• 약학회지
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• 제52권6호
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• pp.514-519
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• 2008

We developed a convenient synthetic route to 3-alkylated 2-phenyl-4-quinolone derivatives (4a-h and 5a-c), which were expected to retain antitumor activity. A series of 2,3-dihydro-2-hydroxy-2-phenyl-4-quinolones (3a-h) was synthesized through dehydration, dealcoholation and hydration using acid-catalyzed one-pot reaction from anilines and ethyl benzoylacetates. 3-Methyl (or 3,3-dimethyl)-2-phenyl-4-quinolone derivatives 4 and 5 were synthesized from 3a-h through the methylation using methyl iodide. Formation of quinolone nucleus was undertaken with p-toluenesulfonic acid (p-TSA) at $90{\sim}110^{\circ}C$ in toluene for 3${\sim}$7.5 hr over the Dean-Stark apparatus. The key intermediates in these preparations are ${\beta}$-ketoesters 2a-h, which can be readily obtained from the corresponding anilines 1a-e by reaction with ethyl bezoylacetates.

• 약학회지
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• 제24권2호
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• pp.135-141
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• 1980

The crystal and molecular structure of 2-methyl-3-(N-trimethyl ammonium)phenol iodide, $C_{10}H_{16}NOI, was determined by X-ray diffraction method. The compound crystallizes in the orthorhombic space group $P_{na2}_{1}$ with a=13.327(3), b=12.496(3), C=7.227(2)A and Z=4. A total of 489 independent observed reflections were collected by the automated Four-circle diffractometer and was solved by heavy atom method and refined by anisotropic block-diagonal least-squares method to the R value of 0.04. The benzene ring is slightly distorted from regular hexagon. The I atom and 2-methyl-3-(N-trimethyl ammonium)phenol group is held together by van der Waals forces in the crystal. Intermolecular hydrogen bond is of the type O-H....I with the length 3.35.angs.. Apart from the hydrogen bonding system the molecules are held together by van der Waals forces in the crystal.

• Nuclear Engineering and Technology
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• 제28권1호
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• pp.44-55
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• 1996

원자력 발전소에서 방사성 요오드를 제거하기 위해 사용되는 원료활성탄과 2%, 5%TEDA(Triethylene-Diamine) 첨착활성탄을 이용하여 원소요오드와 유기요오드인 메틸요오드에 대한 흡착특성을 분석하였다. 여러 흡착 등온식을 선정하여 실험치와 비교함으로서 선정된 흡착 등온식의 적합성 여부를 검증하였다. 흡착평형 실험결과 Dubinin-Astakhov(DA) 등온식이 여러 가지 흡착등온식 가운데 가장 적합한 것으로 나타났다. 흡착표면의 흡착에너지 분포가 불균일(Heterogeneous)하기 때문에 포텐셜 (Potential) 에너지를 근거로 하는 DA등온식이 흡착평형 관계를 보다 정확하게 나타내는 것으로 생각된다. 흡착표면의 불균일성을 확인하기 위해 흡착에너지 분포도를 원료활성탄과 첨착활성탄에 대해 상호 비교하였다 활성탄-요오드 흡착시스템에서 불균일성은 활성탄의 기공구조 분만 아니라 흡착질과 활성탄과의 상호관계에 의해서도 영향을 받게된다 따라서 흡착표면의 불균일성은 활성탄을 첨착함에 따라서 증가하게 되고 원소요오드보다 유기요오드의 경우 불균일성이 더 커지는 것으로 보여진다.

• Fibers and Polymers
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• 제2권1호
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• pp.131-134
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• 2001

Living cationic polymerization behaviors of isobutyl vinyl ehters (IBVE), initiated by iodomethyl methyl ether (IMME)/zinc iodide ($Znl_2$) have been investigated. The polymerization was carried out at 0, -15, and $-30^{\circ}C$ in toluene. It was found that the rate of polymerization increased as the IMME concentration increased and decreased as temperature decreased. 100% conversion was always achieved without exception. Furthermore, the number-average molecular weight ($M_{n}$) of polymers increased in direct proportion to monomer conversion. The molecular weights of polymers were in good agreement with the theoretical values, calculated on the basis that one polymer chain was formed by one IMME molecule and the values of polydispersity index are always less than 1.2, revealing the living nature. The living nature was also confirmed by synthesis of poly(IBVE-b-TBVE) by subsequent monomer addition of t-butyl vinyl ether (TBVE).

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.214-214
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• 2011

The adsorption and reactions of methanol and methyl iodide on ZnO(0001) and ZnO(11-20) single crystal surfaces have been investigated using the temperature programmed desorption (TPD) technique. The interaction of methanol and methyl iodide with ZnO is stronger on the polar ZnO(0001) surface than the non-polar ZnO(11-20) surface. On ZnO(0001), methanol is decomposed to produce formaldehyde and hydrogen. Two desorption features of formaldehyde and hydrogen are observed at around 500 and 580 K. The interaction of methanol and pre-adsorbed hydrogen has been also investigated. The reaction mechanism of methanol on ZnO will be proposed.

• KSBB Journal
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• 제6권2호
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• pp.207-213
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• 1991

In this study poly (1-methyl-4-vinylpyridinium iodide-co-styrene) membrane with pyridinium cation as a fixed carrier was synthesized and the transport characteristics of the membrane was examined over various factors. As the concentration of the fixed carrier in the membrane was increased, the water content was increased. Meanwhile, the counter current of the organic anion and the chloride ion, the following results were obtained. Initial flux of Cl-, organic anion and Na+ decreased with the increasing thickness of membrane, and as the concentration of the fixed carrier increases, the initial flux of Cl- and organic anion increase but the initial flux of Na+ decreased. The flux equation of the organic anion, CCl3COO- was obtained from saturation kinetics as follows;$V_{o}=\frac{(8.67{\times}10^{-5}){\cdot}[NaCl]}{9.63{\times}10^{-2}+[NaCl]} mol/cm^2h$

• 통합자연과학논문집
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• 제10권4호
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• pp.175-191
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• 2017

In organic chemistry amide synthesis is performed through condensation of a carboxylic acid and an amine with releasing one equivalent of water via the corresponding ammonium carboxylate salt. This method is suffering from tedious processes and poor atom-economy due to the adverse thermodynamics of the equilibrium and the high activation barrier for direct coupling of a carboxylic acid and an amine. Most of the chemical approaches to amides formations have been therefore being developed, they are mainly focused on secondary amides. Direct carbonylations of tertiary amines to amides have been an exotic field unresolved, in particular direct carbonylation of trimethylamine in lack of commercial need has been attracted much interests due to the versatile product of N,N-dimethylacetamide in chemical industries and the activation of robust N-C($sp^3$) bond in tertiary amine academically. This review is focused mainly on carbonylation of trimethylamine as one of the typical tertiary amines by transition metals of cobalt, rhodium, platinum, and palladium including the role of methyl iodide as a promoter, the intermediate formation of acyl iodide, the coordination ability of trimethylamine to transition metal catalysts, and any possibility of CO insertion into the bond of Me-N in trimethylamine. In addition reactions of acyl halides as an activated form of acetic acid with amines are reviewed in brief since acyl iodide is suggested as a critical intermediate in those carbonylations of trimethylamine.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2003년도 가을 학술논문집
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• pp.207-214
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• 2003

원자력시설에서 방사성요오드 제거용으로 사용되는 TEDA 침착활성탄의 고온공정에서의 메틸요오드의 제거성능을 은이온제올라이트(AgX)와 상호 비교하였다. $30^{\circ}C~400^{\circ}C$ 온도범위에서 온도에 따른 메틸요오드의 흡착량 및 탈착후 잔존량을 측정한 결과, 비첨착활성탄의 흡착성능은 온도가 증가함에 따라 급격히 감소하지만 TEDA 침착활성탄의 흡착성능은 $100^{\circ}C$부근에서도 AgX와 거의 유사한 값을 나타내었고, 탈착후 잔존량은 $250^{\circ}C$까지도 비침착활성탄에 비하여 매우 높은 값을 유지하였다. 또한 $100^{\circ}C$ 이상의 고온공정에서 AgX 및 TEDA 침착활성탄을 충전한 고정층 파괴특성을 상호 비교하였으며, 반응 생성기체의 분석으로부터 AgX에 의한 메틸요오드 제거 메커니즘을 제안하였다.

• 대한화학회지
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• 제38권5호
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• pp.372-376
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• 1994

Penicillin으로부터 유도된 4-mercaptoazetidin-2-one(2a)은 염기조건에서 불안정하지만 Et3N이나 pyridine 염기하에서 acetyl chloride, methyl chloroformate, ethyl iodoacetate, diethyl azodicarboxylate 등의 친전자체와 반응하여 sulfur에 acetyl, methoxycarbonyl, ethoxycarbonylmethyl, diethoxycarbonylhydrazineo원자단이 부착된 화합물이 된다. 반면 thiol의 methylation은 methyl iodide와의 반응으로 얻을 수 없고 diazomethane을 사용해야 한다. 또한 화합물 2a의 이성질체인 화합물 3a의 반응성도 화합물 2a와 거의 비슷하다.

• 방사성폐기물학회지
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• 제21권2호
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• pp.205-224
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• 2023

The emission of off-gas streams from used fuel recycling is a concern in nuclear energy usage as they contain radioactive compounds, such as, ³H, ¹⁴C, ⁸⁵Kr, ¹³¹I, and ¹²⁹I that can be harmful to human health and environment. Radioactive iodine, ¹²⁹I, is particularly troublesome as it has a half-life of more than 15 million years and is prone to accumulate in human thyroid glands. Organic iodides are hazardous even at very low concentrations, and hence the capture of ¹²⁹I is extremely important. Dynamic adsorption experiments were conducted to determine the efficiency of sodium mordenite, partially exchanged silver mordenite, and fully exchanged silver mordenite for the removal of methyl iodide present at parts per billion concentrations in a simulated off-gas stream. Kinetic analysis of the system was conducted incorporating the effects of diffusion and mass transfer. The possible reaction mechanism is postulated and the order of the reaction and the values of the rate constants were determined from the experimental data. Adsorbent characterization is performed to investigate the nature of the adsorbent before and after iodine loading. This paper will offer a comprehensive understanding of the methyl iodide behavior when in contact with the mordenites.