KR20140121344A - Catalyst for olefin polymerization and method for preparing polyolefin using the same - Google Patents

Abstract

The present invention relates to a catalyst for olefin polymerization containing a new structure of transition metal compound, and a preparing method thereof, and a method for preparing polyolefin using the same. According to the present invention, the catalyst has more improved comonomer insertion capability, and enables the preparation of polyolefin with a wide distribution of molecular weight and with improved processability.

Description

TECHNICAL FIELD The present invention relates to a catalyst for olefin polymerization and a process for producing the same,

The present invention relates to a catalyst for olefin polymerization and a process for producing a polyolefin using the same.

The metallocene catalyst system is known as a catalyst system which is very useful for the copolymerization of ethylene with other alpha-olefins. Examples of the comonomers used in this copolymerization include 1-butene, 1-hexene, 1-octene, and the like.

In particular, along with the improvement of the activity of the Ziegler-Natta catalyst, the development of polyolefins using a variety of single-site catalysts such as Dow's Constrained-Geometry Catlyst (CGC) is under development.

It is known that the CGC exhibits excellent activity even at a high polymerization temperature, permits the production of a polymer having a high molecular weight, and is also excellent in the copolymerization of an alpha-olefin having a large steric hindrance such as 1-hexene or 1-octene.

As described above, the superiority of the CGC is known, and its derivatives have been actively studied as a polymerization catalyst to obtain more improved effects.

However, the compounds known so far have a problem in that they are difficult to apply to practical industrial fields because of the complexity of the synthesis process compared with the performance thereof, or the improved results in terms of copolymerization performance.

Accordingly, the present invention is to provide a catalyst for olefin polymerization, which has improved comonomer incorporation ability and is capable of producing a polyolefin having a broad molecular weight distribution and excellent processability.

The present invention also provides a process for producing a polyolefin using the catalyst.

According to the present invention, there is provided a catalyst for olefin polymerization comprising a transition metal compound represented by the following general formula:

[Chemical Formula 1]

In Formula 1,

M is a Group 4 transition metal;

Q ¹ and Q ² are each independently selected from the group consisting of halogen, alkyl of 1 to 20 carbon atoms, alkenyl of 2 to 10 carbon atoms, alkylaryl of 7 to 40 carbon atoms, arylalkyl of 7 to 40 carbon atoms, allyl of 6 to 20 carbon atoms, Alkylidene of 1 to 20 carbon atoms, alkylalkoxy of 2 to 20 carbon atoms, or arylalkoxy of 7 to 40 carbon atoms;

R ¹ , R ² and R ³ are each independently selected from the group consisting of hydrogen, alkyl of 1 to 20 carbon atoms, alkoxy of 1 to 10 carbon atoms, aryl of 6 to 20 carbon atoms, aryloxy of 6 to 10 carbon atoms, , Alkylaryl having 7 to 40 carbon atoms, arylalkyl having 7 to 40 carbon atoms, arylalkenyl having 8 to 40 carbon atoms, or alkynyl having 2 to 10 carbon atoms; R ¹ and R ² or R ² and R ³ may be connected to each other to form a ring;

A is any one substituent selected from the group consisting of a group represented by the following formula (2), provided that the symbol "*" in the following formula (2) is a linkage of A and a cyclopentadienyl ligand.

(2)

In Formula 1, preferably, M is titanium (Ti), zirconium (Zr), or hafnium (Hf); The Q ¹ and Q ² Are each independently methyl or chlorine; R ¹ , R ² and R ³ may each independently be hydrogen or methyl.

The catalyst for olefin polymerization may further contain a cocatalyst compound.

The catalyst for olefin polymerization may include an inert carrier on which the transition metal compound represented by Formula 1 is supported.

On the other hand, according to the present invention, there is provided a process for producing a polyolefin comprising the step of polymerizing at least one olefin-based monomer in the presence of a catalyst.

The olefinic monomer may be an α-olefin having 2 to 20 carbon atoms, a diolefin having 1 to 20 carbon atoms, a cyclo-olefin having 3 to 20 carbon atoms, or a cycloolefin having 3 to 20 carbon atoms And cyclo-diolefin. The term " cycloolefin "

The polyolefin may have a molecular weight distribution (Mw / Mn) of 40,000 to 1,000,000 and a molecular weight distribution of 2 to 30.

The catalyst according to the present invention makes it possible to produce a polyolefin having improved comonomer incorporation ability, broad molecular weight distribution and excellent workability.

1 to 49 are NMR spectra of Scheme and compounds for synthesis of compounds according to Examples and Comparative Examples of the present invention.

Hereinafter, a catalyst for olefin polymerization according to embodiments of the present invention and a method for producing a polyolefin using the same will be described.

Prior to that, the terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. And, the singular forms used herein include plural forms unless the phrases expressly have the opposite meaning. Also, as used herein, the meaning of "comprising" or "containing" embodies certain features, areas, integers, steps, acts, elements or components, But does not exclude the addition of components.

Meanwhile, the inventors of the present invention have found that, in a process of repeatedly studying a catalyst for olefin polymerization, a transition metal compound having a novel structure in which an aryl group having a side chain containing a heteroatom is introduced into a cyclopentadienyl ligand of a conventional constrained geometry catalyst . Further, it has been confirmed that the transition metal compound can exhibit improved copolymer inserting ability particularly in the olefin polymerization process, and can produce a polyolefin having a wide molecular weight distribution and excellent workability.

According to one embodiment of the present invention, there is provided a catalyst for olefin polymerization comprising a transition metal compound represented by the following Formula 1:

[Chemical Formula 1]

In Formula 1,

M is a Group 4 transition metal;

Q ¹ and Q ² are each independently selected from the group consisting of halogen, alkyl of 1 to 20 carbon atoms, alkenyl of 2 to 10 carbon atoms, alkylaryl of 7 to 40 carbon atoms, arylalkyl of 7 to 40 carbon atoms, allyl of 6 to 20 carbon atoms, Alkylidene of 1 to 20 carbon atoms, alkylalkoxy of 2 to 20 carbon atoms, or arylalkoxy of 7 to 40 carbon atoms;

R ¹ , R ² and R ³ are each independently selected from the group consisting of hydrogen, alkyl of 1 to 20 carbon atoms, alkoxy of 1 to 10 carbon atoms, aryl of 6 to 20 carbon atoms, aryloxy of 6 to 10 carbon atoms, , Alkylaryl having 7 to 40 carbon atoms, arylalkyl having 7 to 40 carbon atoms, arylalkenyl having 8 to 40 carbon atoms, or alkynyl having 2 to 10 carbon atoms; R ¹ and R ² or R ² and R ³ may be connected to each other to form a ring;

A is any one substituent selected from the group consisting of a group represented by the following formula (2), provided that the symbol "*" in the following formula (2) is a linkage of A and a cyclopentadienyl ligand.

(2)

The transition metal compound represented by the above formula (1) may be prepared by reacting a cyclopentadienyl ligand with an aryl group having a side chain containing a heteroatom (hereinafter referred to as' at least one substituent selected from the group represented by the formula (2) Substituent A ') is introduced. Accordingly, the compound represented by the above formula (1) enables the synthesis of a polyolefin having a larger weight average molecular weight and a broader molecular weight distribution than the compound having no side chain aryl group introduced therein.

The compound represented by Formula 1 may exhibit improved comonomer insertion capability in the copolymerization process of the olefin monomer and the alpha-olefin. That is, when a copolymer having an equivalent weight average molecular weight is used as a reference, the copolymer obtained by using the compound represented by the formula (1) as a catalyst has a higher comonomer Can be expressed. Accordingly, the compound represented by the above formula (1) has various physical properties (that is, various properties that can be achieved through control of comonomer content, weight average molecular weight, molecular weight distribution, and the like) Physical properties) of the polyolefin.

According to an embodiment, R ¹ , R ² and R ³ in the compound represented by Formula 1 may be independently substituted or unsubstituted with a substituent including an acetal, ketal or ether group. When R ¹ , R ² and R ³ are substituted with the above-mentioned substituent, they may be more advantageously supported on the surface of the carrier.

According to an embodiment, M is preferably titanium (Ti), zirconium (Zr), or hafnium (Hf) in terms of the activity or reproducibility of the catalyst; The Q ¹ and Q ² Are each independently methyl or chlorine. It is preferable that each of R ¹ , R ² , and R ³ is independently hydrogen or methyl. Each such substituent is advantageous because it is advantageous in controlling the electronic and stereoscopic environment around the center metal (M) and can exhibit higher activity.

Meanwhile, the catalyst for olefin polymerization according to one embodiment may include a cocatalyst compound together with the transition metal compound represented by the formula (1).

The promoter compound may be a conventional compound capable of activating the transition metal compound represented by Formula 1; Preferably one or more compounds selected from the group consisting of the following chemical formulas (3), (4) and (5)

(3)

- [Al (R ³¹ ) -O] _a -

In Formula 3,

R ³¹ is each independently a hydrogen, a halogen radical, a hydrocarbyl radical having 1 to 20 carbon atoms or a hydrocarbyl radical having 1 to 20 carbon atoms substituted with halogen;

a is an integer of 2 or more;

[Chemical Formula 4]

D (R < ^{41 >} ) ₃

In Formula 4,

D is aluminum or boron;

R ⁴¹ is each independently a halogen radical, a hydrocarbyl radical having 1 to 20 carbon atoms or a hydrocarbyl radical having 1 to 20 carbon atoms substituted with halogen.

[Chemical Formula 5]

^{[LH] + [Z (A} ) 4] - or ^{[L] + [Z (A} ) 4] -

In Formula 5,

L is a neutral or cationic Lewis base;

[LH] ⁺ or [L] ⁺ is a Bronsted acid;

H is a hydrogen atom;

Z is a Group 13 element;

A is independently selected from the group consisting of a hydrogen atom, a halogen atom, a hydrocarbyl group having 1 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms, an aryloxy group having 6 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, Alkyl radical.

Here, in order that the above-mentioned co-catalyst compound can exhibit a better activation effect, R ³¹ in the above formula (3) is methyl, ethyl, n-butyl or isobutyl; D in the formula 4 is aluminum, R ⁴¹ is methyl or isobutyl; Or D is boron and R < ⁴¹ > is pentafluorophenyl; [LH] ⁺ in the above formula (5) is a dimethylanilinium cation; [Z (A) ₄ ] ^- is [B (C ₆ F ₅ ) ₄ ] ^- ; [L] ⁺ is preferably [(C ₆ H ₅ ) ₃ C] ⁺ .

The content of the co-catalyst compound is preferably from 1: 1 to 1: 100,000, more preferably from 1: 1 to 1: 100,000 based on the molar ratio of the metal contained in the co-catalyst compound to one mole of the transition metal contained in the transition metal compound represented by the formula 1: 1 to 1: 10,000, more preferably 1: 1 to 1: 1,000.

Meanwhile, the catalyst for olefin polymerization according to one embodiment may include an inert carrier on which the compound represented by Formula 1 is supported. As the carrier, an inorganic or organic carrier common in the art to which the present invention belongs may be used without limitation; Preferably, _{SiO 2, Al 2 O 3,} MgO, MgCl 2, CaCl 2, ZrO 2, TiO 2, B 2 O 3, CaO, ZnO, BaO, ThO 2, SiO 2 -Al 2 O 3, SiO 2 - _{MgO, SiO 2 -TiO 2, SiO} 2 -V 2 O 5, SiO 2 -CrO 2 O 3, may be a SiO ₂ -TiO ₂ -MgO, bauxite, zeolite.

According to another embodiment of the present invention, there is provided a process for producing a polyolefin comprising polymerizing at least one olefin-based monomer in the presence of the above-mentioned catalyst.

The olefin-based monomer may be an α-olefin having 2 to 20 carbon atoms, a diolefin having 1 to 20 carbon atoms, a cyclo-olefin having 3 to 20 carbon atoms, or a cycloolefin having 3 to 20 carbon atoms Cyclo-olefin, substituted or unsubstituted styrene, and the like.

Preferably, the olefinic monomer has a number of carbon atoms of 2 or more, including ethylene, propylene, 1-butene, 1-pentene and 1-hexene. To 20 alpha-olefins; But are not limited to those containing 1,3-butadiene, 1,4-pentadiene and 2-methyl-1,3-butadiene. A diolefin having 1 to 20 carbon atoms; The number of carbons including 3 carbon atoms, including cyclopentene, cyclohexene, cyclopentadiene, cyclohexadiene, norbonene and methyl-2-norbonene, Cyclo-olefin or cyclo-diolefin of from 1 to 20 carbon atoms; Substituted styrene in which an alkyl group, an alkoxy group, a halogen group, an amine group, a silyl group, a haloalkyl group or the like is bonded to a phenyl ring of styrene or styrene; Or a mixture thereof.

The step of polymerizing the olefin-based monomer may be carried out in a slurry phase, a solution phase, a gas phase, or a bulk phase.

When the polymerization step is carried out in a liquid phase or a slurry, the solvent or the olefin-based monomer itself can be used as a medium.

The solvent used in the polymerization step may be selected from the group consisting of butane, isobutane, pentane, hexane, heptane, octane, nonane, decane, Aliphatic hydrocarbon solvents such as undecane, dodecane, cyclopentane, methylcyclopentane, cyclohexane and the like; Aromatic hydrocarbon solvents such as benzene, monochlorobenzene, dichlorobenzene, trichlorobenzene, toluene, xylene, chlorobenzene and the like; Halogenated aliphatic hydrocarbons such as dichloromethane, trichloromethane, chloroethane, dichloroethane, trichloroethane, and 1,2-dichloroethane, menstruum; Or a mixture thereof.

The polymerization may be carried out in a batch type, semi-continuous type or continuous type reaction. The temperature and pressure conditions of the polymerization step may be determined in consideration of the efficiency of the polymerization reaction depending on the kind of the reaction to be applied and the kind of the reactor.

On the other hand, the polyolefin prepared by the above method may have a molecular weight distribution (Mw / Mn) of 2 to 30, or 2.5 to 25, or 2.5 to 22. The polyolefin prepared by the above method may have a weight average molecular weight (Mw) of 40,000 or more, or 40,000 to 1,000,000, or 45,000 to 800,000.

Best Mode for Carrying Out the Invention Hereinafter, preferred embodiments are described to facilitate understanding of the present invention. However, the following examples are intended to illustrate the present invention, but the scope of the present invention is not limited thereto.

Comparative Example  One

The following compound 3 was synthesized according to Scheme shown in Fig. Hereinafter, synthesis of each compound will be described.

[Compound 3]

(1) Synthesis of Compound 1

: To a 250 mL Schlenk flask, 1,2,3,4-tetramethyl-1,3-cyclopentadiene (30 mmol, 3.67 g) was added and dissolved in 30 mL of tetrahydropyran (THF) Lt; / RTI > 1.1 equivalents of n-BuLi (33 mmol, 13.2 mL) was added slowly by syringe, then slowly warmed to room temperature and stirred for 2 hours. After the lithium anion solution was lowered to -78 ° C, 2.5 equivalents of Me ₂ SiCl ₂ (75 mmol, 9 mL) was slowly added thereto by using a syringe, then slowly raised to room temperature and stirred for 15 hours. Remove all solvents under vacuum and extract with n-hexane. After removing the salt from the mixture with a Celite bed, all the solvent was removed under vacuum to obtain Compound 1 of yellow oil at a yield of 77.9% (5.02 g).

(2) Synthesis of Compound 2

: Compound 1 (23.3 mmol, 5 g) was added to a 250 mL Schlenk flask and dissolved in 30 mL of THF, and then the temperature was lowered to -78 ° C using dry ice / acetone. Three equivalents of t-BuNH ₂ were slowly added thereto by using a syringe, and then the temperature was gradually raised to room temperature and stirred for 15 hours. Remove all solvents under vacuum and extract with n-hexane. After removing the salt from the mixture with a Celite bed, all the solvent was removed under vacuum to obtain compound 2 as a sticky pale yellow oil in a yield of 86.1% (5.05 g).

(3) Synthesis of Compound 3

: Compound 2 (7.95 mmol, 2 g) was added to a 250 mL Schlenk flask, dissolved with 30 mL of THF, and then cooled down to -78 ° C using dry ice / acetone. 2.1 equivalents of n-BuLi (16.7 mmol, 6.7 mL) was added slowly by syringe, then slowly warmed to room temperature and stirred for 2 hours. After 2 hours, the lithium anion solution was rapidly added to the THF slurry of 0.98 equivalents of TiCl ₃ (THF) ₃ (7.79 mmol, 2.88 g) previously lowered to -78 ° C using a cannula. The reaction was slowly warmed to room temperature and stirred for 15 hours. The mixed solution was rapidly added dropwise to a 250 mL Schlenk flask containing 1.1 equivalents of AgCl and further stirred for 1 hour. All solvents were removed under vacuum and extracted with n-hexane. After removing the salt from the mixture with a Celite bed, all the solvent was removed under vacuum to obtain a yellowish brown solid compound 3 in a yield of 56.4% (1.65 g).

NMR spectrum of Compound 3 is shown below (see Fig. 2).

_{^{1 H NMR (CDCl 3, 400.13}} MHz): δ 2.22 (s, 6H, Cp (CH 3) 2), 2.12 (s, 6H, Cp (CH 3) 2), 1.42 (s, 9H, N (CH 3 _{) 3), 0.69 (s,} 6H, Si (CH 3) 3).

Comparative Example  2

Ind ₂ HfCl ₂ represented by the following formula was prepared as Comparative Example 2.

[Ind ₂ HfCl ₂ ]

Example  One

The following compound 7 was synthesized according to Scheme shown in FIG. Hereinafter, synthesis of each compound will be described.

[Compound 7]

(1) Synthesis of Compound 4

: 2,3,4-Trimethylcyclopent-2-enone (16.5 mmol, 2.05 g) was added to a 250 mL Schlenk flask and dissolved in 20 mL of THF. A 0.5 M solution of 4- (N, N-dimethyl) aniline magnesium bromide (15 mmol, 30 mL) was added to another 250 mL Schlenk flask using a syringe and dissolved in 30 mL of THF. Was lowered to -78 ° C using dry ice / acetone of 4- (N, N-dimethyl) aniline magnesium bromide solution. The 2,3,4-Trimethylcyclopent-2-enone solution was slowly added to the 4- (N, N-dimethyl) aniline magnesium bromide solution. After slowly raising the temperature to room temperature and stirring for 15 hours, 60 mL of a saturated aqueous NH ₄ Cl solution was added slowly to terminate the reaction, followed by extraction with diethyl ether three times. The obtained organic layer was washed with MgSO ₄ to remove all of the water and all the solvent was removed under vacuum. After dissolving the extract in 15 mL of dichloromethane, a small amount of p-toluenesulfonic acid (p-TsOH) was added at room temperature and stirred for 1 hour. After completion of the reaction, the mixture was extracted three times with diethyl ether. The obtained organic layer was washed with MgSO ₄ to remove all of the water and all the solvent was removed under vacuum. The product was recrystallized with a minimum of ethanol. The obtained product was filtered and impurities were removed with a small amount of cold n-hexane to obtain a pale pink solid compound 4 in a yield of 77.7% (2.65 g).

The NMR spectrum of Compound 4 is shown below (see Figs. 4 and 5).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.25 (d, 2H, J = 8.84 Hz, Ph), 6.75 (d, 2H, J = 8.88 Hz, Ph), 3.15 (t, 2H, J = _{8.42 Hz, Cp (H 2)} ), 2.95 (s, 6H, N (CH 3) 2), 2.06 (t, 3H, J = 2.1 Hz, Cp (CH 3) 3), 1.98 (s, 3H, Cp _{(CH 3) 3), 1.86} (d, 3H, J = 1.04 Hz, Cp (CH 3) 3).

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 148.34, 137.26, 136.54, 135.85, 133.67, 128.23, 126.96, 112.72 (Ph, Cp), 46.74 (N (CH 3) 2), 40.78 (Cp), 13.49, 13.01, 11.23 (Cp (CH 3) 3).

(2) Synthesis of Compound 5

: Compound 5 was applied in the same manner as the synthesis route of Compound 1. With compound 4 (5.7 mmol, 1.3 g) , 1.1 equiv of n-BuLi (6.3 mmol, 2.5 mL) and _{Me 2 SiCl 2 (14.3 mmol,} 1.7 mL) of 2.5 equivalent, colorless with a yield of 89.4% (1.16 g) Of solid compound 5 was obtained.

NMR spectrum of Compound 5 is shown below (see Fig. 6).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.08 (d, 2H, J = 7.44 Hz, Ph), 6.69 (d, 2H, J = 8.4 Hz, Ph), 3.69 (s, 1H, CpH 2 ), 2.94 (s, 6H, N (CH 3) 2), 2.10 (s, 3H, Cp (CH 3) 3), 2.00 (d, 3H, J = 1.64 Hz, Cp (CH 3) 3), 1.88 (t, 3H, J = 1.1 Hz, Cp (CH 3) 3), 0.11 (s, 6H, Si (CH 3) 2).

(3) Synthesis of Compound 6

: Compound 6 was applied in the same manner as the synthesis route of Compound 2. Using the compound 5 (3.44 mmol, 1.1 g) and 3 equivalents of t-BuNH ₂ (10.3 mmol, 1.1 mL), a viscous pale brown oil compound 6 was obtained in a yield of 99.6% (1.22 g).

NMR spectrum of Compound 6 is shown below (see Figs. 7 and 8).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.11 (m, 2H, Ph), 6.73 (m, 2H, Ph), 3.49 (s, 1H, Cp (H)), 2.93 (s, 6H, _{N (CH 3) 2),} 2.06 (s, 3H, Cp (CH 3) 3), 1.99 (d, 3H, J = 1.52 Hz, Cp (CH 3) 3), 1.87 (s, 3H, Cp (CH _{3) 3), 0.96 (s} , 9H, NC (CH 3) 3), 0.16 (s, 3H, Si (CH 3) 2), -0.31 (s, 3H, Si (CH 3) 2).

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 148.96, 138.28, 135.98, 135.36, 135.22, 130.07, 128.03, 112.66, 49.29 (Ph, Cp), 55.46 (NC), 40.94 (N ( CH ₃ ) ₂ ), 33.67 (NC (CH ₃ ) ₃ ), 15.11, 12.64, 11.34 (Cp (CH ₃ ) ₃ ), 0.49, 0.30 (Si (CH ₃ ) ₂ ).

(4) Synthesis of Compound 7

: Compound 7 was applied in the same manner as the synthesis route of Compound 3. To a solution of compound 6 (3.08 mmol, 1.1 g), 2.1 eq. Of n-BuLi (3.4 mmol, 1.4 mL), 0.98 eq. TiCl ₃ (THF) ₃ (3.02 mmol, 1.12 g) and 1.1 eq. g), a reddish brown solid compound 7 was obtained in a yield of 71.4% (0.962 g).

NMR spectrum of Compound 7 is shown below (see Figs. 9 and 10).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.10 (m, 2H, Ph), 6.73 (m, 2H, Ph), 2.93 (s, 6H, N (CH 3) 2), 2.05 (s, _{3H, Cp (CH 3) 3} ), 1.99 (d, 3H, J = 1.48 Hz, Cp (CH 3) 3), 1.87 (s, 3H, Cp (CH 3) 3), 0.95 (s, 9H, NC _{(CH 3) 3), 0.16} (s, 3H, Si (CH 3) 2), -0.31 (s, 3H, Si (CH 3) 2).

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 148.78, 138.12, 135.22, 135.08, 129.92, 127.88, 112.51 (Ph, Cp), 55.33 (NC), 40.78 (N (CH 3) 2 _{), 33.52 (NC (CH 3} ) 3), 11.18, 12.45, 14.95 (Cp (CH 3) 3), 0.14, 0.34 (Si (CH 3) 2).

Example  2

The following compound 11 was synthesized according to Scheme shown in FIG. Hereinafter, synthesis of each compound will be described.

[Compound 11]

(1) Synthesis of Compound 8

: Compound 8 was synthesized in the same manner as in the synthesis route of Compound 4. A white solid compound 8 was obtained in a yield of 83.7% (3.2 g) using 2,3,4-Trimethylcyclopent-2-enone (16.5 mmol, 2.05 g) and 4-methoxyphenyl magnesium bromide solution (15 mmol, 30 mL) .

NMR spectrum of Compound 8 is shown below (see Figs. 12 and 13).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.23 (m, 2H, PhH 2), 6.86 (m, 2H, PhH 2), 3.80 (s, 3H, PhOCH 3), 3.13 (t, 2H, _{J = 1.80 Hz, CpH 2)} , 2.02 (t, 3H, J = 1.72 Hz, Cp (CH 3)), 1.96 (s, 3H, Cp (CH 3)), 1.84 (d, 3H, J = 1.00 Hz , Cp (CH _3)).

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 157.50, 137.67, 137.23, 135.42, 134.33, 130.92, 128.52, 113.70 (Ph, Cp), 55.26 (PhOCH 3), 46.90 (Cp), 13.50, 12.98, 11.23 (Cp ( CH 3) 3).

(2) Synthesis of Compound 9

: Compound 9 was applied in the same manner as the synthesis route of Compound 1. (1.34 g) using compound 8 (4.66 mmol, 1.0 g), 1.1 eq of n-BuLi (5.1 mmol, 2.1 mL) and 2.5 equivalents of Me ₂ SiCl ₂ (11.6 mmol, 1.4 mL) Brown oil compound 9 was obtained.

NMR spectrum of Compound 9 is shown below (see Fig. 14).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.11 (m, 2H, Ph), 6.85 (m, 2H, Ph), 3.80 (s, 3H, PhOCH 3), 3.69 (s, 1H, CpH) , 2.11 (s, 3H, Cp (CH 3)), 2.18 (d, 3H, J = 1.60 Hz, Cp (CH 3)), 1.89 (s, 3H, Cp (CH 3)), 0.10 (s, 3H _{, Si (CH 3)),} 0.13 (s, 3H, Si (CH 3)).

(3) Synthesis of Compound 10

: Compound 10 was applied in the same manner as the synthesis route of Compound 2. Using the compound 9 (4.33 mmol, 1.33 g) and 3 equivalents of t-BuNH ₂ (13.0 mmol, 1.4 mL), a viscous pale yellow oily compound 10 was obtained in a yield of 92.0% (1.37 g).

NMR spectrum of Compound 10 is shown below (see Figs. 15 and 16).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.10 (m, 2H, Ph), 6.85 (m, 2H, Ph), 3.80 (s, 3H, PhOCH 3), 3.49 (s, 1H, CpH) , 2.05 (s, 3H, Cp (CH 3)), 1.97 (d, 3H, J = 1.56 Hz, Cp (CH 3)), 1.89 (s, 3H, Cp (CH 3)), 0.95 (s, 9H _{, NC (CH 3) 3)} , 0.21 (s, 3H, Si (CH 3)), 0.33 (s, 3H, Si (CH 3)).

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 157.68, 137.54, 136.08, 135.88, 135.79, 131.88, 130.21, 113.48 (Ph, Cp), 55.56 (NC), 55.28 (PhOCH 3), 49.18 (Cp), 33.53 (NC (CH 3) 3), 14.97, 12.46, 11.17 (Cp (CH 3) 3), 0.59, 0.01 (Si (CH 3) 2).

(4) Synthesis of Compound 11

: Compound 11 was synthesized in the same manner as the synthesis route of Compound 3. To a solution of compound 10 (3.78 mmol, 1.3 g), 2.1 eq. Of n-BuLi (7.94 mmol, 3.2 mL), 0.98 equivalents of TiCl ₃ (thf) 3 (3.7 mmol, 1.37 g) and 1.1 equivalents of AgCl g) to obtain a dark red solid compound 11 in a yield of 68.4% (1.05 g).

NMR spectrum of Compound 11 is shown below (see Figs. 17 and 18).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 6.81 (m, 4H, Ph), 3.80 (s, 3H, PhOCH 3), 2.26 (s, 3H, Cp (CH 3)), 2.20 (s, _{3H, Cp (CH 3))} , 2.13 (s, 3H, Cp (CH 3)), 1.35 (s, 9H, NC (CH 3) 3), 0.60 (s, 3H, Si (CH 3)), 0.16 (s, 3H, Si (CH 3)).

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 159.46, 147.97, 142.10, 137.73, 137.07, 127.61, 113.03, 104.57 (Ph, Cp), 63.00 (NC), 55.19 (PhOCH 3), _{32.59 (NC (CH 3) 3} ), 16.17, 13.30, 13.29 (Cp (CH 3) 3), 4.90, 4.07 (Si (CH 3) 2).

Example  3

The following compound 15 was synthesized according to Scheme shown in Fig. Hereinafter, synthesis of each compound will be described.

[Compound 15]

(1) Synthesis of Compound 12

2,3,4-trimethylcyclopent-2-enone (6.18 mmol, 0.767 g) was added to a 250 mL Schlenk flask and dissolved in 20 mL of THF. In another 250 mL Schlenk flask, a 0.5 M solution of 4-thioanisolemagnesium bromide (5.88 mmol, 11.8 mL) was added using a syringe and dissolved in THF (30 mL). 4-thioanisolemagnesium bromide solution to -78 < 0 > C using dry ice / acetone. The 2,3,4-trimethylcyclopent-2-enone solution was slowly added to the 4-thioanisolemagnesium bromide solution. After slowly raising the temperature to room temperature and stirring for 15 hours, 30 mL of a saturated aqueous NH ₄ Cl solution was added slowly to terminate the reaction, followed by three extractions with diethyl ether. The obtained organic layer was washed with MgSO ₄ to remove all of the water and all the solvent was removed under vacuum. After dissolving the extract in 15 mL of dichloromethane, a small amount of p-toluenesulfonic acid (p-TsOH) was added at room temperature and stirred for 1 hour. After completion of the reaction, the mixture was extracted three times with diethyl ether. The obtained organic layer was washed with MgSO ₄ to remove all of the water and all the solvent was removed under vacuum. The product was washed with a small amount of cold methanol to remove impurities, and Compound 12, which was a pale-orange solid at a yield of 92.9% (1.26 g), was obtained.

The NMR spectrum of Compound 12 is shown below (see Figs. 20 and 21).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.23 (q, 4H, J = 2.97 Hz, Ph), 3.14 (q, 2H, J = 1.72 Hz, Cp (H 2)), 2.47 (s, 3H, SMe), 2.04 (t , 3H, J = 1.88 Hz, Cp (CH 3) 3), 1.97 (s, 3H, Cp (CH 3) 3), 1.84 (d, 3H, J = 1.12 Hz, Cp (CH _{3) 3).}

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 139.11, 137.38, 135.21, 135.14, 135.12, 134.82, 127.82, 126.9 (Ph, Cp), 46.66 (Cp), 16.21 (SMe), 11.19 , 13.14, 13.54 (Cp (CH 3) 3).

(2) Synthesis of Compound 13

Compound 12 (2.24 mmol, 0.517 g) was added to a 250 mL Schlenk flask, which was then dissolved in 30 mL of THF and then cooled to -78 ° C using dry ice / acetone. 1.1 eq. Of nuLi (2.46 mmol, 1 mL) was added slowly by syringe, then slowly warmed to room temperature and stirred for 2 hours. After the lithium anion solution was cooled to -78 ° C, 2.5 equivalents of Me ₂ SiCl ₂ (5.6 mmol, 0.68 mL) was slowly added thereto by using a syringe, then slowly raised to room temperature and stirred for 15 hours. Remove all solvents under vacuum and extract with n-hexane. After removing the salt from the mixture with a Celite bed, all the solvent was removed under vacuum to obtain a yellow solid compound 13 in a yield of 99.5% (0.72 g).

NMR spectrum of Compound 13 is shown below (see Figs. 22 and 23).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.21 (m, 2H, Ph), 7.12 (m, 2H, Ph), 3.73 (s, 1H, Cp (H)), 2.48 (s, 3H, SMe), 2.12 (s, 3H , Cp (CH 3) 3), 2.02 (d, 3H, J = 1.68 Hz, Cp (CH 3) 3), 1.9 (s, 3H, Cp (CH 3) 3), -0.085, (s, 3H, Si (CH 3) 2), -0.094 (s, 3H, Si (CH 3) 2)).

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 139.6, 137.89, 136.09, 135.89, 134.68, 134.52, 129.38, 126.48 (Ph, Cp), 54.84 (Cp), 15.97 (Cp (CH 3 _{) 3), 14.71 (SMe)} , 11.21, 12.77 (Cp (CH 3) 3), 2.87 (Si (CH 3) 2), -2.33 (Si (CH 3) 2).

(3) Synthesis of Compound 14

Compound 13 (2.27 mmol, 0.735 g) was added to a 250 mL Schlenk flask, which was then dissolved in 30 mL of THF and then cooled to -78 ° C using dry ice / acetone. Three equivalents of t-BuNH ₂ (6.81 mmol, 0.72 mL) was slowly added thereto using a syringe, and the temperature was gradually raised to room temperature, followed by stirring for 15 hours. All solvents were removed under vacuum and extracted with n-hexane. After removing the salt from the mixture with a Celite bed, all the solvent was removed under vacuum to obtain compound 14 as a sticky yellow oil in a yield of 82.9% (0.672 g).

NMR spectrum of Compound 14 is shown below (see FIGS. 24 and 25).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.23 (m, 2H, Ph), 7.14 (m, 2H, Ph), 3.53 (s, 1H, Cp (H)), 2.48 (s, 3H, SMe), 2.08 (s, 3H , Cp (CH 3) 3), 2.01 (d, 3H, J = 1.6 Hz, Cp (CH 3) 3), 1.89 (s, 3H, Cp (CH 3) 3), 0.98 (s, 9H, NC ( CH 3) 3), 0.4 (s, 1H, NH), -0.19 (s, 3H, Si (CH 3) 2), -0.29 (s, 3H, Si (CH 3) ₂ ).

¹³ C ( ¹ H) NMR (CDCl ₃ , 100.61 MHz, ppm):? 137.25, 136.96,136.69,136.88,135.81,134.96,129.55,126.72 (Ph, Cp), 55.47 _{, 33.48 (N (CH 3)} 2), 16.29 Cp (CH 3) 3), 14.98 (SMe), 11.1, 12.52 (Cp (CH 3) 3), -0.069, 0.7 (Si (CH 3) 2).

(4) Synthesis of compound 15

Compound 14 (1.74 mmol, 0.628 g) was added to a 250 mL Schlenk flask, dissolved in 30 mL of THF, and then cooled down to -78 ° C using dry ice / acetone. 2.1 equivalents of n-BuLi (3.65 mmol, 1.46 mL) was slowly added by syringe, then slowly warmed to room temperature and stirred for 2 hours. After 2 hours, the lithium anion solution was quickly added to the THF slurry of 0.98 equivalents of TiCl ₃ (THF) ₃ (1.71 mmol, 0.632 g) previously lowered to -78 ° C using a cannula. The reaction was slowly warmed to room temperature and stirred for 15 hours. The mixed solution was rapidly added dropwise to a 250 mL Schlenk flask containing 1.1 equivalents of AgCl (1.91 mmol, 0.274 g), and the mixture was further stirred for 1 hour. Remove all solvents under vacuum and extract with n-hexane. After removing the salt from the mixture with a Celite bed, all the solvent was removed under vacuum to obtain a dark red crystalline solid compound 15 in a yield of 84.1% (0.683 g).

The NMR spectrum of Compound 15 is shown below (see Figs. 26 and 27).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.16 (d, 2H, J = 6.36 Hz, Ph), 2.48 (s, 3H, SMe), 2.27 (s, 3H, Cp (CH 3) 3) , 2.21 (s, 3H, Cp (CH 3) 3), 2.13 (s, 3H, Cp (CH 3) 3), 1.36 (s, 9H, NC (CH 3) 3), 0.63 (s, 3H, Si _{(CH 3) 2), -0.14} (s, 3H, Si (CH 3) 2).

^{13 C {1 H} NMR (} CDCl 3, 100.61 MHz, ppm): δ 147.23, 142.35, 138.84, 137.69, 137.1, 131.87, 125.24, 104.39 (Ph, Cp), 63.06 (NC), 32.56 (NC (CH 3 _{) 2), 16.71 (SMe)} , 13.24, 13.26, 15.37 (Cp (CH 3) 3), 4.21, 4.87 (Si (CH 3) 2).

Example  4

The following compound 19 was synthesized according to Scheme shown in Fig. Hereinafter, synthesis of each compound will be described.

[Compound 19]

(1) Synthesis of Compound (16)

Compound 16 was obtained by the same method as the synthesis route of compound 12. Compound 2 (16.4 mmol, 2.05 g) and 4-fluorophenylmagnesium bromide (15 mmol, 15 mL) were used in the yield of 80.4% (2.46 g) as a pale yellow solid ≪ / RTI >

The NMR spectrum of Compound 16 is shown below (see FIGS. 29, 30 and 31).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.25 (m, 2H, Ph), 6.97 (m, 2H, Ph), 3.13 (t, 2H, J = 1.64 Hz, Cp (H 2)), 2.02 (s, 3H, Cp ( CH 3) 3), 1.97 (s, 3H, Cp (CH 3) 3), 1.85 (d, 3H, J = 0.8 Hz, Cp (CH 3) 3).

¹³ C ( ¹ H) NMR (CDCl ₃ , 100.61 MHz, ppm): δ 162.14, 159.7, 138.87, 138.86, 137.23, 135, 134.74, 134.2, 134.17, 128.86, 128.78, , 46.91 (Cp), 11.18, 12.95, 13.48 (Cp (CH 3) 3).

_{^{19 F NMR (CDCl 3, 376.5}} MHz, ppm): δ -117.49.

(2) Synthesis of Compound 17

Compound 17 was obtained by the same method as the synthesis route of Compound 13. To yield compound 16 (3.27 mmol, 0.661 g) , 1.1 equiv of n-BuLi (3.59 mmol, 1.44 mL) and 2.5 eq. Of _{Me 2 SiCl 2 94.7% (0.913} g) using a (8.18 mmol, 1.0 mL) Compound 17 as a pale brown oil was obtained.

The NMR spectrum of Compound 17 is shown below (see FIGS. 32, 33 and 34).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.18 (m, 2H, Ph), 7.03 (m, 2H, Ph), 3.73 (s, 1H, Cp (H)), 2.16 (s, 3H, _{Cp (CH 3) 3),} 2.04 (s, 3H, Cp (CH 3) 3), 1.94 (s, 3H, Cp (CH 3) 3), -0.03, (s, 3H, Si (CH 3) 2 ), -0.076 (s, 3H, Si (CH 3) 2).

¹³ C ( ¹ H) NMR (CDCl ₃ , 100.61 MHz, ppm): δ 162.32, 160.37, 139.49, 137.77, 135.92, 134.05, 133.86, 130.41, 130.35, 115.14, 114.97 (Ph, Cp), 55.04 11.13, 12.57, 14.6 (Cp ( CH 3) 3), 2.53 (Si (CH 3) 2), -2.19 (Si (CH 3) 2).

_{^{19 F NMR (CDCl 3, 376.5}} MHz, ppm): δ -117.39.

(3) Synthesis of compound 18

Compound 18 was obtained by the same method as the synthesis route of Compound 14. Compound 17 (3.04 mmol, 0.896 g) and 3 equivalents of t-BuNH ₂ (9.12 mmol, 0.96 mL) were used to obtain compound 18 as a brown oil in a yield of 98.3% (0.987 g).

The NMR spectrum of compound 18 is shown below (see Figs. 35, 36 and 37).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.17 (m, 2H, Ph), 7.02 (m, 2H, Ph), 3.52 (s, 1H, Cp (H)), 2.1 (s, 3H, _{Cp (CH 3) 3),} 2.0 (s, 3H, Cp (CH 3) 3), 1.91 (s, 3H, Cp (CH 3) 3), 1.01 (s, 9H, NC (CH 3) 3), 0.29 (s, 1H, NH) , -0.19, (s, 3H, Si (CH 3) 2), -0.27 (s, 3H, Si (CH 3) 2).

¹³ C { ¹ H} NMR (CDCl ₃ , 100.61 MHz, ppm): δ 162.15, 160.2, 136.99, 136.85, 136.7, 135.77, 135.33, 135.3, 130.57, 130.51, 114.93, 114.76 (Ph, Cp), 55.79 ), 49.23 (Cp), 33.57 (NC (CH 3) 3), 11.14, 12.46, 15 (Cp (CH 3) 3), 0.85 (Si (CH 3) 2), -0.082 (Si (CH 3) 2 ).

_{^{19 F NMR (CDCl 3, 376.5}} MHz, ppm): δ -116.14.

(4) Synthesis of Compound 19

Compound 19 was obtained by the same method as the synthesis route of Compound 15. To a solution of compound 18 (2.96 mmol, 0.978 g), 2.1 eq. Of n-BuLi (6.22 mmol, 2.5 mL), 0.98 eq TiCl ₃ (THF) ₃ (2.9 mmol, 1.07 g) and 1.1 eq. 0.466 g) to give compound 19 as a yellowish brown solid in a yield of 87.4% (1.16 g).

The NMR spectrum of Compound 19 is shown below (Figs. 38, 39 and 40).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 6.98 (m, 4H, Ph), 2.27 (s, 3H, Cp (CH 3) 3), 2.21 (s, 3H, Cp (CH 3) 3) , 2.12 (s, 3H, Cp (CH 3) 3), 1.36 (s, 9H, NC (CH 3) 3), 0.64 (s, 3H, Si (CH 3) 2), -0.18 (s, 3H, Si (CH _{3) 2).}

¹³ C { ¹ H} NMR (CDCl ₃ , 100.61 MHz, ppm): δ 163.63, 161.65, 146.47, 142.42, 137.64, 137.27, 131.29, 131.27, 114.78, 114.61, 104.53 (Ph, Cp), 63.13 _{), 32.54 (NC (CH 3} ) 3), 13.23, 16.71 (Cp (CH 3) 3), 3.98, 4.83 (Si (CH 3) 2).

¹⁹ F NMR (CDCl ₃ , 376.5 MHz, ppm): 隆 -113.55.

Example  5

The following compound 23 was synthesized according to Scheme shown in Fig. Hereinafter, synthesis of each compound will be described.

[Compound 23]

(1) Synthesis of Compound 20

Compound 20 was obtained by the same method as the synthesis route of Compound 12. (2.65 g) was obtained in a yield of 92.9% (23.5 mmol) using 2,3-trimethylcyclopent-2-enone (16.5 mmol, 2.05 g) and 2-thienylmagnesium bromide solution ≪ / RTI >

The NMR spectrum of Compound 20 is shown below (see FIGS. 42 and 43).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.13 (q, 1H, J = 2.07 Hz, Th), 6.99 (q, 1H, J = 2.91 Hz, Th), 6.95 (q, 1H, J = 1.45 Hz, Th), 3.22 ( q, 2H, J = 1.71 Hz, Cp (H 2)), 2.12 (t, 3H, J = 1.76 Hz, Cp (CH 3) 3), 1.97 (s, 3H, Cp _{(CH 3) 3), 1.84} (q, 3H, J = 1.49 Hz, Cp (CH 3) 3).

¹³ C ( ¹ H) NMR (CDCl ₃ , 100.61 MHz, ppm):? 141.27,139.01,137.35,134.45,129.62,127.01,122.28,121.11,46.91 (Ph, Cp), 13.55,13.29,11.14 ₃ ) ₃ ).

(2) Synthesis of Compound 21

Compound 21 was obtained by the same method as the synthesis route of Compound 13. Using 2.20 g (10.0 mmol, 1.9 g), 1.1 equivalents of n-BuLi (11.0 mmol, 4.4 mL) and 2.5 equivalents of Me ₂ SiCl ₂ (25.0 mmol, 3.0 mL) Compound 21 as an orange oil was obtained.

The NMR spectrum of Compound 21 is shown below (see Figs. 44 and 45).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.21 (q, 1H, J = 1.65 Hz, Th), 7.01 (q, 1H, J = 2.64 Hz, Th), 6.84 (t, 1H, J = 1.38 Hz, Th), 3.7 ( s, 1H, Cp (H)), 2.14 (s, 3H, Cp (CH 3) 3), 2.12 (s, 3H, Cp (CH 3) 3), 1.91 (s, _{3H, Cp (CH 3) 3} ), 0.059, (s, 3H, Si (CH 3) 2), -0.056 (s, 3H, Si (CH 3) 2).

¹³ C { ¹ H} NMR (CDCl ₃ , 100.61 MHz, ppm): δ 140.29, 140.17, 137.93, 136.62, 128.22, 127.03, 124.82, 123.87, 56.21 (Ph, Cp), 14.68, 12.84, ₃ ) ₃ , 2.4 (Si (CH ₃ ) ₂ ), and -2.53 (Si (CH ₃ ) ₂ ).

(3) Synthesis of Compound 22

Compound 22 was obtained by the same method as the synthesis route of Compound 14. Compound 22 (6.0 mmol, 1.7 g) and 3 equivalents of t-BuNH ₂ (18.0 mmol, 1.9 mL) were used in the yield of 92.9% (1.78 g) as a viscous pale orange oil.

The NMR spectrum of Compound 22 is shown below (see Figs. 46 and 47).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.18 (d, 1H, J = 3.32 Hz, Th), 7.01 (q, 1H, J = 2.29 Hz, Th), 6.82 (s, br, 1H, Th), 3.51 (s, 1H , Cp (H)), 2.11 (s, 3H, Cp (CH 3) 3), 2.09 (s, 3H, Cp (CH 3) 3), 1.9 (s, 3H, Cp _{(CH 3) 3), 1.07} (s, 9H, NC (CH 3) 3), -0.16, (s, 3H, Si (CH 3) 2), -0.19 (s, 3H, Si (CH 3) 2 ).

¹³ C ( ¹ H) NMR (CDCl ₃ , 100.61 MHz, ppm): δ 141.86, 138.01, 137.44, 135.94, 130.81, 126.89, 124.33, 123.24 (Ph, Cp), 57.11 _{(NC (CH 3) 3)} , 15.05, 12.76, 11.1 (Cp (CH 3) 3), 0.7 (Si (CH 3) 2), -0.56 (Si (CH 3) 2).

(4) Synthesis of Compound 23

Compound 23 was obtained by the same method as the synthesis route of Compound 15. To a solution of compound 22 (5.0 mmol, 1.6 g), 2.1 eq. Of n-BuLi (10.5 mmol, 4.2 mL), 0.98 equivalents of TiCl ₃ (THF) ₃ (4.9 mmol, 1.82 g) and 1.1 equiv. 0.772 g) was used to obtain Compound 23, which was a solid of deep red crystals in a yield of 69.4% (1.51 g).

The NMR spectrum of Compound 23 is shown below (see FIGS. 48 and 49).

_{^{1 H NMR (CDCl 3, 400.13}} MHz, ppm): δ 7.16 (d, 1H, J = 3.4 Hz, Th), 6.98 (q, 1H, J = 2.31 Hz, Th), 6.78 (d, 1H, J = 2.08 Hz, Th), 2.07 ( s, 3H, Cp (CH 3) 3), 2.05 (s, 3H, Cp (CH 3) 3), 1.86 (s, 3H, Cp (CH 3) 3), 1.03 ( _{s, 9H, NC (CH 3} ) 3), -0.21 (s, 3H, Si (CH 3) 2), -0.23 (s, 3H, Si (CH 3) 2).

^{13 C {1H} NMR (CDCl} 3, 100.61 MHz, ppm): δ 141.73, 137.88, 137.33, 135.82, 130.72, 126.8, 124.22, 123.14 (Ph, Cp), 57 (NC), 33.54 (NC (CH 3) _{3), 14.97, 12.68, 11.02} (Cp (CH 3) 3), 0.61, -0.68 (Si (CH 3) 2).

Test Example

Ethylene / 1-octene copolymerization and ethylene / 1-hexane copolymerization were carried out using each of the final compounds according to the Comparative Examples and Examples as catalysts.

Specifically, an appropriate amount of s-MAO was prepared in a 250 mL Schlenk flask and purified toluene (49.5 mL) was introduced through a cannula. The mixture was stirred at a polymerization temperature for a certain period of time, an appropriate amount of 1-octene (or 1-hexene) was added dropwise, and the ethylene monomer was saturated at 1 bar for about 3 minutes. After 3 minutes of ethylene monomer saturation, the reaction was initiated by adding a proper amount of catalyst dissolved in 0.5 mL of toluene. As the reaction progressed, the viscosity of the solution increased, and about 2 mL of the prepared 10% HCl / MeOH solution was added to the syringe to terminate the reaction. The mixture was poured into a 10% HCl / MeOH solution. The obtained polymer was subjected to paper filtration and washed several times with MeOH. The filtered polymer was dried in a vacuum oven at about 60 DEG C for at least 10 hours to obtain a final copolymer.

The measurement results of the physical properties of the copolymer according to the respective steps are shown in Tables 1 and 2 below.

(1) Ethylene / 1-octene copolymerization

Catalyst ^a Comparative Example
One Comparative Example
2 Example
One Example
2 Example
3 Example
4 Example
5 Yield (g) 1.23 1.06 1.88 0.20 0.64 2.79 1.74 Activity
(kg / mol * h) 4920 4240 1500 160 510 2230 1370 Comonomer
contents
(mol%) ^b 12.7 4.45 11.2 17.9 20.9 12.1 12.4 Mw (GPC) ^c 150,000 120,400 325,400 187,000 45,000 177,703 334,000 PDI ^c 2.8 2.8 9.1 22.9 2.82 3.28 4.36

^a Copolymerization condition: [Cat] = 1 μmol (Comparative Example 1, Comparative Example 2); [Cat] = 5 占 퐉 ol (Examples 1 to 5); [MAO] / [Cat] = 2000; toluene = 50 mL; Time = 15 min; Temp. = 75 DEG C; Induction period = 45 min (Examples 1 and 2), 15 min (Examples 3 to 5)

^b Determined by ¹ H NMR

^c Obtained by GPC analysis and calibrated by polystyrene standard

The polymer obtained by the catalyst of Comparative Example 1 (1 μmol) was in the form of a transparent solid having elasticity, and the yield was 1.23 g and the activity was 4920 (kg / molh) over a polymerization time of 3 minutes. The mole fraction was obtained as 12.7%. The polymer obtained in Comparative Example 2 (1 μmol) as a catalyst was obtained as a colorless solid in powder form. The yield was 1.06 g and the activity was 4240 (kg / mol). As can be seen from the obtained polymer, % Of 1-octene mole fraction.

On the other hand, the polymer obtained in Example 1 (5 μmol) was obtained in the form of a colorless tear rubber. The yield was 1.88 g, the activity was 1500 kg / molh and the molar fraction of 1-octene was 11.2% lost. The polymer obtained in Example 2 (5 μmol) as a catalyst was obtained as a colorless solid in the form of powder, the yield was 0.2 g, the activity was 160 kg / molh and the mole fraction of 1-octene was 17.9% lost.

Comparative Example 1 and Comparative Example 2 exhibited a relatively low 1-octene molar fraction or molecular weight as compared with Example 1 or Example 2, although they exhibited relatively high activity. In particular, it was confirmed that Comparative Example 2 is not a suitable catalyst system in the copolymerization of ethylene / 1-octene. In addition, the activity of Example 1 or Example 2 was relatively low, but it was confirmed that a copolymer having a high mole fraction of 1-octene or a molecular weight could be obtained, and thus it could be used as a catalyst system for ethylene / 1-octene copolymerization.

Particularly, in the polymerization process using the catalysts of Examples 1 and 2, a copolymer having a molecular weight distribution that is at least three times and at least seven times greater than that of the catalysts of Comparative Example 1 and Comparative Example 2 is obtained there was.

Further, when the catalyst of Example 1 was used, a copolymer having a large weight average molecular weight could be obtained. In particular, the catalyst of Example 2 has improved comonomer incorporation ability as compared with other compounds, and the copolymer obtained using the same has a high weight average molecular weight and a significantly higher comonomer content.

(2) Ethylene / 1-hexene copolymerization

Catalyst ^a Comparative Example
One Example
One Example
2 Example
3 Example
4 Example
5 Yield (g) 0.94 0.34 0.18 0.83 1.19 0.57 Activity
(kg / mol * h) 3800 280 140 660 950 230 Comonomer
contents
(mol%) ^b 17.5 14.8 14.5 19.3 22.1 34.5 Mw (GPC) ^c 157,000 119,000 215,000 60,000 60,433 109,000 PDI ^c 2.4 14.7 19.8 3.67 2.72 5.58

^a Copolymerization condition: [Cat] = 1 μmol (Comparative Example 1); [Cat] = 5 占 퐉 ol (Examples 1 to 5); [MAO] / [Cat] = 2000; toluene = 50 mL; Time = 15 min; Temp. = 75 DEG C; Induction period = 45 min (Examples 1 and 2), 15 min (Examples 3 to 5)

^b Determined by ¹ H NMR

^c Obtained by GPC analysis and calibrated by polystyrene standard

As can be seen from Table 2, the catalysts of Examples 4 and 5 showed relatively high 1-hexene mole fractions. In addition, the catalyst of Example 4 showed 2-4 times higher activity than the catalyst of the other Examples. It was confirmed that although the catalysts of Examples 4 and 5 have relatively higher silver activity than the catalyst of Comparative Example 1, higher copolymers of 1-hexene mole fractions were obtained.

Claims (9)

1. A catalyst for olefin polymerization comprising a transition metal compound represented by the following formula
[Chemical Formula 1]

In Formula 1,
M is a Group 4 transition metal;
Q ¹ and Q ² are each independently selected from the group consisting of halogen, alkyl of 1 to 20 carbon atoms, alkenyl of 2 to 10 carbon atoms, alkylaryl of 7 to 40 carbon atoms, arylalkyl of 7 to 40 carbon atoms, allyl of 6 to 20 carbon atoms, Alkylidene of 1 to 20 carbon atoms, alkylalkoxy of 2 to 20 carbon atoms, or arylalkoxy of 7 to 40 carbon atoms;
R ¹ , R ² and R ³ are each independently selected from the group consisting of hydrogen, alkyl of 1 to 20 carbon atoms, alkoxy of 1 to 10 carbon atoms, aryl of 6 to 20 carbon atoms, aryloxy of 6 to 10 carbon atoms, , Alkylaryl having 7 to 40 carbon atoms, arylalkyl having 7 to 40 carbon atoms, arylalkenyl having 8 to 40 carbon atoms, or alkynyl having 2 to 10 carbon atoms; R ¹ and R ² or R ² and R ³ may be connected to each other to form a ring;
A is any one substituent selected from the group consisting of a group represented by the following formula (2), provided that the symbol "*" in the following formula (2) is a linkage of A and a cyclopentadienyl ligand.
(2)

The method according to claim 1,
M is titanium (Ti), zirconium (Zr) or hafnium (Hf);
The Q ¹ and Q ² Are each independently methyl or chlorine;
Wherein R ¹ , R ² and R ³ are each independently hydrogen or methyl.
The method according to claim 1,
A catalyst for olefin polymerization further comprising at least one promoter compound selected from the group consisting of the following chemical formulas (3), (4) and (5)
(3)
- [Al (R ³¹ ) -O] _a -
In Formula 3,
R ³¹ is each independently a hydrogen, a halogen radical, a hydrocarbyl radical having 1 to 20 carbon atoms or a hydrocarbyl radical having 1 to 20 carbon atoms substituted with halogen;
a is an integer of 2 or more;
[Chemical Formula 4]
D (R < ^{41 >} ) ₃
In Formula 4,
D is aluminum or boron;
R ⁴¹ is each independently a halogen radical, a hydrocarbyl radical having 1 to 20 carbon atoms or a hydrocarbyl radical having 1 to 20 carbon atoms substituted with halogen.
[Chemical Formula 5]
^{[LH] + [Z (A} ) 4] - or ^{[L] + [Z (A} ) 4] -
In Formula 5,
L is a neutral or cationic Lewis base;
[LH] ⁺ or [L] ⁺ is a Bronsted acid;
H is a hydrogen atom;
Z is a Group 13 element;
A is independently selected from the group consisting of a hydrogen atom, a halogen atom, a hydrocarbyl group having 1 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms, an aryloxy group having 6 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, Alkyl radical.
The method of claim 3,
R ³¹ in Formula 3 is methyl, ethyl, n-butyl or isobutyl;
D in the formula 4 is aluminum, R ⁴¹ is methyl or isobutyl; Or D is boron and R < ⁴¹ > is pentafluorophenyl;
[LH] ⁺ in the above formula (5) is a dimethylanilinium cation; [Z (A) ₄ ] ^- is [B (C ₆ F ₅ ) ₄ ] ^- ; [L] ⁺ is a catalyst for the polymerization of [(C ₆ H ₅ ) ₃ C] ⁺ .
The method according to claim 1,
Wherein the content of the co-catalyst compound is 1: 1 to 1: 100,000 based on the molar ratio of the metal contained in the co-catalyst compound to one mole of the transition metal contained in the transition metal compound represented by the formula (1).
The method according to claim 1,
A catalyst for olefin polymerization, further comprising an inert carrier on which the transition metal compound represented by Formula (1) is supported.
A process for producing a polyolefin comprising polymerizing at least one olefin-based monomer in the presence of the catalyst according to claim 1.
8. The method of claim 7,
The olefinic monomer may be an α-olefin having 2 to 20 carbon atoms, a diolefin having 1 to 20 carbon atoms, a cyclo-olefin having 3 to 20 carbon atoms, Olefins. ≪ RTI ID = 0.0 > 21. < / RTI >
8. The method of claim 7,
Wherein the polyolefin has a weight average molecular weight (Mw) of 40,000 to 1,000,000 and a molecular weight distribution (Mw / Mn) of 2 to 30.

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