TW201418329A - Polyimide and heat-resistant material - Google Patents

Polyimide and heat-resistant material Download PDF

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TW201418329A
TW201418329A TW102131789A TW102131789A TW201418329A TW 201418329 A TW201418329 A TW 201418329A TW 102131789 A TW102131789 A TW 102131789A TW 102131789 A TW102131789 A TW 102131789A TW 201418329 A TW201418329 A TW 201418329A
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polyimine
formula
group
precursor
film
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TWI639633B (en
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Masatoshi Hasegawa
Junichi Ishii
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Nissan Chemical Ind Ltd
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1067—Wholly aromatic polyimides, i.e. having both tetracarboxylic and diamino moieties aromatically bound
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1085—Polyimides with diamino moieties or tetracarboxylic segments containing heterocyclic moieties
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/12—Unsaturated polyimide precursors
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/02—Flame or fire retardant/resistant

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

To provide a polyimide exhibiting excellent heat resistance, and a heat resistant material formed from said polyimide. A polyimide having a repeating unit represented by formula (1). (In formula (1), X1 represents a C6-14 quadrivalent aromatic group which may be substituted with a C6-20 aromatic group, for example, X1 represents a quadrivalent group represented by formulae (2) to (4).)

Description

聚醯亞胺及耐熱性材料 Polyimine and heat resistant materials

本發明係關於聚醯亞胺及耐熱性材料。 This invention relates to polyimine and heat resistant materials.

目前，以各種圖像顯示裝置或太陽能電池之輕量化或改善脆弱性為主要目的，已進行將無機玻璃基板置換成塑膠基板之檢討。然而，獲得具有玻璃普遍之特性亦即無色透明性、優異之低熱膨脹特性及超耐熱性、且大幅改善玻璃之缺點的脆弱性之塑膠基板材料以現行之技術極為困難。 At present, the main purpose of reducing the weight of various image display devices or solar cells or improving the fragility has been to replace the inorganic glass substrate with a plastic substrate. However, it has been extremely difficult to obtain a plastic substrate material having the general characteristics of glass, that is, colorless transparency, excellent low thermal expansion characteristics, and super heat resistance, and greatly improving the fragility of glass.

全芳香族聚醯亞胺由於在既有之樹脂中具有最高之耐熱性(焊接耐熱性)，故適用於以電子領域中為主之各種用途之構件。 Since the wholly aromatic polyimine has the highest heat resistance (weld heat resistance) among the existing resins, it is suitable for various members mainly used in the field of electronics.

然而，以往之聚醯亞胺膜因源自分子構造之電荷移動相互作用而會強烈著色(例如非專利文獻1)，且應各種製程合適性所要求之高度低熱膨脹特性未必足夠。 However, the conventional polyimine film is strongly colored by charge-transfer interaction derived from a molecular structure (for example, Non-Patent Document 1), and the high low-heat expansion property required for various process suitability is not necessarily sufficient.

因此，不將現有之聚醯亞胺膜進行任何改善即直接應用於塑膠基板等之光學構件中有其困難。 Therefore, it is difficult to directly apply it to an optical member such as a plastic substrate without any improvement of the existing polyimide film.

相對於此，藉由於聚醯亞胺之單體的二胺或四羧酸二酐中之一者、或者二者中使用脂環式單體，而顯著妨礙電荷移動相互作用使聚醯亞胺完全無色透明化之技術已被揭示(例如非專利文獻2~4)。 In contrast, by using an alicyclic monomer in one or both of a diamine or a tetracarboxylic dianhydride of a monomer of polyimine, the charge-moving interaction is significantly hindered. A technique of completely colorless and transparent has been disclosed (for example, Non-Patent Documents 2 to 4).

然而，該情況下，由於聚醯亞胺骨架中導入耐熱性差之脂環構造單位，故相較於以往之全芳香族聚醯亞胺，無法避免熱安定性大幅下降。且，導入脂環構造亦導致聚醯亞胺主鏈之直線性降低，故無色透明聚醯亞胺經常無法顯示低熱膨脹特性。 However, in this case, since the alicyclic structure unit having poor heat resistance is introduced into the polyimine skeleton, the thermal stability can be prevented from being largely lowered as compared with the conventional wholly aromatic polyimide. Moreover, the introduction of the alicyclic structure also leads to a decrease in the linearity of the polyimine chain, so that the colorless transparent polyimine often fails to exhibit low thermal expansion characteristics.

據此，完全滿足作為塑膠基板全部要求之特性在材料設計上並不容易。 Accordingly, it is not easy to completely satisfy the requirements of all the requirements as a plastic substrate in material design.

另一方面，依據用途，有時亦要求對於上述特性內若干之被限制要求特性予以特性化之塑膠基板材料。其一例列舉為面發光方式之有機發光二極體(OLED)顯示器中使用之塑膠基板。 On the other hand, depending on the application, a plastic substrate material which is characterized by a plurality of restricted characteristics in the above characteristics may be required. An example of this is a plastic substrate used in a surface-emitting organic light-emitting diode (OLED) display.

現行的底部發光方式之OLED顯示器用途中，由於在塑膠基板上形成發光元件之過程中會經過300℃以上，視情況經過400℃以上之高溫製程，故其步驟中自基板材料本身產生揮發性有機化合物(VOC)時，會有對元件造成深度不良影響之虞。 In the current OLED display of the bottom-emitting type, since the process of forming a light-emitting element on a plastic substrate passes through 300 ° C or more, and a high-temperature process of 400 ° C or higher is used as the case may be, the volatile organic compound is generated from the substrate material itself in the step. When the compound (VOC) is used, there is a problem that the component is adversely affected in depth.

因此，作為OLED用塑膠基板材料，雖已要求同時具有用於儘可能抑制在高溫下產生VOC之極高熱安定性、高度熱尺寸安定性(亦即，低熱膨脹特性)、玻璃普遍之無色透明性及優異膜形成能(膜韌性)之以往所沒有之材料， 但開發以該等全部要求之特性作為目標之樹脂材料之障礙極高。 Therefore, as a plastic substrate material for OLED, it is required to have extremely high thermal stability for suppressing generation of VOC at a high temperature, high thermal dimensional stability (that is, low thermal expansion property), and colorless transparency of glass. And materials that have not been conventionally excellent in film formation energy (film toughness), However, the obstacles to the development of resin materials targeting all of the required characteristics are extremely high.

另一方面，就高精細化等有利性而言，最近，已檢討面發光方式之OLED顯示器。該方式由於係自與塑膠基板相反方向取出自發光層發出之光，故發出之光不通過塑膠基板，故塑膠基板本身著色不成為重大問題。 On the other hand, in terms of advantages such as high definition, recently, a surface-emitting type OLED display has been reviewed. In this method, since the light emitted from the self-luminous layer is taken out from the opposite direction to the plastic substrate, the emitted light does not pass through the plastic substrate, so coloring of the plastic substrate itself does not become a major problem.

因此，面發光方式之OLED顯示器用塑膠基板被要求極高之VOC抑制能(不會自基板材料本身產生VOC之性質，以下同)、極低之線熱膨脹係數(以下稱為CTE)及優異膜形成能(膜韌性)。 Therefore, the surface-emitting type OLED display plastic substrate is required to have extremely high VOC suppression energy (the VOC property is not generated from the substrate material itself, the same applies hereinafter), the extremely low linear thermal expansion coefficient (hereinafter referred to as CTE), and the excellent film. Formation energy (membrane toughness).

然而，甚至是面發光方式之OLED顯示器用塑膠基板所要求之該等要求特性，目前亦未知有能同時達成其全部之實用材料。 However, even these required characteristics required for a plastic substrate for an OLED display of a surface-emitting type are not known at present for all of the practical materials.

為提高VOC抑制能至極限，期望自材料樹脂之構造完全排除脂肪族烴基、硫醚基、碸基、胺基、碳酸酯基、脲基、胺基甲酸酯基、醯胺基、酯基、伸烷基、異亞丙基、伸環己基等之耐熱性差的取代基或連結基。 In order to increase the VOC inhibition energy to the limit, it is desirable to completely exclude aliphatic hydrocarbon groups, thioether groups, mercapto groups, amine groups, carbonate groups, urea groups, urethane groups, guanylamino groups, and ester groups from the structure of the material resin. A substituent or a linking group having poor heat resistance such as an alkyl group, an isopropylidene group or a cyclohexylene group.

另一方面，就展現高度低熱膨脹特性之觀點而言，期望成為極剛直且直鏈之主鏈構造。 On the other hand, from the viewpoint of exhibiting a high degree of low thermal expansion characteristics, it is desirable to have an extremely rigid and linear main chain structure.

而且，就VOC抑制能與低熱膨脹特性之觀點而言，列舉為以下述式(X1)表示之對伸苯基作為重複單位之聚對伸苯基作為理想的分子構造。 Further, from the viewpoint of the VOC suppression energy and the low thermal expansion property, a polyparaphenylene group having a pendant phenyl group as a repeating unit represented by the following formula (X1) is exemplified as an ideal molecular structure.

然而，聚對伸苯基對有機溶劑完全不具溶解性，欲使其聚合時在分子量增加前即產生沉澱，故其聚合反應本身 極為困難。 However, poly(p-phenylene) is completely insoluble in organic solvents, and it is intended to cause precipitation before the molecular weight increases during polymerization, so the polymerization itself Extremely difficult.

相對於此，已報導具有具剛直且直線的主鏈構造之以下述式(X2)表示之重複單位構造之聚醯亞胺，其本身雖完全不溶於一般有機溶劑，但在具有下述式(X3)表示之重複單位構造之醯胺系溶劑可溶性前驅物(聚醯胺酸)之階段，藉由溶液澆鑄法預先成形為薄膜狀，使之在高溫下進行加熱脫水環化反應(醯亞胺化反應)處理，可容易地獲得聚醯亞胺膜，因而使其薄膜顯示極低之CTE(例如非專利文獻6)。 On the other hand, it has been reported that a polyimine having a repeating unit structure represented by the following formula (X2) having a rigid and straight main chain structure is completely insoluble in a general organic solvent, but has the following formula ( X3) The stage of the repeating unit structure of the amide-based solvent-soluble precursor (poly-proline) is preliminarily formed into a film by a solution casting method, and is subjected to a heat dehydration cyclization reaction at a high temperature (imine) The polyimide reaction can easily obtain a polyimide film, and thus the film exhibits an extremely low CTE (for example, Non-Patent Document 6).

聚醯胺酸之優異醯胺系溶劑溶解性係因上述式(X3)中之取代基COOH基之強溶劑合能(salvation energy)所致者(例如非專利文獻6)。 The excellent amide-based solvent solubility of poly-proline is caused by the strong solvent energy of the substituent COOH group in the above formula (X3) (for example, Non-Patent Document 6).

然而，具有以上述式(X2)表示之重複單位構造之高分子，由於高分子鏈彼此幾乎不絡合，故其薄膜經常顯著脆弱化有而完全喪失膜形成能之重大問題(例如非專利文獻5)。 However, since the polymer having the repeating unit structure represented by the above formula (X2) is hardly complexed with each other, the film is often significantly weakened and the film forming energy is completely lost (for example, non-patent literature). 5).

另一方面，就耐熱性之觀點而言，具有與聚醯亞胺匹敵之超耐熱性之聚苯并噁唑亦可成為上述面發光方式之OLED顯示器用塑膠基板材料之候補。 On the other hand, from the viewpoint of heat resistance, polybenzoxazole having superheat resistance comparable to polyimine may also be a candidate for the plastic substrate material for OLED display of the above-described surface light-emitting method.

例如，具有以下述式(X4)表示之重複單位構造之聚苯并噁唑具有適用於上述用途之理想分子構造，亦即不具有所有取代基或連結基，而具有剛直且直線狀之主鏈構造。 For example, polybenzoxazole having a repeating unit structure represented by the following formula (X4) has an ideal molecular structure suitable for the above-mentioned use, that is, a chain which has a straight and straight line without all substituents or linking groups. structure.

與聚醯亞胺同樣，聚苯并噁唑本身由於完全不溶於一般有機溶劑，故若聚苯并噁唑前驅物可溶於溶劑中則經由此製造聚苯并噁唑薄膜在原理上為可能。 Like polybenzimine, polybenzoxazole itself is completely insoluble in common organic solvents, so if the polybenzoxazole precursor is soluble in a solvent, it is possible in principle to produce a polybenzoxazole film. .

然而，為獲得聚苯并噁唑前驅物，預先使單體轉化成活性衍生物之步驟有其必要，與完全不需要此等步驟之聚醯亞胺前驅物之聚合步驟相比較，聚苯并噁唑前驅物之聚合步驟相當繁雜。 However, in order to obtain a polybenzoxazole precursor, it is necessary to previously convert the monomer into a reactive derivative, and the polybenzoic acid is compared with the polymerization step of the polyimine precursor which does not require such a step at all. The polymerization step of the oxazole precursor is quite complicated.

除該點以外，以VOC抑制能與低熱膨脹特性之展現作為目標，如上述式(X4)所例示般，自聚苯并噁唑完全排 除連結基，而以成為剛直且直線性高之主鏈構造之方式進行分子設計時，即便在聚苯并噁唑之前驅物的聚羥基醯胺之階段亦會發生對有機溶劑缺乏溶解性之重大問題(例如非專利文獻7)。 In addition to this point, the VOC inhibition energy and the display of low thermal expansion characteristics are targeted, and as exemplified in the above formula (X4), the self-polybenzoxazole is completely discharged. In addition to the linking group, molecular design is carried out in such a manner as to be a rigid and highly linear main chain structure, even in the stage of polyhydroxyphthalamide, which is preceded by polybenzoxazole, solubility in an organic solvent may occur. A major problem (for example, Non-Patent Document 7).

此係因例如具有以下述式(X5)表示之重複單位構造之聚羥基醯胺之取代基的酚性OH基之溶劑合能較弱所致。 This is because the solvent of the phenolic OH group having a substituent of a polyhydroxyguanamine having a repeating unit structure represented by the following formula (X5) is weak.

依據上述情形，直接應用製造聚醯亞胺膜時通常使用之簡易2階段製膜步驟，亦即，在前驅物漆料之塗佈．乾燥後，進行加熱脫水環化反應之步驟，難以製造聚苯并噁唑膜。 According to the above situation, the simple 2-stage film forming step, that is, the coating of the precursor paint, is usually applied directly when manufacturing the polyimide film. After drying, the step of heating the dehydration cyclization reaction is carried out, and it is difficult to produce a polybenzoxazole film.

如使用聚醯亞胺之情況般，若可獲得適合於簡易之製造步驟(容易前驅物聚合步驟與後續之2階段加熱製膜步驟)，且沒有缺乏耐熱性之取代基或連結基之具有剛直且直線性高的主鏈構造之新穎聚苯并噁唑，則可提供上述技術領域中尤其作為上述塑膠基板材料之有益材料，該等材料尚未知。 As in the case of using polyimine, if a simple manufacturing step (easily a precursor polymerization step and a subsequent two-stage heating film forming step) is obtained, and the substituent or the linking group which lacks heat resistance has rigidity The novel polybenzoxazole having a highly linear main chain structure can provide a useful material especially in the above technical field as a plastic substrate material, and such materials are not known.

[先前技術文獻] [Previous Technical Literature] [非專利文獻] [Non-patent literature]

[非專利文獻1] Prog. Polym. Sci., 26, 259-335(2001) [Non-Patent Document 1] Prog. Polym. Sci., 26, 259-335 (2001)

[非專利文獻2] React. Funct. Polym., 30, 61-69(1996) [Non-Patent Document 2] React. Funct. Polym., 30, 61-69 (1996)

[非專利文獻3] Macromolecules, 32, 4933-4939(1999) [Non-Patent Document 3] Macromolecules, 32, 4933-4939 (1999)

[非專利文獻4] Macromol. Res., 15, 114-128(2007) [Non-Patent Document 4] Macromol. Res., 15, 114-128 (2007)

[非專利文獻5] High Perform. Polym., 21, 709-728(2009) [Non-Patent Document 5] High Perform. Polym., 21, 709-728 (2009)

[非專利文獻6] J. Polym. Sci., Part A, 25, 2479-2491(1987) [Non-Patent Document 6] J. Polym. Sci., Part A, 25, 2479-2491 (1987)

[非專利文獻7] J. Photopolym. Sci. Technol., 17, 253-258(2004) [Non-Patent Document 7] J. Photopolym. Sci. Technol., 17, 253-258 (2004)

本發明係鑑於上述情況而完成者，其目的係提供一種具有低的線熱膨脹係數、高的玻璃轉移溫度、高的耐熱性及高的膜韌性，尤其適用於例如有機EL元件之裝置之基板材料，可有助於元件之輕量化或改善脆弱性之聚醯亞胺。 The present invention has been made in view of the above circumstances, and an object thereof is to provide a substrate material having a low linear thermal expansion coefficient, a high glass transition temperature, high heat resistance, and high film toughness, and is particularly suitable for a device such as an organic EL device. Polyimine which can contribute to the weight reduction of components or improve the vulnerability.

本發明人等為達成上述目的而重複積極檢討之結果，發現由含苯并噁唑基之二胺化合物與芳香族四羧酸二酐衍生，且分子內不具有耐熱性差之取代基或連結基 之以下述式(1)表示之聚醯亞胺尤其顯示出面發光方式之OLED顯示器用塑膠基板材料所要求之特性，亦即極高之VOC抑制能、高度之低熱膨脹特性及優異之膜形成能，銦而完成本發明。 As a result of repeating the positive review, the present inventors have found that a diamine compound containing a benzoxazolyl group and an aromatic tetracarboxylic dianhydride have a substituent or a linking group which does not have poor heat resistance in the molecule. The polyimine represented by the following formula (1) particularly exhibits characteristics required for a surface-emitting type of plastic substrate material for an OLED display, that is, extremely high VOC suppression energy, high low thermal expansion property, and excellent film formation energy. Indium, the present invention has been completed.

亦即，本發明提供下列： That is, the present invention provides the following:

1.一種聚醯亞胺，其具有以式(1)表示之重複單位， (式(1)中，X1表示可經碳原子數6至20之芳香族基取代之碳原子數6至14之四價芳香族基)。 A polyimine having a repeating unit represented by the formula (1), (In the formula (1), X 1 represents a tetravalent aromatic group having 6 to 14 carbon atoms which may be substituted with an aromatic group having 6 to 20 carbon atoms).

2.如1.之聚醯亞胺，其中前述X1係由式(2)至(4)所組成群組選出之至少1種的四價基， 2. The polyimine of 1 , wherein the X 1 is at least one tetravalent group selected from the group consisting of the formulas (2) to (4),

3.如1.或2.之聚醯亞胺，其係使固有黏度為0.3dL/g以上之具有以式(5)表示之重複單位之聚醯亞胺前驅物進行脫水環化而得， (式(5)中，X1表示與前述相同意義)。 3. The polyimine of 1, or 2., which is obtained by dehydrating and cyclizing a polyimine precursor having a repeating unit represented by the formula (5) having an intrinsic viscosity of 0.3 dL/g or more. (In the formula (5), X 1 represents the same meaning as described above).

4.一種耐熱性材料，其係由如1.至3.中任一項之聚醯亞胺所構成。 A heat-resistant material which is composed of the polyimine of any one of 1. to 3.

5.一種耐熱性薄膜，其係由如4.之耐熱性材料所構成。 A heat-resistant film comprising a heat-resistant material such as 4.

6.如5.之耐熱性薄膜，其厚度為1至100μm。 6. A heat-resistant film according to 5., which has a thickness of from 1 to 100 μm.

7.如5.或6.之耐熱性薄膜，其具有15ppm/K以下之線熱膨脹係數，370℃以上之玻璃轉移溫度，及在氮氣環境中，570℃以上之5%重量減少溫度及20%以上之斷裂伸長率。 7. A heat-resistant film according to 5. or 6. having a linear thermal expansion coefficient of 15 ppm/K or less, a glass transition temperature of 370 ° C or more, and a 5% weight reduction temperature of 570 ° C or more and a 20% in a nitrogen atmosphere. The above elongation at break.

8.一種光電轉換元件、發光元件或電子電路用之基板，其係由5.至7.中任一項之耐熱性薄膜所構成。 A substrate for a photoelectric conversion element, a light-emitting element, or an electronic circuit, which is composed of the heat-resistant film of any one of 5. to 7.

9.一種漆料，其包含具有以式(5)表示之重複單位之聚醯亞胺前驅物， (式(5)中，X1表示可經碳原子數6至20之芳香族基取代之碳原子數6至14之四價芳香族基)。 A paint comprising a polyimine precursor having a repeating unit represented by formula (5), (In the formula (5), X 1 represents a tetravalent aromatic group having 6 to 14 carbon atoms which may be substituted with an aromatic group having 6 to 20 carbon atoms).

10.如9.之漆料，其中前述X1係由式(2)至(4)所組成群組選出之至少1種的四價基， 10. The paint of 9, wherein the X 1 is at least one tetravalent group selected from the group consisting of the formulas (2) to (4),

11.如9.或10.之漆料，其中前述聚醯亞胺前驅物之固有黏度為0.3dL/g以上。 11. The paint of 9, or 10. wherein the polythenimine precursor has an intrinsic viscosity of 0.3 dL/g or more.

12.一種耐熱性薄膜之製造方法，其特徵為將9.至11.中任一項之漆料塗佈於基板上，使之在350℃以上加熱。 A method for producing a heat-resistant film, characterized in that the paint of any one of 9. to 11. is applied onto a substrate and heated at 350 ° C or higher.

13.一種聚醯亞胺前驅物，其係具有以式(5)表示之重複單位， (式(5)中，X1表示可經碳原子數6至20之芳香族基取代之碳原子數6至14之四價芳香族基)。 A polyimine precursor having a repeating unit represented by the formula (5), (In the formula (5), X 1 represents a tetravalent aromatic group having 6 to 14 carbon atoms which may be substituted with an aromatic group having 6 to 20 carbon atoms).

14.如13.之聚醯亞胺前驅物，其固有黏度為0.3dL/g 以上。 14. A polyimide precursor such as 13. having an intrinsic viscosity of 0.3 dL/g. the above.

本發明之聚醯亞胺不僅具備用以實現極高熱安定性、高度尺寸安定性所必要之非常低的線熱膨脹係數，且兼具非常高的玻璃轉移溫度及優異之膜韌性。因此，本發明之聚醯亞胺適於近年來被要求該等特性之光電轉換元件、發光元件、影像顯示裝置等之電子裝置的基板材料，尤其是OLED顯示器用塑膠基板材料，可助於機器之輕量化或改善脆弱性。 The polyimine of the present invention not only has a very low linear thermal expansion coefficient necessary for achieving extremely high thermal stability and high dimensional stability, but also has a very high glass transition temperature and excellent film toughness. Therefore, the polyimide of the present invention is suitable for a substrate material of an electronic device such as a photoelectric conversion element, a light-emitting element, or an image display device which requires such characteristics in recent years, in particular, a plastic substrate material for an OLED display, which can assist a machine Lighten or improve vulnerability.

圖1係實施例1所記載之聚醯亞胺前驅物薄膜之FT-IR光譜。 Fig. 1 is an FT-IR spectrum of a polyimide film precursor film described in Example 1.

圖2係實施例1所記載之聚醯亞胺薄膜之FT-IR光譜。 2 is an FT-IR spectrum of the polyimide film described in Example 1.

以下針對本發明加以詳細說明。 The invention is described in detail below.

〈聚醯亞胺〉 Polyethylenimine

本發明之聚醯亞胺具有以式(1)表示之重複單位。 The polyimine of the present invention has a repeating unit represented by the formula (1).

式(1)中，X1表示可經碳原子數6~20之芳香族基取代之碳原子數6~14之四價芳香族基。 In the formula (1), X 1 represents a tetravalent aromatic group having 6 to 14 carbon atoms which may be substituted with an aromatic group having 6 to 20 carbon atoms.

此種碳原子數6~14之四價芳香族基之具體例列舉為苯-1,2,4,5-四基、苯-1,2,3,4-四基、萘-1,2,3,4-四基、萘-1,2,5,6-四基、萘-1,2,6,7-四基、萘-1,2,7,8-四基、萘-2,3,5,6-四基、萘-2,3,6,7-四基、萘-1,4,5,8-四基、聯苯-2,2’,3,3’-四基、聯苯-2,3,3’,4’-四基、聯苯-3,3’,4,4’-四基、蒽-1,2,3,4-四基、蒽-1,2,5,6-四基、蒽-1,2,6,7-四基、蒽-1,2,7,8-四基、蒽-2,3,6,7-四基、菲-1,2,3,4-四基、菲-1,2,5,6-四基、菲-1,2,6,7-四基、菲-1,2,7,8-四基、菲-1,2,9,10-四基、菲-2,3,5,6-四基、菲-2,3,6,7-四基、菲-2,3,9,10-四基、菲-3,4,5,6-四基、菲-3,4,9,10-四基、苯基醚-3,3’,4,4’-四基、氫醌-二苯二酸酐-四基等。重複單位中之X1可相同亦可不同。 Specific examples of such a tetravalent aromatic group having 6 to 14 carbon atoms are benzene-1,2,4,5-tetrayl, benzene-1,2,3,4-tetrayl, naphthalene-1,2. , 3,4-tetrayl, naphthalene-1,2,5,6-tetrayl, naphthalene-1,2,6,7-tetrayl, naphthalene-1,2,7,8-tetrayl, naphthalene-2 ,3,5,6-tetrayl, naphthalene-2,3,6,7-tetrayl, naphthalene-1,4,5,8-tetrayl,biphenyl-2,2',3,3'-four Base, biphenyl-2,3,3',4'-tetrayl,biphenyl-3,3',4,4'-tetrayl, 蒽-1,2,3,4-tetrayl, 蒽-1 , 2,5,6-tetrayl, 蒽-1,2,6,7-tetrayl, 蒽-1,2,7,8-tetrayl, 蒽-2,3,6,7-tetrayl, phenanthrene -1,2,3,4-tetrayl, phenanthrene-1,2,5,6-tetrayl, phenanthrene-1,2,6,7-tetrayl, phenanthrene-1,2,7,8-tetrayl Philippine-1,2,9,10-tetrayl, phenanthrene-2,3,5,6-tetrayl, phenanthrene-2,3,6,7-tetrayl, phenanthrene-2,3,9,10- Tetrakis, phenanthrene-3,4,5,6-tetrayl, phenanthrene-3,4,9,10-tetrayl, phenyl ether-3,3',4,4'-tetrayl, hydroquinone-di Phthalic anhydride - tetrayl and the like. The X 1 in the repeating unit may be the same or different.

該等中，X1較好為苯-1,2,4,5-四基、萘-1,2,3,4-四基、萘-1,2,5,6-四基、萘-1,2,6,7-四基、萘-1,2,7,8-四基、萘-2,3,5,6-四基、聯苯-2,2’,3,3’-四基、聯苯-2,3,3’,4’-四基、聯苯-3,3’,4,4’-四基，更好為下述式(2)~(4)之任一者。 Among these, X 1 is preferably benzene-1,2,4,5-tetrayl, naphthalene-1,2,3,4-tetrayl, naphthalene-1,2,5,6-tetrayl, naphthalene- 1,2,6,7-tetrayl, naphthalene-1,2,7,8-tetrayl, naphthalene-2,3,5,6-tetrayl,biphenyl-2,2',3,3'- Tetrakisole, biphenyl-2,3,3',4'-tetrayl, biphenyl-3,3',4,4'-tetrayl, more preferably as the following formula (2) to (4) One.

本發明之聚醯亞胺之重複構造中之碳原子數6~14之四價芳香族基的芳香環上之任意氫原子亦可經碳原子數6~20之芳香族基取代。 Any hydrogen atom on the aromatic ring of the tetravalent aromatic group having 6 to 14 carbon atoms in the repeating structure of the polyimine of the present invention may be substituted with an aromatic group having 6 to 20 carbon atoms.

該種碳原子數6~20之芳香族基之具體例列舉為苯基、1-萘基、2-萘基、1-蒽基、2-蒽基、9-蒽基、1-菲基、2-菲基、3-菲基、4-菲基、9-菲基等。 Specific examples of the aromatic group having 6 to 20 carbon atoms are phenyl, 1-naphthyl, 2-naphthyl, 1-indenyl, 2-indenyl, 9-fluorenyl, 1-phenanthryl, 2-phenanthryl, 3-phenanthryl, 4-phenanthryl, 9-phenanthryl and the like.

〈聚醯亞胺前驅物〉 <Polyimide precursors>

本發明之聚醯亞胺可由具有以下述式(5)表示之重複單位之聚醯亞胺前驅物製造。 The polyimine of the present invention can be produced from a polyimine precursor having a repeating unit represented by the following formula (5).

(式(5)中，X1表示與上述相同之意義)。 (In the formula (5), X 1 represents the same meaning as described above).

製造具有以上述式(5)表示之重複單位之聚醯亞胺前驅物之方法並無特別限制，可使用習知方法。更具 體而言，係藉由例如以下方法獲得。 A method of producing a polyimine precursor having a repeating unit represented by the above formula (5) is not particularly limited, and a conventional method can be used. More In general, it is obtained by, for example, the following method.

首先，使以下述式(8)表示之二胺(對應於以後述方法所得之以式(6)表示之二胺)溶解於溶劑中，於其中緩慢添加以下述式(7)表示之四羧酸二酐，且使用機械攪拌機，在0~100℃、較好在20~60℃攪拌0.5~100小時，較好1~72小時。 First, a diamine represented by the following formula (8) (a diamine represented by the formula (6) obtained by a method described later) is dissolved in a solvent, and a tetracarboxylic acid represented by the following formula (7) is slowly added thereto. The acid dianhydride is stirred at 0 to 100 ° C, preferably at 20 to 60 ° C for 0.5 to 100 hours, preferably 1 to 72 hours, using a mechanical stirrer.

(式(7)中，X1表示與上述相同之意義)。 (In the formula (7), X 1 represents the same meaning as described above).

此時，以式(8)表示之二胺與以式(7)表示之酸二酐之物質量(mol)比，相對於二胺1，酸二酐可為0.8~1.1左右，但較好為0.9~1.1左右，更好為0.95~1.05左右。 In this case, the ratio of the mass of the diamine represented by the formula (8) to the acid dianhydride represented by the formula (7) may be from 0.8 to 1.1 with respect to the diamine 1, but preferably It is about 0.9~1.1, preferably about 0.95~1.05.

又，反應溶劑中之單體(二胺及酸二酐)之濃度為5~50質量%，較好為10~40質量%。藉由以該單體濃度範圍進行聚合，可充分確保單體及聚合物之溶解性，可獲得均一高聚合度之聚醯亞胺前驅物之溶液。 Further, the concentration of the monomer (diamine and acid dianhydride) in the reaction solvent is 5 to 50% by mass, preferably 10 to 40% by mass. By carrying out the polymerization in the monomer concentration range, the solubility of the monomer and the polymer can be sufficiently ensured, and a solution of a polypyridamine precursor having a uniform high degree of polymerization can be obtained.

就本發明之耐熱性薄膜韌性之觀點而言，聚醯亞胺前驅物之聚合度宜儘可能高，因此，期望將反應溶劑中之單 體濃度設為5~50質量%，較好為10~40質量%而調製聚醯亞胺前驅物。 From the viewpoint of the toughness of the heat-resistant film of the present invention, the degree of polymerization of the polyimide precursor is preferably as high as possible, and therefore, it is desirable to treat the single in the reaction solvent. The polyimine precursor is prepared by setting the bulk concentration to 5 to 50% by mass, preferably 10 to 40% by mass.

又，於聚醯亞胺前驅物之聚合度過度增加，而難以攪拌聚合溶液之情況時，亦可以與反應所用之溶劑相同之溶劑適當稀釋。 Further, when the degree of polymerization of the polyimide precursor is excessively increased and it is difficult to stir the polymerization solution, it may be appropriately diluted with the same solvent as the solvent used for the reaction.

另外，就本發明之耐熱性薄膜之韌性及其製造所用之漆料之處理性之觀點而言，聚醯亞胺前驅物之固有黏度較好為0.3dL/g以上，更好為0.3~5.0dL/g之範圍內。 Further, the intrinsic viscosity of the polyimide precursor is preferably 0.3 dL/g or more, more preferably 0.3 to 5.0, from the viewpoint of the toughness of the heat-resistant film of the present invention and the paint used for the production thereof. Within the range of dL/g.

成為本發明對象之聚醯亞胺，就展現極高熱安定性之觀點而言，在使聚醯亞胺聚合時，係使用不含苯基以外之所有取代基或醚基以外之所有連結基之芳香族四羧酸二酐。即使使用例如少量之脂環式四羧酸二酐亦會有顯著損及熱安定性之虞而不佳。 The polyimine which is the object of the present invention uses all the substituents other than the substituents other than the phenyl group or the ether group in the polymerization of the polyimine. Aromatic tetracarboxylic dianhydride. Even the use of, for example, a small amount of alicyclic tetracarboxylic dianhydride may cause a significant deterioration in thermal stability.

作為該芳香族四羧酸二酐若為滿足上述條件者則無特別限制，舉例為均苯四酸二酐、苯-1,2,3,4-四羧酸二酐、萘-1,2,3,4-四羧酸二酐、萘-1,2,5,6-四羧酸二酐、萘-1,2,6,7-四羧酸二酐、萘-1,2,7,8-四羧酸二酐、萘-2,3,5,6-四羧酸二酐、萘-2,3,6,7-四羧酸二酐、萘-1,4,5,8-四羧酸二酐、聯苯-2,2’,3,3’-四羧酸二酐、聯苯-2,3,3’,4’-四羧酸二酐、聯苯-3,3’,4,4’-四羧酸二酐、蒽-1,2,3,4-四羧酸二酐、蒽-1,2,5,6-四羧酸二酐、蒽-1,2,6,7-四羧酸二酐、蒽-1,2,7,8-四羧酸二酐、蒽-2,3,6,7-四羧酸二酐、菲-1,2,3,4-四羧酸二酐、菲-1,2,5,6-四羧酸二酐、菲-1,2,6,7- 四羧酸二酐、菲-1,2,7,8-四羧酸二酐、菲-1,2,9,10-四羧酸二酐、菲-2,3,5,6-四羧酸二酐、菲-2,3,6,7-四羧酸二酐、菲-2,3,9,10-四羧酸二酐、菲-3,4,5,6-四羧酸二酐、菲-3,4,9,10-四羧酸二酐、4,4’-氧基二苯二甲酸二酐、氫醌-二苯二酸酐等。該等可單獨使用，亦可組合2種以上使用。 The aromatic tetracarboxylic dianhydride is not particularly limited as long as it satisfies the above conditions, and examples thereof include pyromellitic dianhydride, benzene-1,2,3,4-tetracarboxylic dianhydride, and naphthalene-1,2. , 3,4-tetracarboxylic dianhydride, naphthalene-1,2,5,6-tetracarboxylic dianhydride, naphthalene-1,2,6,7-tetracarboxylic dianhydride, naphthalene-1,2,7 , 8-tetracarboxylic dianhydride, naphthalene-2,3,5,6-tetracarboxylic dianhydride, naphthalene-2,3,6,7-tetracarboxylic dianhydride, naphthalene-1,4,5,8 -tetracarboxylic dianhydride, biphenyl-2,2',3,3'-tetracarboxylic dianhydride, biphenyl-2,3,3',4'-tetracarboxylic dianhydride, biphenyl-3, 3',4,4'-tetracarboxylic dianhydride, indole-1,2,3,4-tetracarboxylic dianhydride, indole-1,2,5,6-tetracarboxylic dianhydride, hydrazine-1, 2,6,7-tetracarboxylic dianhydride, indole-1,2,7,8-tetracarboxylic dianhydride, indole-2,3,6,7-tetracarboxylic dianhydride, phenanthrene-1,2, 3,4-tetracarboxylic dianhydride, phenanthrene-1,2,5,6-tetracarboxylic dianhydride, phenanthrene-1,2,6,7- Tetracarboxylic dianhydride, phenanthrene-1,2,7,8-tetracarboxylic dianhydride, phenanthrene-1,2,9,10-tetracarboxylic dianhydride, phenanthrene-2,3,5,6-tetracarboxylic acid Acid dianhydride, phenanthrene-2,3,6,7-tetracarboxylic dianhydride, phenanthrene-2,3,9,10-tetracarboxylic dianhydride, phenanthrene-3,4,5,6-tetracarboxylic acid Anhydride, phenanthrene-3,4,9,10-tetracarboxylic dianhydride, 4,4'-oxydiphthalic dianhydride, hydroquinone-diphenyl dianhydride, and the like. These may be used alone or in combination of two or more.

上述芳香族四羧酸二酐中，獲得本發明之聚醯亞胺時，就展現低熱膨脹性之觀點而言，及取得容易性或成本之觀點而言，較好使用具有剛直且直線構造之四羧酸二酐，亦即均苯四羧酸二酐、3,33',4,4'-聯苯四羧酸二酐、2,3,6,7-萘四羧酸二酐作為四羧酸二酐成分。此時，該等四羧酸二酐之含量為全部四羧酸二酐使用量之50~100莫耳%，較好為70~100莫耳%。 In the aromatic tetracarboxylic dianhydride, when the polyimine of the present invention is obtained, from the viewpoint of exhibiting low thermal expansion property, and from the viewpoint of availability and cost, it is preferred to use a straight and straight structure. Tetracarboxylic dianhydride, that is, pyromellitic dianhydride, 3,33', 4,4'-biphenyltetracarboxylic dianhydride, 2,3,6,7-naphthalenetetracarboxylic dianhydride as four A carboxylic acid dianhydride component. In this case, the content of the tetracarboxylic dianhydride is 50 to 100 mol%, preferably 70 to 100 mol%, based on the total amount of the tetracarboxylic dianhydride.

就展現本發明之聚醯亞胺之極高熱安定性之觀點而言，亦可部分使用不含苯基以外之所有取代基或醚基以外之所有連結基之芳香族二胺作為含上述式(8)所例示之苯并噁唑基之二胺的共聚合成分。但，即使例如少量使用脂環式二胺亦有顯著損及熱安定性之虞故不佳。 From the viewpoint of exhibiting the extremely high heat stability of the polyimine of the present invention, an aromatic diamine having no substituent other than the phenyl group or all of the linking groups other than the phenyl group may be partially used as the above formula ( 8) A copolymerization component of the benzoxazolyl diamine exemplified. However, even if a small amount of the alicyclic diamine is used, for example, it is not preferable for the thermal stability.

該種芳香族二胺只要在上述條件之範圍內即無特別限制，列舉為對-苯二胺、間-苯二胺、鄰-苯二胺、4,4’-二胺基二苯基醚、3,4'-二胺基二苯基醚、3,3'-二胺基二苯基醚、2,4’-二胺基二苯基醚、2,2’-二胺基二苯基醚、聯苯胺、1,4-雙(4-胺基苯氧基)苯、1,3-雙(4-胺基苯氧基)苯、1,3-雙(3-胺基苯氧基)苯、4,4'-雙(4-胺基苯氧基)聯 苯、對-聯三苯二胺等。且，該等可單獨使用，亦可併用2種以上。該等之共聚合二胺成分之使用量為全部二胺使用量之0~30莫耳%，較好為0~10莫耳%。 The aromatic diamine is not particularly limited as long as it is within the above conditions, and is exemplified by p-phenylenediamine, m-phenylenediamine, o-phenylenediamine, and 4,4'-diaminodiphenyl ether. , 3,4'-diaminodiphenyl ether, 3,3'-diaminodiphenyl ether, 2,4'-diaminodiphenyl ether, 2,2'-diaminodiphenyl Ether, benzidine, 1,4-bis(4-aminophenoxy)benzene, 1,3-bis(4-aminophenoxy)benzene, 1,3-bis(3-aminophenoxy) Benzo, 4,4'-bis(4-aminophenoxy) linkage Benzene, p-terphenylene diamine, and the like. Further, these may be used alone or in combination of two or more. The amount of the copolymerized diamine component used is 0 to 30 mol%, preferably 0 to 10 mol%, based on the total amount of the diamine used.

本發明之使聚醯亞胺前驅物聚合時使用之溶劑較好使用N,N-二甲基甲醯胺、N,N-二甲基乙醯胺、N-甲基-2-吡咯烷酮、二甲基亞碸、3-甲氧基-N,N-二甲基丙醯胺、3-正丁氧基-N,N-二甲基丙醯胺、3-第二丁氧基-N,N-二甲基丙醯胺、3-第三丁氧基-N,N-二甲基丙醯胺等之非質子性溶劑，但若原料單體與生成之聚醯亞胺前驅物溶解沒有問題，則其構造並無特別限定。 The solvent used in the polymerization of the polyimine precursor of the present invention is preferably N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, or the like. Methyl sulfoxide, 3-methoxy-N,N-dimethylpropanamide, 3-n-butoxy-N,N-dimethylpropanamide, 3-second butoxy-N, An aprotic solvent such as N-dimethylpropionamide or 3-tert-butoxy-N,N-dimethylpropionamide, but if the starting monomer and the formed polyimine precursor are dissolved, The problem is not particularly limited in its construction.

例如，可使用N,N-二甲基甲醯胺、N,N-二甲基乙醯胺、N-甲基-2-吡咯烷酮等醯胺溶劑、γ-丁內酯、γ-戊內酯、δ-戊內酯、γ-己內酯、ε-己內酯、α-甲基-γ-丁內酯等環狀酯溶劑、碳酸伸乙酯、碳酸伸丙酯等碳酸酯溶劑、三乙二醇等二醇系溶劑、間-甲酚、對-甲酚、3-氯酚、4-氯酚等酚系溶劑、苯乙酮、1,3-二甲基-2-咪唑啶酮、環丁碸、二甲基亞碸等。 For example, a decylamine solvent such as N,N-dimethylformamide, N,N-dimethylacetamide or N-methyl-2-pyrrolidone, γ-butyrolactone or γ-valerolactone can be used. , a cyclic ester solvent such as δ-valerolactone, γ-caprolactone, ε-caprolactone, α-methyl-γ-butyrolactone, a carbonate solvent such as ethyl carbonate or propyl carbonate, and the like a diol solvent such as ethylene glycol, a phenol solvent such as m-cresol, p-cresol, 3-chlorophenol or 4-chlorophenol, acetophenone or 1,3-dimethyl-2-imidazolidone , Cyclobutane, dimethyl hydrazine and the like.

另外，亦可部分地使用酚、鄰-甲酚、乙酸丁酯、乙酸乙酯、乙酸異丁酯、丙二醇單甲醚乙酸酯、四氫呋喃、二乙二醇二甲醚、甲基異丁基酮、二異丁基酮、環己酮、甲基乙基酮、丙酮、丁醇、乙醇、二甲苯、甲苯、氯苯等一般溶劑。 In addition, phenol, o-cresol, butyl acetate, ethyl acetate, isobutyl acetate, propylene glycol monomethyl ether acetate, tetrahydrofuran, diethylene glycol dimethyl ether, methyl isobutyl may also be partially used. General solvents such as ketone, diisobutyl ketone, cyclohexanone, methyl ethyl ketone, acetone, butanol, ethanol, xylene, toluene, chlorobenzene.

本發明之聚醯亞胺前驅物之聚合溶液亦可直接使用以製造本發明之耐熱性薄膜，亦可使用滴加於大量 之水或甲醇等弱溶劑中，經過濾．乾燥獲得聚醯亞胺前驅物，使之再度溶解於溶劑(前述之聚醯亞胺前驅物之製造中使用之溶劑等)中而成者以製造本發明之耐熱性薄膜。又，上述聚醯亞胺前驅物之聚合溶液及使聚醯亞胺前驅物再度溶解於溶劑中而成者之任一種均為含聚醯亞胺前驅物之漆料，且為本發明之對象。 The polymerization solution of the polyimine precursor of the present invention can also be used as it is to produce the heat-resistant film of the present invention, and can also be used in a large amount. In water or methanol and other weak solvents, filtered. The heat-sensitive film of the present invention is produced by drying to obtain a polyimide precursor and re-dissolving it in a solvent (a solvent used in the production of the above-mentioned polyimide precursor). Further, any one of the polymerization solution of the polyimine precursor and the polyimine precursor re-dissolved in a solvent is a paint containing a polyimide precursor, and is an object of the present invention. .

〈耐熱性薄膜(聚醯亞胺薄膜)〉 <Heat-resistant film (polyimine film)>

本發明之耐熱性薄膜可藉由使以上述方法獲得之聚醯亞胺前驅物進行加熱脫水環化反應(醯亞胺化反應)而製造。 The heat-resistant film of the present invention can be produced by subjecting a polyimide precursor obtained by the above method to a heat dehydration cyclization reaction (oxime imidization reaction).

亦即，本發明之耐熱性薄膜係如下般製造。 That is, the heat resistant film of the present invention is produced as follows.

將含本發明之聚醯亞胺前驅物之漆料澆鑄於玻璃、銅、鋁、不銹鋼、矽等之基板上，在烘箱中，於40~180℃，較好於50~150℃乾燥，製作聚醯亞胺前驅物薄膜。 The paint containing the polyimine precursor of the present invention is cast on a substrate of glass, copper, aluminum, stainless steel, tantalum or the like, and dried in an oven at 40 to 180 ° C, preferably 50 to 150 ° C. Polyimine precursor film.

在基板上，於真空中、氮氣等惰性氣體中、或者空氣中加熱所得聚醯亞胺前驅物薄膜，獲得本發明之耐熱性薄膜(聚醯亞胺薄膜)。 The obtained polyimide film precursor film is heated on a substrate in a vacuum, an inert gas such as nitrogen, or air to obtain a heat-resistant film (polyimine film) of the present invention.

此時，加熱溫度就完成醯亞胺化之觀點而言為200℃以上，較好為250℃以上，就抑制生成之聚醯亞胺膜熱分解之觀點而言為450℃以下，較好為430℃以下。 In this case, the heating temperature is 200° C. or higher, preferably 250° C. or higher from the viewpoint of completion of the imidization, and is 450° C. or less from the viewpoint of suppressing thermal decomposition of the produced polyimide film. Below 430 °C.

此外，醯亞胺化雖宜在真空中或惰性氣體中進行，但若不使醯亞胺化溫度太高則亦可在空氣中進行。 Further, the ruthenium imidization is preferably carried out in a vacuum or in an inert gas, but it may be carried out in the air if the ruthenium imidization temperature is not too high.

醯亞胺化反應亦可藉由在吡啶或三乙胺等3 級胺存在下，將聚醯亞胺前驅物膜浸漬於含乙酸酐等脫水環化試藥之溶液中進行而取代熱處理。 The ruthenium imidization reaction can also be carried out by using pyridine or triethylamine. In the presence of a hydrazine, the polyimine precursor film is immersed in a solution containing a dehydrating cyclization reagent such as acetic anhydride instead of heat treatment.

且，亦可將該等脫水環化試藥預先在室溫下投入於含聚醯亞胺前驅物之漆料中並攪拌，且使之澆鑄於上述基板上並乾燥，而製作經部分醯亞胺化之聚醯亞胺前驅物，使其進一步進行如上述之熱處理而獲得聚醯亞胺膜。 Further, the dehydrated cyclization reagent may be previously put into a paint containing a polyimide precursor at room temperature and stirred, and cast on the substrate and dried to prepare a partial yam. The aminated polyimide precursor is further subjected to heat treatment as described above to obtain a polyimide film.

含本發明之聚醯亞胺前驅物之漆料藉由塗佈於金屬箔例如銅箔上並乾燥後，藉由上述條件醯亞胺化，可獲得金屬層與聚醯亞胺膜之層合體。再者藉由使用氯化鐵水溶液等之蝕刻液將金屬層蝕刻成期望之電路狀，可製造無接著劑型可撓性基板。 The lacquer containing the polyimine precursor of the present invention can be obtained by coating on a metal foil such as a copper foil and drying, and then iodizing the above conditions to obtain a laminate of a metal layer and a polyimide film. . Further, by etching the metal layer into a desired circuit shape by using an etching solution such as an aqueous solution of ferric chloride, a non-adhesive type flexible substrate can be produced.

本發明之耐熱性薄膜之厚度並無特別限定，只要依據使用目的決定適當厚度即可，但若使用該耐熱性薄膜本身作為有機太陽能電池或矽太陽能電池之光電轉化元件、有機EL元件之發光元件、電路電子基板時，較好為1~100μm左右。 The thickness of the heat-resistant film of the present invention is not particularly limited as long as the appropriate thickness is determined depending on the purpose of use, but the heat-resistant film itself is used as a photoelectric conversion element of an organic solar cell or a tantalum solar cell, and a light-emitting element of an organic EL element. When the circuit electronic substrate is used, it is preferably about 1 to 100 μm.

以上說明之本發明之耐熱性薄膜可由本發明之具有優異膜形成能之聚醯亞胺前驅物輕易地製造，由於具有極高之VOC抑制能與高度之低熱膨脹特性，故可較好地用作為有機EL元件、液晶顯示元件或有機太陽能電池等之基板中之耐熱性薄膜。 The heat-resistant film of the present invention described above can be easily produced from the polyimine precursor having excellent film forming ability of the present invention, and can be preferably used because of its extremely high VOC suppression energy and low thermal expansion property. A heat resistant film in a substrate such as an organic EL element, a liquid crystal display element, or an organic solar cell.

〈含苯并噁唑基之二胺(以下亦稱為含BO之二胺)之合成〉 <Synthesis of a benzoxazolyl-containing diamine (hereinafter also referred to as a BO-containing diamine)>

本發明之聚醯亞胺前驅物及聚醯亞胺係如前述由其單體的四羧酸二酐與含BO之二胺獲得。 The polyimine precursor of the present invention and the polyimine are obtained as described above from the monomeric tetracarboxylic dianhydride and the BO-containing diamine.

本發明中使用之含BO基之二胺係以下述式(8)表示。 The BO group-containing diamine used in the present invention is represented by the following formula (8).

以上述式(8)表示之含BO基之二胺係使用以下述式(9)表示之雙(鄰-胺基苯酚)作為起始原料而合成。 The BO group-containing diamine represented by the above formula (8) is synthesized by using bis(o-aminophenol) represented by the following formula (9) as a starting material.

以下，針對使用3,3’-二羥基聯苯胺(以下稱為p-HAB)作為雙(鄰-胺基苯酚)時之含BO基之二胺的合成分法，針對其順序之一例加以例示，但合成方法並無特別限制，可應用習知方法。 Hereinafter, a synthetic method of a BO group-containing diamine when 3,3'-dihydroxybenzidine (hereinafter referred to as p-HAB) is used as bis(o-aminophenol) will be exemplified for an example of the sequence. However, the synthesis method is not particularly limited, and a conventional method can be applied.

首先，在3頸燒瓶中，將p-HAB溶解於經脫水之醯胺系溶劑中，於其中添加吡啶作為脫氧劑，以隔墊蓋密封設為A液。 First, in a 3-necked flask, p-HAB was dissolved in a dehydrated guanamine-based solvent, and pyridine was added thereto as a deoxidizing agent, and sealed with a septum cap to be a liquid A.

接著，於梨型燒瓶中，使p-HAB之2倍莫耳量的4- 硝基苯甲醯氯溶解於與A液同樣之溶劑中，且以隔墊蓋密封設為B液。 Next, in a pear-shaped flask, 4-fold molar amount of p-HAB was made 4- Nitrobenzidine chloride was dissolved in the same solvent as the solution A, and sealed with a septum cap to be a liquid B.

接著，使A液在冰浴中冷卻，邊以轉子攪拌邊以注射筒將B液少量地添加於A液中，添加結束後持續攪拌數小時，合成二醯胺體。 Next, the liquid A was cooled in an ice bath, and while the rotor was stirred, the liquid B was added to the liquid A in a small amount in a syringe, and after stirring, the mixture was stirred for several hours to synthesize a diamine.

接著，移開冰浴，在室溫攪拌數小時後，於該反應溶液中添加適當量之對-甲苯磺酸以完成脫水環化反應，且以200℃之油浴進行回流數小時。 Next, the ice bath was removed, and after stirring at room temperature for several hours, an appropriate amount of p-toluenesulfonic acid was added to the reaction solution to complete the dehydration cyclization reaction, and the mixture was refluxed for several hours in an oil bath at 200 °C.

以過濾收集所生成之沉澱物且以水重複洗淨後，在100℃真空乾燥12小時，合成以下述式(10)表示之二硝基體。 The resulting precipitate was collected by filtration, washed repeatedly with water, and dried under vacuum at 100 ° C for 12 hours to synthesize a dinitro compound represented by the following formula (10).

接著，於3頸燒瓶中，將以上述式(10)表示之二硝基體溶解於醯胺系溶劑中，且添加適當量之Pd/C作為觸媒，在氫氣氛圍中於室溫~150℃進行還原反應1~24小時。反應進行可藉薄層層析追蹤。 Next, in a 3-necked flask, the dinitrogen represented by the above formula (10) is dissolved in a guanamine-based solvent, and an appropriate amount of Pd/C is added as a catalyst in a hydrogen atmosphere at room temperature to 150 ° C. The reduction reaction is carried out for 1 to 24 hours. The reaction can be followed by thin layer chromatography.

反應結束後，藉過濾分離Pd/C後，將濾液緩慢滴加於大量水中，析出產物。藉過濾收集沉澱物且以水重複洗淨後，在100℃真空乾燥12小時。視需要亦可自適當溶 劑再結晶進行高純度化。 After the completion of the reaction, Pd/C was separated by filtration, and the filtrate was slowly added dropwise to a large amount of water to precipitate a product. The precipitate was collected by filtration and washed repeatedly with water, and dried under vacuum at 100 ° C for 12 hours. Dissolve as needed The agent is recrystallized for high purity.

據此，獲得可使用於本發明之聚醯亞胺前驅物之聚合的以下述式(6)表示之含BO基之二胺。 According to this, a BO group-containing diamine represented by the following formula (6) which can be used for the polymerization of the polyimine precursor of the present invention is obtained.

[實施例] [Examples]

以下，以實施例具體說明本發明，但本發明並不限於該等實施例。又，以下之例中之物性值係藉以下方法測定。 Hereinafter, the present invention will be specifically described by way of examples, but the invention is not limited to the examples. Further, the physical property values in the following examples were measured by the following methods.

〈紅外線吸收光譜〉 <Infrared absorption spectrum>

使用傅立葉轉換紅外線分光光度計(日本分光公司製之FT-IR5300)，以KBr片法測定含有BO基之二胺的紅外線吸收光譜。且藉透過法測定聚醯亞胺前驅物膜及聚醯亞胺膜(約5μm厚)之紅線吸收光譜。 The infrared absorption spectrum of the BO-containing diamine was measured by a KBr sheet method using a Fourier transform infrared spectrophotometer (FT-IR5300, manufactured by JASCO Corporation). The red line absorption spectrum of the polyimide precursor film and the polyimide film (about 5 μm thick) was measured by a transmission method.

〈1H-NMR光譜〉 < 1 H-NMR spectrum>

使用日本電子公司製之NMR分光光度計(ECP400)，於氘化二甲基亞碸中測定含BO基之二胺之1H-NMR光譜。 The 1 H-NMR spectrum of the BO group-containing diamine was measured in a deuterated dimethyl hydrazine using an NMR spectrophotometer (ECP400) manufactured by JEOL.

〈示差掃描熱量分析(熔點及熔解曲線)〉 <Differential scanning calorimetry (melting point and melting curve)>

含BO基之二胺之熔點及熔解曲線係使用Bruker AXS公司製之示差掃描熱量分析裝置(DSC3100)，在氮氣氛圍中，以升溫速度2℃/分鐘測定。熔點愈高熔解波峰愈陡峭表示純度愈高。 The melting point and melting curve of the BO group-containing diamine were measured using a differential scanning calorimeter (DSC3100) manufactured by Bruker AXS Co., Ltd. under a nitrogen atmosphere at a temperature elevation rate of 2 ° C/min. The higher the melting point, the steeper the melting peak, indicating the higher the purity.

〈固有黏度〉 Intrinsic viscosity

使用Ostwald黏度計，在30℃測定0.5質量%之聚醯亞胺前驅物溶液。 A 0.5% by mass polyimide precursor solution was measured at 30 ° C using an Ostwald viscometer.

〈玻璃轉移溫度(Tg)〉 <glass transition temperature (T g )>

使用Bruker AXS公司製之熱機械分析裝置(TMA4000)，以動態黏彈性測定，由頻率0.1Hz、升溫速度5℃/分鐘之損失能量曲線之波峰溫度求出聚醯亞胺膜(20μm厚)之玻璃轉移溫度。 Using a thermomechanical analyzer (TMA4000) manufactured by Bruker AXS Co., Ltd., a polyimine film (20 μm thick) was obtained by dynamic viscoelasticity measurement from the peak temperature of the loss energy curve at a frequency of 0.1 Hz and a temperature increase rate of 5 ° C/min. Glass transfer temperature.

〈線熱膨脹係數：CTE〉 <Line thermal expansion coefficient: CTE>

使用Bruker AXS公司製之熱機械分析裝置(TMA4000)，藉由熱機械分析，由荷重0.5g/膜厚1μm、升溫速度5℃/分鐘下之試驗片之伸長度，以100~200℃之範圍之平均值求出聚醯亞胺膜(20μm厚度)之CTE。 Using a thermomechanical analyzer (TMA4000) manufactured by Bruker AXS Co., Ltd., by thermomechanical analysis, the elongation of the test piece at a load of 0.5 g/film thickness of 1 μm and a temperature increase rate of 5 ° C/min was in the range of 100 to 200 ° C. The average value of the CTE of the polyimide film (20 μm thickness) was determined.

〈5%重量減少溫度(Td 5)〉 <5% weight reduction temperature (T d 5 )>

使用Bruker AXS公司製之熱重量分析裝置(TG-DTA2000)，測定在氮氣中或空氣中，以升溫速度10℃/分鐘之升溫過程中，聚醯亞胺膜(20μm厚度)之初期重量減少5%時之溫度。該值愈高表示熱安定性愈高。 A thermogravimetric analyzer (TG-DTA2000) manufactured by Bruker AXS Co., Ltd. was used to measure the initial weight reduction of the polyimide film (20 μm thickness) during heating at a heating rate of 10 ° C / min in nitrogen or air. The temperature at %. The higher the value, the higher the thermal stability.

〈彈性率、斷裂伸長率、斷裂強度〉 <elasticity, elongation at break, breaking strength>

使用東洋BALDWIN公司製之拉伸試驗機(Tensilon UTM-2)，針對聚醯亞胺試驗片(3mm×30mm×20μm厚)實施拉伸試驗(延伸速度：8mm/分鐘)，由應力-變形曲線之初期梯度求出彈性率，由薄膜斷裂時之伸長率求出斷裂伸長率(%)。斷裂伸長率愈高，意指薄膜之韌性愈高。 A tensile test (extension speed: 8 mm/min) was carried out on a polyimide test piece (3 mm × 30 mm × 20 μm thick) using a tensile tester (Tensilon UTM-2) manufactured by Toyo BALDWIN Co., Ltd., from the stress-strain curve The modulus of elasticity was determined from the initial gradient, and the elongation at break (%) was determined from the elongation at break of the film. The higher the elongation at break, the higher the toughness of the film.

[合成例1] [Synthesis Example 1] 〈含BO基之二胺之合成〉 <Synthesis of a diamine containing a BO group>

於3頸燒瓶中，將p-HAB(和歌山精化公司製，2.61g，12mmol)溶解於經充分脫水之N-甲基-2-吡咯烷酮(以下稱為NMP)(81mL)中，於其中添加吡啶(2.9mL，36mmol)作為脫氧劑，以隔墊蓋密封設為A液。接著於另一梨形燒瓶中，使4-硝基苯甲醯氯(4.49g，24mmol)溶解於NMP(17mL)中，以隔墊蓋密封設為B液。使A液在冰浴中冷卻，邊以轉子攪拌邊以注射器將B液少量地添加於A液中，添加結束後持續攪拌3小時，合成二醯胺體。 In a 3-necked flask, p-HAB (2.61 g, 12 mmol, manufactured by Wakayama Seika Co., Ltd.) was dissolved in a sufficiently dehydrated N-methyl-2-pyrrolidone (hereinafter referred to as NMP) (81 mL), and added thereto. Pyridine (2.9 mL, 36 mmol) was used as a deoxidizer, and was sealed with a septum cap to be a liquid A. Next, in a separate pear-shaped flask, 4-nitrobenzhydrazin chloride (4.49 g, 24 mmol) was dissolved in NMP (17 mL), and sealed with a septum lid to be liquid B. The liquid A was cooled in an ice bath, and the liquid B was added to the liquid A in a small amount by a syringe while stirring with a rotor. After the completion of the addition, the mixture was continuously stirred for 3 hours to synthesize a diamine.

接著移開冰浴，在室溫攪拌數小時後，於該反應溶液中添加適量之對-甲苯磺酸(1.90g，11mmol)以完 成脫水環化反應，在200℃之油浴中進行回流3小時。藉過濾回收所生成之沉澱物且以水洗淨。此時，重複洗淨直到於洗液中適當添加1%硝酸銀水溶液時未見到白色沉澱為止，完全去除氯化物離子。再以乙醇洗淨後，在100℃真空乾燥12小時，以收率81%獲得熔點401℃之黃色針狀結晶。 After removing the ice bath and stirring at room temperature for several hours, an appropriate amount of p-toluenesulfonic acid (1.90 g, 11 mmol) was added to the reaction solution. The mixture was dehydrated and cyclized, and refluxed in an oil bath at 200 ° C for 3 hours. The resulting precipitate was recovered by filtration and washed with water. At this time, the washing was repeated until the white precipitate was not observed when the 1% silver nitrate aqueous solution was appropriately added to the washing liquid, and the chloride ions were completely removed. After washing with ethanol, it was dried under vacuum at 100 ° C for 12 hours to obtain a yellow needle-like crystal having a melting point of 401 ° C in a yield of 81%.

所得產物由於幾乎不溶於DMSO-d6或CDCl3中，故無法進行1H-NMR測定，但其紅外線吸收光譜在1605cm-1處顯示BO基C=N伸縮振動帶，在1518/1348cm-1處顯示硝基伸縮振彎曲，未見到醯胺C=O伸縮振動帶或酚性O-H伸縮振動帶。 Since the resulting product is hardly soluble in DMSO-d 6 or 3 in CDCl3, it can not be measured 1 H-NMR, infrared absorption spectrum display but BO group at 1605cm -1 of the C = N stretching vibration band at 1518 / 1348cm -1 The nitro stretching vibration was observed, and no guanamine C=O stretching vibration band or phenolic OH stretching vibration band was observed.

由該等之結果，認為所得產物為以下述式(10)表示之二硝基體。 From the results of the above, the obtained product is considered to be a dinitro group represented by the following formula (10).

接著於3頸燒瓶中，使以上述式(10)表示之二硝基體(6.13g，11.9mmol)溶解於NMP(250mL)中，添加Pd/C(0.63g)作為觸媒，在氫氣氛圍中於100℃進行還原反應15小時。反應進行係以薄層層析追蹤。反應結束後，藉過濾分離Pd/C後，將濾液緩慢滴加於大量水中析出產 物。藉由過濾回收沉澱物，以水重複洗淨後，在100℃真空乾燥12小時，以粗製產物收率82%獲得茶色粉末。為進一步提高純度，而自γ-丁內酯進行再結晶，最後在100℃真空乾燥12小時獲得熔點354℃之茶色板狀晶。 Next, a dinitrogen (6.13 g, 11.9 mmol) represented by the above formula (10) was dissolved in NMP (250 mL) in a 3-neck flask, and Pd/C (0.63 g) was added as a catalyst in a hydrogen atmosphere. The reduction reaction was carried out at 100 ° C for 15 hours. The reaction was followed by thin layer chromatography. After the reaction is completed, the Pd/C is separated by filtration, and the filtrate is slowly added dropwise to a large amount of water for precipitation. Things. The precipitate was recovered by filtration, washed repeatedly with water, and dried under vacuum at 100 ° C for 12 hours to obtain a brown powder in a crude product yield of 82%. In order to further increase the purity, recrystallization was carried out from γ-butyrolactone, and finally, vacuum drying at 100 ° C for 12 hours was carried out to obtain a brown plate crystal having a melting point of 354 ° C.

所得產物之紅外線吸收光譜在3454/3380/3210cm-1處顯示胺基N-H伸縮振動帶，在1621/1607cm-1處顯示BO基C=N伸縮振動帶，在1499cm-1處顯示1,4-伸苯基伸縮振動帶，並未發現硝基伸縮振動帶或醯胺C=O伸縮振動帶。 The infrared absorption spectrum of the resulting product / 3210cm -1 displayed at the NH stretching vibration band of an amine group in 3454/3380, / 1607cm -1 displayed at the BO group with C = N stretching vibration at 1621, 1499cm -1 displayed at the 1,4 The phenyl stretching vibration band was not observed, and the nitro stretching vibration band or the guanamine C=O stretching vibration band was not found.

由該紅外線吸收光譜之結果與下述1H-NMR光譜及元素分析之結果，確認所得產物為以下述式(6)表示之含BO基之二胺。 From the results of the infrared absorption spectrum and the results of the following 1 H-NMR spectrum and elemental analysis, it was confirmed that the obtained product was a BO group-containing diamine represented by the following formula (6).

1H-NMR光譜(400MHz,DMSO-d6,δ,ppm)：8.06(s,2H)，7.90-7.88(d,4H)，7.75-7.71(m,4H)，6.72-6.70(d,4H)，6.04(s,4H) 1 H-NMR spectrum (400 MHz, DMSO-d 6 , δ, ppm): 8.06 (s, 2H), 7.90-7.88 (d, 4H), 7.75-7.71 (m, 4H), 6.72-6.70 (d, 4H) ), 6.04(s,4H)

元素分析：推定值C；74.63%,H；4.34%,N；13.39%，分析值C；74.41%,H；4.47%,N；13.26%。 Elemental analysis: Putative value C; 74.63%, H; 4.34%, N; 13.39%, analytical value C; 74.41%, H; 4.47%, N; 13.26%.

〈聚醯亞胺前驅物之聚合、醯亞胺化及聚醯亞胺膜之特性評價〉 <Polymerization of yttrium imine precursors, ruthenium imidization and evaluation of properties of polyimide membranes> [實施例1] [Example 1]

將以上述式(6)表示之含BO基之二胺5mmol饋入經充分乾燥之附攪拌機之密閉反應容器中，在約50℃下溶解於以分子篩4A充分脫水之NMP中之後，放冷至室溫，於該溶液中添加2,3,6,7’-萘四羧酸二酐(JFE化學公司製，以下稱為NTDA)粉末5mmol(全部溶質濃度：13質量%)。隨後，在室溫攪拌72小時，獲得含均勻黏稠聚醯亞胺前驅物之溶液(聚醯亞胺前驅物溶液)。 5 mmol of the BO group-containing diamine represented by the above formula (6) is fed into a sufficiently dried mixer vessel, and dissolved in NMP sufficiently dehydrated with molecular sieve 4A at about 50 ° C, and then allowed to cool to To the solution, 2,3,6,7'-naphthalenetetracarboxylic dianhydride (manufactured by JFE Chemical Co., Ltd., hereinafter referred to as NTDA) powder 5 mmol (all solute concentration: 13% by mass) was added to the solution. Subsequently, the mixture was stirred at room temperature for 72 hours to obtain a solution (polyimine precursor solution) containing a uniform viscous polyimide precursor.

在NMP中，於30℃、以0.5質量%之濃度，藉由Ostwald黏度計測定之聚醯亞胺前驅物之固有黏度為1.15dL/g。 In NMP, the intrinsic viscosity of the polyimide precursor as measured by an Ostwald viscometer at a concentration of 0.5% by mass at 30 ° C was 1.15 dL/g.

將上述聚醯亞胺前驅物塗佈於玻璃基板上，以熱風乾燥機在80℃乾燥3小時，製作聚醯亞胺前驅物膜。 The above polyimide precursor was applied onto a glass substrate, and dried at 80 ° C for 3 hours in a hot air dryer to prepare a polyimide film.

圖1顯示所得聚醯亞胺前驅物薄膜之紅外線吸收光譜。觀測到在2600cm-1附近之寬吸收帶(氫鍵性COOH基O-H伸縮振動帶)、1711cm-1處之氫鍵性COOH基C=O伸縮振動帶、1678cm-1(肩部)/1530cm-1處之醯胺基C=O伸縮振動帶、1501cm-1處之1,4-伸苯基伸縮振動帶，另一方面，未見到源自單體之胺基N-H伸縮振動帶或四羧酸二酐之酸酐基C=O伸縮振動帶，確認生成目標之聚醯亞胺 前驅物。 Figure 1 shows the infrared absorption spectrum of the obtained polyimide precursor film. Was observed in the vicinity of 2600cm -1 broad absorption band (hydrogen-bonding group COOH OH stretching vibration band), hydrogen-bonding COOH group C = O stretching vibration band of -1 1711cm, 1678cm -1 (shoulder) / 1530cm - A guanamine - based C=O stretching vibration band at one position and a 1,4-phenylene stretching vibration band at 1501 cm -1 . On the other hand, no amine-based NH stretching vibration band or tetracarboxylic acid derived from a monomer was observed. The acid anhydride group C=O stretching vibration band of the acid dianhydride confirmed that the target polyimine precursor was formed.

接著，使聚醯亞胺前驅物膜於每玻璃基板上在250℃下過熱1小時，接著在真空中於350℃過熱1小時進行熱醯亞胺化後，為去除殘留應力而自基板剝離再於真空中於400℃進行熱處理1小時，獲得膜厚20μm之柔軟聚醯亞胺膜。 Next, the polyimide film was superheated on the glass substrate at 250 ° C for 1 hour, and then subjected to hot iridization in a vacuum at 350 ° C for 1 hour, and then peeled off from the substrate to remove residual stress. The heat treatment was carried out at 400 ° C for 1 hour in a vacuum to obtain a soft polyimide film having a film thickness of 20 μm.

圖2顯示以相同條件另外製作之聚醯亞胺膜之紅外線吸收光譜。在3046cm-1處觀測到芳香族C-H伸縮振動帶，在1777/1721cm-1處觀測到醯亞胺基C=O伸縮振動帶，在1618cm-1處觀測到BO基C=N伸縮振動帶，在1501cm-1處觀測到1,4-伸苯基伸縮振動帶，在1356cm-1處觀測到醯亞胺基N-C(芳香族)伸縮振動帶，另一方面，未見到源自COOH基或醯胺基之吸收帶，故確認醯亞胺化完成，生成目標之聚醯亞胺。 Fig. 2 shows an infrared absorption spectrum of a polyimide film produced separately under the same conditions. Observed at 3046cm -1 to aromatic CH stretching vibration band, observed acyl imino C = O stretching band at 1777 / 1721cm -1, BO group C were observed at 1618cm -1 = N stretching vibration band, observed at 1501cm -1 to a stretching vibration band of 1,4-phenylene, imino acyl observed NC (aromatic) stretching vibration band at 1356cm -1, on the other hand, not seen from COOH group or The absorption band of the guanamine group confirms that the ruthenium imidization is completed to form the target polyimine.

所得聚醯亞胺膜對於任何有機溶劑均未顯示完全溶解性。針對聚醯亞胺膜(膜厚20μm)進行動態黏彈性測定之結果，在408℃觀測到玻璃轉移點。線熱膨脹係數顯示8.4ppm/K之極低值。此認為係起因於本發明之聚醯亞胺之主鏈構造極剛直且直線性高，且因熱醯亞胺步驟中聚醯亞胺主鏈相對於薄膜面以平行方向顯著配置所致者。5%重量減少溫度在氮氣中為603℃，在空氣中為592℃，可知所得聚醯亞胺具有極高之熱安定性。進一步評價機械特性之結果，拉伸彈性率(楊氏係數)為3.8GPs，斷裂伸長率為39%，亦保持優異之膜韌性。表1彙總物性值。 The obtained polyimide film showed no complete solubility for any organic solvent. The glass transition point was observed at 408 ° C as a result of dynamic viscoelasticity measurement of the polyimide film (film thickness: 20 μm). The linear thermal expansion coefficient shows an extremely low value of 8.4 ppm/K. It is considered that the main chain structure of the polyimine of the present invention is extremely straight and highly linear, and is mainly caused by a prominent arrangement of the polyimine main chain in the parallel direction with respect to the film surface in the thermal imine step. The 5% weight loss temperature was 603 ° C in nitrogen and 592 ° C in air, and it was found that the obtained polyimine had extremely high thermal stability. As a result of further evaluation of the mechanical properties, the tensile modulus (Young's modulus) was 3.8 GPs, and the elongation at break was 39%, and excellent film toughness was also maintained. Table 1 summarizes the physical property values.

[實施例2] [Embodiment 2]

除了使用相同莫耳量之3,3’,4,4’-聯苯四羧酸二酐(和光純藥公司製，以下稱為BPDA)替代NTDA作為四羧酸二酐成分以外，餘根據實施例1所記載之方法使聚醯亞胺前驅物聚合，進行製膜、熱醯亞胺化、膜物性評價。表1中示出物性。與實施例1所記載之聚醯亞胺同樣，顯示優異之特性。 In addition to the use of the same molar amount of 3,3',4,4'-biphenyltetracarboxylic dianhydride (manufactured by Wako Pure Chemical Industries, Inc., hereinafter referred to as BPDA) instead of NTDA as the tetracarboxylic dianhydride component, In the method described in Example 1, the polyimide precursor was polymerized, and film formation, thermal imidization, and film physical property evaluation were performed. Physical properties are shown in Table 1. As in the case of the polyimine described in Example 1, excellent properties were exhibited.

又，表中，ND表示在室溫~500℃為止之動態黏彈性測定中未檢測出玻璃轉移。 Further, in the table, ND indicates that no glass transition was detected in the dynamic viscoelasticity measurement from room temperature to 500 °C.

[實施例3] [Example 3]

除了使用相同莫耳量之均苯四酸二酐(三菱瓦斯化學公司製，以下稱為PMDA)替代NTDA作為四羧酸二酐成分以外，餘根據實施例1所記載之方法使聚醯亞胺前驅物聚合，進行製膜、熱醯亞胺化、膜物性評價。表1示出物性。與實施例1所記載之聚醯亞胺同樣，顯示優異之特性。 Except that the same molar amount of pyromellitic dianhydride (manufactured by Mitsubishi Gas Chemical Co., Ltd., hereinafter referred to as PMDA) was used instead of NTDA as the tetracarboxylic dianhydride component, the polyimine was obtained according to the method described in Example 1. The precursor was polymerized, and film formation, thermal imidization, and film physical property evaluation were performed. Table 1 shows the physical properties. As in the case of the polyimine described in Example 1, excellent properties were exhibited.

[比較例1] [Comparative Example 1]

除了使用相同莫耳量之PMDA作為四羧酸二酐成分，使用相同莫耳量之對-苯二胺作為二胺成分以外，餘根據實施例1所記載之方法進行聚合、製膜、熱醯亞胺化，製作聚醯亞胺膜。該聚醯亞胺膜顯示極低之 CTE(2.8ppm/K)，但極為脆弱且斷裂伸長率為0%。且，該薄膜容易因彎曲而斷裂。此係起因於該聚醯亞胺系之棒狀主鏈構造者，故聚合物鏈間幾乎沒有絡合之故。 Polymerization, film formation, and enthalpy were carried out according to the method described in Example 1, except that the same molar amount of PMDA was used as the tetracarboxylic dianhydride component, and the same molar amount of p-phenylenediamine was used as the diamine component. Imine to produce a polyimide film. The polyimide film shows extremely low CTE (2.8 ppm/K), but extremely fragile and elongation at break is 0%. Moreover, the film is easily broken by bending. This is due to the fact that the polyimine-based rod-shaped main chain structure has almost no complexation between the polymer chains.

[比較例2] [Comparative Example 2]

除了使用相同莫耳量之PMDA作為四羧酸二酐成分，使用相同莫耳量之4,4’-氧基二苯胺作為二胺成分以外，餘根據實施例1所記載之方法進行聚合、製膜、熱醯亞胺化，且進行膜物性評價。該聚醯亞胺膜顯示極高之玻璃轉移溫度(408℃)，斷裂伸長率85%及具有優異之韌性，但CTE為42.8ppm/K，未顯示低的熱膨脹特性。 The polymerization was carried out according to the method described in Example 1, except that the same molar amount of PMDA was used as the tetracarboxylic dianhydride component, and the same molar amount of 4,4'-oxydiphenylamine was used as the diamine component. The film, hot hydrazine imidization, and film property evaluation. The polyimide film exhibited an extremely high glass transition temperature (408 ° C), an elongation at break of 85%, and excellent toughness, but a CTE of 42.8 ppm/K, which did not exhibit low thermal expansion characteristics.

Claims (14)

一種聚醯亞胺，其具有以式(1)表示之重複單位， (式(1)中，X1表示可經碳原子數6至20之芳香族基取代之碳原子數6至14之四價芳香族基)。 a polyimine having a repeating unit represented by the formula (1), (In the formula (1), X 1 represents a tetravalent aromatic group having 6 to 14 carbon atoms which may be substituted with an aromatic group having 6 to 20 carbon atoms). 如請求項1之聚醯亞胺，其中前述X1係由式(2)至(4)所組成群組選出之至少1種的四價基， The polyimine of claim 1, wherein the X 1 is at least one tetravalent group selected from the group consisting of the formulas (2) to (4), 如請求項1或2之聚醯亞胺，其係使固有黏度為0.3dL/g以上之具有以式(5)表示之重複單位之聚醯亞胺前驅物進行脫水環化而得， (式(5)中，X1表示與前述相同意義)。 The polyimine of claim 1 or 2, which is obtained by dehydrating and cyclizing a polyimine precursor having a repeating unit represented by formula (5) having an intrinsic viscosity of 0.3 dL/g or more. (In the formula (5), X 1 represents the same meaning as described above). 一種耐熱性材料，其係由請求項1至3中任一項之聚醯亞胺所構成。 A heat resistant material comprising the polyamidene of any one of claims 1 to 3. 一種耐熱性薄膜，其係由請求項4之耐熱性材料所構成。 A heat resistant film comprising the heat resistant material of claim 4. 如請求項5之耐熱性薄膜，其厚度為1至100μm。 The heat resistant film of claim 5, which has a thickness of from 1 to 100 μm. 如請求項5或6之耐熱性薄膜，其具有15ppm/K以下之線熱膨脹係數，370℃以上之玻璃轉移溫度，及在氮氣環境中，570℃以上之5%重量減少溫度及20%以上之斷裂伸長率。 The heat-resistant film of claim 5 or 6, which has a linear thermal expansion coefficient of 15 ppm/K or less, a glass transition temperature of 370 ° C or more, and a 5% weight reduction temperature of 570 ° C or more and 20% or more in a nitrogen atmosphere. Elongation at break. 一種光電轉換元件、發光元件或電子電路用之基板，其係由請求項5至7中任一項之耐熱性薄膜所構成。 A substrate for a photoelectric conversion element, a light-emitting element, or an electronic circuit, which is composed of the heat-resistant film of any one of claims 5 to 7. 一種漆料，其包含具有以式(5)表示之重複單位之聚醯亞胺前驅物， (式(5)中，X1表示可經碳原子數6至20之芳香族基取代之碳原子數6至14之四價芳香族基)。 A paint comprising a polyimine precursor having a repeating unit represented by the formula (5), (In the formula (5), X 1 represents a tetravalent aromatic group having 6 to 14 carbon atoms which may be substituted with an aromatic group having 6 to 20 carbon atoms). 如請求項9之漆料，其中前述X1係由式(2)至(4)所組成群組選出之至少1種的四價基， The paint of claim 9, wherein the X 1 is at least one tetravalent group selected from the group consisting of the formulas (2) to (4), 如請求項9或10之漆料，其中前述聚醯亞胺前驅物具有0.3dL/g以上之固有黏度。 The paint of claim 9 or 10, wherein the polybenzamine precursor has an intrinsic viscosity of 0.3 dL/g or more. 一種耐熱性薄膜之製造方法，其特徵為將請求項9至11中任一項之漆料塗佈於基板上，使之在350℃以上加熱。 A method for producing a heat-resistant film, characterized in that the paint of any one of claims 9 to 11 is applied onto a substrate and heated at 350 ° C or higher. 一種聚醯亞胺前驅物，其係具有以式(5)表示之重複單位， (式(5)中，X1表示可經碳原子數6至20之芳香族基取代之碳原子數6至14之四價芳香族基)。 A polyimine precursor having a repeating unit represented by the formula (5), (In the formula (5), X 1 represents a tetravalent aromatic group having 6 to 14 carbon atoms which may be substituted with an aromatic group having 6 to 20 carbon atoms). 如請求項13之聚醯亞胺前驅物，其固有黏度為0.3dL/g以上。 The polyamidene precursor of claim 13 has an intrinsic viscosity of 0.3 dL/g or more.
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