• Journal of the Korean Applied Science and Technology
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• v.15 no.2
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• pp.41-48
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• 1998

The catalytic oxidations of several cycloolefins in $CH_2Cl_2$ were been investigated using Mn(III)-, Fe(III)-porphyrin complexes as a catalyst and sodium hypochlorite as a terminal oxidant. Porphyrins were $(p-CH_3O)TTP,\;(p-CH_3)TTP,$ TPP, (p-F)TPP, (p-Cl)TPP and $(F_{20})TPP$ (TPP = tetraphenylporphyrin), and olefins were cyclopentene, cyclohexene and cycloheptene. The substrate conversion yield was discussed according to the substituent effects of metalloporphyrin. The conversion yield of substrate by changing the substituent of TPP increased in the order of $p-CH_3O$ < $p-CH_3$ < H < p-F < p-Cl, which was consistent with the sequence of $4{\sigma}$ values of TPP. The conversion of cycloalkene followed the order of $C_5\;<\;C_6\;<\;C_7$.

• Journal of the Korean Applied Science and Technology
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• v.21 no.1
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• pp.76-88
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• 2004

The catalytic oxidation reaction of several cycloolefins in $CH_2Cl_2$ have been investigated using non-redox metalloporphyrin(M = Ga(III), In(III) and TI(III) complexes as a catalyst and sodium hypochlorite as a terminal oxidant. Porphyrins were $(p-CH_3O)$TPP, $(p-CH_3)$TPP, TPP, (p-F)TPP, (p-Cl)TPP and $(F_{20})$TPP (TPP=5,10,15,20-tetraphenyl-21H,23H-porphyrin) and olefins were cyclopentene, cyclohexene, cycloheptene and cyclooctene, The substrate conversion yield(%) was investigated according to the radius effect of non-redox metal ion, substituent effect and hindrance effect of metalloporphyrin. The conversion yield of cycloolefin was in the following order : $C_5$ < $C_6$ < $C_7$ = $C_8$.

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.155-155
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• 2006

The most commercially and academically advanced catalysts of late transition metals are diimine complexes based on Pd(II)/Ni(II) and bis(imino)pyridyl complexes based on Fe(II)/Co(II). It is well known that the former systems yield branched polyethylenes and the latter linear PEs. In this presentation, effect of extremely bulky ligands with electron withdrawing/donating substituents at a remote position from Ni(II) metal center and of using multi-nuclear homo or hetero multi-metal on the ethylene polymerization is to be paged.

• Journal of the Korean Chemical Society
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• v.25 no.3
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• pp.172-176
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• 1981

The formation of $C_2-C_{10}$ hydrocarbons from methanol over shape-selective ZSM-5 zeolite catalysts is studied. It seems that $C_2-C_5$ olefins formed from methanol via dimethylether are transformed further to higher hydrocarbons containing higher concentration of aromatics by the acid sites of ZSM-5. Unique cross linked channel structure and its hydrophobicity seems to be mainly responsible for its high activity of ZSM-5 catalyst for the conversion of methanol.

• Macromolecular Research
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• v.16 no.1
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• pp.36-44
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• 2008

A series of polysiloxanes containing alkylsulfonyl side groups were synthesized using a polymer analogous reaction beginning from poly(methylhydrosiloxane) and the corresponding olefins. These polymers showed a mesomorphic behavior with smectic liquid crystalline phases. The chemical and physical properties of these polymers were examined using nuclear magnetic resonance spectroscopy, gel permeation chromatography, differential scanning calorimetry, optical polarizing microscopy, and X-ray diffraction.

• Archives of Pharmacal Research
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• v.28 no.2
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• pp.151-158
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• 2005

Palladium(II)-catalyzed carboxylation of chiral olefins 6a-d has been examined under various conditions. In the weak basic condition ($K_{2}CO_3$), 7a-d were obtained in good yields. Alternatively, in the strong basic condition, pyrrolidinones 8a-d were obtained resulting in excellent yields and with high diastereoselectivity.

• YAKHAK HOEJI
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• v.43 no.5
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• pp.566-571
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• 1999

(1H-1,2,4-Triazolyl) methy-4-(sub). phenyl-5-methyl-1,3-dioxolan-2-yliden (3) derivatives were synthesized and tested for their antifungal activities. The designed compounds with a 1,2,4-triazolylmethyl group at the 4-position of 1,3-dioxolan-2-yliden moiety were synthesized by reaction of difluorinated olefins(2) with (2R, 3R)-2-(2,4-dihalophenyl)-1-(1H-1,2,4-triazol-l-yl) butane-2,3-diol (1). These compounds were tested for in vitro antifungal activities against 16 fungi species. The MIC values were determined by the micro broth dilution method. In general, 1,3-dioxolan-2-yliden derivatives showed antifungal activities in vitro. Among them, (4R, 5R)-4-(2,4-difluorophenyl)-5-methyl-2-[1-(3,4-methylenedioxypheny)meth-ylidene)-1,3-dioxolon-4-yl(1H-1,2,4-triazollyl)methane showed superior antifungal activities to fluconazol and ketoconazol.

• Proceedings of the Membrane Society of Korea Conference
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• 2003.07a
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• pp.137-138
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• 2003

The worldwide annual production of polyolefins amounted to 60 million tons in 2000. During the process, 1-2 wt% of the olefin monomers have been emitted and flared into the air, causing the huge energy consumption and severe carbon dioxide emission. Recently, membrane process has been proved to be the most competitive among other separation processes in terms of cost of equipments, energy consumption and safety in this application. The performance of membrane process highly depends on the membrane properties and thus, it is very important to develop good membrane materials and composite membranes. We prepared PMDS dense and composite membranes and studied basic permeation behaviors of a series of olefins(ethylene, propylene, 1 -butylene), nitrogen and hydrogen as model gases.

• Proceedings of the Membrane Society of Korea Conference
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• 2004.05a
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• pp.211-215
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• 2004

Olefins are the most important feedstock in the petrochemical industry and thus the separation of olefin/paraffin mixtures is crucial to that industry. At present, this separation is mostly carried out using cryogenic distillation processes that require enormous capital investment and have high operational costs.(omitted)

• Bulletin of the Korean Chemical Society
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• v.17 no.7
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• pp.625-630
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• 1996

The cobalt-substituted polyoxotungstate [(CoPW11O39)5-] has been used as a catalyst in olefin epoxidation and alkane hydroxylation reactions. The epoxidation of olefins by iodosylbenzene in CH3CN yielded epoxides predominantly with trace amounts of allylic oxidation products. cis-Stilbene was streoselectively oxidized to cis-stilbene oxide with small amounts of trans-stilbene oxide and benzaldehyde formation. The epoxidation of carbamazepine (CBZ) by potassium monopersulfate in aqueous solution gave the corresponding CBZ 10,11-oxide product. Other transition metal-substituted polyoxotungstates (M=Mn2+, Fe2+, Ni2+, and Cu2+) were inactive in the CBZ epoxidation reaction. The cobalt-substituted polyoxotungstate also catalyzed the oxidation of alkanes with m-chloroperbenzoic acid to give the corresponding alcohols and ketones. The presence of CH2Br2 in the hydroxylation of cyclohexane afforded the formation of bromocyclohexane, suggesting the participation of cyclohexyl radical. In the 18O-labeled water experiment, there was no incorporation of 18O into the cyclohexanol product when the hydroxylation of cyclohexane by MCPBA was carried out in the presence of H218O. Some mechanistic aspects are discussed as well.