• 제목/요약/키워드: Alkyl acetate

검색결과 29건 처리시간 0.011초

알킬술폰이 삽입된 층상구조의 염기성 초산구리의 합성과 구조 (The structure and synthesis of intercalation compounds between layered basic copper acetate and alkyl sulfonates)

  • 조영식;허영덕
    • 한국결정성장학회지
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    • 제8권3호
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    • pp.431-434
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    • 1998
  • 층상구조를 가진 염기성 초산구리, $Cu(OH)(CH_3COO){cdot}H_2O$를 합성하였다. 또한 음이온 치환반응을 통해서 alkyl sulfonate를 염기성 초산구리에 삽입시켰다. X-선 회절 데이터와 alkyl sulfonate의 분자의 크기를 비교하여 층간 삽입된 초산구리의 공간배열을 확인하였다.

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비닐 아세테이트/알킬메타크릴레이트계 공중합과 등온건조속도 (Isothermal Drying Rate and Copolymerization of Vinyl Acetate/Alkyl Methacrylates)

  • 김민성;설수덕
    • 폴리머
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    • 제33권3호
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    • pp.230-236
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    • 2009
  • 비닐 아세테이트/알킬메타크릴레이트계 에멀젼 공중합에서 반응온도, 개시제의 종류와 농도, 보호콜로이드인 PVA의 종류와 농도, 공단량체인 MMA, EMA의 조성비를 변화시키며 중합하였다. 제조된 공중합체인 poly(vinyl acetate-co-methyl methacrylate)(PVAc/PMMA), poly(vinyl acetate-co-ethyl methacrylate)(PVAc/PEMA)를 수분 측정기를 사용하여 100, 130, 150, 180, $200^{\circ}C$에서 등온건조 시키고, 그 건조 특성을 고찰하여 다음과 같은 결론을 얻었다. 등온법으로 얻은 중합체 고형화 과정의 활성화 에너지는 PVAc/PMMA> PVAc/PEMA> PVAc의 순으로 공단량체의 곁사슬의 탄소수 증가에 따라 감소하였다. 접착박리강도는 동일한 조성의 공중합체에서 보호콜로이드 함량에 비례하여 증가하였고, 내수 접착박리강도는 최적의 보호콜로이드 함량에서 공단량체의 종류와 함량에 따라 PVAc/PMMA>PVAc/PEMA>PVAc 순이다.

비닐아세테이트/알킬아크릴레이트계 에멀젼 공중합과 등온 열분해 특성 (Characteristics of Isothermal Analysis and Emulsion Copolymerization of Vinyl Acetate/Alkyl Acrylate)

  • 조대훈;최성일;설수덕
    • 접착 및 계면
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    • 제13권2호
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    • pp.64-72
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    • 2012
  • 비닐아세테이트와 알킬아크릴레이트계 에멀젼공중합에서 개시제인 ammonium persulfate (APS)의 농도, 보호 콜로이드인 poly(vinyl alcohol) (PVA)의 종류와 농도, 공단량체인 methyl acrylate (MA), ethyl acrylate (EA), n-butyl acrylate (BA)의 혼합비를 변화시켜 중합하였다. 제조된 poly(vinyl acetate-co-methyl acrylate) (PVAc/PMA), poly(vinyl acetate-co-ethyl acrylate) (PVAc/PEA), poly(vinyl acetate-co-n-butyl acrylate) (PVAc/PBA)에 대하여 다음과 같은 결론을 얻었다. 등온 열분해법으로 $100{\sim}200^{\circ}C$ 영역에서 구한 비닐아세테이트와 알킬아크릴레이트 공중합체에 대한 등온 열분해 활성화에너지는 PVAc/PMA > PVAc/PEA > PVAc/PBA이었으며, 플라스마 처리 전과 후의 접착박리강도는 PVAc/PMA > PVAc/PEA > PVAc/PBA의 순이었다.

Bis (\beta$-amino-alkyl-oxo) oxalate 유도체의 납 중독 해독에 관한 연구 (Studies on the Bis (amino-alkyl-oxo) Oxalate Derivatives As a Antidote of Lead poisoning)

  • 최선아;유미례;노영수;정성현;정세영
    • Environmental Analysis Health and Toxicology
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    • 제4권3_4호
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    • pp.1-6
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    • 1989
  • The effects of his ($\beta$-amino-ethyl-oxo) oxalate and bis ($\alpha$-amino-methyl-oxo) oxalate on the toxicity of lead acetate in rast were examined. Rats were given intraperitoneally at the dose of lead acetate 45 mg/kg. The exposure of lead acetate showed the 70% decrease of ALAD ($\delta$-amino levulinic acid dehydratase) activity in red blood cell. In vivo 122 mg/kg administration of bis ($\beta$-amino-ethyl-oxo) oxalate and bis ($\alpha$-amino-methyl-oxo) oxalate showed the 50% increase of ALAD activity, whereas 149 mg/kg administeration of Ca-EDTA had no effect. In vitro, the same results were obtained. Both compounds had hemolytic activity at concentrations higher than that required for showing the 50% ALAD activity increase in vivo.

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팔라듐 촉매를 이용한 Aryl Conjugated Enamides의 합성 (Palladium Catalyzed Synthesis of Aryl Conjugated Enamides)

  • 홍영택;이종태;유철모;김진일
    • 대한화학회지
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    • 제29권3호
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    • pp.287-294
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    • 1985
  • Acrylamide, N-alkyl substituted acrylamides and N,N-diethylacrylamide를 트리에틸아민과 palladium acetate-triorthotolyl phosphine 촉매 존재하에서 브롬화 방향족화합물들과 비닐화 반응을 실시하여 여러 기능기로 치환된 aryl conjugated enamides를 합성하였다. 이들 반응은 모두 선택적으로 진행되어 (E)-이성질체의 aryl conjugated enamides를 생성하였다. N-alkyl substituted acrylamides는 브롬화 방향족화합물들과의 반응에서 acrylamide와 N,N-diethylacrylamide보다 더 좋은 반응성을 나타내어 생성물들을 높은 수득율로 얻을 수 있었다. 또한 브롬화 방향족화합물이 전자받기 기능기로 치환된 경우에 좋은 반응성을 나타냈으며 전자 주기 기능기를 갖는 경우 acrylamide와 N,N-diethylacrylamide와의 반응에서는 반응이 전혀 진행되지 않거나 낮은 반응성을 나타냈다.

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Triton X 系를 乳化劑로 하는 Vinyl Acetate 의 乳化重合 (Emulsion Polymerization of Vinyl Acetate with Triton-X as Emulsifier)

  • 정기현;한상구
    • 대한화학회지
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    • 제6권1호
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    • pp.19-24
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    • 1962
  • In the emulsion polymerization of vinyl acetate with Triton-X(Alkyl-aryl-polyether alcohol) and polyvinyl alcohol as emulsifier, some relations between the conditions of polymerization and the polymerization rate, polymerization degree and stability of the emulsion are studied and discussed.

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메틸 2-클로로-2-(메틸티오)아세트산을 이용한 치환페놀류로부터 2(3H)-벤조푸란온 유도체의 합성 (Synthesis of 2(3H)-Benzofuranone Derivatives from Substituted Phenols Using Methyl 2-chloro-2-(methylthio)acetate)

  • 최홍대;김미헌;신상훈;손병화
    • 약학회지
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    • 제40권6호
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    • pp.640-645
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    • 1996
  • 5-Alkyl-2(3H)-benzofuranones(3a-e) were prepared from Friedel-Crafts reaction of 4-alkylphenols with methyl 2-chloro-2-(methylthio)acetae(1) followed by the treatment of zinc du st-acetic acid. The reaction of disubstituted phenols with 1 in the presence of stannic chloride afforded 3-methyltWa-2(3H)-benzofuranone derivatives(11a-c), which were readily converted into 2(3H)-benzofuranone derivatives(12a-c) by desulfurization with zinc dust-acetic acid.

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Soluble Single-Molecule Magnet: Mn12-stearate.

  • 박치동;정둑영
    • Bulletin of the Korean Chemical Society
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    • 제22권6호
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    • pp.611-615
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    • 2001
  • A new polynuclear complex of manganese stearate has been prepared by substitution of acetate with stearic acid. The stearate ion with long alkyl chain was used to isolate molecular $Mn_{12}$ cluster from each other. The $Mn_{12}$-stearate compound prepared is soluble in most organic solvents and resistant against water catalyzed reduction. The $Mn_{12}$-stearate compound shows similar electrochemical, magnetic properties to the pristine $Mn_{12}$-acetate.

Potential Functional Role of Phenethylamine Derivatives in Inhibiting Dopamine Reuptake: Structure-Activity Relationship

  • Dooti Kundu;Anlin Zhu;Eunae Kim;Suresh Paudel;Choon-Gon Jang;Yong Sup Lee;Kyeong-Man Kim
    • Biomolecules & Therapeutics
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    • 제31권1호
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    • pp.108-115
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    • 2023
  • Numerous psychotropic and addictive substances possess structural features similar to those of β-phenethylamine (β-PEA). In this study, we selected 29 β-PEA derivatives and determined their structure-activity relationship (SAR) to their ability to inhibit dopamine (DA) reuptake; conducted docking simulation for two selected compounds; and identified their potential functionals. The compounds were subdivided into arylethylamines, 2-(alkyl amino)-1-arylalkan-1-one derivatives and alkyl 2-phenyl-2-(piperidin-2-yl)acetate derivatives. An aromatic group, alkyl group, and alkylamine derivative were attached to the arylethylamine and 2-(alkyl amino)-1-arylalkan-1-one derivatives. The inhibitory effect of the compounds on dopamine reuptake increased in the order of the compounds substituted with phenyl, thiophenyl, and substituted phenyl groups in the aromatic position; compounds with longer alkyl groups and smaller ring-sized compounds at the alkylamine position showed stronger inhibitory activities. Docking simulation conducted for two compounds, 9 and 28, showed that the (S)-form of compound 9 was more stable than the (R)-form, with a good fit into the binding site covered by helices 1, 3, and 6 of human dopamine transporter (hDAT). In contrast, the (R, S)-configuration of compound 28 was more stable than that of other isomers and was firmly placed in the binding pocket of DAT bound to DA. DA-induced endocytosis of dopamine D2 receptors was inhibited when they were co-expressed with DAT, which lowered extracellular DA levels, and uninhibited when they were pretreated with compound 9 or 28. In summary, this study revealed critical structural features responsible for the inhibition of DA reuptake and the functional role of DA reuptake inhibitors in regulating D2 receptor function.