JP6851093B2 - 低誘電率を有するポリマー及びポリマーの誘電率を低下させるための分子構造設計法 - Google Patents
低誘電率を有するポリマー及びポリマーの誘電率を低下させるための分子構造設計法 Download PDFInfo
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- 229920000642 polymer Polymers 0.000 title claims description 36
- 238000000034 method Methods 0.000 title claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 31
- 239000000463 material Substances 0.000 claims description 27
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 235000010290 biphenyl Nutrition 0.000 claims description 13
- 239000004305 biphenyl Substances 0.000 claims description 13
- 239000004642 Polyimide Substances 0.000 claims description 6
- 125000006267 biphenyl group Chemical group 0.000 claims description 6
- 229920001721 polyimide Polymers 0.000 claims description 6
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 claims description 4
- 239000002657 fibrous material Substances 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 claims 1
- QHHKLPCQTTWFSS-UHFFFAOYSA-N 5-[2-(1,3-dioxo-2-benzofuran-5-yl)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)(C(F)(F)F)C(F)(F)F)=C1 QHHKLPCQTTWFSS-UHFFFAOYSA-N 0.000 claims 1
- 125000006617 triphenylamine group Chemical group 0.000 claims 1
- 229920006254 polymer film Polymers 0.000 description 35
- 239000002861 polymer material Substances 0.000 description 9
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 101100046775 Arabidopsis thaliana TPPA gene Proteins 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 238000009776 industrial production Methods 0.000 description 3
- 230000010354 integration Effects 0.000 description 3
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- 230000008054 signal transmission Effects 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000004377 microelectronic Methods 0.000 description 1
- 101150100677 polo gene Proteins 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- 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
- C08G73/1039—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors comprising halogen-containing substituents
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- 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
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- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
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- C08J2379/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2361/00 - C08J2377/00
- C08J2379/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Formation Of Insulating Films (AREA)
- Laminated Bodies (AREA)
- Organic Insulating Materials (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Description
式中、X1は、下記構造式からなる群より選択されるいずれかであり(ただし、0≦n<10):
Y1は、下記構造式からなる群より選択されるいずれかであり(ただし、0≦n<10):
Zは、下記構造式からなる群より選択されるいずれかであり(ただし、0≦m<10):
前記側鎖構造は、一般構般式I又はIIのうち一つ又は二つ以上を有する。
Zは、下記構造式からなる群より選択されるいずれかであり(ただし、0≦m<10):
式中、X1は、下記構造式からなる群より選択されるいずれかであり(ただし、0≦n<10):
Y1は、下記構造式からなる群より選択されるいずれかであり(ただし、0≦n<10):
Zは、下記構造式からなる群より選択されるいずれかであり(ただし、0≦m<10):
実施例1
本実施例におけるポリマーフィルムTmBPPAの分子構造は、以下の通りである。
Claims (5)
- 分子構造が主鎖構造と側鎖構造から構成される低誘電率を有するポリマーであって、前記主鎖構造は、トリフェニルアミン又はトリフェニルメタンと、6FDA(2,2−ビス(3,4−アンヒドロジカルボキシフェニル)ヘキサフルオロプロパン)又はPMDA(ピロメリット酸無水物)構造を含むポリイミドであり、前記側鎖構造は主鎖構造に結合するベンゼン環又はビフェニルセグメントを有し、かつ、ベンゼン環又はビフェニル基のメタ位に剛直な直鎖構造を有する置換基を有し、前記側鎖構造は、一般構造式I又はIIのうち一つ又は二つ以上を有することを特徴とする、低誘電率を有するポリマー。
式中、X 1 は、下記構造式からなる群より選択されるいずれかであり(ただし、0≦n<10):
Y 1 は、下記構造式からなる群より選択されるいずれかであり(ただし、0≦n<10):
Zは、下記構造式からなる群より選択されるいずれかであり(ただし、0≦m<10):
- 前記ポリマーは、粉末材料、繊維材料、又はフィルム材料であることを特徴とする、請求項1記載の低誘電率を有するポリマー。
- 低誘電ポリマー材料の製造に適用する、請求項1記載の低誘電率を有するポリマー。
- 主鎖構造がトリフェニルアミン又はトリフェニルメタンと、6FDA(2,2−ビス(3,4−アンヒドロジカルボキシフェニル)ヘキサフルオロプロパン)又はPMDA(ピロメリット酸無水物)構造を含むポリイミドであるポリマーに側鎖構造を導入し、前記側鎖構造が主鎖構造に結合するベンゼン環又はビフェニルセグメントを有し、前記側鎖構造は、一般構造式I又はIIのうち一つ又は二つ以上を有し、かつ、ベンゼン環又はビフェニル基のメタ位に剛直な直鎖構造を有する置換基を有することを特徴とする、ポリマーの誘電率を低下できる分子構造設計法。
式中、X 1 は、下記構造式からなる群より選択されるいずれかであり(ただし、0≦n<10):
Y 1 は、下記構造式からなる群より選択されるいずれかであり(ただし、0≦n<10):
Zは、下記構造式からなる群より選択されるいずれかであり(ただし、0≦m<10):
- 前記ポリマーは、粉末材料、繊維材料、又はフィルム材料であることを特徴とする、請求項4記載のポリマーの誘電率を低下できる分子構造設計法。
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CN201710083465.1A CN107057065B (zh) | 2017-02-16 | 2017-02-16 | 具有低介电常数的聚合物及降低聚合物介电常数的分子结构设计方法 |
CN201710083465.1 | 2017-02-16 | ||
PCT/CN2018/074891 WO2018149303A1 (zh) | 2017-02-16 | 2018-02-01 | 具有低介电常数的聚合物及降低聚合物介电常数的分子结构设计方法 |
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CN111082055B (zh) * | 2019-12-12 | 2020-12-29 | 华南师范大学 | 二联三苯胺-酰亚胺聚合物在锂电池正极制备中的应用 |
JP7438790B2 (ja) * | 2020-03-04 | 2024-02-27 | 東レ・デュポン株式会社 | 接着剤付きポリイミドフィルムおよびフラットケーブル |
WO2021251052A1 (ja) * | 2020-06-09 | 2021-12-16 | Dic株式会社 | 硬化性樹脂、硬化性樹脂組成物、及び、硬化物 |
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US4937165A (en) * | 1989-04-03 | 1990-06-26 | Xerox Corporation | Photoconductive imaging members with N,N-bis(biarylyl)aniline charge transport polymers |
US4959288A (en) * | 1989-04-03 | 1990-09-25 | Xerox Corporation | Photoconductive imaging members with diaryl biarylylamine copolymer charge transport layers |
US5403908A (en) * | 1989-10-06 | 1995-04-04 | Idemitsu Kosan Company, Limited | Aryl styrene-based copolymer |
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US11370886B2 (en) | 2022-06-28 |
US20190367678A1 (en) | 2019-12-05 |
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