阅读说明：本技术 包含光敏部分的嵌段共聚物 (Block copolymers comprising photoactive moieties ) 是由 朴鲁振 金进坤 崔青龙 尹圣琇 于 2019-01-23 设计创作，主要内容包括：本申请可以提供嵌段共聚物及其用途。本申请可以提供嵌段共聚物及其用途。本申请的嵌段共聚物可以具有优异的自组装特性或相分离特性,并且同时具有能够改变首先形成的自组装结构的特性,或者提供能够在聚合物膜中形成相分离结构的图案的嵌段共聚物。(The present application can provide block copolymers and uses thereof. The present application can provide block copolymers and uses thereof. The block copolymer of the present application may have excellent self-assembly characteristics or phase separation characteristics and simultaneously have characteristics capable of changing a self-assembly structure formed first, or provide a block copolymer capable of forming a pattern of a phase separation structure in a polymer film.)

1. A block copolymer comprising a first polymer segment, a second polymer segment, and a third polymer segment,

wherein the block copolymer has a star structure in which three polymer segments are covalently bonded to one point of attachment while sharing the point,

the linking group linking at least one of the three polymer segments to the point of attachment is a cleavable linking group, an

At least one of the first polymer segment through the third polymer segment comprises vinylpyridine units.

2. The block copolymer according to claim 1, wherein two polymer segments of the first polymer segment to the third polymer segment are the same as each other, another polymer segment is different from the two polymer segments, and a polymer segment different from the two polymer segments contains a vinylpyridine unit.

3. The block copolymer according to claim 2, wherein in the segments that are identical to each other in the first polymer segment to the third polymer segment, 50% or more of constituent monomer units are identical to each other, and the difference of the identical monomers in the respective segments is within 20% by weight.

4. The block copolymer according to claim 2, wherein in the same segment as each other of the first polymer segment to the third polymer segment, a deviation in solubility parameter of each polymer segment is within 10%.

5. The block copolymer of claim 2, wherein either of two of the first to third polymer segments that are identical to each other are connected to the point of attachment by the cleavable linker.

6. The block copolymer of claim 1, wherein any of the first polymer segment through the third polymer segment comprises vinylpyridine units and the other two segments comprise styrene units.

7. The block copolymer of claim 1, wherein the cleavable segment comprises a 2-nitrobenzyl, coumarinyl, or pyrenylalkyl group.

8. The block copolymer of claim 1, wherein the number average molecular weight is in the range of 1000 to 1000000.

9. The block copolymer of claim 1, wherein the molecular weight distribution is in the range of 1.01 to 2.

10. A polymer film comprising the self-assembling block copolymer of claim 1.

11. The polymer film of claim 10, wherein two or more phase separated structures selected from the group consisting of: spherical structures, columnar structures, helical structures, and layered structures.

12. The polymer film of claim 10, wherein one of the first through third polymer segments in the block copolymer is mixed with a block copolymer comprising two other segments in a broken state.

13. The polymer film of claim 12, wherein the polymer segments in the broken state comprise styrene units.

14. A method for forming a polymer film on a substrate, the polymer film comprising the self-assembled block copolymer of claim 1, the method comprising the steps of:

using the block copolymer of claim 1 to achieve a first phase separated structure; and cleaving cleavable linking groups of the block copolymer that achieve the first phase separated structure,

wherein after the step of breaking, a second phase separation structure different from the first phase separation structure is formed in the polymer film.

15. The method for forming a polymer film according to claim 14, wherein the first phase separation structure includes a spherical structure, and the second phase separation structure includes a columnar structure.

Technical Field

This application claims benefit of the filing date of korean patent application No. 10-2018-0010050, filed on 26.1.2018, the disclosure of which is incorporated herein by reference in its entirety.

The present application relates to block copolymers comprising a photoactive moiety.

Background

The block copolymer has a molecular structure in which polymer blocks having different chemical structures are linked via covalent bonds. The block copolymer may form a periodically arranged structure such as a sphere, a column, a helix, or a layer by phase separation. The domain size of the structure formed by the self-assembly phenomenon of the block copolymer can be widely controlled and various types of structures can be manufactured, so that the block copolymer can be applied to high-density magnetic storage media, nanowire manufacturing, various next-generation nano devices (e.g., quantum dots or metal dots or magnetic recording media), or patterning by photolithography, and the like.

Disclosure of Invention

Technical problem

Block copolymers and uses thereof are provided.

Technical scheme

The present application relates to block copolymers. In the present application, the term block copolymer is a copolymer in which two polymer segments different from each other are linked by a covalent bond.

In the present application, the fact that two polymer segments are the same means a case corresponding to any one of the following three cases. First, (1) when the kinds of monomer units contained as main components are the same as each other in any two polymer segments, or (2) when 50% or more, 55% or more, 60% or more, 65% or more, 70% or more, 75% or more, 80% or more, 85% or more, or 90% or more of the kinds of monomer units contained in the two polymer segments are common, and the weight ratio deviation of the common monomer units in each polymer segment is within 30%, within 25%, within 20%, within 15%, within 10%, or within 5%, the two polymer segments may be regarded as the same. Here, it may be appropriate for the ratio of the common monomer units to satisfy both polymer segment modes. For example, if any polymer segment 1 has monomer units of A, B, C, D and F and the other polymer segment 2 has monomer units of D, F, G and H, the common monomer units in the polymer segments 1 and 2 are D and F, with a common ratio of 40% in the position of the polymer segment 1 (100 × 2/5) because two of the five in total are common, but the ratio is 50% in the position of the polymer segment 2 (100 × 2/5). Therefore, in this case, the two polymer segments may be regarded as being different because the common ratio is not less than 50% in only the polymer segment 2. On the other hand, the weight ratio deviation of the co-monomers is the percentage of the value where the major weight ratio minus the minor weight ratio divided by the minor weight ratio. For example, in the above case, if the weight ratio of the D monomer units in the segment 1 is about 40% based on 100% of the total weight ratio of all the monomer units in the segment 1, and the weight ratio of the D monomer units in the segment 2 is about 30% based on 100% of the total weight ratio of all the monomer units in the segment 2, the weight ratio deviation may be approximately 33% (═ 100 × (40-30)/30). If the comonomer units are two or more in both segments, in order to make them the same segment, when a deviation of weight ratio is within 30% is satisfied for all the comonomers or for the monomer unit as a main component, it may be considered as a comonomer.

In another example, two segments may be considered identical even if the solubility parameters of any two segments are within 30%, within 25%, within 20%, within 15%, within 10%, or within 5%. As in the case of the weight ratio deviation, the deviation is the percentage of the value where the small solubility parameter is divided by the large solubility parameter minus the small solubility parameter.

Each polymer segment identified as being the same by the above criteria may be a different type of polymer (e.g., either segment is in the form of a block copolymer and the other segment is in the form of a random copolymer), but it may also be suitably the same type of polymer.

In the present application, any of the three criteria may be considered to be the same if they are met. For example, even if the solubility parameter deviates by more than 30%, it may be the same segment when the ratio of the co-monomers is 50% or more and the weight ratio deviation is 30% or less, and vice versa. Conversely, when all three criteria are not met, they may be considered different segments.

In the present specification, the fact that a certain component is contained as a main component in the main body means the case where: the weight ratio of the components contained therein is 55% or more, 60% or more, 65% or more, 70% or more, 75% or more, 80% or more, 85% or more, or 90% or more, and in this case, the upper limit of the ratio is not particularly limited, and it may be, for example, about 100%. For example, the fact that component a is contained as a main component in component B is the case: the weight of component a contained in the relevant component B is within the above range based on the total weight of component B.

The block copolymers of the present application comprise at least a first polymer segment, a second polymer segment, and a third polymer segment. The three segments may be the same or different from each other, but the case where all three segments are the same is not included. In one example, the block copolymer may have a star structure in which three polymer segments are covalently bonded to one point of attachment while sharing the point. Such block copolymers are also known in the art as so-called heteroarm block copolymers. The block copolymer of the present application may also have additional polymer segments as long as it contains at least three segments. In one example, the block copolymer of the present application can have 3 to 10, 3 to 8, 3 to 6, 3, or 4 segments.

In block copolymers, at least one of the three polymer segments may be connected to the point of attachment by a so-called cleavable linker. In the present application, a cleavable linking group means a linking group that can be cleaved by an external action such as heat application or light irradiation. Such linking groups are well known.

The applicant has confirmed that in the block copolymer having a star structure as above, a self-assembled structure can be formed by connecting at least one polymer segment by a cleavable linking group, and then the relevant self-assembled structure can be changed as described below. For example, without being limited by theory, it is considered that when a cleavable linking group is cleaved by an external action after a self-assembled structure is formed by applying a block copolymer comprising three segments, a blend of the cleaved segment and the remaining block copolymer is formed, and curvature at the interface of separated phases in a phase separation structure generated by the formed blend is changed, whereby the phase separation structure is changed.

In particular, the applicant has found that by making at least any one of the three polymer segments, i.e., the first polymer segment to the third polymer segment, contain a vinylpyridine unit, a block copolymer in which conversion between a spherical structure and a columnar structure is efficiently performed can be obtained. In particular, the block copolymer having the above structure may be a block copolymer: a globular structure is formed when all three segments are linked to each other, whereas a columnar structure is achieved when the cleavable linking groups are separated. The segment containing a vinylpyridine unit may contain a vinylpyridine unit as a main component.

In order to achieve the above action more effectively, any one of the first polymer segment to the third polymer segment in the block copolymer may be different from the other two polymer segments. In one example, two polymer segments in the first through third polymer segments in the block copolymer can be the same as each other, and the other polymer segment can be different from the two polymer segments. In such a structure, the segments connected by the cleavable linking group may be either of two polymer segments identical to each other. In this case, when the broken segment in the blend formed by the breaking is mixed with any one of the segments in the remaining block copolymer which realizes the phase separation structure and is immiscible with the other segment, a new structure of the phase separation structure can be realized.

The specific kind of each segment in the block copolymer is not particularly limited. For example, the first polymer segment to the third polymer segment may each be selected from the following segments to satisfy the above condition: polyvinylpyrrolidone segments, polylactic acid segments, polyvinylpyridine segments, polystyrene segments (e.g., polystyrene or polytrimethylsilylstyrene), polyalkylene oxide segments (e.g., polyethylene oxide), polybutadiene segments, polyisoprene segments, polyolefin segments (e.g., polyethylene) or poly (alkyl (meth) acrylate) segments (e.g., polymethyl methacrylate).

In one example, the polymer segment that is different from the two polymer segments can be a polymer segment that includes vinylpyridine units. Further, in this case, the two polymer segments different from the polymer segment containing the vinylpyridine unit may each contain a styrene unit, and such a styrene unit may be contained as a main component.

In the present application, the type of the cleavable linking group that links the polymer segments is not particularly limited, and known cleavable linking groups may be applied. For example, the linking group is a photocleavable linking group, which may be a linking group containing 2-nitrobenzyl, coumarinyl, pyrenylalkyl, or the like, as known linking groups. Such linkers are well known, and methods of joining segments by applying such linkers are also known. In the present application, a suitable linking group can be selected and used among these known linking groups without limitation.

The number average molecular weight (Mn) of the block copolymer may be, for example, in the range of 1000 to 1000000. In the present specification, the term number average molecular weight is a conversion value to standard polystyrene measured using GPC (gel permeation chromatography), and the term molecular weight herein means a number average molecular weight unless otherwise specified. In another example, the molecular weight (Mn) can be, for example, 5000 or greater, 10000 or greater, 50000 or greater, 100000 or greater, 300000 or greater, 400000 or greater, or 500000 or greater. In another example, the molecular weight (Mn) may be approximately 900000 or less, 800000 or less, or 700000 or less. The polydispersity (Mw/Mn) of the block copolymer may be in the range of 1.01 to 2. In another example, the polydispersity may be about 1.05 or greater, or about 1.1 or greater. In another example, the polydispersity may be about 1.5 or less.

Within this range, the block copolymer may exhibit suitable self-assembly characteristics. The number average molecular weight of the block copolymer and the like can be adjusted in consideration of a desired self-assembled structure and the like.

When the block copolymer contains at least the first segment to the third segment, the ratio of each segment in the block copolymer is not particularly limited, and may be appropriately selected in consideration of the desired self-assembly characteristics. For example, as described above, when any two of the first segment to the third segment are the same segment and the other is a different segment, the ratio of one different segment in the block copolymer may be in the range of 10 mol% to 90 mol%.

The method for producing the block copolymer of the present application is not particularly limited, and known methods may be applied.

For example, a block copolymer can be produced by a CLP (controlled/living polymerization) method using monomers forming each segment. For example, there are the following methods: an anionic polymerization method in which a block copolymer is synthesized by using an organic rare earth metal complex as a polymerization initiator or by using an organic alkali metal compound as a polymerization initiator in the presence of an inorganic acid salt (e.g., an alkali metal or an alkaline earth metal); an anionic polymerization method in which a block copolymer is synthesized by using an organic alkali metal compound as a polymerization initiator in the presence of an organoaluminum compound; atom Transfer Radical Polymerization (ATRP) using an atom transfer radical polymerization agent as a polymerization initiator; ARGET (activator regenerated by electron transfer) Atom Transfer Radical Polymerization (ATRP) which uses an atom transfer radical polymerization agent as a polymerization initiator but performs polymerization under an organic or inorganic reducing agent that generates electrons; ICAR (initiator continuous activator regeneration) atom transfer radical polymerization; polymerization via reversible addition-fragmentation chain transfer (RAFT) using an inorganic reducing agent and a reversible addition-fragmentation chain transfer agent; or a method using an organic tellurium compound as an initiator, and the like, and an appropriate method can be selected and applied among these methods.

In this process, an initiator, a chain transfer agent, or a block copolymer in which a protecting group or the like is used may be applied to form a star structure, and a known method for introducing a cleavable linking group may also be performed.

The present application also relates to polymer films comprising the block copolymers. The polymer film can be used in various applications, for example, in various electric or electronic components, a patterning process, a recording medium (such as a magnetic storage medium and a flash memory), or a biosensor, and the like.

In one example, the block copolymer in the polymer film can achieve periodic structures, including spherical, columnar, helical, lamellar, and the like, by self-assembly.

For example, the first segment or the second segment in the block copolymer or another segment in the other segments covalently bonded thereto may form a regular structure such as a lamellar shape or a columnar shape.

In one example, the phase separation structure in the block copolymer may be a structure in which two or more of the above-described structures are present together. As described above, such a structure may be formed by the following process: after the self-assembled structure is first formed by applying the block copolymer of the present application, the cleavable linking group is cleaved. Thus, in this case, one of the first to third polymer segments may be mixed in a broken state with a block copolymer containing two other segments in the polymer film.

In one example, the spherical structure may be realized in a state or a portion in which the first segment to the third segment are all linked in the polymer film, and the columnar structure may be realized in a state or a portion in which one of the first polymer segment to the third polymer segment is mixed with a block copolymer including the other two segments in a broken state.

Here, the polymer segment mixed with the block copolymer including the other two segments in a broken state may be a segment including a styrene unit.

The present application also relates to methods for forming polymer films using the block copolymers. The method can include forming a polymer film comprising the block copolymer in a self-assembled state on a substrate. For example, the method may include the following processes: a layer of a block copolymer or a coating liquid in which a block copolymer is diluted in an appropriate solvent is formed on a substrate by coating or the like, and if necessary, the layer is aged or heat-treated.

The aging or heat treatment may be based on, for example, the phase transition temperature or glass transition temperature of the block copolymer, and may be performed, for example, at a temperature higher than the glass transition temperature or phase transition temperature. The time for performing this heat treatment is not particularly limited, and the treatment may be performed, for example, in the range of about 1 minute to 72 hours, but the time may be changed as needed. The heat treatment temperature of the polymer film may be, for example, about 100 ℃ to 250 ℃, but this may be changed in consideration of the block copolymer to be used.

In another example, the formed layer may also be subjected to solvent aging in a non-polar solvent and/or a polar solvent for about 1 minute to 72 hours at room temperature.

In one example, a method for forming a polymer film may include the steps of: a first phase-separated structure is realized using the above block copolymer; and cleaving the cleavable linking group of the block copolymer that realizes the first phase separation structure, and as described above, a second phase separation structure different from the first phase separation structure may be formed in the polymer film by the cleaving step. In this case, the method of cleaving the cleavable linking group is not particularly limited, and an appropriate method may be selected in consideration of the kind of the linking group applied.

In one example, the first phase separation structure may be a spherical structure and the second phase separation structure may be a columnar structure.

Such breaking may be performed in the entire polymer film, or may be performed only in a part by a mask or the like. Each of the first phase separation structure and the second phase separation structure may be selected from any one of a spherical structure, a columnar structure, a helical structure, and a layered structure.

The present application also relates to a patterning method. For example, the method may include the following processes: any segment of the block copolymer is selectively removed from a laminate having a substrate and a polymer film formed on a surface of the substrate and comprising the self-assembled block copolymer. The method may be a method of forming a pattern on a substrate. For example, the method can include forming a polymer film comprising a block copolymer on a substrate, selectively removing one or more blocks of the block copolymer present in the film, and then etching the substrate. In this way, a fine pattern of, for example, a nanometer order can be formed. In addition, various types of patterns, such as nanorods or nanopores, may be formed by the above-described method according to the shape of the block copolymer in the polymer film. If necessary, a copolymer or a homopolymer, etc., which is different from the block copolymer, may be mixed for pattern formation. The type of the substrate applied to this method is not particularly limited and may be selected as needed, for example, silicon oxide or the like may be applied.

For example, the method can form nanoscale patterns of silicon oxide that exhibit high aspect ratios. For example, after forming a polymer film on silicon oxide and selectively removing any block of a block copolymer (which is in a state in which the block copolymer in the polymer film forms a predetermined structure), the silicon oxide may be etched by various means such as reactive ion etching or the like to achieve various shapes including patterns of nanorods or nanopores or the like.

The method for selectively removing any one segment in the block copolymer in the above method is not particularly limited, and for example, a method of removing a relatively soft block by irradiating a polymer film with an appropriate electromagnetic wave (e.g., ultraviolet rays or the like) can be used. In this case, the ultraviolet irradiation conditions are determined according to the type of the block in the block copolymer, and the method may be performed, for example, by irradiating with ultraviolet rays having a wavelength of about 254nm for 1 minute to 60 minutes.

In addition, after the ultraviolet irradiation, a step of treating the polymer film with an acid or the like to further remove the segment decomposed by the ultraviolet ray may be further performed.

Further, the step of etching the substrate using the polymer film in which the blocks are selectively removed as a mask is not particularly limited, and it may be performed, for example, by using CF₄A reactive ion etching step of/Ar ion or the like is performed, and after this process, a step of removing the polymer film from the substrate by oxygen plasma treatment or the like may also be performed.

Advantageous effects

The present application can provide block copolymers and uses thereof. The block copolymer of the present application may have excellent self-assembly characteristics or phase separation characteristics and simultaneously have characteristics capable of changing a self-assembly structure formed first, or provide a block copolymer capable of forming a pattern of a phase separation structure in a polymer film.

Drawings

Fig. 1 to 10 are analysis results of the compounds or polymers produced in the preparation examples.

FIG. 11 is a GPC curve of the polymer (D) in example 1 before and after ultraviolet irradiation.

Fig. 12 is a TEM image of a sample of polymer (D) of example 2 before uv irradiation.

Fig. 13 is a TEM image of a sample of the polymer (D) of example 2 after ultraviolet irradiation, in which the small image at the upper left is a TEM image taken in the vertical direction.

FIG. 14 is a SAXS plot of a sample of polymer (D) from example 2 prior to UV irradiation.

FIG. 15 is a SAXS plot after UV irradiation of a sample of polymer (D) of example 2.

FIG. 16 is a cross-sectional AFM image of a thin film sample of Polymer (D) in example 3 before UV irradiation.

FIG. 17 is a cross-sectional AFM image of a thin film sample of Polymer (D) in example 3 after UV irradiation.

FIG. 18 is an SEM image of polymer (D) in example 4 before UV irradiation, and the film sample was transformed into metal nanoparticles.

Fig. 19 is an SEM image of example 4, the thin film sample having been converted into metal nanoparticles.

Detailed Description

Hereinafter, the present application will be described in detail by way of examples, but the scope of the present application is not limited by the following examples.

NMR measurement

NMR analysis was performed at room temperature using NMR spectrometers including a Varian Unity Inova (500MHz) spectrometer with a triple resonant 5mm probe. The analytes were dissolved in a solvent for NMR measurement (CDCl)₃) To a concentration of about 10mg/ml and chemical shifts are expressed in ppm.

< abbreviations of application >

br is broad, s is singlet, d is doublet, dd is doublet, t is triplet, dt is doublet, q is quartet, p is quintet, and m is multiplet.

GPC (gel permeation chromatography)

The number average molecular weight (Mn) and molecular weight distribution were measured using GPC (gel permeation chromatography). Analytes such as block copolymers of examples or comparative examples or large initiators were placed in 5mL vials and diluted in THF (tetrahydrofuran) to a concentration of about 1 mg/mL. Then, the standard sample for calibration and the sample to be analyzed were filtered through a syringe filter (pore size: 0.45 μm), and then measured. ChemStation from Agilent Technologies was used as an analytical procedure, and the elution time of the sample was compared with a calibration curve to obtain a weight average molecular weight (Mw) and a number average molecular weight (Mn), respectively, and a molecular weight distribution was calculated from the ratio thereof (Mw/Mn). The measurement conditions of GPC are as follows.

< GPC measurement conditions >

The instrument comprises the following steps: 1200 series from Agilent Technologies

Column: two PLgel mixed B from Polymer Laboratories were used

Solvent: THF (tetrahydrofuran)

Column temperature: 35 deg.C

Sample concentration: injection of 1mg/mL, 200. mu.L

Standard samples: polystyrene (Mp: 3900000, 723000, 316500, 52200, 31400, 7200, 3940, 485)

Preparation example 1.

The compound of the following formula 1 (5- (4-bromobutoxy) -2-nitrophenyl) methanol) was prepared in the following manner. 5g (29.6mmol) of 5-hydroxy-1-nitrobenzyl alcohol was dissolved in 200mL of acetonitrile, to which was then added an aqueous solution of sodium hydride (2.16g, 90mmol) while stirring at 0 ℃. The resulting yellow precipitate was filtered and dissolved in DMF (150 mL). After complete dissolution, dibromobutane (7.03g, 32.56mmol) was slowly added at room temperature. After 12 hours of the reaction, distilled water was poured to terminate the reaction, and the reaction was extracted with ethyl acetate. The extract was purified by column chromatography to obtain a compound of the following formula 1. FIG. 1 shows the results of analysis of this compound.

[ formula 1]

< results of NMR analysis >

¹H-NMR(400MHz，CDCl₃)：d8.06(d，1H)；d7.12(s，1H)；d6.78(d，1H)；d4.88(s，2H)；d4.02(t，2H)；d3.32(t，2H)；d3.20(s，1H)；d1.98(p，2H)；d1.90(p，2H).

Preparation example 2.

The compound of the following formula 2 (5- (4-azidobutoxy) -2-nitrophenyl) methanol) was prepared in the following manner. The compound of formula 1 in preparation example 1 (8.5g, 27.9mmol) and sodium azide (2.36g, 36.3mmol) were dissolved in a mixed solvent of acetone and distilled water (6: 1), and refluxed at 65 ℃ under a nitrogen atmosphere to obtain the objective product. FIG. 2 shows the results of analysis of this compound.

[ formula 2]

< results of NMR analysis >

¹H-NMR(400MHz，CDCl₃)：d8.06(d，1H)；d7.12(s，1H)；d6.78(d，1H)；d5.52(s，2H)；d4.02(t，2H)；d3.32(t，2H)；d3.20(s，1H)；d1.98(p，2H)；d1.90(p，2H).

Preparation example 3.

A compound of the following formula 3 (5- (4-azidobutoxy) -2-nitrophenyl-2-bromo-2-methylpropionate) was prepared in the following manner. The compound of formula 2 in preparation example 2 (7.19g, 27.0mmol) was dissolved in THF (tetrahydrofuran), and 2-bromo-2-methylpropanoyl bromide (7.45g, 32.4mmol) was added while stirring with triethylamine (3.24g, 32.0mmol) at 40 ℃ under a nitrogen atmosphere. Salts generated during the reaction were filtered off, and the residue was purified by column chromatography to obtain a compound of the following formula 3. FIG. 3 shows the results of analysis of this compound.

[ formula 3]

< results of NMR analysis >

¹H-NMR(400MHz，CDCl₃)：d8.06(d，1H)；d7.12(s，1H)；d6.78(d 1H)；d5.52(s，2H)；d4.02(t，2H)；d3.32(t，2H)；d1.99(s，6H)；d1.98(p，2H)；d1.90(p，2H).

Preparation example 4.

A compound of the following formula 4 (1-bromo-4- (1-phenylvinyl) benzene) was prepared in the following manner. Methyltriphenylphosphine bromide (7.2g, 20mmol) and potassium tert-butoxide (2.3g, 20mmol) were placed in THF (tetrahydrofuran) (50mL) and THF (tetrahydrofuran) (35mL) with p-bromobenzophenone (3.4g, 17mmol) dissolved therein was slowly added while stirring at room temperature and the mixture was allowed to react for 3 hours. After the reaction, a saturated aqueous ammonium chloride solution was added to terminate the reaction, and the reaction mixture was extracted with diethyl ether to obtain the compound of formula 4 as a product. FIG. 4 shows the results of analysis of this compound.

[ formula 4]

< results of NMR analysis >

¹H-NMR(400MHz，CDCl₃)：d7.33(d，2H)；d7.19(d，5H)；d7.05(d，2H)；d5.32(d，2H).

Preparation example 5.

A compound of the following formula 5 (tert-butyldimethyl ((4- (1-phenylvinyl) phenyl) ethynyl) silane) was prepared in the following manner. The compound of formula 4 in preparation example 4 (3.89g, 15mmol) was completely dissolved in piperidine (50mL), and tert-butyldimethylsilylacetylene (2.53g, 18mmol) was then added thereto. Then, the reaction was allowed to proceed at 50 ℃ for 24 hours, followed by filtration and extraction with hexane, and then the extract was purified by column chromatography to obtain a compound of formula 5. FIG. 5 shows the results of analysis of this compound.

[ formula 5]

< results of NMR analysis >

¹H-NMR(400MHz，CDCl₃)：d7.33(d，2H)；d7.19(d，5H)；d7.05(d，2H)；d5.32(d，2H)；d1.03(s，9H)；d0.22(d，6H).

Preparation example 6

Polymer (A) of the following formula 6 was synthesized. Using the compound of formula 3 in production example 3 (50mg) as an initiator, and stirring at 90 ℃ under a nitrogen atmosphere, a reaction solution in which styrene (6mL), copper (I) bromide (18mg) and PMDETA (N, N', N ", N ″ -pentamethyldiethylenetriamine, 24 μ L) were mixed was freeze-melted three times and polymerized. The polymer solution was passed through an alumina column to remove the catalyst and precipitated in methanol to obtain a powder of polymer (a). The number average molecular weight (Mn) of polymer (A) was about 12000 and the molecular weight distribution (Mw/Mn) was about 1.18. Fig. 6 shows the measurement results of the polymer (a).

[ formula 6]

Preparation example 7.

Polymer (B) of the following formula 7 was synthesized. Lithium chloride (0.3g) and THF (80mL) were placed in the reactor under an argon atmosphere and stirred at-78 deg.C to allow them to dissolve sufficiently. Subsequently, 86. mu.L of a 1.2M concentration sec-butyllithium solution was added, and purified styrene (3.0g) was added thereto. After stirring well for about 1 hour, the compound of formula 5 in preparation example 5 was added. Then, 2-vinylpyridine (2VP) (1.25g) was added and stirred for about 1 hour, and then the reaction was terminated with 2-propanol to obtain polymer (B). The number average molecular weight (Mn) of polymer (B) was about 45000 and the molecular weight distribution (Mw/Mn) was about 1.20. Further, the mass fraction of the polystyrene segment in the polymer (B) was about 72%. FIG. 7 shows the result of GPC measurement of the polymer (B).

[ formula 7]

Preparation example 8.

Synthesizing a polymer (C) of the following formula 8 in which TBDMS as a protecting group is removed from the polymer (B) of the above formula 7. The polymer (B) of preparation example 7 was completely dissolved in THF and sufficiently degassed with nitrogen, and 10mL of a tetrabutylammonium fluoride solution (1.0M in THF) was added thereto and stirred at room temperature for 12 hours. After the reaction, THF was removed and the solvent was changed to chloroform, and the reaction was purified by column chromatography. As shown in FIG. 8, it was confirmed that the reaction corresponded to Si (CH) contained in the protective group in the polymer (B)₃) The peak of (d) of (2) disappears.

[ formula 8]

Preparation example 9.

The polymer (A) and the polymer (C) were coupled to synthesize a hetero-arm block copolymer having three polymer segment arms (polymer (D)). 0.1g (1.2 equivalents) of the polymer (A) and 0.25g (1.0 equivalent) of the polymer (C) were sufficiently dissolved in 5ml of THF, followed by deaeration with nitrogen. After PMDETA (N, N', N "-pentamethyldiethylenetriamine, 24mL) and copper (I) bromide (18mg) were sequentially charged into the reactor, the reactor was sealed and stirred at room temperature for 2 days, and then the remaining polymer (a) was removed by purification to obtain polymer (D). The number average molecular weight (Mn) of polymer (D) was about 60000 and the molecular weight distribution (Mw/Mn) was about 1.20. Further, the mass fraction of the polystyrene segment in the polymer (D) was about 80%. Fig. 9 is a GPC measurement result of the polymer (D), and fig. 10 is a result of comparing NMR before and after the reaction.

[ formula 9]