• 제목/요약/키워드: Michael Addition

검색결과 153건 처리시간 0.023초

광경화형 자가광개시 아크릴레이트의 경화특성 및 도막물성 (Curing and Coating Properties of Photo-Curable Self-Photoinitiating Acrylate)

  • 한아람;홍진후;김현경
    • 접착 및 계면
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    • 제15권1호
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    • pp.22-30
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    • 2014
  • 본 연구는 자가광개시형 아크릴레이트를 Michael addition 반응을 이용하여 합성하고 자유라디칼, 양이온 및 하이브리드 시스템을 통해 배합-경화-물성 상관관계를 유도하여 이들의 경화물성, 표면 물성을 Photo-DSC, 진자경도, 연필경도 및 내오염성 측정을 이용하여 평가하였다. 그 결과, 자유라디칼 반응형 모노머 첨가를 통해 경화 특성의 향상을 유도할 수 있었으나, 일정량 이상의 모노머 첨가 시 반응성 저하로 인해 경화성이 오히려 저하되었으며, 이는 자유라디칼 반응형 모노머에 의한 이동성의 향상이 SPIA의 경화 향상에는 한계가 있음을 확인하였다. 자유 라디칼 광개시제에 의한 자유 라디칼의 생성과 자가광개시 반응에 의한 자유라디칼이 동시에 연속적으로 반응에 참여되어 우수한 경화 특성을 보였으며, 양이온 시스템을 접목한 하이브리드 시스템의 경우 양이온계 광개시제와 양이온계 모노머가 라디칼 생성과 확산까지 촉진 시켜 우수한 경화특성을 보이며, 라디칼 중합에 비해 산소에 의한 영향이 적은 양이온 중합의 영향으로 표면물성을 비롯한 도막 물성 또한 가장 우수하였다.

Kinetic Study on Michael-type Reactions of 1-Phenyl-2-propyn-1-one with Alicyclic Secondary Amines: Effect of Medium on Reactivity and Mechanism

  • Hwang, So-Jeong;Park, Youn-Min;Um, Ik-Hwan
    • Bulletin of the Korean Chemical Society
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    • 제29권10호
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    • pp.1911-1914
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    • 2008
  • Second-order rate constants (kN) have been measured for Michael-type addition reactions of a series of alicyclic secondary amines to 1-phenyl-2-propyn-1-one (2) in MeCN at 25.0 ${\pm}$ 0.1 ${^{\circ}C}$. All the amines studied are less reactive in MeCN than in $H_2O$ although they are more basic in the aprotic solvent by 7-9 p$K_a$ units. The Bronsted-type plot is linear with $\beta_{nuc}$ = 0.40, which is slightly larger than that reported previously for the corresponding reactions in $H_2O$ ($\beta_{nuc}$ = 0.27). Product analysis has shown that only E-isomer is produced. Kinetic isotope effect is absent for the reactions of 2 with morpholine and deuterated morpholine (i.e., $k^H/k^D$ = 1.0). Thus, the reaction has been concluded to proceed through a stepwise mechanism, in which proton transfer occurs after the rate-determining step. The reaction has been suggested to proceed through a tighter transition state in MeCN than in H2O on the basis of the larger $\beta_{nuc}$ in the aprotic solvent. The nature of the transition state has been proposed to be responsible for the decreased reactivity in the aprotic solvent.

항암항생제 11-Deoxy-$\beta$-rhodomycinone의 합성 (Total Synthesis of 11-Deoxy-$\beta$-rhodomycinone Antitumor Antibiotics)

  • 노영쇠;강혼수;신홍식
    • 약학회지
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    • 제37권6호
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    • pp.555-560
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    • 1993
  • Methyl 3-[(phenylsulfonyl)methyl]-1, 4, 8-trimethoxy-2-naphthoate(7) preparad by 3 steps was condensed with 5-ethyl-2-cyclohexen-1-one(8) to afford the teracyclic aromatic ring system compound 10, which was stepwise converted into the precursor of 11-Deoxy-$\beta$-rhodomycinone by means of various functional groups transformation.

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Efficient One-Pot Synthesis of Acridinediones by Indium(III) Triflate-Catalyzed Reactions of β-Enaminones, Aldehydes, and Cyclic 1,3-Dicarbonyls

  • To, Quang Huy;Lee, Yong-Rok;Kim, Sung-Hong
    • Bulletin of the Korean Chemical Society
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    • 제33권4호
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    • pp.1170-1176
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    • 2012
  • An efficient one-pot synthesis of acridinediones by $In(OTf)_3$-catalyzed reactions was developed starting from ${\beta}$-enaminones, aldehydes, and cyclic 1,3-diketones. The key strategies of these reactions involve domino Knoevenagel condensation/Michael addition/cyclodehydration reaction.

Kinetics and Thermodynamic Studies on the Reaction of Cysteine with Cinnamaldehyde

  • Kim, Tae-Rin;Yun, Se-Joon;Park, Byung-Bin
    • Bulletin of the Korean Chemical Society
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    • 제7권1호
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    • pp.25-29
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    • 1986
  • The reaction of cysteine with cinnamaldehyde have been studied kinetically and thermodynamically. It was found that the reaction proceeds in two steps; formation of the monoadduct by a Michael type addition followed by the nucleophilic attack of the second cysteine to the carbonyl carbon of the monoadduct to afford the thiazolidine derivative. A reaction profile for the reaction of cysteine with cinnamaldehyde was constructed based on the thermodynamic parameters analyzed for the forward and the reverse reactions. It was assumed that the second step of this reaction accompanies an intermediate, a Schiff base.

Henry Fayol's 14 Principles of Management: Implications for Libraries and Information Centres

  • Uzuegbu, C.P.;Nnadozie, C.O.
    • Journal of Information Science Theory and Practice
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    • 제3권2호
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    • pp.58-72
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    • 2015
  • This paper focuses generally on the ‘fourteen principles of management’ by Henri Fayol. However, it specifically analyses their application to and implications for libraries and information centres. An extensive review of published works on management generally, and library management in particular, was conducted. This yielded vital insights on the original meaning and later modifications of these principles, as well as their application in the management of various organisations. Consequently, the strengths and weaknesses of these principles were examined to determine their suitability in libraries and information centres. Inferences, illustrations, and examples were drawn from both developed and developing countries which gives the paper a global perspective. Based on available literature, it was concluded that Fayol’s principles of management are as relevant to libraries as they are in other organisations. The paper, therefore, recommends that in addition to modifying some aspects to make these principles more responsive to the peculiar needs of libraries, further research should be undertaken to expand the breadth of these principles and ascertain their impacts on the management of information organisations.

Furfurylidene acetophenone유도체에 대한 Thiourea의 친핵성 첨가반응 메카니즘과 그 반응속도론적 연구 (The Kinetics and Mechanism of the Nucleophilic Addition of Thiourea for Furfurylidene Acetophenone derivatives)

  • 이기창;목갑영;오세영;류정욱
    • 한국응용과학기술학회지
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    • 제14권1호
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    • pp.27-32
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    • 1997
  • Furfurylidene acetophenone derivatives were synthesis, it was measured that nucleophilic addition made use of UV at a wide pH 1.0${\sim}$13.0 range in 30% dioxane-$H_2O$ solution, 25$^{\circ}C$. On the basis of general base catalysis, substitutent effect, confirmation of nucleophilic addition products, it was measured the reaction rate of furfurylidene acetophenone derivatives for the pH change. It may be concluded that a part was unrelated to pH and another part was in proportion to concentration of hydroxide ion: Above pH 10.0. sulfide anion adds to the double bond (Michael type addition), a part having no concern with pH, addition reaction to double bond is initiated by addition of neutral thiourea molecule. From the result of measurement the reaction rate, nucleophilic addition of furfurylidene acetophenone derivatives confirmed to the irreversible first order. Through measurement the substituent effect. It found that reaction rate was accelerated by electron attracting group. On the basis of these findings, nucleophilic addition of thiourea for the furfurylidene acetophenone derivative was proposed a fitting mechanisms.

Indium and Gallium-Mediated Addition Reactions

  • Lee, Phil-Ho
    • Bulletin of the Korean Chemical Society
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    • 제28권1호
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    • pp.17-28
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    • 2007
  • Indium and gallium have emerged as useful metals in organic synthesis as a result of its intriguing chemical properties of reactivity, selectivity, and low toxicity. Although indium belongs to a main metal in group 13, its first ionization potential energy is very low and stable in H2O and O2. Therefore, indium-mediated organic reactions are of our current interest. On the basis of these properties of indium, many efficient indium-mediated organic reactions have been recently developed, such as the addition reactions of allylindium to carbonyl and iminium groups, the indium-mediated synthesis of 2-(2-hydroxyethyl)homoallenylsilanes, the indiummediated allylation of keto esters with allyl halides, sonochemical Reformatsky reaction using indium, the indium-mediated selective introduction of allenyl and propargyl groups at C-4 position of 2-azetidinones, the indium-mediated Michael addition and Hosomi-Sakurai reactions, the indium-mediated β-allylation, β- propargylation and β-allenylation onto α,β-unsaturated ketones, the highly efficient 1,4-addition of 1,3-diesters to conjugated enones by indium and TMSCl, and the intramolecular carboindation reactions. Also, we found gallium-mediated organic reactions such as addition reactions of propargylgallium to carbonyl group and regioselective allylgallation of terminal alkynes.

2-Phenyl-4H,5H-3-methyl-3-thiazolinium Perchlorate 유도체의 가수분해 반응 메카니즘에 관한 반응속도론적 연구 (Kinetic Studies on the Mechanism of Hydrolysis of 2-Phenyl-4H,5H-3-methyl-3-thiazolinium Perchlorate Derivatives)

  • 김태린;이소영;한만소;변상용;이석희
    • 대한화학회지
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    • 제44권2호
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    • pp.120-126
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    • 2000
  • 2-PhenyI-4H,5H-3-methyl-3-thiazolinium perchlorate(PTP)유도체들의 가수분해속도상수를 수용액에서 자외선 분광법으로 측정하여 넓은 pH 범위에서 적용될 수 있는 속도식을 구하였다. pH에 따른 속도상수의 변화, 가수분해 생성물의 확인, 일반염기 및 치환기 효과 등을 바탕으로 반응 메카니즘을 제안하였다. 즉 pH 4.0 이하에서는 물분자의 첨가가 일어나 가수분해가 진행되며, pH 9.0 이상에서는 전형적인 Michael type의 반응이 일어나며, pH $4.5{\sim}8.0$ 사이에서는 이들 두 반응이 경쟁적으로 일어남을 알았다.

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