• 제목/요약/키워드: m-Nitroaniline

검색결과 13건 처리시간 0.027초

Catalytic Reduction of ortho- and meta-Nitroaniline by Nickel Oxide Nanoparticles

  • Jeon, Sugyeong;Ko, Jeong Won;Ko, Weon Bae
    • Elastomers and Composites
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    • 제55권3호
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    • pp.191-198
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    • 2020
  • Nickel oxide (NiO) nanoparticles were synthesized by a reaction of nickel nitrate hexahydrate (Ni(NO3)2·6H2O) and sodium hydroxide (NaOH). The synthesized NiO nanoparticles were examined with X-ray diffraction, scanning electron microscopy, Raman spectroscopy, and ultraviolet-visible (UV-vis) spectroscopy. The NiO nanoparticles were used as the catalyst for the reduction of o- and m-nitroaniline to phenylenediamine. The reduction rate of m-nitroaniline was faster than that of o-nitroaniline. The reduction rate for both o- and m-nitroaniline increased as the reaction temperature increased. The rate of reduction for nitroaniline followed a pseudo first-order reaction rate law.

1-알콕시-4-니트로아닐린들의 糖度에 關한 硏究 (Sweet Taste Mechanism of 1-Alkoxy-4-nitroaniline)

  • 김의락;전무식;채영복
    • 대한화학회지
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    • 제17권6호
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    • pp.391-394
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    • 1973
  • 반실험적인 양자역학 이론인 extended Huckel theory를 nitroaniline, 1-methoxy-4-nitroaniline과 1-ethoxy-4-nitroaniline에 적용하여 정량적으로 변화하는 sweetness기구를 구명코져 nitroaniline을 coplanar로 두고 ortho치환체의 geometrical rotation을 시켰을 때 charge density와 sweetness와의 상관관계를 설명하였다.

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유기결정 meta-Nitroaniline(mNA)의 과냉법에 의한 단결정 성장과 극성 외형의 이상성 (Supercooled melt growth and abnormal polar morphology of meta-Nitroaniline(mNA))

  • 류기한;윤춘섭
    • 한국결정성장학회지
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    • 제7권3호
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    • pp.349-358
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    • 1997
  • 비선형 광학 유기물질 meta-Nitroaniline(mNA)의 고품질 단결정을 과냉법을 사용하여 성장시키는데 처음으로 성공 하였다. 정제한 mNA를 녹인 뒤, 0.1 K의 일정한 과냉각 상태에서 종자 결정을 도입하여 하루 동안 크기가 약 $20{\times}15{\times}15 \textrm {mm}^3인 우수한 품질의 단결정을 성장시켰다. 성장된 결정의 전체적인 외형상 특징은 한쪽 방향으로만 성장했다는 것이다. 성장한 방향으로는 잘 발달된 {111}면과 {021}면으로 형성되어 있으나, 성장하지 않을 반대쪽 방향으로는 결정면이 생기기 않았다. 결정 성장이 이루어지는 방향은 파이로 전기적 방법으로 측정한 결과, [001] 방향으로 판명되었다. 성장된 결정의 결함 구조 특성은 싱크로트론 X-선 topography를 이용하여 조사하였으며, 비선형 광학 특성은 2차 조화파 변환 효율 및 광손상 문턱 값 측정으로 조사하였다.

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Synthesis of Gold Nanoparticles Using Fullerene Oxide and Their Catalytic Activity for Reduction of 4-Nitroaniline

  • Park, Geun Wook;Ko, Jeong Won;Ko, Weon Bae
    • Elastomers and Composites
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    • 제54권2호
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    • pp.105-109
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    • 2019
  • Gold nanoparticles were synthesized by reacting potassium tetrachloroaurate ($KAuCl_4$), potassium carbonate ($K_2CO_3$), and isopropyl alcohol in the presence of fullerene oxide [$C_{60}(O)_n$, $n{\geq}1$], which was, in turn, prepared from [$C_{60}$] fullerene and m-chloroperoxybenzoic acid under refluxing conditions. The crystallinity and morphology of the prepared gold nanoparticles were confirmed by UV-vis spectroscopy, X-ray diffraction, and scanning electron microscopy. The activity of the gold nanoparticles in the reduction of 4-nitroaniline was measured in order to determine its capability as a catalyst.

항응고성의 3-(N-Arylamino)-1,4-Naphthoquinone 유도체 합성(III) (Synthesis of Anticoagulant 3-(N-Aryalmino)-1,4-Naphthoquinones(III))

  • 유충규
    • 약학회지
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    • 제34권6호
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    • pp.422-428
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    • 1990
  • 2,3-Dibromo-1,4-naphthoquinone was reacted with p-aminobenzoic acid, 2-aminopyridine, 2-amino-4-metylpyridine, m-nitroaniline, sulfathiazol, p-chloroaniline, phenetidine and 2-bromo-3-(N-arylamino)-1,4-naphthoquinones($1{\sim}8$). 2,3-Epoxy-2,3-dihydro-1,4-naphthoquinone was also reacted with p-amonobenzoic acid, p-toluidine, p-chloroaniline, m-chloroaniline, m-nitroaniline, p-phenetidine, N,N-dimethyl-1,4-pheylenediamine as a ring opening and dehydogenation to form 2-hydroxy-3-(N-arylamino)-naphthoquinones ($9{\sim}16$) in good yield. These new compounds($1{\sim}16$) are expected to have a biological activities such as anticoagulant and cytotoxic.

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Epoxy 樹脂에 關한 硏究 (第 1 報) Naphthylamines 及 Aromatic amines 과 Epichlorohydrin과의 重合物에 關하여 (Studies on Epoxy Resins (Part 1) Polymerization of Epichlorohydrin with Naphthylamines)

  • 심정섭;홍성일
    • 대한화학회지
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    • 제5권1호
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    • pp.60-65
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    • 1961
  • Nowadays, it is a well-known fact that the epoxy resins play an important role in the industrial field of plastics because of their excellent properties. Although studies on the polymers of epichlorohydrin with phenols, up-to-date, were various, there were only a few wokrs on the polymers of epichlorohydrin with amines. Therefore the experiments are carried out about the polymerization of epichlorohydrin with ${\alpha}-, {\beta}$-naphtylamine, o-, m-, p-toluidine, and o-, m-, p-nitroaniline. Examining the polymerization processes and the differences in the properties of the polymers, we obtained the following conclusions. 1) ${\alpha}$-naphthylamine, ${\beta}$-naphthylamine, o-toluidine, m-toluidine and p-toluidine react with epichlorohydrin to form polymers but o-, m-, and p-nitroaniline do not make polymers with epichlorohydrin. 2) As polymerization times after adding sodium hydroxide and refluxing again 3hrs. are suitable for ${\alpha}$-naphthylamine-epichlorohydrin, 3.5hrs. for${\beta}$-naphthylamine-epichlorohydrin, and 4hrs, for m-toluidine-epichlorohydrin. 3) Method for determining molecular weight of these polymers by the titration of end group is applicable to the polymers having D.P. less than about 200 for ${\alpha}$-, ${\beta}$-naphthylamine-epichlorohydrin and those having D.P. less than 18 for m-toluidine-epichlorohydrin. 4) Gererally, these polymers get special colors so that these need proper pigmentation to use as molding compounds.

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2, 2'-methylene-bis-(3, 4, 6-trichloroacetoxy benzene)의 nitroaniline 계 mannich bases에 관한 연구 I. 합성 및 항균성 (Studies on Nitroaniline derivative of 2, 2'-methylene-bis-(3, 4, 6-trichloroacetoxy benzene by Mannich reaction Part I. Synthesis and Antimicrobial activity)

  • 유주현;김유삼;김종호;양융
    • 한국식품과학회지
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    • 제6권1호
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    • pp.6-11
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    • 1974
  • Four new compounds; 2,2'-methylene-bis [3, 4, 6-trichloro ${{\beta}-(o-nitroanilino)$ propionoxy} benzene]; m.p. $200{\sim}202^{\circ}C,\;C_{31}H_{22}O_8N_4Cl_6$ 2,2'-methylene-bis [3, 4, 6-trichloro ${{\beta}-(p-nitroanilino)$ propionoxy} benzene]; m.p. $168-170^{\circ}C,\;C_{31}H_{22}O_8N_4Cl_6$ : 2,2'-Methylene-bis [3, 4, 6-trichloro ${{\beta}-(o-chloro-p-nitroanilino)$ propionoxy} benzene]; m.p. $170.5-172.5^{\circ}C,\;C_{31}H_{20}O_8N_4Cl_8$ : 2,2'-Methylene-bis [3, 4, 6-trichloro ${{\beta}-(c-methyl-p-nitroanilino)$ propionoxy} benzene]; m.p. $163-164^{\circ}C,\;C_{33}H_{26}O_8N_4Cl_6$-were synthesized by Mannich reaction from 2,2'-Methylene-bis (3, 4, 6-trichloroacetoxy benzene) and their antimicrobial activities against the microorganisms Staphylococcus aureus, Escherichia coli, Bacillus subtilis Natto, Brevibacterium ammoniagenes, Candida tropicalis, Rhodotorula glutinis, Pseudomonas ovalis, Aspergillus candidus Link, Aspergillus awamori Nakazawa. Aspergillus niger var. Tieghem, Aspergillus usami Sakakuchi, Penicillium notatum-were tested. 2,2'-methylene-bis [3, 4, 6-trichloro ${{\beta}-(o-nitroanilino)$ propionoxy} benzene] showed a strong antimicrobial activity against Bacilus subtilis Natto and Brevibacterium ammoniagenes.

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Pd/C촉매하 파라니트로아닐린 수소첨가에 의한 고순도 파라페닐렌디아민의 합성공정 (Synthesis of High Purity p-Phenylenediamine from p-Nitroaniline by Catalytic Hydrogenation)

  • 조철군;정광보
    • 공업화학
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    • 제10권8호
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    • pp.1210-1215
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    • 1999
  • Pd/C촉매가 부유되어 있는 3상 슬러리 반응기에서 원료 p-nitroaniline(PNA)를 수소 첨가시켜 고순도의 p-phenylenediamine(PPD)를 합성하는 최적 반응조건을 구하였다. 수소첨가 반응시 활성점에서 수소부족을 줄이고 불순물의 생성을 감소시킬 수 있도록, 기체-액체, 액체-촉매사이의 물질전달 저항을 최소화하고 표면반응속도가 율속할 수 있게 반응조건을 설정하였다. 이 반응조건은 온도 $60^{\circ}C$, 압력 60~70 psig, 촉매농도 1~2 g-cat/L일 때가 최적이었으며, 반응속도는 PNA 농도에 0차, 수소 반응압력에 1차를 각각 보여주었으며, 총괄반응속도식은 $R_A=6.44{\times}10^6{\cdot}H{\cdot}P{\cdot}m{\cdot}$exp(-4659/T)로 나타났다.

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Synthesis of Carbobenzoxy-alanyl-thiaarginine (thialysine) benzyl ester and kinetic Studies with Trypsin

  • 홍남주;장성훈;진동훈
    • Bulletin of the Korean Chemical Society
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    • 제19권6호
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    • pp.689-695
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    • 1998
  • Carbobenzoxy-alanyl-thiaarginine benzyl ester and carbobenzoxy-alanyl-thialysine benzyl ester were synthesized in solution. Kinetic studies were carried out using three different analytical methods, semi-classical method, progress curve analysis and competitive spectrophotometry. In competitive spectrophotometry, carbobenzoxy-valyl-glycyl-arginyl-p-nitroaniline was used as a detector. Kinetic constants such as $K_m$ and $V_{max}$ measured by competitive spectrophotometry are almost the same as those values measured by semi-classical method. Colorimetric Ellman's assays showed the thio-peptido mimetics to be a suitable substrates for trypsin. Kinetic studies with trypsin gave $K_m$ of 2.33 mM and $k_{cat}$ of $1.50{\times}10^5\;min^{-1}$ for carboxy-alanyl-thiaarginine benzyl ester and $K_m$ of $3.41{\times}10^{-3}\; Mm\; and\; k_{cat}\; of\; 520{\times}102\; min^{-1}$ for carbobenzoxy-alanyl-thialysine benzyl ester, respectively. Kinetic constants $(K_m=2.04{\times}10^{-2}\; mM, K_{cat}=4.42{\times}10^3 \;min^{-1})$ for natural substrate, carbobenzoxy-alanyl-lysine benzyl ester, were also evaluated by competitive spectrophotometry in order to compare the mode of binding on trypsin.

합성화학물질들의 유전독성평가(Ⅷ) -마우스의 골수세포를 이용한 8종 합성화학물질들의 생체내 소핵시험- (Evaluation of the Genetic Toxicity of Synthetic Chemicals (Ⅷ) - In vivo Bone Marrow Micronucleus Assay of 8 Synthetic Chemicals in Mice -)

  • Ryu, Jae-Chun;Kim, Kyung-Ran;Kim, Youn-Jung
    • Environmental Analysis Health and Toxicology
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    • 제18권2호
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    • pp.137-143
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    • 2003
  • 합성화학물질들이 환경중에 유입되어 인체에는 물론 환경생태계에 많은 영향을 미치고 있어 이들의 유해성 검증은 매우 중요한 일이라 할 수 있다. 실제 산업체에서 사용되는 수많은 화학물질들의 유전적 손상 유발유무는 더욱이 중요한 일이라 할 수 있다. 이에 산업체 공정과정에서 널리 사용되는 것으로 알려진 8종의 합성화학물질에 대해 마우스의 골수세포를 이용한 in vivo 소핵시험을 수행하여, 소핵형성 유발유무를 관찰하였다. 양성대조군으로 사용된 mitomycin는 음성대조군과 비교시 유의하게 소핵을 유발하는 반면, 비교적 마우스에서 높은 50% 치사량을 보이는 phenylisocyanate, m-aminochlorobenzene 및 2-chloro-4-nitroaniline 등의 합성물질들을 비롯한 나머지 5종의 물질들은 본 실험결과 통계적으로 유의하게 소핵을 유발하지 않는 것을 관찰 할 수 있었다.