KR970042937A - Electrochromic Composition - Google Patents

Electrochromic Composition Download PDF

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KR970042937A
KR970042937A KR1019950048832A KR19950048832A KR970042937A KR 970042937 A KR970042937 A KR 970042937A KR 1019950048832 A KR1019950048832 A KR 1019950048832A KR 19950048832 A KR19950048832 A KR 19950048832A KR 970042937 A KR970042937 A KR 970042937A
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South Korea
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group
carbon atoms
alkyl
cyano
substituted
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KR1019950048832A
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Korean (ko)
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KR100345508B1 (en
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박주옥
조영환
최준영
우경근
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김익명
삼성코닝 주식회사
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K9/00Tenebrescent materials, i.e. materials for which the range of wavelengths for energy absorption is changed as a result of excitation by some form of energy
    • C09K9/02Organic tenebrescent materials

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)

Abstract

음극환원성분의 음이온으로 (C6H5)3BCN-을 사용하여 제조된 본 발명의 일렉트로크로믹 조성물은 장기간 사용하여도 분충현상이 발생하지 않아 색깔이 균일하게 나타나며, 발, 소색시 걸리는 시간이 짧은 효과가 있다.The electrochromic composition of the present invention prepared using (C 6 H 5 ) 3 BCN- as the anion of the negative electrode reduction component does not produce insecticidal phenomenon even after long-term use, and the color appears uniformly. This has a short effect.

Description

일렉트로크로믹 조성물Electrochromic Composition

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (3)

하기한 성분을 포함하는 일렐트로크로믹 장치용 일렉트로크로믹 조성물.An electrochromic composition for an eletrochromic device comprising the following component. 1)하기한 양이온,음이온을 포함하는 음극환원성분1) Cathode reduction component containing the following cation and anion ①하기의 구조식 Ⅰ및 / 또는 Ⅱ로 이루어진 양이온① cations consisting of the following structural formulas I and / or II (상기식에서 R21,R22는 탄소수 1 내지 10개인 알킬기,CI,Br,시아노,탄소수 1 내지 4개인 알킬기로 이루어진 그룹에서 선택되는 기로 치환된 페닐기 및 CI,Br,시아노,탄소수 1 내지 4개인 알킬기로 이루어진 그룹에서 선택되는 기로 치환된 벤질기로 이루어진 그룹에서 선택된다.)(In the formula, R 21 , R 22 is a phenyl group substituted with a group selected from the group consisting of alkyl group having 1 to 10 carbon atoms, CI, Br, cyano, alkyl group having 1 to 4 carbon atoms and CI, Br, cyano, 1 to 1 carbon atoms). Is selected from the group consisting of benzyl groups substituted with groups selected from the group consisting of four alkyl groups.) (상기식에서 R21,R22는 탄소수 1 내지 10개인 알킬기,CI,Br,시아노,탄소수 1 내지 4개인 알킬기로 이루어진 그룹에서 선택되는 기로 치환된 페닐기 및 CI,Br,시아노,탄소수 1 내지 4개인 알킬기로 이루어진 그룹에서 선택되는 기로 치환된 벤질기로 이루어진 그룹에서 선택되고, R31은 탄소수 1 내지 10개인 알킬기이다.)(In the formula, R 21 , R 22 is a phenyl group substituted with a group selected from the group consisting of alkyl group having 1 to 10 carbon atoms, CI, Br, cyano, alkyl group having 1 to 4 carbon atoms and CI, Br, cyano, 1 to 1 carbon atoms). Is selected from the group consisting of benzyl groups substituted with a group selected from the group consisting of four alkyl groups, R 31 is an alkyl group having 1 to 10 carbon atoms.) ②(C6H5)3BCN-을 포하하는 음이온② anion containing (C 6 H 5 ) 3 BCN- 2)하기의 구조식 Ⅰ,Ⅱ,Ⅲ,Ⅳ 및 Ⅴ로 이루어진 그룹에서 선택되는 둘 이하의 양극산화성분2) up to two anodization components selected from the group consisting of the following structural formulas: I, II, III, IV and V (상기식에서 R41,R42,R43및 R44는 수소,탄소수 1 내지 10개인 알킬기,CI,Br,시아노,탄소수 1 내지 4개인 알킬기로 이루어진 그룹에서 선택되는 기로 치환된 페닐기 및 CI,Br,시아노,탄소수 1 내지 4개인 알킬기로 이루어진 그룹에서 선택되는 기로 치환된 벤질기로 이루어진 그룹에서 선택된다.)(Wherein R 41 , R 42 , R 43 and R 44 are hydrogen, a phenyl group substituted with a group selected from the group consisting of 1 to 10 carbon atoms, CI, Br, cyano, alkyl group having 1 to 4 carbon atoms and CI, It is selected from the group consisting of benzyl groups substituted with a group selected from the group consisting of Br, cyano, alkyl groups having 1 to 4 carbon atoms.) (상기식에서 R53,R55는 수소,R21,R22는 탄소수 1 내지 10개인 알킬기,CI,Br,시아노,탄소수 1 내지 4개인 알킬기로 이루어진 그룹에서 선택되는 기로 치환된 페닐기 및 CI,Br,시아노,탄소수 1 내지 4개인 알킬기로 이루어진 그룹에서 선택되는 기로 치환된 벤질기로 이루어진 그룹에서 선택된다.)(Wherein R 53 , R 55 is hydrogen, R 21 , R 22 is an alkyl group having 1 to 10 carbon atoms, CI, Br, cyano, a phenyl group and CI substituted with a group selected from the group consisting of alkyl groups having 1 to 4 carbon atoms, It is selected from the group consisting of benzyl groups substituted with a group selected from the group consisting of Br, cyano, alkyl groups having 1 to 4 carbon atoms.) (상기식에서, R61,R62,R63,R64는 페닐기,탄소수 1 내지 10개인 알킬기로 이루어진 그룹에서 선택되고, R65,R66은 수소,탄소수 1 내지 10개인 알킬기로 이루어진 그룹에서 선택된다.)Wherein R 61 , R 62 , R 63 , R 64 are selected from the group consisting of phenyl group, alkyl group having 1 to 10 carbon atoms, and R 65 , R 66 are selected from the group consisting of hydrogen, alkyl group having 1 to 10 carbon atoms do.) (상기식에서, R71은 산소,탄소수 1 내지 10개인 알킬기로 이루어진 그룹에서 선택되고, R75는 수소,탄소수 1 내지 6개인 다아미노 알킬기로 이루어진 그룹에서 선택된다. 또한 R72,R73,R74는 수소,알킬,페닐,탄소수 1 내지 6개인 벤질기로 이루어진 그룹에서 선택된다.)(Wherein, R 71 is selected from the group consisting of oxygen, C 1 -C 10 alkyl group, R 75 is selected from the group consisting of hydrogen, C 1 to 6 is an aminoalkyl group. In addition, R 72, R 73, R 74 is selected from the group consisting of hydrogen, alkyl, phenyl, benzyl groups having 1 to 6 carbon atoms.) 3)프로필렌 카보네이트, γ-부티로락톤을 포함하는 용매3) propylene carbonate, solvent containing γ-butyrolactone 제1항에 있어서, 상기 음극환원성분의 농도가 0.01∼0.1M, 양극산화성분의 농도가 0.01∼0.1M인 일렉트로크로믹 조성물.The electrochromic composition according to claim 1, wherein the concentration of the cathode reduction component is 0.01 to 0.1 M and the concentration of the anodization component is 0.01 to 0.1 M. 제1항에 있어서, 상기 R21,R22,R31,R41,R43,R44,R53,R|55,R61,R62,R63,R64,R65,R66,R71,R72,R73,R74및 R75는 메틸기인 일렉트로크로믹 조성물.The compound of claim 1, wherein R 21 , R 22 , R 31 , R 41 , R 43 , R 44 , R 53 , R | 55. R 61 , R 62 , R 63 , R 64 , R 65 , R 66 , R 71 , R 72 , R 73 , R 74 and R 75 are methyl groups.
KR1019950048832A 1995-12-12 1995-12-12 Electrochromic composition KR100345508B1 (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR980009421A (en) * 1996-07-30 1998-04-30 안기훈 Multicolor electrochromic composition and multicolor electrochromic device
KR980009422A (en) * 1996-07-30 1998-04-30 안기훈 Multicolor electrochromic composition and multicolor electrochromic device
KR980009420A (en) * 1996-07-30 1998-04-30 안기훈 Multicolor electrochromic composition and multicolor electrochromic device

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR980009421A (en) * 1996-07-30 1998-04-30 안기훈 Multicolor electrochromic composition and multicolor electrochromic device
KR980009422A (en) * 1996-07-30 1998-04-30 안기훈 Multicolor electrochromic composition and multicolor electrochromic device
KR980009420A (en) * 1996-07-30 1998-04-30 안기훈 Multicolor electrochromic composition and multicolor electrochromic device

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