KR100911970B1 - 할로겐화 방향족 화합물, 이 화합물의 (공)중합체, 및 이 (공)중합체를 포함하는 프로톤 전도막 - Google Patents
할로겐화 방향족 화합물, 이 화합물의 (공)중합체, 및 이 (공)중합체를 포함하는 프로톤 전도막 Download PDFInfo
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- KR100911970B1 KR100911970B1 KR1020030003913A KR20030003913A KR100911970B1 KR 100911970 B1 KR100911970 B1 KR 100911970B1 KR 1020030003913 A KR1020030003913 A KR 1020030003913A KR 20030003913 A KR20030003913 A KR 20030003913A KR 100911970 B1 KR100911970 B1 KR 100911970B1
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- LZXRLBAASXQZKZ-UHFFFAOYSA-N CC(C)C(C)(CCC1)CC1C(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Oc(cc1)ccc1Oc(cc1)ccc1Oc(cc1)ccc1Oc1ccccc1)=O)=O Chemical compound CC(C)C(C)(CCC1)CC1C(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Oc(cc1)ccc1Oc(cc1)ccc1Oc(cc1)ccc1Oc1ccccc1)=O)=O LZXRLBAASXQZKZ-UHFFFAOYSA-N 0.000 description 1
- ANZPRJHYMGCFCL-UHFFFAOYSA-N CC(c(cc1)ccc1C(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Cl)=O)=O)=O)Cl Chemical compound CC(c(cc1)ccc1C(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Cl)=O)=O)=O)Cl ANZPRJHYMGCFCL-UHFFFAOYSA-N 0.000 description 1
- 0 CC*C1CC(*)(CC(C)(C)CC(C2)(C3)*4CC4)*2C(*)NC(C)=C[*@](*)C3(C)CC(C*)C1 Chemical compound CC*C1CC(*)(CC(C)(C)CC(C2)(C3)*4CC4)*2C(*)NC(C)=C[*@](*)C3(C)CC(C*)C1 0.000 description 1
- BNIFRBBEXXKBLE-UHFFFAOYSA-N O=C(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Oc(cc1)ccc1Oc1ccccc1)=O)c(cc1)ccc1Oc(cc1)ccc1C(c1cc(Cl)ccc1Cl)=O Chemical compound O=C(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Oc(cc1)ccc1Oc1ccccc1)=O)c(cc1)ccc1Oc(cc1)ccc1C(c1cc(Cl)ccc1Cl)=O BNIFRBBEXXKBLE-UHFFFAOYSA-N 0.000 description 1
- GWDNRMYBHBDYNH-UHFFFAOYSA-N O=C(c(cc1)ccc1Oc(cc1)ccc1S(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Cl)=O)(=O)=O)c(cc1)ccc1Cl Chemical compound O=C(c(cc1)ccc1Oc(cc1)ccc1S(c(cc1)ccc1Oc(cc1)ccc1C(c(cc1)ccc1Cl)=O)(=O)=O)c(cc1)ccc1Cl GWDNRMYBHBDYNH-UHFFFAOYSA-N 0.000 description 1
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- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
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- C07C45/70—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
- C07C45/71—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
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- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
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- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
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- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/4012—Other compound (II) containing a ketone group, e.g. X-Ar-C(=O)-Ar-X for polyetherketones
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- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
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Abstract
Description
실 시 예 | 프로톤 전도성 | 인장 강도 특성 | 내열수성 | 펜톤 시약 내성 | 열적 성질 | ||||
탄성률 | 항복 강도 | 인장 강도 | 신장률 | 동적 점탄성 | 열분해 온도 | ||||
(S/cm) | (GPa) | (MPa) | (MPa) | (%) | |||||
2 | 0.14 | 3.1 | 72 | 72 | 65 | ○ | ○ | >150℃ | >250℃ |
3 | 0.10 | 3.2 | 72 | 76 | 56 | ○ | ○ | >150℃ | >250℃ |
Claims (10)
- 하기 화학식 1로 표시되는 할로겐화 방향족 화합물.<화학식 1>식 중, A는 독립적으로 >C=O, -CONH-, -(CF2)p- (여기에서, p는 1 내지 10의 정수이다), -C(CF3)2-, -COO-, -SO- 및 -SO2-로 이루어지는 군으로부터 선택되는 전자 흡인성의 기이고, B는 독립적으로 -O-, -S-, -CH=CH-, -C≡C-, 하기 화학식 4 및 화학식 5로 이루어지는 군으로부터 선택되는 전자 공여성 원자 또는 2가의 기이고, X는 독립적으로 염소 원자, 요오드 원자 또는 브롬 원자이고, Z는 페닐기 또는 p-톨릴기이고, R1 내지 R19는 동일하거나 상이하며, 수소 원자, 불소 원자, 메틸기, 에틸기, 트리플루오로메틸기 또는 펜타플루오로에틸기이고, a, b는 1 이상의 정수이다.<화학식 4><화학식 5>
- 제1항에 있어서, 상기 화학식 1 중의 전자 흡인성의 기 A가 >C=O이고, 또한, 전자 공여성의 원자 B가 -O-인 것을 특징으로 하는 할로겐화 방향족 화합물.
- 제1항에 있어서, 2,5-디클로로-4'-[4-{4-(4-페녹시)페녹시}벤조일]페녹시벤조페논인 화합물.
- 제4항에 있어서, 상기 화학식 2 중의 전자 흡인성의 기 A가 >C=O이고, 또한, 전자 공여성의 원자 B가 -O-인 것을 특징으로 하는 폴리아릴렌계 (공)중합체.
- 제4항 또는 제5항에 있어서, 화학식 2로 표시되는 반복 단위 이외에 2가의 방향족기를 포함하는 반복 단위를 더 갖는 공중합체인 것을 특징으로 하는 폴리아릴렌계 (공)중합체.
- 제6항에 있어서, 상기 2가의 방향족기를 포함하는 반복 단위가 화학식 3으로 표시되는 단위인 것을 특징으로 하는 폴리아릴렌계 (공)중합체.<화학식 3>식 중, A는 독립적으로 >C=O, -CONH-, -(CF2)p- (여기에서, p는 1 내지 10의 정수이다), -C(CF3)2-, -COO-, -SO- 및 -SO2-로 이루어지는 군으로부터 선택되는 전자 흡인성의 기이고, B는 독립적으로 -O-, -S-, -CH=CH-, -C≡C-, 하기 화학식 4 및 화학식 5로 이루어지는 군으로부터 선택되는 전자 공여성 원자 또는 2가의 기이고, R20 내지 R27은 동일하거나 상이하며, 수소 원자, 불소 원자, 알릴기, 트리플루오로메틸기 또는 펜타플루오로에틸기이고, n은 0 또는 1 이상의 정수이다.<화학식 4><화학식 5>
- 제4항 또는 제5항에 있어서, 분자 중에 술폰산기를 더 갖는 것을 특징으로 하는 폴리아릴렌계 (공)중합체.
- 제8항에 있어서, 술폰산기를 0.5 내지 3.0 밀리그램 당량/g 함유하는 것을 특징으로 하는 폴리아릴렌계 (공)중합체.
- 제8항에 기재된 술폰산기를 갖는 폴리아릴렌 (공)중합체를 포함하는 프로톤 전도막.
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JP2002013450 | 2002-01-22 | ||
JPJP-P-2002-00013450 | 2002-01-22 |
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KR20030063216A KR20030063216A (ko) | 2003-07-28 |
KR100911970B1 true KR100911970B1 (ko) | 2009-08-13 |
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KR1020030003913A KR100911970B1 (ko) | 2002-01-22 | 2003-01-21 | 할로겐화 방향족 화합물, 이 화합물의 (공)중합체, 및 이 (공)중합체를 포함하는 프로톤 전도막 |
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US (1) | US6833426B2 (ko) |
EP (1) | EP1329444B1 (ko) |
KR (1) | KR100911970B1 (ko) |
DE (1) | DE60332404D1 (ko) |
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DE10126432A1 (de) * | 2001-05-31 | 2002-12-05 | Bayer Ag | Fluor enthaltende Bisphenole, deren Herstellung, deren Vor- und Zwischenprodukte sowie die Verwendung der Fluor enthaltenden Bisphenole |
JP3867029B2 (ja) * | 2002-08-20 | 2007-01-10 | Jsr株式会社 | プロトン伝導膜の製造方法 |
CN1708270A (zh) * | 2002-10-29 | 2005-12-14 | 转化医药公司 | 丙泊酚与半胱氨酸 |
US7544433B2 (en) | 2002-11-18 | 2009-06-09 | Honda Motor Co., Ltd. | Electrode structure for polymer electrolyte fuel cells, and polymer electrolyte fuel cell using the same |
JP4068988B2 (ja) * | 2003-02-20 | 2008-03-26 | Jsr株式会社 | 電解膜−電極基板複合体の製造方法 |
JP4135558B2 (ja) * | 2003-05-21 | 2008-08-20 | Jsr株式会社 | スルホン酸基を有するポリアリーレンおよびその製造方法、ならび直接メタノール型燃料電池用プロトン伝導膜 |
JP4428181B2 (ja) | 2003-10-07 | 2010-03-10 | Jsr株式会社 | ニトリル型疎水性ブロックを有するスルホン化ポリマーおよび固体高分子電解質 |
JP2005162772A (ja) | 2003-11-28 | 2005-06-23 | Jsr Corp | プロトン伝導体組成物およびプロトン伝導膜 |
DE602004016469D1 (de) | 2003-12-09 | 2008-10-23 | Honda Motor Co Ltd | Membran-Elektroden-Einheit und Polymer-Elektrolytbrennstoffzelle enthaltend diesselbe |
US7615300B2 (en) * | 2005-08-30 | 2009-11-10 | The Board of Regents University and Community College System of Nevada on Behalf of the University of Nevada | Development of novel proton-conductive polymers for proton exchange membrane fuel cell (PEMFC) technology |
KR100896339B1 (ko) | 2005-12-02 | 2009-05-07 | 고려대학교 산학협력단 | 유-무기 복합 양성자 전도성 고분자 막, 그 제조방법 및 그고분자막을 채용한 연료전지 |
JP2007291243A (ja) * | 2006-04-25 | 2007-11-08 | Jsr Corp | フルオレン骨格を有する芳香族化合物およびスルホン酸基を有するポリアリーレン |
US10435504B2 (en) | 2014-11-18 | 2019-10-08 | Rensselaer Polytechnic Institute | Polymers and methods for their manufacture |
US11236196B2 (en) | 2014-11-18 | 2022-02-01 | Rensselaer Polytechnic Institute | Polymers and methods for their manufacture |
US11621433B2 (en) | 2016-12-20 | 2023-04-04 | Rensselaer Polytechnic Institute | Proton exchange membrane material and methods of making the same |
US20200238272A1 (en) | 2017-07-06 | 2020-07-30 | Rensselaer Polytechnic Institute | Ionic functionalization of aromatic polymers for ion exchange membranes |
KR20210122231A (ko) | 2018-11-26 | 2021-10-08 | 렌슬러 폴리테크닉 인스티튜트 | 인산 음이온-사차 암모늄 이온 쌍 배위 고분자 막 |
CA3159447A1 (en) | 2019-11-25 | 2021-06-03 | Ziyang HOU | Membrane electrode assembly for cox reduction |
US11465139B2 (en) | 2020-03-20 | 2022-10-11 | Rensselaer Polytechnic Institute | Thermally stable hydrocarbon-based anion exchange membrane and ionomers |
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US5071448A (en) * | 1990-12-05 | 1991-12-10 | Union Carbide Industrial Gases Technology Corporation | Semipermeable membranes based on certain sulfonated substituted polysulfone polymers |
DE19909028A1 (de) * | 1999-03-02 | 2000-09-07 | Aventis Res & Tech Gmbh & Co | Sulfonierte aromatische Polymere, Membran enthaltend diese Polymeren, Verfahren zu deren Herstellung und deren Verwendung |
DE60116678T2 (de) | 2000-03-29 | 2006-08-24 | Jsr Corp. | Polyarylen Kopolymer und Protonen leitende Membran |
JP3956661B2 (ja) * | 2001-03-30 | 2007-08-08 | Jsr株式会社 | ハロゲン化芳香族化合物、該化合物の重合体、及び該重合体からなるプロトン伝導膜 |
JP3698067B2 (ja) | 2001-03-30 | 2005-09-21 | Jsr株式会社 | 電子吸引性基および電子供与性基を有するモノマー、それを用いた共重合体、ならびにプロトン伝導膜 |
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- 2003-01-21 KR KR1020030003913A patent/KR100911970B1/ko active IP Right Grant
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- 2003-01-21 US US10/347,336 patent/US6833426B2/en not_active Expired - Lifetime
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US6833426B2 (en) | 2004-12-21 |
DE60332404D1 (de) | 2010-06-17 |
US20030173547A1 (en) | 2003-09-18 |
EP1329444B1 (en) | 2010-05-05 |
EP1329444A1 (en) | 2003-07-23 |
KR20030063216A (ko) | 2003-07-28 |
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