• 제목/요약/키워드: Hydrazine Hydrate

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액상-환원법으로 초미세 Cu 분말 제조 시 반응 조건의 영향 (The Influence of Reaction Conditions on the Preparation of Ultra Fine Cu Powders with Wet-reduction Process)

  • 박영민;진형호;김상렬;박홍채;윤석영
    • 한국재료학회지
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    • 제14권11호
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    • pp.790-794
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    • 2004
  • Ultra-fine Copper particles for a conductive paste in electric-electronic field were prepared using wet-reduction process with hydrazine hydrate ($N_{2}H_4{\cdot}H_{2}O$) as a reductor. The effect of reaction conditions such as the amount of dispersion ($Na_{4}O_{7}P_2{\cdot}10H_{2}O$) and reductor ($N_{2}H_4{\cdot}H_{2}O$) on the particle size and shape for the prepared Cu powders was investigated. The quantity of dispersion and reductor varied from 0 to 0.0025 M and from 5 to 40 ml at a reaction temperature of $70^{\circ}C$, respectively. The particle size, shape, and structure for the obtained Cu particles were characterized by means of XRD, SEM, TEM, EDS and TGA. The aggregation of Cu particles was reduced with relatively increasing of the amount of dispersion at fixed other reaction conditions. The smaller Cu particle with size of approximately 300nm was obtained from 0.032 M $CuSO_4$ with adding of 0.0025 M $Na_{4}O7P_2{\cdot}10H_{2}O$ and 40ml $N_{2}H_4{\cdot}H_{2}O$ at a reaction temperature of $70^{\circ}C$.

Azomethine계 화합물의 분광학적 특성과 전기적 특성에 관한 연구 (The study on the spectroscopic and electrical properties of Azomethine compounds)

  • 백대진;오원춘;고영신
    • 분석과학
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    • 제8권3호
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    • pp.249-258
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    • 1995
  • Polyazine, polyazomethine ( I ) 및 ( II )는 각각 p-benzoquinone과 hydrazine hydrate, p-phenylenediamine, 그리고 diaminomaleonitrile을 dimethylsulfoxide(DMSO)하에서 중합하여 얻었다. Polyazine, polyazomethine ( I ) 및 ( II )의 IR spectra 분석결과 $1600cm^{-1}$ 부근에서 Schiff base의 특성 peak인 -C=N-를 확인하였다. 또한 각 polyazine, polyazomethine ( I ) 및 ( II )를 conc. $H_2SO_4$에 용해시켜 UV/VIS spectrum 측정결과 protonate (>$C\limits^{\small\oplus}=NH-$)에 해당되는 것으로 생각되는 흡수 band가 300nm 부근에서 나타났으며 350~415nm 부근에서 전하이동전이와 같은 흡수로 생각되는 흡수 band가 나타났다. Polyazine, Polyazomethine ( I ) 및 ( II )의 자체 전기전도도는 약 $10^{-14}{\sim}10^{-11}{\Omega}^{-1}cm^{-1}$로 나타났으며 $I_2$를 도핑한 후 최고 전기전도도가 $10^{-2}{\Omega}^{-1}cm^{-1}$ 정도로 약 $10^{12}{\sim}10^9$배 향상되었다.

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Synthesis and Biological Activities of Some New 3,6-Disubstituted 1,2,4-Triazolo[3,4-b]1,3,4-thiadiazole Derivatives

  • Rafiq, Muhammad;Saleem, Muhammad;Hanif, Muhammad;Maqsood, Muhammad Rizwan;Rama, Nasim Hasan;Lee, Ki-Hwan;Seo, Sung-Yum
    • Bulletin of the Korean Chemical Society
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    • 제33권12호
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    • pp.3943-3949
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    • 2012
  • A series of aromatic hydrazides 3a-j were prepared by refluxing esters 2a-j with hydrazine hydrate in methanol, which were prepared by the esterification of 1a-j. Acetohydrazides 3a-j upon treatment with carbon disulfide and methanolic potassium hydroxide yielded potassium dithiocarbazate salts 4a-j, which on refluxing with hydrazine hydrate yielded substituted 4-amino-5-aryl-3H-1,2,4-triazole-3-thiones 5a-j. The target compounds 6a-j were synthesized by condensing furan-3-carboxylic acid in the presence of polyphosphoric acid under reflux. The structures of newly synthesized compounds were characterized by IR, $^1H$ NMR, $^{13}C$ NMR, elemental analysis and mass spectrometric studies. All the synthesized compounds were screened for their urease, acetylcholine esterase inhibition, antioxidant and alkaline phosphatase inhibition activity. Almost all of the compounds 6a-j showed good to excellent activities against urease and acetylcholine esterase more than the reference drugs. Compounds 6f and 6g were more potent scavenger of free radicals than the reference n-propyl gallate. Compound 6b and 6h showed excellent activities of alkaline phosphatase as compare to the reference $KH_2PO_4$.

관능기화 그래핀 및 환원된 그래핀 옥사이드의 합성과 특성분석 (Syntheses and Characterizations of Functionalized Graphenes and Reduced Graphene Oxide)

  • 문현곤;장진해
    • 폴리머
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    • 제35권3호
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    • pp.265-271
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    • 2011
  • Hummers와 Offeman 방법을 이용하여 흑연으로부터 graphene oxide(GO)를 합성하였다. Hydrazine hydrate를 사용하여 GO를 환원시켜 reduced graphene oxide (RGO)를 합성하였으며, 말단에 amine이 치환된 유기화제를 사용하여 관능기화 그래핀을 합성하였다. 합성된 GO, RGO, 그리고 관능기화 그래핀의 구조를 확인하기 위하여 FTIR과 $^{13}C$ NMR를 이용하였다. 합성된 시료들의 안정성, 모폴로지 및 다양한 유기용매 내에서의 분산도를 각각 조사하였다. AFM 사진으로부터 GO와 RGO는 한층 또는 두층 두께의 그래핀으로 이루어졌으며, 관능기화 그래핀들의 평균두께는 약 2.26~3.30 nm임을 알았다. 관능기화 그래핀들의 열 안정성은 RGO보다 낮았다. 관능기화 그래핀들은 용액상태에서 흑연의 특성 피크가 관찰되지 않는 것으로 보아 클로로포름과 톨루엔에 좋은 분산성을 가지는 것으로 확인되었다.

$\gamma$,$\gamma$,$\gamma$-Trichloroethylidene-m-Nitroacetophenone과 Hydrazine 들의 반응 (Reactions of $\gamma$,$\gamma$,$\gamma$-Trichloroethylidene-m-Nitroacetophenone with Hydrazines)

  • 이윤영;송석주
    • 대한화학회지
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    • 제17권1호
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    • pp.25-30
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    • 1973
  • $\gamma$,$\gamma$,$\gamma$-Trichloroethylidene-m-Nitroacetophenone과 phenylhydrazine및 치환된 phenylhydrazine들과의 반응으로 2,6-disubstituted-3-pyridazinone들을 합성하였으며 2,4-dinitrophenylhydrazine과의 반응에서는 hydrazone을 중간체로 분리하였다. hydrazinehydrate와의 반응에서는 3-(mnitrophenyl)-5-trichloromethyl-2-pyrazoline이 좋은 수득률로 얻어졌다. 또한$\gamma$,$\gamma$,$\gamma$-trichloroethylidene-m-nitroacetophenone과 치환된 phenylhydrazine과의 반응에서 phenyl기에 결합된 치환기의 효과를 검토하였다.

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습식 환원법에 의한 Ni 분말 합성시 반응조건의 영향 (The Effect of Reaction Conditions on the Preparation of Ni Powder Using Wet Chemical Reduction Process)

  • 김동현;박영민;김이중;진형호;박홍채;윤석영
    • 한국재료학회지
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    • 제14권10호
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    • pp.725-730
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    • 2004
  • Nickel ultrafine powder have been synthesized by chemical reduction of aqueous $NiSO_4$ with hydrazine at various reaction conditions. The effect of reaction conditions such as the amount of surfactant and reductor, and reaction temperature on the particle size and shape was investigated by the mean of XRD, SEM and SEM-PSA. Experiments showed that the ratio of $N_{2}H_4/Ni$ and the reaction temperature were affected on the particle size of the nickel powder. The average particle size of synthesized nickel powder increased with increasing reaction temperature regardless of the ratio of $N_{2}H_4/Ni$. Also the surfactant could influence the size and agglomeration of ultrafine powder with the reaction temperature.

새로운 펩티드 유사체인 5-aminobenzimidazoles의 합성 (New Antibacterial Peptide Analogs of 5-Aminobenzimidazoles)

  • Gondal, Humaira Y.;Mashooda, H.;Ali, Muhammad
    • 대한화학회지
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    • 제55권4호
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    • pp.650-655
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    • 2011
  • 새로운 펩티드 유사체인 5a-c를 5-amino benzimidazoles 2a-c과 L-phenylalanine과의 커플링반응에 의해 합성하였다. Phenylalanine의 amine 부분을 phthalic anhydride로 보호하고, 나머지 작용기인 carboxylic acid를 염소화시켜서 hthaloyl-Lphenylalanyl chloride 4를 합성한 다음에, 화합물 2a-c와 반응시켜서 화합물 5a-c를 합성하였다. 얻어진 화합물 5a-c를 hydrazine으로 반응시켜서 새로운 펩티드 유사체인 6a-c를 합성하였으며, 얻어진 화합물에 대한 항균성을 측정하였다.

Electron Impact Ionization Mass Spectra of 3-Substituted-2-hydroxy-4(3H)-quinazolinones

  • El Deen, I.M.;Abd El Fattah, M.E.
    • Bulletin of the Korean Chemical Society
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    • 제24권4호
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    • pp.473-478
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    • 2003
  • 3-Amino-2-hydroxy-4(3H)-quinazolinone (3) was prepared via condensation of 1 with hydrazine hydrate. Treatment of 3 with appropriate acid in $POCl_3$, ethyl chloroacetate and activated olefinic compounds in DMF yielded the corresponding 3-(substituted)amino-2-hydroxy-4(3H)-quinazolinones 4, 5 and 6. The electron impact ionization mass spectra of compounds 3 and 4 show a weak molecular ion peak and a base peak of m/z 146 resulting from a cleavage fragmentation. The compounds 5 and 6 give a characteristic fragmentation pattern with a very stable fragment of benzopyrazolone (m/z 132).

Synthesis, Reactions and Antimicrobial Activity of 2-Amino-4-(8-quinolinol-5-yl)-1-(p-tolyl)-pyrrole-3-carbonitrile

  • Abdel-Mohsen, Shawkat A.
    • Bulletin of the Korean Chemical Society
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    • 제26권5호
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    • pp.719-728
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    • 2005
  • A novel 2-amino-4-(8-quinolinol-5-yl)-1- (p-tolyl)-pyrrole-3-cabonitrile (2) was obtained by the reaction of 2-[2-bromo-1-(8-hydroxyquinolin-5-yl)-ethylidene]-malononitrile (1) with p-toluidene. The new synthon compound (2) could be annelated to the corresponding pyrrolo[2,3-d]pyrimidines (4, 6, 7, 26-28), triazolo[1,5-c]pyrrolo[3,2-e]pyrimidines (10, 29, 30), pyrrolo[2,3-c]pyrazoles (11-15), pyrrolo[1,2-a]pyrrolo[3,2-e] pyrimidine (17) and imidazo[1,2-c]pyrrolo[3,2-e]pyrimidines (18-25) via the reaction with some reagents such as acetic anhydride, formamide, triethyl orthoformate, hydrazine hydrate, hydroxylamine, ethylenediamine, carbon disulfide and phosphorus oxychloride. Chemical and spectroscopic evidences for the structures of these compounds are presented. The antifungal and antibacterial activity of the newly synthesized comounds were evaluated.

Rapid One-pot, Four Component Synthesis of Pyranopyrazoles Using Heteropolyacid Under Solvent-free Condition

  • Chavan, Hemant V.;Babar, Santosh B.;Hoval, Rahul U.;Bandgar, Babasaheb P.
    • Bulletin of the Korean Chemical Society
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    • 제32권11호
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    • pp.3963-3966
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    • 2011
  • A series of pyranopyrazoles, was efficiently synthesized via one-pot, four component reaction of ethyl acetoacetate, hydrazine hydrate, aldehydes and malononitrile in the presence of catalytic amount silicotungstic acid under solvent free condition. NOE experiments confirmed that the product exist exclusively in the 2H form. The present protocol offers the advantages of clean reaction, short reaction time, high yield, easy purification and economic availability of the catalyst.