further mixed with Li[B(C6F5)4] (Lithium[tetrakis-(pentafluorophenyl)borate], also known as LiFABA), or PhNMe2[B(C6F5)4], which are examples of an activator, activating the catalyst so as to obtain an activated and/or cationic catalyst.
In a further step, the activated catalyst is mixed, still in the solvent cyclohexane, with isoprene (monomers) and norbornene (monomers) so as to obtain the isoprene-norbornene copolymer. In this example, polymerization takes place at a temperature of 40° C. Other temperatures are in principle possible. The cis-1,4 isoprene units, 3,4 isoprene units and norbornene units in Reaction Scheme A are typically not distributed in blocks of such types of units. Rather, these units may partially alternate and/or be random. Molecular weights (Mn) typically obtained by the method in accordance with an embodiment of the invention are within a range of 100,000 g/mol to 900,000 g/mol.
It is noted that a person skilled in the art could polymerize the copolymer with the above description and knowledge of Reaction Scheme A. Alternative examples of catalysts disclosed herein may be used. Merely for the sake of providing specific examples, further non-limiting details are provided below. It is emphasized that multiple of the provided details could be adapted according to available equipment and chemistry and/or with regard to the scale of polymer needed. It is also noted that the above scheme is shown for the example of isoprene-norbornene. However, it can for instance also involve butadiene-norbornene in accordance with another embodiment of the present invention.
A non-limiting example is given for isoprene/norbornene/Ti(L2)Cl2/triisobutylaluminum/lithium (or dimethylanilinium) tetrakis-perfluorophenylborate, at a molar ratio of 180/20/1/5/1. The solution of a catalyst was prepared by adding 5 cquiv. of triisobutylaluminum (1.1 M solution in toluene) to Ti(L2)Cl2 in a Schlenk flask and stirring for about 1 hour at room temperature, followed by the addition of the resultant solution to 1 equiv. of lithium (or dimethylanilinium) tetrakis-perfluorophenylborate in a polymerization flask and stirring for 5 minutes at room temperature. The polymerization was initiated by the addition of isoprene-norbornene solution (6.67 M in cyclohexane, 90:10 comonomer ratio) to an activated catalyst. The reaction mixture was allowed to stir for the required time at 40° C. The resulting copolymer was precipitated in acidic methanol (5% hydrochloric acid), filtered, and washed with acetone. Then the polymer was dried under vacuum (0.3 mbar) at 55° C. The yield was calculated based on the dried polymer.
Another non-limiting example is given for isoprene/norbornene/Catalyst 1/triisobutylaluminum/lithium tetrakis-perfluorophenylborate at a molar ratio of 180/20/1/5/1. The solution of activated Catalyst 1 was prepared by adding 0.5 mmol of triisobutylaluminum (0.45 ml, 1.1 M solution in toluene) to 0.1 mmol, 79.4 mg of Catalyst 1 (FW=794) in a Schlenk flask and stirring for 1 hour at room temperature, followed by the addition of the resultant solution to 0.1 mmol, 64.8 mg of lithium tetrakis-perfluorophenylborate (FW=648) in a polymerization flask and stirring for 5 minutes at room temperature. The polymerization was initiated by the addition of 18 mmol of isoprene and 2 mmol of norbornene (3 ml, 6.67 M cyclohexane solution) to the activated catalyst. The reaction mixture was allowed to stir for the required time at 40° C. The resulting copolymer was precipitated in acidic methanol (5% hydrochloric acid), filtered, and washed with acetone. After that the polymer was dried under vacuum (0.3 mbar) at 55° C. The yield was calculated based on the dried polymer.
Still another non-limiting example is given for isoprene/norbornene/Catalyst 3/triisobutylaluminum/dimethylanilinium tetrakis-perfluorophenylborate at a molar ratio of 180/20/1/5/1. The solution of activated Catalyst 3 was prepared by adding 0.5 mmol of triisobutylaluminum (0.45 ml, 1.1 M solution in toluene) to 0.1 mmol, 70.9 mg of Catalyst 1 (FW=709) in a Schlenk flask and stirring for 1 hour at room temperature, followed by the addition of the resultant solution to 0.1 mmol, 80.1 mg of dimethylanilinium tetrakis-perfluorophenylborate (FW=801) in a polymerization flask and stirring for 5 minutes at room temperature. The polymerization was initiated by the addition of 18 mmol of isoprene and 2 mmol of norbornene (3 ml, 6.67 M cyclohexane solution) to the activated catalyst. The reaction mixture was allowed to stir for the required time at 40° C. The resulting copolymer was precipitated in acidic methanol (5% hydrochloric acid), filtered, and washed with acetone. After that the polymer was dried under vacuum (0.3 mbar) at 55° C. The yield was calculated based on the dried polymer.
As for the polymerization process, with regard to suitable catalysts, there are various ways to prepare those in accordance with embodiments of the invention. Some non-limiting ways are demonstrated herein below. However, a person skilled in the art would be able to synthesize such materials using different steps, chemicals, conditions and equipment upon reading the present description.
In a first non-limiting example of preparing a catalyst, a homoligand Titanium complexe [(L1)2TiCl2] is prepared. To a stirred 0.1 M solution of substituted salicylidene aldimine, (E)-2,4-di-tert-butyl-6-(((4-methoxyphenyl)imino)methyl)phenol (678 mg, 2 mmol, in 20 mL of anhydrous tetrahydrofuran (THF)) the BuLi (2 mmol, 0.8 mL of 2.5 M solution in hexane) is added at −60° C. under inert atmosphere. The resulting solution is stirred for 1 h at −60° C., whereupon TiCl4 (1 mmol, 1 mL of 1 M solution in toluene) is added. The mixture is allowed to warm to room temperature (22° C.) and stirring is continued for 2-3 hours. After removal of all volatiles under reduced pressure, the residue is dissolved in 20 mL of the mixture of anhydrous CH2Cl2 and cyclohexane (1:1 by volume). The precipitate is filtered off and the volume of the filtrate is reduced 10 times before placing in a freezer for crystallization. After 10-15 h at −18° C., the titanium complex is obtained as deep red crystals that are filtered under inert atmosphere and dried at 22° C./0.3 mbar for 20 h.
In a second non-limiting example, heteroligand Titanium complexes [(L1L2)TiCl2] are prepared. To a stirred 0.1 M solution of substituted salicylidene aldimine, (E)-2,4-di-tert-butyl-6-(((4-methoxyphenyl)imino)methyl)phenol (Ligand 1, L1) (339 mg, 1 mmol) in 10 mL of anhydrous tetrahydrofuran (THF)) the BuLi (1 mmol, 0.4 mL of 2.5 M solution in hexane) is added dropwise at −60° C. under inert atmosphere. The resulting solution is stirred for 1 h at −60° C., whereupon it is warmed up to 0° C. and Me3SiCl (0.13 mL, 1 mmol) is added dropwise. The mixture is allowed to further warm up to room temperature, is stirred for 1 h at room temperature and then is again cooled down to −50° C. To thus obtained solution the TiCl4 (1 mmol, 1 mL of 1 M solution in toluene) is added dropwise at −50° C. The mixture is stirred for 1 h −50° C. to form a monoligated titanium complex. Then, a second substituted salicylidene aldimine, (E)-2-(tert-butyl)-6-((phenylimino)methyl)phenol (Ligand 2, L2), (253 mg, 1 mmol) is deprotonated in a separate flask with BuLi (1 mmol, 0.4 mL of 2.5 M solution in hexanes) in 10 mL of anhydrous THF using exactly the same procedure as for Ligand 1. The obtained solution of lithiated Ligand 2 is added to the solution of monoligated titanium complex via cannula at −50° C. The mixture is allowed to warm to room temperature and the stirring is continued overnight. After removal of all the volatiles under reduced pressure, the residue is dissolved in 20 mL of a mixture of anhydrous CH2Cl2 and cyclohexane (1:1 by volume) (same volume as in the reaction). The precipitate is filtered off and the volume of the filtrate is reduced 10 times before placing in the freezer for crystallization. After 10-15 h at −18° C., the titanium complex is obtained as crystals that are filtered under inert atmosphere and dried at room temperature/0.3 mbar for 20 h.
In a third non-limiting example, heteroligand dinuclear titanium complexes [(L1)2(L2)Ti2Cl4] are prepared. To a stirred 0.1 M solution of substituted salicylidene aldimine (Ligand 1, L1) (1 mmol) in 10 mL of anhydrous tetrahydrofuran (THF)) BuLi (1 mmol, 0.4 mL of 2.5 M solution in hexane) is added dropwise at −60° C. under inert atmosphere. The resulting solution is stirred for 1 h at −60° C., whereupon it is warmed up to 0° C. and Me3SiCl (0.13 mL, 1 mmol) is added dropwise. The mixture is allowed to further warm up to room temperature, is stirred for 1 h at room temperature and then is again cooled down to −50° C. To thus obtained solution the TiCl4 (1 mmol, 1 mL of 1 M solution in toluene) is added dropwise at −50° C. The mixture is stirred for 1 h −50° C. to form a monoligated titanium complex. Then, a second difunctional substituted salicylidene aldimine (Ligand 2, L2), (0.5 mmol) is deprotonated in a separate flask with BuLi (1 mmol, 0.4 mL of 2.5 M solution in hexanes) in 10 mL of anhydrous THF using exactly the same procedure as for Ligand 1. The obtained solution of lithiated Ligand 2 is added to the solution of monoligated titanium complex via cannula at −50° C. The mixture is allowed to warm to room temperature and the stirring is continued overnight. After removal of all the volatiles under reduced pressure, the residue is dissolved in 20 mL of a mixture of anhydrous CH2Cl2 and cyclohexane (1:1 by volume) (same volume as in the reaction). The precipitate is filtered off and the volume of the filtrate is reduced 10 times before placing in the freezer for crystallization. After 10-15 h at −18° C., the titanium complex is obtained as crystals that are filtered under inert atmosphere and dried at room temperature/0.3 mbar for 20 h.
Variations in the present invention are possible in light of the description of it provided herein. While certain representative embodiments and details have been shown for the purpose of illustrating the subject invention, it will be apparent to those skilled in this art that various changes and modifications can be made therein without departing from the scope of the subject invention. It is, therefore, to be understood that changes can be made in the particular embodiments described which will be within the full intended scope of the invention as defined by the following appended claims.
