TW201811846A - Cyclic olefin-based copolymer and method of preparing the same - Google Patents

Abstract

The present invention relates to a cyclic olefin-based copolymer and a process for preparing the same. More specifically, the present invention relates to a cyclic olefin-based copolymer containing three repeating units having a specific functional group in a predetermined ratio, and the above copolymer exhibits low dielectric characteristics and thus can be applied to a semiconductor substrate, a printed circuit board, and the like.

Description

Cyclic olefin polymer and preparation method thereof

Korean Patent Application No. 10-2016-0097090, filed on July 29, 2016, and Korean Patent Application No. 10-2017-0090791, filed on July 18, 2017 The disclosure is hereby incorporated by reference in its entirety.

The present invention relates to a cyclic olefin copolymer having a lower dielectric character and a process for the preparation thereof.

Due to the current increase in demand for high performance electronic devices, higher frequencies are required in the field of using semiconductor substrates and printed circuit boards. Since the transmission loss of the electrical signal in the high frequency region is proportional to the dielectric loss and frequency, the transmission loss increases toward the higher frequency region, which adversely affects the performance, durability, and manufacturing yield of the electronic device. Therefore, reducing these shortcomings requires the development of materials with lower dielectric constants and lower dielectric loss (lower dielectric loss factor) characteristics.

In the field of conventional communication and networking, polyphenylene ether is also used as a lower dielectric material, but there is a problem of maneuverability due to breakage of the prepreg, and heat resistance is still insufficient.

Therefore, there is still a need to develop materials having lower dielectric constants and lower dielectric loss characteristics while having sufficient mechanical properties.

[technical problem]

It is an object of the present invention to provide a cyclic olefin copolymer having lower dielectric characteristics such as lower dielectric constant and lower dielectric loss.

Another object of the present invention is to provide a process for preparing a cyclic olefin copolymer.

[Technical Solutions]

One embodiment of the present invention provides a cyclic olefin copolymer comprising a repeating unit represented by the following Chemical Formula 1, a repeating unit represented by the following Chemical Formula 2, and a repeating unit represented by the following Chemical Formula 3, wherein the chemical formula 1 represents The repeating unit is contained in an amount of 15 mol% to 60 mol% based on the total amount of all the repeating units of the chemical formula 1 to the chemical formula 3.

Another embodiment of the present invention provides a process for producing a cyclic olefin copolymer, comprising the steps of: allowing a monomer represented by the following Chemical Formula 4 and a monomer represented by the following Chemical Formula 5 to contain a Group 10 transition metal; The precatalyst, an anionic cocatalyst coordinated to the metal of the precatalyst, and a ligand containing a Group 15 element are polymerized; and the polymer is reacted with a peroxyacid to perform epoxidation.

The cyclic olefin copolymer according to a specific embodiment of the present invention and a method for producing the same will be described in more detail below.

According to an embodiment of the present invention, there is provided a cyclic olefin copolymer comprising a repeating unit represented by the following Chemical Formula 1, a repeating unit represented by the following Chemical Formula 2, and a repeating unit represented by the following Chemical Formula 3, wherein The repeating unit represented by Chemical Formula 1 is contained in an amount of from 15 mol% to 60 mol% based on the total amount of all the repeating units of Chemical Formulas 1 to 3. [Chemical Formula 1] In the above formula 1, p is an integer of 0 to 4, and R ₁ to R ₄ are each independently hydrogen or an epoxy group substituted or unsubstituted with an alkyl group having 1 to 4 carbon atoms, or R ₁ And at least one selected from the group consisting of R ₂ and R ₃ and R ₄ may be bonded to each other to form an epoxy group, with the proviso that the case where all of R ₁ to R ₄ are hydrogen. [Chemical Formula 2] In Formula 2, q is an integer of 0 to 4, R ₅ to R _{8 are} each independently alkyl having 1 to 4 carbon atoms is a hydrogen or a substituted or unsubstituted vinyl group, or R ₅ and by the At least one selected from the group consisting of R ₆ and R ₇ and R ₈ may be bonded to each other to form an alkylidene group, with the proviso that the case where R ₅ to R ₈ are all hydrogen is excluded. [Chemical Formula 3] In the above formula 3, r and m are each independently an integer of 0 to 4, each R is independently hydrogen; halogen; substituted or unsubstituted C _1-20 alkyl; substituted or unsubstituted C _1-20 ether; substituted or unsubstituted C _1-20 alkoxy group; or substituted or unsubstituted C _{2 -60} heterocyclic ring containing at least one of O, N, Si and S.

As used herein, the term "substituted or unsubstituted" means unsubstituted or substituted with one or more substituents selected of the group consisting of the following: halo; hydroxy; C _3-60 cycloalkyl group, and .

In the present specification, examples of the halogen group include fluorine, chlorine, bromine or iodine.

Further, in the present specification, the alkyl group may be linear or branched, and the number of carbon atoms thereof is not particularly limited, but is preferably from 1 to 20. Specific examples of the alkyl group include, but are not limited to, methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, t-butyl, 1 -Methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methyl Pentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n-heptyl, 1-methylhexyl, cyclopentylmethyl, Cyclohexylmethyl, octyl, n-octyl, trioctyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-decyl, 2,2-dimethylheptyl , 1-ethyl-propyl, 1,1-dimethyl-propyl, isohexyl, 2-methylpentyl, 4-methylhexyl, 5-methylhexyl and the like.

In the present specification, the heterocyclic group is a heterocyclic group containing at least one of O, N, Si and S as a hetero atom, and the number of carbon atoms thereof is not particularly limited, but is preferably from 2 to 60. Examples of heterocyclic groups include, but are not limited to, thienyl, furyl, pyrrolyl, imidazolyl, thiazolyl, oxazolyl, dioxolyl, oxadiazolyl, triazolyl, pyridyl , bipyridyl, pyrimidinyl, triazinyl, triazolyl, acridine, pyridazinyl, pyrazinyl, quinolinyl, quinazolinyl, quinoxalinyl, pyridazinyl, pyridopyrimidinyl , pyridopyridyl, pyrazinopyrazinyl, isoquinolyl, decyl, oxazolyl, benzoxazolyl, benzimidazolyl, benzothiazolyl, benzoxazolyl, benzene And thienyl, dibenzothiophenyl, benzofuranyl, morpholinyl, thiazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, benzothiazolyl, phenothiazine, dibenzo Furanyl and its analogous groups.

The present inventors have conducted intensive studies for obtaining materials having lower dielectric constant and lower dielectric loss characteristics, and have found through experiments that a repeating unit having an epoxy group is contained in a predetermined ratio, having a vinyl group or an alkylene group. The copolymer of the repeating unit and the repeating unit having an aliphatic functional group has a dielectric constant of 2.6 or less at 10 GHz (GHz), that is, has a lower dielectric characteristic, thereby completing the present invention.

More specifically, the repeating unit represented by Chemical Formula 1 in the cyclic olefin copolymer contains an epoxy group, and when the proportion of the repeating unit represented by Chemical Formula 1 becomes high, the degree of curing and the adhesion strength may increase, but dielectric Features may be reduced. Further, when the proportion of the repeating unit containing a vinyl group represented by Chemical Formula 2 becomes high, the lower dielectric constant and dielectric loss characteristics can be improved. Further, when the proportion of the repeating unit containing the aliphatic functional group represented by Chemical Formula 3 becomes high, the dielectric characteristics of the copolymer to be produced are improved, but the degree of cure and solubility of the resin may be lowered.

Therefore, it is necessary for the cyclic olefin-based copolymer to adjust the repeating unit represented by Chemical Formula 1 to Chemical Formula 3 at an appropriate ratio, and if the repeating unit represented by Chemical Formula 1 is expressed in relation to the chemical formula 1 to Chemical Formula 3 Preferably, the total amount of the repeating unit is from 15% by mole to 60% by mole, preferably from 20% by mole to 50% by mole, more preferably from 25% by mole to 40% by mole. The copolymer exhibits a lower dielectric constant and lower dielectric loss characteristics. If the proportion of the repeating unit represented by Chemical Formula 1 exceeds the above range, the dielectric characteristics may be poor, or physical properties such as adhesion and durability may not be sufficient for use in the fields of communication and networking.

In the repeating unit represented by Chemical Formula 1, R ₁ to R ₄ are each independently hydrogen or The functional group represented, or at least one selected from the group consisting of R ₁ , R ₂ , R ₃ and R ₄ , may be bonded to each other to form an epoxy group. Here, n is an integer of 0 to 4, and R is hydrogen or an alkyl group having 1 to 4 carbon atoms, which is limited to the case where R ₁ to R ₄ are all hydrogen.

Further, in the repeating unit represented by Chemical Formula 2, R ₅ to R ₈ are each independently hydrogen or The functional group represented, or at least one selected from the group consisting of R ₅ and R ₆ and R ₇ and R ₈ may be bonded to each other to form an alkylene group. Here, n is an integer of 0 to 4, and R is hydrogen or an alkyl group having 1 to 4 carbon atoms, which is limited to the case where R ₅ to R ₈ are all hydrogen.

In the repeating unit represented by Chemical Formula 3, each R may be independently hydrogen; halogen; substituted or unsubstituted C _1-20 alkyl; substituted or unsubstituted C _1-20 ether; substituted or An unsubstituted C _1-20 alkoxy group; or a substituted or unsubstituted C _{2 -60} heterocyclic ring containing at least one of O, N, Si and S. Preferably, a substituted or unsubstituted C _1-20 ether or a substituted or unsubstituted C _{2 -60} heterocyclic ring containing at least one of O, N, Si and S may be used.

Specific, as in the chemical formula of R 3 via substituted or non-substituted C _1-20 ethers may be substituted by C _1-20 alkoxy the C _1-20 alkyl group. Specific examples of substituted by C _1-20 alkoxy C _1-20 alkyl comprises _1-10 alkoxy substituted by C of C _1-10 alkyl, substituted by words more particularly a C _1-3 alkoxy group C _1-3 alkyl. A preferred example of the C _1-20 alkyl group substituted by a C _1-20 alkoxy group includes a methoxymethyl group.

Further, the _C2-60 heterocyclic ring containing at least one of O, N, Si and S which is substituted or unsubstituted in R in Chemical Formula 3 may be a functional group represented by the following Chemical Formula 7. [Chemical Formula 7] In the above formula 7, at least one of A ₁ and A ₂ is O, N, Si or S, and the rest is carbon, and t is 1 or an integer greater than 1 or an integer from 1 to 5, and "*" and The same carbon atom forms a bond. In Chemical Formula 7, "*" forms a bond with the same carbon atom, thereby forming a ring structure. That is, when the functional group of Chemical Formula 7 is introduced as R in Chemical Formula 3, the repeating unit of Chemical Formula 3 may have a spiro ring structure in which two different rings are linked to each other via one carbon atom.

Preferably, in Chemical Formula 7, A ₁ is O, A ₂ is carbon, t is 1, and "*" may be an oxetane functional group which forms a bond with the same carbon atom. Further, in Chemical Formula 7, A ₁ and A ₂ are O, t is 2, and "*" may be a 1,3-dioxane functional group which forms a bond with the same carbon atom.

Further, the cyclic olefin copolymer may have a weight average molecular weight of from about 1,000 g/m to 100,000 g/mole, preferably from about 1,500 g/m to 50,000 g/m, more preferably about 2,500 g/ Moor to 10,000 g/mole.

In order to produce a copolymer having a low molecular weight of from 2,500 g/m to 10,000 g/m as described above, it is preferred to use a large volume of phosphine as the organic ligand in the catalyst structure.

When the weight average molecular weight of the cyclic olefin copolymer is in the range of 2,500 gram/mol to 10,000 gram/mol, it is possible to prevent excessive viscosity increase by mixing with other materials for film formation to prepare a composition. And therefore ensure excellent fluidity. Specifically, the composition containing the cyclic olefin copolymer may have a viscosity of 40 centipoise to 100 centipoise or 40 under the condition that the ratio of the solid content to the solvent exceeds 1 (solid content/solvent > 1). From centipoise to 80 centipoise.

When the weight average molecular weight of the cyclic olefin copolymer exceeds the range mentioned above, the viscosity and fluidity of the film-forming composition do not satisfy an appropriate level, thereby making it difficult to obtain a clean coated surface and forming A coating film of constant thickness. Therefore, errors may occur when measuring electrical and physical properties.

As used herein, the weight average molecular weight means the weight average molecular weight as measured by the GPC method relative to polystyrene. In the process of measuring the weight average molecular weight measured by the GPC method with respect to polystyrene, a generally known analysis device, a detector such as a refractive index detector, and an analytical column can be used. Conditions commonly used for temperature, solvent, and flow rate can be used. Specific examples of the measurement conditions include a temperature of 30 ° C, tetrahydrofuran (THF), and a flow rate of 1 mL/min.

Meanwhile, the glass transition temperature of the cyclic olefin copolymer may be about 255 ° C or higher, or 255 ° C to 300 ° C, or 268 ° C or higher than 268 ° C, or 268 ° C to 300 ° C, or 268 ° C to 280 ° C. The glass transition temperature can be confirmed by DSC measurement data or the like. For example, a method of measuring the glass transition temperature by using a cyclic olefin copolymer at 300 ° C for 5 minutes, slowly cooling to room temperature, and a heating rate of 10 ° C / minute can be used. Rescan it. The glass transition temperature of the salty cyclic olefin copolymer is attributed to the chemical structure of the copolymer. As the glass transition temperature of the copolymer increases, the CTE value decreases while increasing the modulus at high temperatures. Therefore, the thermal stability of the last manufactured CCL or PCB can be improved.

The cured product of the cyclic olefin copolymer may have a dielectric constant (Dk) of about 2.6 or less, or about 2.3 to 2.6 at 10 GHz. A dielectric network analyzer (Agilent Technologies) was used to measure the dielectric constant at 10 GHz. When the dielectric constant exceeds 2.7, the insulation characteristics are not good, and the transmission loss increases in the high frequency region. Therefore, it may adversely affect the performance, durability, and manufacturing yield of the electronic device.

Further, the cured product of the cyclic olefin copolymer may have a dielectric loss factor (Df) at 10 GHz of about 0.007 or less, preferably 0.002 to 0.007, and more preferably 0.003 to 0.007. The dielectric loss factor is measured by the same equipment and method as in the dielectric constant measurement method.

Further, the cured product of the cyclic olefin copolymer has a copper foil adhesion strength of 0.6 kgf/cm or more than 0.6 kgf/cm, or 0.6 kgf/cm to 1.0 kgf/cm, or 0.8 kgf/cm to 1.0 kgf/cm. Examples of the method for measuring the adhesion strength of the copper foil are not particularly limited, but for example, the laminate between the cured product of the cyclic olefin copolymer and the copper foil having a thickness of 35 μm is cut into a width. After a rectangular shape of 10 mm, it can be measured by using a tensile strength tester (ZWICK) to grasp the end of the copper foil and peel it off from the substrate layer at an angle of 90° and a speed of 50 mm/min. The required force (peel strength) is used to calculate the adhesion strength of the copper foil.

In the cured product of the cyclic olefin copolymer, when the adhesion strength of the copper foil is excessively reduced to less than 0.6 kgf/cm, a copper clad laminate (CCL) is prepared using a prepreg and a copper foil. It is easily peeled off, thereby making it difficult to manufacture a product. Even if a product is manufactured, it is difficult to ensure reliability.

On the other hand, according to another embodiment of the present invention, there is provided a process for producing a cyclic olefin copolymer comprising the steps of: a monomer represented by the following Chemical Formula 4 and a monomer represented by the following Chemical Formula 5 Polymerization of a pre-catalyst comprising a Group 10 transition metal, an anionic cocatalyst coordinated to said metal of said precatalyst, and a ligand comprising a Group 15 element; and reacting said polymer with a peroxyacid To perform epoxidation. [Chemical Formula 4] In the above formula 4, q is an integer of 0 to 4, and R ₅ to R ₈ are each independently hydrogen or an alkyl group substituted or unsubstituted with an alkyl group having 1 to 4 carbon atoms, or R ₅ and At least one selected from the group consisting of R ₆ and R ₇ and R ₈ may be bonded to each other to form an alkylene group, with the proviso that the case where R ₅ to R ₈ are all hydrogen. [Chemical Formula 5] In the above formula 5, r and m are each independently an integer of 0 to 4, each R is independently hydrogen; halogen; substituted or unsubstituted C _1-20 alkyl; substituted or unsubstituted C _1-20 ether; substituted or unsubstituted C _1-20 alkoxy group; or substituted or unsubstituted C _{2 -60} heterocyclic ring containing at least one of O, N, Si and S.

As described above, the inventors confirmed through experiments that the cyclic olefin copolymer produced according to the method described above contains a repeating unit having an epoxy group, a repeating unit having a vinyl group or an alkylene group in a predetermined ratio, and A repeating unit having an aliphatic functional group, and which not only has a lower dielectric constant and a lower dielectric loss characteristic, but also exhibits a higher peel strength.

In the repeating unit represented by Chemical Formula 5, each R may independently be hydrogen; halogen; substituted or unsubstituted C _1-20 alkyl; substituted or unsubstituted C _1-20 ether; substituted or the unsubstituted C _1-20 alkoxy group; or a substituted or unsubstituted containing the O, N, Si and S, at least one of the C _2-60 heterocycle. Preferably, a substituted or unsubstituted C _1-20 ether or a substituted or unsubstituted C _{2 -60} heterocyclic ring containing at least one of O, N, Si and S may be used.

Specific, as in the chemical formula of R 5 is substituted or non-substituted C _1-20 ethers may be substituted by C _1-20 alkoxy the C _1-20 alkyl group. Specific examples of substituted by C _1-10 alkoxy C _1-20 alkyl comprises _1-10 alkoxy substituted by C of C _1-10 alkyl, substituted by words more particularly a C _1-3 alkoxy group C _1-3 alkyl. A preferred example of the C _1-20 alkyl group substituted by a C _1-20 alkoxy group includes a methoxymethyl group.

Further, as the R in Formula 5 is a substituted or unsubstituted containing the O, N, Si and S, at least one of the C _2-60 heterocyclic ring may be represented by the following Chemical Formula 7 of functional groups. [Chemical Formula 7] In the above formula 7, at least one of A ₁ and A ₂ is O, N, Si or S, and the rest is carbon, and t is 1 or an integer greater than 1 or an integer from 1 to 5, and "*" and The same carbon atom forms a bond. In Chemical Formula 7, "*" forms a bond with the same carbon atom, thereby forming a ring structure. That is, when the functional group of Chemical Formula 7 is introduced as R in Chemical Formula 3, the repeating unit of Chemical Formula 3 may have a spiro ring structure in which two different rings are linked to each other via one carbon atom.

Preferably, the chemical formula 7 may be a functional group in which A ₁ is O, A ₂ is carbon, t is 1, and "*" may be an oxetane functional group which forms a bond with the same carbon atom. Further, the chemical formula 7 may be a functional group in which A ₁ and A ₂ are O, t is 2, and "*" forms a bond with the same carbon atom.

The step of polymerizing the monomers represented by Chemical Formula 4 and Chemical Formula 5 is carried out on a precatalyst containing a Group 10 transition metal, an anionic cocatalyst coordinated to the metal of the precatalyst, and a ligand containing a Group 15 element. Exist in the presence. The Group 10 transition metal precatalyst may comprise at least one precatalyst selected from the group consisting of palladium dichloride (PdCl ₂ ), palladium dibromide (PdBr ₂ ), allyl palladium chloride dimer. ([(allyl)Pd(Cl)] ₂ ), palladium acetate ((CH ₃ CO ₂ ) ₂ Pd), palladium acetylacetonate ([CH ₃ COCH=C(O-)CH ₃ ] ₂ Pd ), [PdCl(NB)O(CH ₃ )] ₂ , bis(dibenzylideneacetone)palladium ((diphenylmethyleneacetone) ₂ Pd), tris(diphenylmethyleneacetone)dipalladium ( (diphenylmethyleneacetone) ₃ Pd ₂ ), palladium nitrate (Pd(NO ₃ ) ₂ ) and NiBr(NP(CH ₃ ) ₃ ) ₄ .

The anionic cocatalyst capable of weakly coordinating with the metal of the precatalyst can be represented by the following Chemical Formula 6: [Cat] [Ani] In the above formula 6, [Cat] is any one selected from the group consisting of the following: a hydrogen cation, a Group 1 metal cation, a Group 2 metal cation, a transition metal cation, and an organic group containing the cation, and [Ani] is any one selected from the group consisting of borate, aluminum. Acidate, [SbF ₆ ]-, [PF ₆ ]-, [AsF ₆ ]-, perfluoroacetate ([CF ₃ CO ₂ ]-), perfluoropropionate ([C ₂ F ₅ CO ₂ ]-), Perfluorobutyrate ([CF ₃ CF ₂ CF ₂ CO ₂ ]-), perchlorate ([ClO ₄ ]-), p-toluenesulfonate ([p-CH ₃ C ₆ H ₄ SO ₃ ]-), [SO ₃ CF ₃ ]-, halogen-substituted or unsubstituted borobenzene and carborane.

Further, the ligand containing the Group 15 element has an electron stabilizing ability and can function to activate the transition metal compound thermally and chemically, while increasing the solubility of the transition metal compound in an organic solvent. Specific examples of the ligand containing a Group 15 element include an aliphatic, alicyclic or aromatic phosphine or phosphite, preferably at least one ligand selected from the group consisting of: (2-hydroxyl) Phenyl)diphenylphosphine, tris(furan-2-yl)phosphine, bis(diphenylphosphino)methane, bis(diphenylphosphino)ethane, phosphite tris(2,4-di- Tributyl phenyl ester), tris(o-tolyl)phosphine, tris(p-tolyl)phosphine, tri-1-naphthylphosphine, tributylphosphine, tetrafluoroborate, triphenylphosphine, tricyclohexylphosphine , triphenyl phosphite, 1,2-(diphenylphosphino)ethane, tributylphosphine, triphenylphosphine oxide, and 1,2-(diphenylphosphino)butane.

More preferably, at least one selected from the group consisting of (2-hydroxyphenyl)diphenylphosphine, tris(2-yl)phosphine, bis(diphenylphosphino)methane, bis (two) Phenylphosphino)ethane, tris(2,4-di-t-butylphenyl)phosphite, tris(o-tolyl)phosphine, tris(p-tolyl)phosphine, tri-1-naphthylphosphine, Tributylphosphine and tetrafluoroborate, which have a bulky structure for the manufacture of low molecular weight copolymers.

Further, the step of polymerizing the monomer may be carried out at a temperature of from 50 ° C to 200 ° C, or from 70 ° C to 150 ° C, or from 90 ° C to 140 ° C, or from 100 ° C to 135 ° C.

Next, a step of reacting a polymer produced by polymerizing the monomers represented by Chemical Formula 4 and Chemical Formula 5 with a peroxyacid to carry out epoxidation can be performed.

In this case, the peroxyacid may comprise at least one peroxyacid selected from the group consisting of peroxybenzoic acid, peroxyacetic acid, peroxyformic acid, peroxyphthalic acid, peroxypropionic acid, Peroxybutyric acid, trifluoro-peroxyacetic acid, and hydrogen peroxide.

In the step of performing the epoxidation, the molar ratio between the polymer and the peroxyacid may be from about 1:0.1 to 1:5, preferably from about 1:0.2 to 1:3. The molar ratio between the polymer and the peroxyacid is related to the ratio of each repeating unit of the cyclic olefin copolymer to be produced. When the polymer and the peroxyacid are reacted in the above molar ratio, a cyclic olefin copolymer containing 15 mol% to 60 mol% of the repeating unit represented by Chemical Formula 1 of one example can be produced.

Alternatively, the epoxidation reaction can be carried out at a temperature of about 50 ° C or less, preferably about 0 ° C to 40 ° C.

[Advantageous]

According to the present invention, there can be provided a cyclic olefin copolymer which exhibits a lower dielectric constant and a lower dielectric loss characteristic, and thus can be applied to a semiconductor substrate, a printed circuit board, and the like.

The invention will be described in more detail below by means of examples. However, these examples are provided for illustrative purposes only and are not to be construed as limiting the scope of the invention to these examples. < Example and Comparative Example > Example 1

(Step 1) 22.8 g of 5-ethylidene-2-norbornene, 77.2 g 1,2,3,4,4a,5,8,8a-eight were added to a 250 ml Schlenk flask. Hydrogen-2-methyl-1,4:5,8-dimethylnaphthalene and 250 g of xylene. The temperature was raised to 130 ° C while purging with N ₂ . Dissolving 0.022 g of palladium dichloride (PdCl ₂ ), 0.036 g of trinaphthylphosphine (P(1-nap) 3 ) and 0.025 g of silver tetrafluoroborate (AgBF ₄ ) in 6 ml of dichloromethane, and The solution was added and allowed to react at 130 ° C for 16 hours with stirring. After the reaction, the reaction mixture was poured into an excess of methanol to obtain a white polymer precipitate. The precipitate was filtered through a glass funnel, and the collected solid was dried in a vacuum oven at 30 ° C for 24 hours to obtain a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 5010 g/mole, PDI = 1.95, yield 48%).

(Step 2) 20 g of the copolymer obtained in the step 1 was dissolved in 60 g of dichloromethane. While stirring, the temperature was lowered to 0 ° C, and 1.18 g of m-chloroperoxybenzoic acid (mCPBA) was slowly added dropwise. After stirring for 1 hour, the temperature was raised to room temperature, and then reacted for 5 hours. After the reaction, the reaction mixture was filtered, and the obtained reaction solution was poured into an excess of methanol to obtain a white solid precipitate. The precipitate was filtered through a glass funnel, and the collected solid was dried in a vacuum oven at 30 ° C for 24 hours to obtain an epoxide conversion of 90% and a repeating unit of Chemical Formula 1: a repeating unit of Chemical Formula 2: Chemical Formula 3 The repeat unit had a molar ratio of 2.7:0.3:7 (Mw = 5,300 g/mole, PDI = 1.95, yield 90%). Example 2

(Step 1) except that the amount used was changed to 31.5 g of 5-ethylidene-2-norbornene, 68.5 g of 1,2,3,4,4a,5,8,8a-octahydro-2-methyl- In the same manner as in the first step of Example 1, except that 1,4:5,8-dimethylnaphthalene, 0.022 g of PdCl ₂ , 0.037 g of P(1-nap) ₃ and 0.026 g of AgBF ₄ were obtained. Repeating unit: a repeating unit of Chemical Formula 3 having a molar ratio of 4:6 (Mw = 5,015 g/mole, PDI = 1.95, yield 48%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 1 of Example 1 except that the content of mCPBA was changed to 1.63 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5,305 g/mole, PDI = 1.96, yield 89%). Example 3

(Step 1) In place of 72.9 grams of 5-ethoxy-2-norbornene, 0.027 grams of PdCl ₂ , 0.042 grams of P(1-nap) _3, and 0.029 grams of AgBF ₄ instead of 27.15 grams of 5-ethylidene-2- Norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene and reacted at 125 ° C, A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 5,500 g/mole, PDI = 2.02, yield 51%) ).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.40 gram: the repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 5,750 g/m, PDI = 2.02, yield 86%). Example 4

(Step 1) In place of 63.4 g of 5-ethoxy-2-norbornene, 0.027 g of PdCl ₂ , 0.043 g of P(1-nap) ₃ and 0.030 g of AgBF ₄ instead of 36.7 g of 5-ethylidene-2- Norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene and reacted at 125 ° C, A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1: a repeating unit of Chemical Formula 3 having a molar ratio of 4:6 (Mw = 5,450 g/mole, PDI = 2.02, yield 51%) ).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.90 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5800 g/mole, PDI = 2.02, yield 86%). Example 5

(Step 1) Instead of using 76.4 grams of 5-butoxy-2-norbornene, 0.023 grams of PdCl ₂ , 0.037 grams of P(1-nap) _3, and 0.026 grams of AgBF ₄ instead of 23.7 grams of 5-ethylidene-2- Norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene and reacted at 125 ° C, A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 5,800 g/mole, PDI = 2.00, yield 53%) ).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.22 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: 0.3:7 copolymer (Mw = 5900 g/mole, PDI = 2.01, yield 85%). Example 6

(Step 1) Instead of using 67.5 g of 5-butoxy-2-norbornene, 0.024 g of PdCl ₂ , 0.038 g of P(1-nap) ₃ and 0.026 g of AgBF ₄ instead of 32.6 g of 5-ethylidene-2- Norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene and reacted at 125 ° C, A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1: a repeating unit of Chemical Formula 3 having a molar ratio of 4:6 (Mw = 5,800 g/mole, PDI = 2.01, yield 52%) ).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.68 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5950 g/mole, PDI = 2.01, yield 85%). Example 7

(Step 1) Instead of using 72.9 grams of 5-(methoxymethyl)-2-norbornene, 0.027 grams of PdCl ₂ , 0.042 grams of P(1-nap) _3, and 0.029 grams of AgBF ₄ instead of 27.15 grams of 5-AB Base-2-norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene and react at 125 ° C Further, a repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 5700 g/mole, PDI = 2.00, Yield 52%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.40 gram: the repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: 0.3:7 copolymer (Mw = 5850 g/mole, PDI = 2.01, yield 86%). Example 8

(Step 1) In place of 63.4 g of 5-(methoxymethyl)-2-norbornene, 0.027 g of PdCl ₂ , 0.043 g of P(1-nap) ₃ and 0.030 g of AgBF ₄ instead of 36.7 g of 5-AB Base-2-norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene and react at 125 ° C Further, a repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1: a repeating unit of Chemical Formula 3 having a molar ratio of 4:6 (Mw = 5,750 g/m, PDI = 2.00, Yield 52%).

(Step 2) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.90 g: the repeating unit of Chemical Formula 3: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5900 g/mole, PDI = 2.00, yield 86%). Example 9

(Step 1) except that 72.6 g of spiro [bicyclo[2,2,1]hept-5-ene-2,2'-oxetane], 0.027 g of PdCl ₂ , 0.040 g of P(1-nap) _{3 was used.} And 0.029 g of AgBF ₄ instead of 27.4 g of 5-ethylidene-2-norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5, A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1 except that 8-dimethylnaphthalene was reacted at 125 ° C: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 ( Mw = 4500 g/mole, PDI = 2.10, yield 40%).

(Step 2) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 2.83 g: The repeating unit of Chemical Formula 3: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: 0.3:7 copolymer (Mw = 4700 g/mole, PDI = 2.11, yield 85%). Example 10

(Step 1) except that 63.0 g of spiro [bicyclo[2,2,1]hept-5-ene-2,2'-oxetane], 0.026 g of PdCl ₂ , 0.040 g of P(1-nap) _{3 was used.} And 0.028 g of AgBF ₄ instead of 37.0 g of 5-ethylidene-2-norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5, A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1 except that 8-dimethylnaphthalene was reacted at 120 ° C: a repeating unit of Chemical Formula 3 having a molar ratio of 4:6 ( Mw = 4400 g/m, PDI = 2.08, yield 41%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 3.93 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 4650 g/mole, PDI = 2.09, yield 83%). Example 11

(Step 1) except that 74.7 g of spiro[5,5-(1',3'-dioxane)-2-norbornene], 0.025 g of PdCl ₂ , 0.039 g of P(1-nap) ₃ and 0.027 g were used. AgBF ₄ replaces 25.3 grams of 5-ethylidene-2-norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-two A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1 except that the reaction was carried out at 120 ° C. The repeating unit of Chemical Formula 3 had a molar ratio of 3:7 (Mw = 5000). G/m, PDI = 2.05, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.31 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 5300 g/mole, PDI = 2.07, yield 88%). Example 12

(Step 1) except that 65.5 g of spiro[5,5-(1',3'-dioxane)-2-norbornene], 0.026 g of PdCl ₂ , 0.040 g of P(1-nap) ₃ and 0.028 g were used. AgBF ₄ replaces 34.5 grams of 5-ethylidene-2-norbornene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-two A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1 except that the reaction was carried out at 120 ° C. The repeating unit of Chemical Formula 3 had a molar ratio of 4:6 (Mw = 5000). G/m, PDI = 2.06, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.78 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5300 g/mole, PDI = 2.06, yield 87%). Example 13

(Step 1) Instead of using 24.7 grams of 2-norbornene, 0.035 grams of PdCl ₂ , 0.055 grams of P(1-nap) ₃ and 0.038 grams of AgBF ₄ instead of 25.3 grams of 5-ethylidene-2-norbornene and 1, In the same manner as in the first step of Example 1, except that 2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene was obtained. Repeating unit of 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 6000 g/mole, PDI = 2.10, yield 55%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.83 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 6100 g/mole, PDI = 2.10, yield 90%). Example 14

(Step 1) In place of 54.0 g of 2-norbornene, 0.034 g of PdCl ₂ , 0.054 g of P(1-nap) ₃ and 0.037 g of AgBF ₄ instead of 46.0 g of 5-ethylidene-2-norbornene and 1, In the same manner as in the first step of Example 1, except that 2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene was obtained. Repeating unit of 2: a repeating unit of Chemical Formula 3 having a molar ratio of 4:6 (Mw = 6050 g/mole, PDI = 2.11, yield 55%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 2.38 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 6100 g/mole, PDI = 2.11, yield 89%). Example 15

(Step 1) Instead of using 77.6 g of 5-n-hexyl-2-norbornene, 0.022 g of PdCl ₂ , 0.035 g of P(1-nap) ₃ and 0.024 g of AgBF ₄ instead of 22.4 g of 5-ethylidene-2-nor Borneene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene, in step 1 with Example 1 In the same manner, a repeating unit of Chemical Formula 2 was obtained: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 5950 g/mole, PDI = 2.10, yield 54%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.16 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 6050 g/mole, PDI = 2.11, yield 90%). Example 16

(Step 1) In addition to using 69.0 g of 5-n-hexyl-2-norbornene, 0.023 g of PdCl ₂ , 0.036 g of P(1-nap) ₃ and 0.025 g of AgBF ₄ instead of 31.0 g of 5-ethylidene-2-nor Borneene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene, in step 1 with Example 1 In the same manner, a repeating unit of Chemical Formula 2 was obtained: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 6000 g/mole, PDI = 2.10, yield 54%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.60 gram: the repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 6100 g/mole, PDI = 2.10, yield 90%). Example 17

(Step 1) Instead of using 74.5 grams of 5-n-hexyl-2-norbornene, 0.025 grams of PdCl ₂ , 0.040 grams of P(1-nap) _3, and 0.028 grams of AgBF ₄ instead of 25.6 grams of 5-ethylidene-2-nor Borneene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene, in step 1 with Example 1 In the same manner, a repeating unit of Chemical Formula 2 was obtained: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 5900 g/mole, PDI = 2.09, yield 56%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.32 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 6000 g/mole, PDI = 2.09, yield 90%). Example 18

(Step 1) Instead of using 65.2 grams of 5-n-hexyl-2-norbornene, 0.026 grams of PdCl ₂ , 0.041 grams of P(1-nap) _3, and 0.028 grams of AgBF ₄ instead of 34.8 grams of 5-ethylidene-2-nor Borneene and 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene, in step 1 with Example 1 In the same manner, a repeating unit of Chemical Formula 2 was obtained: a repeating unit of Chemical Formula 3 having a molar ratio of 4:6 (Mw = 5900 g/mole, PDI = 2.10, yield 56%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.80 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 6000 g/mole, PDI = 2.10, yield 90%). Example 19

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 5000 g/mole, PDI = 1.95, yield 48%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 5300) G/m, PDI = 1.97, yield 90%). Example 20

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 2 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 4:6 (Mw = 5005 g/mole, PDI = 1.95, yield 47%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 2: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 5310) G/m, PDI = 1.95, yield 90%). Example 21

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 3 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 5410 g/mole, PDI = 2.01, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 3: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 5650) G/m, PDI = 2.01, yield 86%). Example 22

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 4 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 4:6 (Mw = 5,450 g/mole, PDI = 2.00, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 4: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 5610) G/m, PDI = 2.01, yield 87%). Example 23

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 5 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 5700 g/mole, PDI = 2.00, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 5: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 5,800) G/m, PDI = 2.00, yield 87%). Example 24

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 6 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 4:6 (Mw = 5720 g/mole, PDI = 2.00, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 6: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 5810) G/mole, PDI = 2.00, yield 86%). Example 25

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 7 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 5,740 g/mole, PDI = 1.98, yield 50%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 7: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 5,800) G/m, PDI = 1.98, yield 85%). Example 26

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 8 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 4:6 (Mw = 5700 g/mole, PDI = 1.98, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 8: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 5,800) G/m, PDI = 1.98, yield 86%). Example 27

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 9 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 4,600 g/mole, PDI = 2.10, yield 40%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 9: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 4700) G/m, PDI = 2.10, yield 82%). Example 28

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 10 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a 4:6 molar ratio (Mw = 4400 g/mole, PDI = 2.08, yield 41%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 10: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 4600) G/m, PDI = 2.08, yield 83%). Example 29

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 11 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 5100 g/mole, PDI = 2.05, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 11: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 5250) G/m, PDI = 2.06, yield 90%). Example 30

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 12 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 4:6 (Mw = 5120 g/mole, PDI = 2.05, yield 49%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 12: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 5300) G/m, PDI = 2.05, yield 90%). Example 31

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 13 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 5900 g/mole, PDI = 2.09, yield 54%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 13: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 5950) G/m, PDI = 2.09, yield 89%). Example 32

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 14 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 4:6 (Mw = 5870 g/mole, PDI = 2.08, yield 55%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 14: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 5940) G/m, PDI = 2.08, yield 90%). Example 33

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 15 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 6000 g/mole, PDI = 2.10, yield 53%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 15: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 6040) G/m, PDI = 2.10, yield 87%). Example 34

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 16 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 4:6 (Mw = 6050 g/mole, PDI = 2.11, yield 53%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 16: A repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 6100) G/m, PDI = 2.11, yield 87%). Example 35

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 17, except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 3:7 (Mw = 5,800 g/mole, PDI = 2.10, yield 57%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 17: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 2.7:0.3:7 (Mw = 5860) G/m, PDI = 2.11, yield 89%). Example 36

(Step 1) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 18 except that 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene: Chemical Formula The repeating unit of 3 had a molar ratio of 4:6 (Mw = 5840 g/mole, PDI = 2.09, yield 57%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 18: a repeating unit of Chemical Formula 2: a repeating unit of Chemical Formula 3 having a molar ratio of 3.6:0.4:6 (Mw = 5900) G/m, PDI = 2.10, yield 90%). Example 37

(Step 1) except that 24.8 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 75.2 g 1,2,3 , 4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene, 0.022 g PdCl ₂ , 0.035 g P(1-nap) ₃ and 0.024 g AgBF _{Except for 4} , a repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 1: a repeating unit of Chemical Formula 3 having a molar ratio of 3:7 (Mw = 5100 g/mole, PDI = 1.97) , yield 48%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.15 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 5300 g/mole, PDI = 1.99, yield 88%). Example 38

(Step 1) except that 34.0 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 66.1 g 1,2,3 , 4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethylnaphthalene, 0.022 g PdCl ₂ , 0.036 g P(1-nap) ₃ and 0.025 g AgBF than _4, the same procedures as in example 1 of the embodiment 1 is obtained in the repeating unit of the formula: a repeating unit of chemical formula 3 molar ratio of 4: 6 copolymer (Mw = 5150 g / mole, PDI = 1.97 , yield 48%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 1 except that the content of mCPBA was changed to 1.57 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5300 g/mole, PDI = 1.97, yield 88%). Example 39

(Step 1) except that 29.4 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 70.6 g of 5-ethoxyl. Repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 3 except that -2-norbornene, 0.026 g of PdCl ₂ , 0.041 g of P(1-nap) ₃ and 0.028 g of AgBF ₄ were used: The repeat unit had a molar ratio of 3:7 (Mw = 5300 g/mole, PDI = 2.00, yield 49%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 3 except that the content of mCPBA was changed to 1.36 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: 0.3:7 copolymer (Mw = 5500 g/mole, PDI = 2.00, yield 84%). Example 40

(Step 1) except that 39.3 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 60.8 g of 5-ethoxyl. A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 3 except that -2-norbornene, 0.026 g of PdCl ₂ , 0.041 g of P(1-nap) ₃ and 0.029 g of AgBF ₄ were used: Chemical Formula 3 The repeat unit had a molar ratio of 4:6 (Mw = 5300 g/mole, PDI = 1.99, yield 48%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 3 except that the content of mCPBA was changed to 1.82 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5520 g/mole, PDI = 1.99, yield 86%). Example 41

(Step 1) except that 25.7 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 74.4 g of 5-butoxy A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 5 except that -2-norbornene, 0.023 g of PdCl ₂ , 0.036 g of P(1-nap) ₃ and 0.025 g of AgBF ₄ were used: The repeating unit had a molar ratio of 3:7 (Mw = 5600 g/mole, PDI = 2.00, yield 50%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 5 except that the content of mCPBA was changed to 1.19 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: 0.3:7 copolymer (Mw = 5700 g/mole, PDI = 2.02, yield 87%). Example 42

(Step 1) except that 35.0 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 65.0 g of 5-butoxy A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 5 except that -2-norbornene, 0.023 g of PdCl ₂ , 0.037 g of P(1-nap) ₃ and 0.025 g of AgBF ₄ were used: Chemical Formula 3 The repeat unit had a molar ratio of 4:6 (Mw = 5700 g/mole, PDI = 2.01, yield 50%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 5 except that the content of mCPBA was changed to 1.62 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5750 g/mole, PDI = 2.01, yield 86%). Example 43

(Step 1) except that 29.4 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 70.6 g of 5-methoxyl. Repeating units of Chemical Formula 2 were obtained in the same manner as in Step 1 of Example 7 except that methyl-2-norbornene, 0.026 g of PdCl ₂ , 0.041 g of P(1-nap) _3, and 0.028 g of AgBF ₄ were used: The repeating unit of 3 had a molar ratio of 3:7 (Mw = 5,800 g/mole, PDI = 2.01, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 7 except that the content of mCPBA was changed to 1.36 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 5850 g/mole, PDI = 2.02, yield 89%). Example 44

(Step 1) except that 39.3 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 60.7 g of 5-methoxyl. Repeating units of Chemical Formula 2 were obtained in the same manner as in Step 1 of Example 7 except that methyl-2-norbornene, 0.026 g of PdCl ₂ , 0.041 g of P(1-nap) _3, and 0.029 g of AgBF ₄ were used: The repeating unit of 3 had a molar ratio of 4:6 (Mw = 5,800 g/mole, PDI = 2.00, yield 53%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 7 except that the content of mCPBA was changed to 1.82 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5840 g/mole, PDI = 2.01, yield 88%). Example 45

(Step 1) except that 27.4 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 72.6 gro[5,5 - (1',3'-dioxane)-2-norbornene, 0.024 g of PdCl ₂ , 0.038 g of P(1-nap) _3, and 0.027 g of AgBF ₄ in the same manner as in step 1 of Example 11. The repeating unit of Chemical Formula 2 was obtained in such a manner that the repeating unit of Chemical Formula 3 had a molar ratio of 3:7 (Mw = 5150 g/mole, PDI = 2.03, yield 52%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 11 except that the content of mCPBA was changed to 1.27 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: 0.3:7 copolymer (Mw = 5300 g/mole, PDI = 2.03, yield 86%). Example 46

(Step 1) except that 37.1 grams of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 63.1 grams of snail [5,5 - (1',3'-dioxane)-2-norbornene, 0.025 g of PdCl ₂ , 0.039 g of P(1-nap) _3, and 0.027 g of AgBF ₄ in the same manner as in step 1 of Example 11. The repeating unit of Chemical Formula 2 was obtained in such a manner that the repeating unit of Chemical Formula 3 had a molar ratio of 4:6 (Mw = 5100 g/mole, PDI = 2.05, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 11 except that the content of mCPBA was changed to 1.72 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5300 g/mole, PDI = 2.05, yield 88%). Example 47

(Step 1) except that 37.9 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 62.1 g of 2-norbornene. In the same manner as in the first step of Example 13, except that 0.033 g of PdCl ₂ , 0.053 g of P(1-nap) ₃ and 0.037 g of AgBF ₄ were obtained, the repeating unit of the chemical formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was obtained. It was a copolymer of 3:7 (Mw = 5900 g/mole, PDI = 2.12, yield 52%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 13 except that the content of mCPBA was changed to 1.76 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 6000 g/mole, PDI = 2.12, yield 84%). Example 48

(Step 1) except that 48.8 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 51.3 g 2-norbornene In the same manner as in the first step of Example 13, except that 0.032 g of PdCl ₂ , 0.051 g of P(1-nap) ₃ and 0.035 g of AgBF ₄ were obtained, the repeating unit of the chemical formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was obtained. It was a 4:6 copolymer (Mw = 5800 g/mole, PDI = 2.13, yield 51%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 13 except that the content of mCPBA was changed to 2.26 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5850 g/mole, PDI = 2.14, yield 84%). Example 49

(Step 1) except that 24.4 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 75.6 g of 5-n-hexyl- In the same manner as in Step 1 of Example 15, a repeating unit of Chemical Formula 2 was obtained except 2-norbornene, 0.022 g of PdCl ₂ , 0.034 g of P(1-nap) ₃ and 0.024 g of AgBF ₄ : repeat of Chemical Formula 3 The unit had a molar ratio of 3:7 (Mw = 6000 g/mole, PDI = 2.10, yield 52%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 15 except that the content of mCPBA was changed to 1.13 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: Copolymer of 0.3:7 (Mw = 6100 g/mole, PDI = 2.10, yield 88%). Example 50

(Step 1) except that 33.4 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 66.7 g of 5-n-hexyl- In the same manner as in Step 1 of Example 15, a repeating unit of Chemical Formula 2 was obtained except 2-norbornene, 0.022 g of PdCl ₂ , 0.035 g of P(1-nap) ₃ and 0.024 g of AgBF ₄ : repeat of Chemical Formula 3 The molar ratio of the unit was 4:6 (Mw = 6000 g/mole, PDI = 2.11, yield 52%).

(Step 2) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 2 of Example 15 except that the content of mCPBA was changed to 1.15 g: The repeating unit of Chemical Formula 3: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 6050 g/mole, PDI = 2.11, yield 86%). Example 51

(Step 1) except that 27.7 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 72.3 g of 5-n-butyl group. Repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 17 except that -2-norbornene, 0.024 g of PdCl ₂ , 0.039 g of P(1-nap) ₃ and 0.027 g of AgBF ₄ were used: Chemical Formula 3 The repeating unit had a molar ratio of 3:7 (Mw = 5,800 g/mole, PDI = 2.10, yield 54%).

(Step 2) A repeating unit of Chemical Formula 1 was obtained in the same manner as in Step 2 of Example 17 except that the content of mCPBA was changed to 1.28 g: The repeating unit of Chemical Formula 2: the molar ratio of the repeating unit of Chemical Formula 3 was 2.7: 0.3:7 copolymer (Mw = 5850 g/mole, PDI = 2.11, yield 85%). Example 52

(Step 1) except that 37.3 g of 5-(1'-methylvinyl)-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 62.7 g of 5-n-butyl A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 1 of Example 17 except that -2-norbornene, 0.025 g of PdCl ₂ , 0.039 g of P(1-nap) ₃ and 0.027 g of AgBF ₄ were used: Chemical Formula 3 The repeat unit had a molar ratio of 4:6 (Mw = 5800 g/mole, PDI = 2.10, yield 56%).

(Step 2) A repeating unit of Chemical Formula 2 was obtained in the same manner as in Step 2 of Example 17 except that the content of mCPBA was changed to 1.73 g: The repeating unit of Chemical Formula 3: the molar ratio of the repeating unit of Chemical Formula 3 was 3.6: 0.4:6 copolymer (Mw = 5900 g/mole, PDI = 2.10, yield 88%). Comparative example 1

(Step 1) except that 83.7 grams of 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 16.4 grams of 2-norbornene, 300 grams of xylene, 0.031 Repeating units of 5-vinyl-2-norbornene were obtained in the same manner as in Step 1 of Example 13 except for gram of PdCl ₂ , 0.049 g of P(1-nap) ₃ and 0.034 g of AgBF ₄ : 2-lower The repeating unit of norbornene has a molar ratio of 8:2 (Mw = Mw = 3000 g/mole, PDI = 2.05, yield 40%).

(Step 2) A copolymer having an epoxide conversion of 94% was obtained in the same manner as in Step 2 of Example 13 except that the content of mCPBA was changed to 4.52 g (Mw = 3250 g/m, PDI = 2.05, yield 88%). Comparative example 2

(Step 1) To a 250 ml Schlenk flask was added 74.9 g of 5-vinyl-2-norbornene, 25.2 g of 2-norbornene, and 250 g of xylene. The temperature was raised to 130 ° C while purging with N ₂ . 0.032 g of palladium dichloride (PdCl ₂ ), 0.050 g of tricyclohexylphosphine (P(Cy) 3 ), and 0.035 g of silver tetrafluoroborate (AgBF ₄ ) were dissolved in 6 ml of dichloromethane, and added thereto. The solution was described and allowed to react at 130 ° C for 16 hours with stirring. After the reaction, the reaction mixture was poured into an excess of methanol to obtain a white polymer precipitate. The precipitate was filtered through a glass funnel, and the collected solid was dried in a vacuum oven at 30 ° C for 24 hours to obtain a repeating unit of 5-vinyl-2-norbornene: a molar unit of 2-norbornene repeating unit The ratio was 7:3 copolymer (Mw = 5500 g/mole, PDI = 2.00, yield 60%).

(Step 2) A copolymer having an epoxide conversion of 100% was obtained in the same manner as in the step 2 of Example 1 except that the content of mCPBA was changed to 4.30 g (Mw = 5650 g/m, PDI = 2.50, yield 88%). Comparative example 3

(Step 1) except that the amount used was changed to 92.0 g of 5-ethylidene-2-norbornene, 8.0 g of 2-norbornene, 150 g of xylene, 0.030 g of PdCl ₂ , and 0.048 g of P(1-Cy). ₃ and 0.233 g of AgBF ₄ were obtained in the same manner as in the step 1 of Example 13 to obtain a repeating unit of 5-ethylidene-2-norbornene: the molar ratio of the repeating unit of 2-norbornene was 9 Copolymer of :1 (Mw = 24000 g/mole, PDI = 3.00, yield 76%).

(Step 2) A copolymer having an epoxide conversion of 90% was obtained in the same manner as in the step 2 of Example 13 except that the content of mCPBA was changed to 4.30 g (Mw = 24,500 g/m, PDI = 3.00, yield 90%). Comparative example 4

(Step 1) except that 8.81 g of 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 91.2 g of 5-(methoxymethyl)-2- Repeating units of Chemical Formula 2 were obtained in the same manner as in Step 1 of Example 7 except for norbornene, 300 g of xylene, 0.031 g of PdCl ₂ , 0.049 g of P(1-nap) _3, and 0.034 g of AgBF ₄ : The molar ratio of the repeating unit of 3 was 1:9 copolymer (Mw = 5000 g/mole, PDI = 2.05, yield 40%).

(Step 2) A copolymer having an epoxide conversion of 54% was obtained in the same manner as in Step 2 of Example 7 except that the content of mCPBA was changed to 0.5 g (Mw = 5100 g/mole, PDI = 2.05, yield 88%). Comparative example 5

(Step 1) except that 67.0 g of 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 33.0 g of 5-(methoxymethyl)-2- Repeating units of Chemical Formula 2 were obtained in the same manner as in Step 1 of Example 7 except for norbornene, 300 g of xylene, 0.031 g of PdCl ₂ , 0.049 g of P(1-nap) _3, and 0.034 g of AgBF ₄ : The molar ratio of the repeating unit of 3 was 7:3 copolymer (Mw = 5100 g/mole, PDI = 2.05, yield 42%).

(Step 2) A copolymer having an epoxide conversion of 95% was obtained in the same manner as in the step 2 of Example 7 except that the content of mCPBA was changed to 7.2 g (Mw = 5100 g/mole, PDI = 2.05, yield 88%). Comparative example 6

(Step 1) except that 88.7 g of 5-vinyl-2-norbornene was used instead of 5-ethylidene-2-norbornene and the amount used was changed to 11.3 g of 5-(methoxymethyl)-2- Repeating units of Chemical Formula 2 were obtained in the same manner as in Step 1 of Example 7 except for norbornene, 300 g of xylene, 0.032 g of PdCl ₂ , 0.050 g of P(1-nap) ₃ and 0.035 g of AgBF ₄ : The molar ratio of the repeating unit of 3 was 9:1 copolymer (Mw = 5100 g/mole, PDI = 2.05, yield 45%).

(Step 2) A copolymer having an epoxide conversion of 97% was obtained in the same manner as in Step 2 of Example 7 except that the content of mCPBA was changed to 7.2 g (Mw = 5,350 g/m, PDI = 2.06, yield 90%). < Experimental example >

40 g of the cyclic olefin copolymer prepared in the examples and comparative examples, 60 g of cyanate resin (Nanozine-375, Nanoco Technologies) and 0.4 g of initiator (diisopropyl peroxide) Benzene, Sigma-Aldrich was dissolved in a cyclohexanone solvent to give a solid content of 50% to prepare a varnish.

50 g of an inorganic filler (SC2050-HMN, Admatechs) and 21 g of cyclohexanone solvent were placed in a ball mill and ball milled for 2 hours to disperse the inorganic filler. Subsequently, the dispersed inorganic filler was mixed with the previously prepared varnish to prepare a slurry. The slurry thus prepared was immersed in a glass fiber (L-1067, UNITIKA), and then subjected to hot air drying to prepare a prepreg. After laminating the two prepregs thus prepared, a copper foil having a thickness of 35 μm was placed on both sides. The copper foil was laminated, and then heated at 220 ° C using a press and pressed for 90 minutes to manufacture a circuit board having a thickness of 170 μm. The cyclic olefin copolymers used in each of the production examples and comparative preparation examples are shown in Table 1 below. [Table 1]

Subsequently, the glass transition temperature (Tg), copper foil adhesion strength, dielectric constant, and dielectric loss factor of the resin composition prepared as described above were measured on the substrate fabricated above.

The DSC (TA Instruments) was used to measure the glass transition temperature, and the copper foil adhesion strength of the sample was measured in the form of a 90 peel strength. Specifically, the peel strength can be calculated by preparing a laminate sample in which a copper foil having a thickness of 35 μm and a substrate are sequentially formed, and the laminate sample is cut into a width of 10 by a physical stimulus. Rectangular shape of millimeters, and the force required to grasp the end of the cut copper foil using a tensile strength tester (ZWICK) and peel it off from the substrate layer at an angle of 90° and a speed of 50 mm/min. (peel strength).

In addition, a vector network analyzer (Agilent Technologies, Inc.) was used to measure the dielectric constant (Dk) and dielectric loss factor (Df) of the sample at 10 GHz. Subsequently, the content of each component and the known dielectric constant value were used to calculate the single dielectric constant value of the cyclic olefin copolymer of the examples and comparative examples.

The measurement results are summarized in Tables 2 to 5 below. [Table 2] [table 3] [Table 4] [table 5]

The cyclic olefin copolymer comprising a repeating unit containing an epoxy group, a repeating unit containing a vinyl group or an ethylene group, and a repeating unit containing an aliphatic functional group according to the present invention has a single dielectric constant of 2.6 or less, And the dielectric loss factor is 0.007 or less than 0.007, that is, exhibits excellent low dielectric characteristics. In the case where a prepreg is used as the insulating layer, the insulating characteristics are better as the values of the dielectric constant and the dielectric loss factor are lowered. As the dielectric constant and dielectric loss factor increase, the insulation characteristics decrease. Therefore, the transmission loss increases in the high frequency region, thereby adversely affecting the performance, durability, and manufacturing yield of the electronic device.

Further, it can be confirmed from the above experimental examples that the cyclic olefin copolymer exhibits a higher copper foil adhesion strength of 0.6 kgf/cm or more than 0.6 kgf/cm. When the adhesion strength of the copper foil is less than 0.6 kgf/cm, it is easily peeled off when the CCL is prepared using the prepreg and the copper foil, thereby making it difficult to manufacture the product, and even if the product is manufactured, it is difficult to ensure reliability.

However, when not containing all three types of repeating units or repeating units containing an epoxy group exceeding the above ratio, the dielectric characteristics, glass transition temperature or adhesion strength may be lowered.

In particular, it was confirmed that since the cyclic olefin copolymers of Examples 25 to 28 used in Preparation Example 5 to Preparation Example 8 contained a repeating unit containing an ether functional group or a heterocyclic functional group, it was excellent. The dielectric characteristics have a higher glass transition temperature of 268 ° C and a higher copper foil adhesion strength of 0.80 kgf / cm or greater than 0.80 kgf / cm. As described above, confirmation that including specific functional groups allows for a significantly higher copper foil adhesion strength while maintaining lower dielectric characteristics.

On the other hand, in order to compare the viscosity according to the molecular weight, the viscosity of the varnish obtained in Preparation Example 5 to Preparation Example 8 was measured by using a TV-25 viscometer (TOKI Sangkyo), and The results are shown in Table 6 below. [Table 6]

As shown in Table 6, the varnish obtained in Preparation Example 5 to Preparation Example 8 contained a cyclic olefin copolymer having a molecular weight of 2,500 g/mTorr to 10,000 g/mole, and thus was able to maintain 1000 cps or less. Lower viscosity of 1000 centipoise. Thus, there is an advantage that it is easy to manufacture a prepreg.

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Claims (16)

A cyclic olefin copolymer comprising a repeating unit represented by Chemical Formula 1, a repeating unit represented by Chemical Formula 2, and a repeating unit represented by Chemical Formula 3, wherein the repeating unit represented by Chemical Formula 1 is relative to From Chemical Formula 1 to Chemical Formula 3 The total amount of all repeating units represented is from 15 mol% to 60 mol% in the cyclic olefin copolymer: [Chemical Formula 1] Wherein, in Chemical Formula 1, p is an integer of 0 to 4, and R ₁ to R ₄ are each independently hydrogen or an epoxy group substituted or unsubstituted with an alkyl group having 1 to 4 carbon atoms, or R ₁ and R _2, and R ₃ and R ₄ groups consisting of at least one composition selected from the each other to form an epoxy group, with the proviso that excluded the case where R ₁ to R ₄ are hydrogen; [chemical formula 2] Wherein, in Chemical Formula 2, q is an integer of 0 to 4, and R ₅ to R ₈ are each independently hydrogen or an alkyl group substituted or unsubstituted with an alkyl group having 1 to 4 carbon atoms, or R ₅ And at least one selected from the group consisting of R ₆ and R ₇ and R ₈ are bonded to each other to form an alkylidene group, the limitation being that the case where R ₅ to R ₈ are all hydrogen is excluded; 3] Wherein, in Chemical Formula 3, r and m are each independently an integer of 0 to 4, and each R is independently hydrogen, halogen, substituted or unsubstituted C _1-20 alkyl, substituted or unsubstituted a C _1-20 ether, a substituted or unsubstituted C _1-20 alkoxy group, or a substituted or unsubstituted C _{2 -60} heterocyclic ring containing at least one of O, N, Si and S. The cyclic olefin copolymer according to claim 1, wherein the cyclic olefin copolymer has a weight average molecular weight (measured by GPC) of from 2,500 g/m to 10,000 g/mole. . The cyclic olefin copolymer according to claim 1, wherein R in the chemical formula 3 is a substituted or unsubstituted C _1-20 ether, or a substituted or unsubstituted O, N, A C _2-60 heterocyclic ring of at least one of Si and S. The cyclic olefin copolymer according to claim 1, wherein R in the chemical formula 3 is a substituted C _1-20 alkyl group substituted by a C _1-20 alkoxy group. The cyclic olefin copolymer according to claim 1, wherein R in the chemical formula 3 is a functional group represented by the following Chemical Formula 7: [Chemical Formula 7] Wherein, in Chemical Formula 7, at least one of A ₁ and A ₂ is O, N, Si or S, the remainder is carbon, t is an integer of 1 or greater, and "*" forms a bond with the same carbon atom. . The cyclic olefin copolymer according to claim 1, wherein the cured product of the cyclic olefin copolymer has a copper foil adhesive strength of 0.6 kgf/cm or more and 0.6 kgf/cm or more. The cyclic olefin copolymer according to claim 1, wherein the cured product of the cyclic olefin copolymer has a dielectric constant of 2.6 or less at 10 GHz. The cyclic olefin copolymer according to claim 1, wherein the cured product of the cyclic olefin copolymer has a dielectric loss factor of 107 or less at 10 GHz. A method for producing a cyclic olefin copolymer, comprising: arranging a monomer represented by Chemical Formula 4 and a monomer represented by Chemical Formula 5 in a precatalyst containing a Group 10 transition metal, and a metal of the precatalyst Polymerization in the presence of an anionic cocatalyst and a ligand containing a Group 15 element; and reacting the polymer with a peroxyacid to perform an epoxidation reaction, [Chemical Formula 4] Wherein, in Chemical Formula 4, q is an integer of 0 to 4, and R ₅ to R ₈ are each independently hydrogen or an alkyl group substituted or unsubstituted with an alkyl group having 1 to 4 carbon atoms, or R ₅ And at least one selected from the group consisting of R ₆ and R ₇ and R ₈ are bonded to each other to form an alkylene group, which is limited to the case where R ₅ to R ₈ are all hydrogen; [Chemical Formula 5] In Chemical Formula 5, r and m are each independently an integer of 0 to 4, and each R is independently hydrogen, halogen, substituted or unsubstituted C _1-20 alkyl, substituted or unsubstituted C _{1 a -20} ether, a substituted or unsubstituted C _1-20 alkoxy group, or a substituted or unsubstituted C _{2 -60} heterocyclic ring containing at least one of O, N, Si and S. A process for producing a cyclic olefin copolymer as described in claim 9, wherein R in the chemical formula 5 is a substituted or unsubstituted C _1-20 ether, or a substituted or unsubstituted A C _2-60 heterocyclic ring containing at least one of O, N, Si, and S. The method for producing a cyclic olefin copolymer according to claim 9, wherein R in the chemical formula 5 is a substituted C _1-20 alkyl group substituted by a C _1-20 alkoxy group. The method for producing a cyclic olefin copolymer according to claim 9, wherein R in the chemical formula 5 is a functional group represented by Chemical Formula 7: [Chemical Formula 7] Wherein, in Chemical Formula 7, at least one of A ₁ and A ₂ is O, N, Si or S, the remainder is carbon, t is an integer of 1 or greater, and "*" forms a bond with the same carbon atom. . The method for producing a cyclic olefin copolymer according to claim 9, wherein the precatalyst comprises at least one selected from the group consisting of palladium dichloride (PdCl ₂ ), Palladium bromide (PdBr ₂ ), allyl palladium dimer chloride ([(allyl)Pd(Cl)] ₂ ), palladium acetate ((CH ₃ CO ₂ ) ₂ Pd), acetylpyruvate Palladium ([CH ₃ COCH=C(O-)CH ₃ ] ₂ Pd), [PdCl(NB)O(CH ₃ )] ₂ , bis(diphenylmethyleneacetone)palladium ((diphenylmethyleneacetone) ₂ Pd), tris(diphenylmethyleneacetone)dipalladium ((diphenylmethyleneacetone) ₃ Pd ₂ ), palladium nitrate (Pd(NO ₃ ) ₂ ) and NiBr(NP(CH ₃ ) ₃ ) ₄ . The method for producing a cyclic olefin copolymer according to claim 9, wherein the ligand containing a Group 15 element comprises at least one selected from the group consisting of: (2 Hydroxyphenyl)diphenylphosphine, tris(furan-2-yl)phosphine, bis(diphenylphosphino)methane, bis(diphenylphosphino)ethane, phosphite tris(2,4-di- Tert-butyl phenyl ester), tris(o-tolyl)phosphine, tris(p-tolyl)phosphine, tri-1-naphthylphosphine, tributylphosphine, tetrafluoroborate, triphenylphosphine, tricyclohexyl Phosphine, triphenyl phosphite, 1,2-(diphenylphosphino)ethane, tributylphosphine, triphenylphosphine oxide, and 1,2-(diphenylphosphino)butane. The method for producing a cyclic olefin copolymer according to claim 9, wherein the peroxyacid comprises at least one selected from the group consisting of peroxybenzoic acid, peracetic acid, Peroxyformic acid, peroxyphthalic acid, peroxypropionic acid, peroxybutyric acid, trifluoro-peroxyacetic acid, and hydrogen peroxide. The method for producing a cyclic olefin copolymer according to claim 9, wherein in the step of performing the epoxidation reaction, a molar ratio between the polymer and the peroxyacid It is 1:0.1 to 1:5.