JP5590491B2 - Polymer compound, polymer organic semiconductor material and organic semiconductor device - Google Patents

Description

  The present invention relates to a polymer compound, a polymer organic semiconductor material, and an organic semiconductor device.

  Organic semiconductor materials are indispensable materials for manufacturing organic devices such as organic transistors, organic EL, and organic thin-film solar cells. In particular, in recent years, the demand for soluble organic semiconductor materials that can be applied to printable electronics (organic device technology manufactured by a coating process such as a spin coat method or an ink jet method) is rapidly increasing. Among these, polymer materials (semiconductor polymers) are superior to low-molecular materials in terms of film-forming properties and film quality, and are attracting the most attention in printable electronics.

  Semiconductor materials are required to have high charge mobility. In the case of an organic polymer material, the movement of electrons due to hopping between polymer main chains is dominant, so the organic polymer material is required to have a strong intermolecular interaction (Non-patent Document 1).

  In recent years, since organic compounds used in pigments have strong intermolecular interactions, their use as organic semiconductor materials has begun to be studied. For example, Non-Patent Document 2 discloses an organic semiconductor material that uses quinacridone that is used in red pigments.

Two-dimensional charge transport in self-organized, high-mobility conjugated polymers; Sirringhaus, P.A. J. et al. Brown, R.A. H. Friend, M .; M.M. Nielsen, K.M. Bechgaard, B.M. M.M. W. Langeveld-Voss, A .; J. et al. H. Spieling, R.M. A. J. et al. Janssen, E .; W. Meijer, P.A. Herwig, D.H. M.M. de Leeuw; Nature 1999, 401, 685-688. Novel White Electroluminescent Single Polymer Derived from Fluorene and Quinacridone; Ju Liu, Baoxiang Gao, Yanxiang Cheng, Zhiyuan Xie, Yanhou Geng, Lixiang Wang, Xiabin Jing, and Fosong Wang; Macromolecules 2008,41,1162-1167

  The polymer compound disclosed in Non-Patent Document 1 is a compound obtained by polymerizing quinacridone using fluorene as a linking group. Since fluorene has a benzene ring (6-membered ring) at both ends, steric hindrance occurs due to overhang of hydrogen or the like bonded to the benzene ring. This steric hindrance weakens intermolecular interactions, making it difficult to improve charge mobility.

  The present invention has been made in view of the above-described matters, and an object thereof is to provide a polymer compound, a polymer organic semiconductor material, and an organic semiconductor device exhibiting good charge mobility.

（一般式（１）及び（２）中、Ｒはそれぞれ独立して水素、又はアルキル基であり、Ｘ^１１〜Ｘ^１６及びＸ^２１〜Ｘ^２６は、同一又は異なって、炭素若しくは窒素原子を示し、炭素の場合は置換基として水素、ハロゲン原子、又はアルキル基のいずれかを有する。Ｚは一般式（３）で表される構造である。）

（一般式（３）中Ｘ^３１〜Ｘ^３４は、同一又は異なって、炭素若しくは窒素原子を示し、炭素の場合は置換基として水素、ハロゲン原子、アルキル基、アルコキシ基、アルコキシカルボニル基、又はアルキルカルボニル基のいずれかを有し、Ｙは２価の複素環基を示し、ｎは０又は正の整数を表す。） The polymer compound according to the first aspect of the present invention is:
It is represented by the following general formula (1) or (2).

(In General Formulas (1) and (2), each R is independently hydrogen or an alkyl group, and X ^{11 to} X ¹⁶ and X ^{21 to} X ²⁶ are the same or different and represent a carbon or nitrogen atom. In the case of carbon, it has any one of hydrogen, a halogen atom, and an alkyl group as a substituent. Z is a structure represented by the general formula (3).)

(In formula (3), X ^{31 to} X ³⁴ are the same or different and each represents a carbon or nitrogen atom, and in the case of carbon, hydrogen, a halogen atom, an alkyl group, an alkoxy group, an alkoxycarbonyl group, or an alkyl as a substituent. Any of carbonyl groups, Y represents a divalent heterocyclic group, and n represents 0 or a positive integer.)

Further, it is preferably represented by the following general formula (4) or (5).

The polymer organic semiconductor material according to the second aspect of the present invention is
It contains the above polymer compound.

The organic semiconductor device according to the third aspect of the present invention is
It contains the above organic semiconductor material.

  The polymer compound according to the present invention is a compound obtained by polymerizing quinacridones using a cyclic compound having a 5-membered ring such as a thiophene ring as a linking group. Since the five-membered ring has less steric hindrance than the benzene ring, it forms a good molecular arrangement. For this reason, the intermolecular interaction is high, and the movement of electrons by hopping tends to occur between the polymer main chains. By using this polymer compound as an organic semiconductor material, an organic semiconductor device exhibiting good charge mobility can be obtained.

It is (A) sectional drawing and (B) top view which show the structure of the FET element used for the Example. It is a graph which shows the transfer characteristic of the FET element which used the high molecular compound (P1) in the Example. It is a graph which shows the output characteristic of the FET element using the high molecular compound (P1) in the Example. It is a graph which shows the transfer characteristic of the FET element which used the high molecular compound (P2) in the Example. It is a graph which shows the output characteristic of the FET element which used the high molecular compound (P2) in the Example.

(Polymer compound)
The polymer compound according to the present embodiment is represented by the general formula (1) or (2).

In general formulas (1) and (2), each R is independently hydrogen or an alkyl group, and X ^{11 to} X ¹⁶ and X ^{21 to} X ²⁶ are the same or different and each represents a carbon or nitrogen atom. In the case of carbon, it has either a hydrogen atom, a halogen atom or an alkyl group as a substituent.

  When R is an alkyl group, it may be a linear or branched alkyl group, preferably having 6 to 30 carbon atoms, more preferably 8 to 24 carbon atoms.

X ¹¹ is to X ¹⁶ and ^X 21 ^{to X 26} is a carbon, when the substituent on the carbon of a halogen atom, preferably a chlorine atom or a fluorine atom, more preferably a fluorine atom.

When X ^{11 to} X ¹⁶ and X ^{21 to} X ²⁶ are carbon and the substituent on the carbon is an alkyl group, it may be either a linear or branched alkyl group, and the number of carbon atoms is 6 to 30 Preferably, it is 8-24.

In the general formulas (1) and (2), Z is a structure represented by the general formula (3).

In the general formula (3), X ^{31 to} X ³⁴ are the same or different and each represents a carbon or nitrogen atom. In the case of carbon, hydrogen, a halogen atom, an alkyl group, an alkoxy group, an alkoxycarbonyl group, or an alkyl as a substituent. It has either a carbonyl group, Y represents a divalent heterocyclic group, and n represents 0 or a positive integer.

When X ^{31 to} X ³⁴ are carbon and the substituent on the carbon is a halogen atom, a chlorine atom or a fluorine atom is preferable, and a fluorine atom is more preferable.

When X ^{31 to} X ³⁴ are carbon and the substituent on the carbon is an alkyl group, it may be either a linear or branched alkyl group, and preferably has 6 to 30 carbon atoms, and 8 to 24 More preferably.

When X ^{31 to} X ³⁴ are carbon and the substituent on the carbon is an alkoxy group, the alkyl group portion may be either linear or branched, and preferably has 6 to 30 carbon atoms. 8 to 24 is more preferable.

When X ^{31 to} X ³⁴ are carbon and the substituent on the carbon is an alkoxycarbonyl group, the alkyl group moiety may be linear or branched, and the carbon number is 6 to 30 Preferably, it is 8-24.

When X ^{31 to} X ³⁴ are carbon and the substituent on the carbon is an alkylcarbonyl group, the alkyl group portion may be either linear or branched, and the carbon number is 6 to 30 Preferably, it is 8-24.

  In formula (3), Y is not particularly limited, but for example, structures represented by the following formulas (6) to (16) are preferable.

式（６）〜（１６）中、Ｒは水素またはアルキル基であり、アルキル基は直鎖状又は分岐状のいずれの形状でもよく、炭素数は６〜３０であることが好ましく、８〜２４であることがより好ましい。

In the formulas (6) to (16), R is hydrogen or an alkyl group, and the alkyl group may be linear or branched, and preferably has 6 to 30 carbon atoms, and 8 to 24 It is more preferable that

  In formula (3), n is preferably 0 or 1.

Especially, it is preferable that a high molecular compound is represented by either General formula (4) or (5).

  In general formulas (4) and (5), R is an alkyl group, which may be linear or branched, and preferably has 6 to 30 carbon atoms, and preferably 8 to 24 carbon atoms. More preferred.

  In general formulas (4) and (5), Z has the same meaning as Z in general formulas (1) and (2).

  The polymer compound according to this embodiment is a polymer compound obtained by polymerizing a quinacridone bonded with a cyclic compound having a five-membered ring such as thiophene. Quinacridones are compounds that are mainly used as red pigments and polarize within the molecule, and therefore have strong intermolecular interactions. For this reason, it is useful as a skeleton of an organic semiconductor.

  And since the high molecular compound is a form in which a cyclic compound having a five-membered ring is bonded between quinacridones, compared to a case where a dry compound having a benzene ring is bonded between quinacridones, Steric hindrance is alleviated. Thereby, a highly oriented molecular arrangement is formed, electron transfer is easily caused by hopping between polymer main chains, and it is useful as an organic semiconductor material exhibiting good charge mobility.

  Furthermore, Y in Z represented by the general formula (3) in the general formulas (1), (2), (4) and (5) is thiazolothiazole, benzobisthiazole, benzooxadiazole, benzothiadiazole , Thiadiazolopyridine, thiadiazolopyridazine, thienopyrrole dione, phthalimide, diketopyrrolopyrrole, naphthalene dicarboximide, these are acceptors, while quinacridones are donors -It becomes an acceptor type high molecular compound. In the donor-acceptor type, since the polarization in the polymer main chain is increased, the intermolecular interaction is further increased and a better charge mobility is exhibited.

  In the polymer compound according to the present embodiment, when the energy level of the highest occupied orbit (HOMO) is −5.0 eV or less, that is, when the ionization potential is 5.0 eV or more, deterioration due to oxidation in the atmosphere. Can be prevented, and stability is increased.

  HOMO energy level is measured by cyclic voltammetry using polymer solution or thin film (Efficient two layer leds on a polymer blend basis; Jorn Pommerehne, Horst Vestweber, Werner Guss, Rainer F. Mahrt, Heinz Bassler, Michael Porsch, Jorg Daub; Advanced Materials 1995, 7, 551-554) or photoelectron spectroscopy using a thin film (for example, atmospheric photoelectron spectrometer AC-2 manufactured by Riken Keiki Co., Ltd.).

  The polymer organic semiconductor material contains at least one polymer compound represented by the general formula (1), (2), (3) or (4) described above. The polymer organic semiconductor material may be composed of only one compound represented by the general formula (1), (2), (3) or (4), or a mixture obtained by combining these compounds. Other substances may be included as long as the properties of the compound represented by formula (1), (2), (3) or (4) are not impaired. Alternatively, the electric field mobility may be adjusted by doping impurities using a known method.

  The organic semiconductor device is a device formed using the above-described polymer organic semiconductor material. As this organic semiconductor device, for example, a thin film transistor having an organic semiconductor layer, a light emitting device having an organic carrier transport layer and / or a light emitting layer, and a photoelectric conversion having a mixed thin film of the organic semiconductor and an n-type organic semiconductor as an organic semiconductor layer. An element etc. are mentioned.

  As an organic semiconductor layer of the photoelectric conversion element, an n-type organic semiconductor mixed with the polymer compound according to the present invention includes a fullerene derivative. Here, examples of fullerene include C60 fullerene, C70 fullerene, and C84 fullerene. A fullerene derivative indicates a compound in which at least a part of these fullerenes is modified, and [6,6] -Phenyl-C61- Butyric Acid Methyl Ester ([60] PCBM), [6,6] Diphenyl-C62-bis (Butylic acid methyl ester) (Bis [60] PCBM), Phenyl-C71-Butyric-Acid-Meth-Ethyl- [Methyl70] ), Phenyl-C85-Butyric-Acid-Methyl Ester ([84] PCBM), [6,6] -Phenyl-C61-Butylic Acid Butyl Est. er ([60] PCBB), [6,6] -Phenyl-C61-Butyric Acid Octyl Ester ([60] PCBO), Thienyl-C61-Butyric-Acyl-Methyl Ester ([60] ThCBO), and the like. By using a mixed thin film with these n-type semiconductors, a more efficient photoelectric conversion element can be obtained.

  Except for using the organic semiconductor material according to the present embodiment described above, known materials and structures can be employed and are not particularly limited.

  It does not specifically limit as a manufacturing method of an organic semiconductor device, A conventionally well-known various manufacturing method can be used. Among them, a solution method can be used as a method of disposing the polymer organic semiconductor material on a support. The solution method is a method for preparing a semiconductor device by dissolving the polymer organic semiconductor material in various organic solvents and forming an organic thin film on a support by a coating method, a spin coating method, an ink jet method or the like. Since the high molecular organic semiconductor material exhibits good solubility in an organic solvent as described above, the welding method is suitably applied.

  As described above, since the semiconductor layer can be formed by a solution method, an organic semiconductor device can be manufactured at a low cost without requiring a vapor deposition process in the case of using silicon or a low molecular organic semiconductor material.

  In addition, since a polymer organic semiconductor material is used, it is superior in flexibility and light in weight as compared with a semiconductor device using silicon. This is also effective for application to lightweight displays, smart tags, and the like.

  A polymer compound was synthesized, an FET (Field Effect Transistor) element was created using the obtained polymer compound, and transistor characteristics were verified. Hereinafter, although the specific manufacturing method of a high molecular compound and the manufacturing method of FET element are illustrated in order, it is not limited to these.

(Synthesis of Compound (1))
Under a nitrogen atmosphere, quinacridone (3.12 g, 10 mmol), 2-decyl-1-bromotetradecane (33.3 g, 80 mmol) and potassium carbonate (27.64 g, 200 mmol) were mixed with NMP (150 mL) at 180 ° C. Stir for 12 hours. After cooling to room temperature, 100 mL of chloroform was added and stirred for 30 minutes, and the precipitate was filtered off.

  The filtrate was washed with 2N hydrochloric acid (150 mL). Washing with hydrochloric acid was performed three times in total. Further, it was washed with water (100 mL). Washing with water was performed three times in total.

  The organic layer was dried over anhydrous magnesium sulfate and filtered, and then the solvent was distilled off under reduced pressure. The obtained solid was purified by silica gel column chromatography using chloroform as a developing solvent, and then recrystallized from ethanol to obtain Compound (1) (3.64 g) as orange crystals.

The above reaction formula is shown below.

(Synthesis of Compound (2))
Compound (1) (3.95 g, 4.02 mmol) and sodium acetate (0.86 g, 10.45 mmol) were mixed with acetic acid (100 mL), and bromine (0.6 mL, 11.7 mmol) was slowly added dropwise.

  The reaction was stirred at reflux for 3 hours. After cooling to room temperature and adding saturated aqueous sodium hydrogen carbonate solution (200 mL), the organic layer was extracted with chloroform (50 mL). Extraction with chloroform was performed three times in total. Further, the extracted organic layer was washed with water (50 mL). Washing with water was performed three times in total.

  The organic layer was dried over anhydrous magnesium sulfate and filtered, and then the solvent was distilled off under reduced pressure. The obtained solid was purified by silica gel column chromatography using chloroform as a developing solvent, and then recrystallized from acetone to obtain Compound (2) (4.02 g) as orange crystals.

The above reaction formula is shown below.

(Synthesis of polymer compound (P1))
Under a nitrogen atmosphere, chlorobenzene (20 ml) was added to the three-necked flask and degassed for 30 minutes. Pd ₂ (dba) ₃ .CHCl ₃ (4.1 mg, 0.004 mmol, 2 mol%), P (o-tolyl) ₃ (4.9 mg, 0.016 mmol, 8 mol%), Compound (2) (228 mg, 0 .2 mmol), 5,5′-bis (trimethyltin) -2,2′-bithiophene (98 mg, 0.2 mmol) was added, and the mixture was refluxed and stirred for 3 days.

  The reaction solution was poured into a mixed solution of methanol (200 mL) and hydrochloric acid (5 mL) and stirred for 3 hours.

  The deposited precipitate was collected by filtration, heated and washed with methanol and hexane, and extracted with chloroform.

The chloroform solution was concentrated, this solution was poured into methanol, and the deposited precipitate was collected by filtration to obtain a polymer compound (P1) (185 mg) as a reddish brown solid. The number average molecular weight in terms of polystyrene of the polymer compound (P1) was 1.2 × 10 ⁴ , and the weight average molecular weight was 3.5 × 10 ⁴ .

The above reaction formula is shown below.

(Synthesis of polymer compound (P2))
Under a nitrogen atmosphere, chlorobenzene (20 mL) was added to the three-necked flask and degassed for 30 minutes.

Pd ₂ (dba) ₃ .CHCl ₃ (2.1 mg, 0.002 mmol, 2 mol%), P (o-tolyl) ₃ (2.4 mg, 0.008 mmol, 8 mol%), Compound (2) (114 mg, 0 0.1 mmol), 5,5 ″ -bis (trimethyltin) -2,2 ′: 5 ′, 2 ″ -terthiophene (57.4 mg, 0.1 mmol) was added, and the mixture was refluxed and stirred for 3 days.

  The reaction solution was poured into a mixed solution of methanol (200 mL) and hydrochloric acid (5 mL) and stirred for 3 hours.

  The deposited precipitate was collected by filtration, heated and washed with methanol and hexane, and extracted with chloroform.

The chloroform solution was concentrated, this solution was poured into methanol, and the deposited precipitate was collected by filtration to obtain a polymer compound (P2) (88 mg) as a reddish brown solid. The number average molecular weight in terms of polystyrene of the polymer compound (P2) was 1.2 × 10 ⁴ , and the weight average molecular weight was 2.7 × 10 ⁴ .

The above reaction formula is shown below.

(Evaluation of transistor characteristics of polymer compound (P1))
The transistor characteristics of the polymer compound (P1) were measured by fabricating the FET device shown in FIG.

  After thoroughly cleaning a highly doped n-type silicon substrate having a 200 nm silicon oxide film to be a gate electrode, the surface of the silicon oxide film on the substrate is treated with silane using perfluorodecyltriethoxysilane (FDTS). did.

  The polymer compound (P1) is dissolved in orthodichlorobenzene to prepare a 3 g / L solution, filtered through a membrane filter, and then applied to the surface-treated substrate by spin coating to a polymer compound (P1) of about 50 nm. A thin film was prepared. This thin film was heated at 150 ° C. for 30 minutes in a nitrogen atmosphere.

  Next, gold was vacuum-deposited to produce a source electrode and a drain electrode having a channel length of 50 μm and a channel width of 1.5 mm on the polymer thin film.

  When the transistor characteristics of the fabricated device were measured by changing the gate voltage Vg to 20 to −60 V and the source-drain voltage Vd to 0 to −60 V, the transfer characteristics (reversible characteristics) shown in FIG. The output characteristics shown in 3 were obtained.

With respect to the transfer characteristics, a drain current (Id) of −0.10 mA was obtained at Vg = −50 V and Vd = −60 V. From this characteristic, the field effect mobility was calculated to be 0.27 cm ² / Vs.

(Evaluation of transistor characteristics of polymer compound (P2))
The transistor characteristics of the polymer compound (P2) were measured by fabricating the FET element shown in FIG.

  After thoroughly cleaning a highly doped n-type silicon substrate having a 200 nm silicon oxide film to be a gate electrode, the surface of the silicon oxide film on the substrate is treated with silane using perfluorodecyltriethoxysilane (FDTS). did.

  The polymer compound (P2) is dissolved in orthodichlorobenzene to prepare a 3 g / L solution, filtered through a membrane filter, and then applied to the surface-treated substrate by spin coating to a polymer compound (P2) of about 50 nm. A thin film was prepared.

  This thin film was heated at 150 ° C. for 30 minutes in a nitrogen atmosphere. Next, gold was vacuum-deposited to produce a source electrode and a drain electrode having a channel length of 50 μm and a channel width of 1.5 mm on the polymer thin film.

  When the transistor characteristics of the fabricated device were measured by changing the gate voltage Vg to 20 to −60 V and the source-drain voltage Vd to 0 to −60 V, the transfer characteristics (reversible characteristics) shown in FIG. The output characteristics shown in 5 were obtained.

With respect to the transfer characteristics, a drain current (Id) of -0.154 mA was obtained at Vg = -50 V and Vd = -60 V. From this characteristic, the field effect mobility was calculated to be 0.25 cm ² / Vs.

  The polymer compound according to the present invention is a compound obtained by polymerizing a quinacridone and a cyclic compound having a 5-membered ring such as a thiophene ring. Quinacridones have strong intermolecular interactions due to intramolecular polarization, and the use of a five-membered ring as a polymer linking group reduces steric hindrance compared to the case where the linking group is a six-membered ring such as a benzene ring. Intermolecular interaction is further increased, and electron hopping between polymer main chains is likely to occur. Therefore, it is expected to be used as an organic semiconductor device exhibiting good charge mobility when used as a polymer organic semiconductor material.

Claims (4)

A polymer compound represented by the following general formula (1) or (2):

(In the general formulas (1) and (2), each R is independently hydrogen or an alkyl group, X ^{11 to} X ¹⁶ and X ^{21 to} X ²⁶ are the same or different and represent a carbon or nitrogen atom, In the case of carbon, it has any one of hydrogen, a halogen atom, and an alkyl group as a substituent, and Z is a structure represented by the general formula (3).

(In formula (3), X ^{31 to} X ³⁴ are the same or different and each represents a carbon or nitrogen atom, and in the case of carbon, hydrogen, a halogen atom, an alkyl group, an alkoxy group, an alkoxycarbonyl group, or an alkyl as a substituent. Any of carbonyl groups, Y represents a divalent heterocyclic group, and n represents 0 or a positive integer.) The polymer compound according to claim 1, which is represented by any one of the following general formulas (4) and (5).

  A polymer organic semiconductor material comprising the polymer compound according to claim 1.   An organic semiconductor device comprising the polymer organic semiconductor material according to claim 3.

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