• 제목/요약/키워드: Azo compounds

검색결과 44건 처리시간 0.023초

Pyrazole과 Pyrazolotriazole 유도체의 합성 및 특성 연구 (Synthesis, Fastness and Spectral Properties of Some New Azo Pyrazole and Pyrazolotriazole Derivatives)

  • Rizk, Hala F.;El-Badawi, Mahmoud A.;Ibrahim, Seham A.;El-Borai, Mohamed A.
    • 대한화학회지
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    • 제54권6호
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    • pp.737-743
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    • 2010
  • 5-Amino-1,3-diaryl-pyrazoles 1a-c 와 다양한 aryl amine의diazonium salts를 반응시켜서 1,3-diaryl-5-amino-4-arylazopyrazoles 3a-l을 합성하였으며, 몇 가지 화합물은 5-amino-1,3-diaryl-4-nitroso-1H-pyrazoles 2a-c와 aryl amine의 diazonium salts를 반응시켜서 얻었다. 합성한 azo 유도체 화합물 3a-l을 DMF 용매 속에서 cupric acetate와 산화반응시켜서 2,4,6-triaryl-2,4-dihydropyrazolo [4,3-d]-1,2,3-triazoles 4a-l을 합성하였으며, 합성한 cyclic triazoles에 대한 형광 특성을 측정하였다. 한편, Diazotization of sodium nitrite/ortho-phosphoric acid 조건에서 5-amino-1,3-diaryl-1H-pyrazoles 1a-c를 diazotization화 반응시킨 다음에, aryl amines과 반응시켜서 o-aminoazo compounds 5a-f를 합성하였다. 합성한 화합물 5a-f를 pyridine/cupric acetate 반응 조건에서 반응시켜서 triazole 6a-f들을 합성하였으며, 얻어진 화합물 6a-f을 aryl diazonium salts과 반응시켜서 화합물 7a-j을 합성하였다. 합성한 염료 화합물을 polyesters에 분산염료와 정착성을 측정하였다.

지방족 할로겐화합물의 활성슬러지와 해안저질 및 점토에서의 흡탈착 특성 (Sorption/Desorption Characteristics of Halogenated Aliphatic Compounds from Activated Sludge, Sediment, and Clay)

  • 김종오;박종석;최연돈
    • 한국환경과학회지
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    • 제11권9호
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    • pp.961-969
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    • 2002
  • This study was performed : 1) to establish the experimental analysis conditions for the sorption and desorption of toxic organic contaminants to/from the activated sludge, sediment, and clay, and 2) to determine the sorption and desorption equilibrium coefficients of some representative halogenated aliphatic compounds. Through the preliminary sorption test using Azo dye, a setting of quantitative experimental conditions to determine the sorption and desorption characteristics was decided as follows; equilibration time of 180 minutes, centrifuge for 15 minutes at 5000$\times$g, and 500mg/$\ell$ of TOC concentration. The sorption and desorption characteristics of halogenated aliphatic compounds onto activated sludge, sediment and clay could be described very well using the Freundlich isotherm. The preference of the average sorption capacity of the overall compounds showed in the sequence sediment 0.26mg/g, clay 0.23mg/g, and activated sludge 0.11 mg/g. The desorption rate of the sorbed compounds onto activated sludge, sediment and clay was approximately 89.8%, 35.3%, and 66.4%, respectively.

Synthesis, Structure Investigation and Dyeing Assessment of Novel Bisazo Disperse Dyes Derived from 3-(2'-Hydroxyphenyl)-1-phenyl-2-pyrazolin-5-ones

  • Metwally, M.A.;Bondock, S.;El-Desouky, S.I.;Abdou, M.M.
    • 대한화학회지
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    • 제56권3호
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    • pp.348-356
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    • 2012
  • In an attempt to find a new class of bisazo disperse dyes with better dyeing properties, a series of novel bisazo dyestuffs based on 4-arylhydrazono-3-(2'-hydroxyphenyl)-1-phenyl-2-pyrazolin-5-ones $\mathbf{3a-f}$ were prepared by diazocoupling of p-nitrophenyl diazonium chloride with 4-arylhydrazono-3-(2'-hydroxyphenyl)-1-phenyl-2-pyrazolin-5-ones $\mathbf{2a-f}$. Compounds $\mathbf{3a-f}$ were subsequently reacted with acetic anhydride in the presence of p-toluenesulfonic acid afford the corresponding O-acetyl derivatives $\mathbf{4a-f}$. The latter products as well as spectral data indicated that compounds $\mathbf{3a-f}$ exist predominantly in the azo-hydrazone tautomeric form (H) as the ZE-configuration. Additionally, two series of the synthesized dyes $\mathbf{3a-f}$ and $\mathbf{4a-f}$ were applied as disperse dyes for dyeing polyester fabrics and their fastness properties were evaluated. Also the position of color in CIELAB coordinates ($L^*$, $a^*$, $b^*$, $H^*$, $C^*$*) was assessed.

나노구조 단분자막의 전기적 특성 (Electrical Characteristics of Nano-Structural Monolayer)

  • 최용성;조장훈;송진원;이경섭
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2006년도 추계학술대회 논문집 Vol.19
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    • pp.166-167
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    • 2006
  • Dendrimers represent a new class of synthetic macromolecules characterized by a regularly branched treelike structure. Multiple branching yields a large number of chain ends that distinguish dendrimers from conventional star-like polymers and microgels. The azobenzene dendrimer is one of the dendrimeric macromolecules that include the azo-group exhibiting a photochromic character. Due to the presence of the charge transfer element of the azo-group and its rod-shaped structure, these compounds are expected to have potential interest in electronics and photoelectronics, especially in nonlinear optics. In the present paper, we give pressure stimulation to organic thin films and detect the induced displacement current. Functional photoisometrization organic molecular the photo-stimulus to organic monomolecular L-films and LB films of dendrimer and 8A5H were performed. The 8A5H organic monolayer in case of pressure stimulus occurred that positive course but in case of the photo-stimulus compared positive and negative. It is assumed that generation forms of displacement current were measured when photo-stimulus for Impression.

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DLPC 인지질 단분자막의 변위전류 특성 (Displacement Current Characteristics of DLPC Lipid Monolayer)

  • 최용성;송진원;이경섭
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2006년도 추계학술대회 논문집 전기물성,응용부문
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    • pp.10-11
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    • 2006
  • The azobenzene dendrimer is one of the dendrimeric macromolecules that include the azo-group exhibiting a photochromic character. Due to the presence of the charge transfer element of the azo-group and its rod-shaped structure, these compounds are expected to have potential interest in electronics and photoelectronics, especially in nonlinear optics. In the present paper, we give pressure stimulation to organic thin films and detect the induced displacement current. Functional photoisometrization organic molecular the photo-stimulus to organic monomolecular L films and LB films of dendrimer and SASH were performed. The SASH organic monolayer in case of pressure stimulus occurred that positive course but in case of the photo-stimulus compared positive and negative. It is assumed that generation forms of displacement current were measured when photo-stimulus for impression.

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Synthesis, Tautomeric Structure, Dyeing Characteristics, and Antimicrobial Activity of Novel 4-(2-Arylazophenyl)-3-(2-hydroxyphenyl)-1-phenyl-2-pyrazolin-5-ones

  • Metwally, M.A.;Bondock, S.A.;El-Desouky, S.I.;Abdou, M.M.
    • 대한화학회지
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    • 제56권1호
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    • pp.82-91
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    • 2012
  • Novel azopyrazolin-5-one dyes 4a-f were synthesized by the regioselective reaction of phenylhydrazine with 2,3,4-chromantrione-3-arylhydrazones 2a-f. The acid dissociation constants $pK_a$ for the series prepared were determined and correlated by the Hammett equation. The results of such correlation together with the spectral data indicated that the studied compounds exist predominantly in the hydrazone keto structure, (D) as the Z-configuration. The dyes were applied to polyester fabrics, affording orange-yellow shades and assessments of their dyeing performance are considered. Further, the compounds 4a-f were screened for their antimicrobial activity against various microorganisms.

Azo계 유기화합물의 폴라로그래프법적 거동 (제3보). 아세토니트릴중에서 Benzeneazoresorcinol의 환원 (Polarographic Behavior of Azo Series Organic Compounds (III). Reduction of Benzeneazoresorcinol in Acetonitrile)

  • 이흥락;배준웅
    • 대한화학회지
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    • 제28권2호
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    • pp.130-134
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    • 1984
  • 반양성자성 용매인 아세토니트릴 중에서 benzeneazoresorcinol (BAR)의 폴라로그래프법적 거동을 직류 폴라로그래프법과 정전위전기량법으로 조사하였다. $1.0{\times} 10^{-2}$몰농도의 과염소산 테트라에틸암모늄의 아세토니트릴 용액 중에서 BAR은 1전자 4단계의 환원과정을 거쳐 아민 화합물로 환원되었다. 각 환원파는 비교적 확산 지배적이었고, 가역성은 나쁜 편이었다

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히드라진과 질산니켈-아연과의 반응에서 얻은 활성화시킨 촉매를 이용한 방향족 니트로화합물의 환원 (Reduction of Nitroarenes with Hydrazine Monohydrate by Activated Nickel Nitrate-Zinc Catalyst)

  • 윤태호;표상현;박문규;한병희
    • 대한화학회지
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    • 제38권5호
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    • pp.397-403
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    • 1994
  • 질산니켈과 아연을 에탄올 용매하에서 환류반응시켜 얻은 활성화시킨 촉매는 히드라진 존재하에서 방향족 니트로화합물을 주로 아족시 화합물로 환원시켜 주었다. 그러나 질산니켈 대신 염화니켈을 사용하여 얻은 촉매는 같은 조건하에서 단지 방향족 아민만을 얻을 수 있었다. 활성화시키지 않고, 방향족 니트로화합물, 염화니켈이나 질산니켈, 아연 그리고 히드라진 혼합물을 환류반응 시킬 때는 낮은 수율의 아조, 아족시와 아민 화합물을 얻을 수 있었다.

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MECC법과 Ion-Pairing 크로마토그래피법을 이용한 염료성분의 분석 (Analysis of dye components using MECC and ion-pairing chromatography)

  • 정혁
    • 분석과학
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    • 제19권1호
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    • pp.31-38
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    • 2006
  • Ion-Paring을 이용한 고성능 액체 크로마토그래피법과 계면활성제를 완충용액에 섞어서 사용하는 미셀 모세관 전기영동법(micellar electrokinetic capillary chromatography, MECC)을 이용하여 아조염료의 합성성분이면서 동시에 독성을 나타내는 분해물인 H-acid, J-acid, ${\gamma}$-acid, orthanilic acid, sulfanilic acid 그리고 2-naphthylamine-1,5-disulfonic acid 등의 디아조 성분에 대하여 분석을 수행하였다. 같은 방법으로 Acid Orange 7, Acid Orange 5, Acid Blue 92 등의 산성염료와 Direct Red 80 등의 직접염료와 같은 반응성 염료 및 Calcion에 대한 분리를 시도한 결과 모든 염료에 대한 완전한 분리를 얻었으며, 특히 각 염료의 환원용액을 H-acid, J-acid, ${\gamma}$-acid, orthanilic acid, sulfanilic acid 혹은 2-naphthylamine-1,5-disulfonic acid 등의 표준물질과 비교 분석한 결과 사용한 각 염료의 디아조 혹은 커플링 성분을 완벽하게 분석할 수 있음을 알 수 있었고, 따라서 Ion-Pair 크로마토그래피법과 모세관 전기영동법은 미지의 염료에 대한 성분확인 및 디아조 혹은 커플링 성분분석에 응용할 수 있음을 보였다.