WO2012148090A3 - Obtention de diamine ayant une nouvelle structure contenant un groupe fonctionnel terpyridine ou phénanthroline et son utilisation - Google Patents

Obtention de diamine ayant une nouvelle structure contenant un groupe fonctionnel terpyridine ou phénanthroline et son utilisation Download PDF

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Publication number
WO2012148090A3
WO2012148090A3 PCT/KR2012/002367 KR2012002367W WO2012148090A3 WO 2012148090 A3 WO2012148090 A3 WO 2012148090A3 KR 2012002367 W KR2012002367 W KR 2012002367W WO 2012148090 A3 WO2012148090 A3 WO 2012148090A3
Authority
WO
WIPO (PCT)
Prior art keywords
terpyridine
phenanthroline
functional group
diamine
production
Prior art date
Application number
PCT/KR2012/002367
Other languages
English (en)
Korean (ko)
Other versions
WO2012148090A2 (fr
Inventor
원종찬
오재범
박노균
정현민
김용석
정택모
김병각
Original Assignee
한국화학연구원
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 한국화학연구원 filed Critical 한국화학연구원
Publication of WO2012148090A2 publication Critical patent/WO2012148090A2/fr
Publication of WO2012148090A3 publication Critical patent/WO2012148090A3/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • C07D213/22—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing two or more pyridine rings directly linked together, e.g. bipyridyl
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)

Abstract

L'invention concerne un composé diamine qui contient un groupe fonctionnel terpyridine ou phénanthroline, et son procédé d'obtention. Le composé diamine contenant un groupe fonctionnel terpyridine ou phénanthroline selon la présente invention présente les avantages consistant en ce qu'il permet de former un polymère par réaction avec un monomère tel qu'un dianhydride, un acide dicarboxylique ou un diester, et en ce que la structure terpyridine ou phénanthroline composée du groupe fonctionnel peut former une liaison de coordination avec un métal, de façon telle que le composé peut être utilisé comme catalyseur ou comme matériau diélectrique qui en fait usage et peut être utilisé dans des domaines où des groupes fonctionnels, qui peuvent se lier avec des paires d'électrons non partagés, peuvent être ajoutés de diverses manières.
PCT/KR2012/002367 2011-04-27 2012-03-30 Obtention de diamine ayant une nouvelle structure contenant un groupe fonctionnel terpyridine ou phénanthroline et son utilisation WO2012148090A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR1020110039621A KR101311767B1 (ko) 2011-04-27 2011-04-27 터피리딘 또는 페난쓰롤린 기능기를 함유하는 새로운 구조의 디아민의 제조와 이의 응용
KR10-2011-0039621 2011-04-27

Publications (2)

Publication Number Publication Date
WO2012148090A2 WO2012148090A2 (fr) 2012-11-01
WO2012148090A3 true WO2012148090A3 (fr) 2012-12-20

Family

ID=47072848

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2012/002367 WO2012148090A2 (fr) 2011-04-27 2012-03-30 Obtention de diamine ayant une nouvelle structure contenant un groupe fonctionnel terpyridine ou phénanthroline et son utilisation

Country Status (2)

Country Link
KR (1) KR101311767B1 (fr)
WO (1) WO2012148090A2 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108659221B (zh) * 2018-05-30 2022-01-11 江西师范大学 一种高介电常数的含联三吡啶单元的聚酰亚胺金属络合物及其制备方法

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108659220B (zh) * 2018-05-30 2021-05-04 江西师范大学 一种含联三吡啶结构的聚酰亚胺及其制备方法
CN108530344B (zh) * 2018-05-30 2023-11-03 江西师范大学 一种含有联三吡啶结构的芳香二胺及其合成方法
CN109320730B (zh) * 2018-09-21 2021-04-16 重庆师范大学 钡-有机配位聚合物、其制备方法及其在离子检测和绿光复合膜制备中的应用
CN113512000A (zh) * 2021-04-29 2021-10-19 河南阿尔法医药科技有限公司 一种规模化生产4’-溴-2,2’:6’,2”-三联吡啶的方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002092766A2 (fr) * 2001-05-11 2002-11-21 Ibc Advanced Technologies, Inc. Compositions et methodes de separation de bases aminees aromatiques heterocycliques, de nucleosides, de nucleotides et de sequences nucleotidiques

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1489155A4 (fr) * 2002-03-22 2006-02-01 Idemitsu Kosan Co Materiau pour dispositifs electroluminescents organiques et dispositifs electroluminescents organiques produits avec ce materiau
KR100747312B1 (ko) * 2005-07-15 2007-08-07 엘지전자 주식회사 전자 전달 화합물 및 그 유기전계발광소자

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002092766A2 (fr) * 2001-05-11 2002-11-21 Ibc Advanced Technologies, Inc. Compositions et methodes de separation de bases aminees aromatiques heterocycliques, de nucleosides, de nucleotides et de sequences nucleotidiques

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
BILJANA BOZIC-WEBER ET AL.: "Evaluation of polynuclear dendrons as photosensitizers for dye-sensitized solar cells", ENERGY & ENVIRONMENTAL SCIENCE, vol. 2, no. 3, 2009, pages 299 - 305 *
EDWIN C. CONSTABLE ET AL.: "''Metal-Directed Synthesis and Photophysical Studies of Trinuclear V-Shaped and Pentanuclear X-Shaped Ruthenium and Osmium Metallorods and Metallostars Based upon 4'-(3,5-Dihydroxyphenyl)-2,2':6',2''-terpyridine Divergent Units''", CHEMISTRY-A EUROPEAN JOURNAL, vol. 11, no. 13, 2005, pages 4024 - 4034 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108659221B (zh) * 2018-05-30 2022-01-11 江西师范大学 一种高介电常数的含联三吡啶单元的聚酰亚胺金属络合物及其制备方法

Also Published As

Publication number Publication date
WO2012148090A2 (fr) 2012-11-01
KR101311767B1 (ko) 2013-09-26
KR20120121677A (ko) 2012-11-06

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