• Korean Chemical Engineering Research
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• 제57권1호
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• pp.124-132
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• 2019

출발물질로서 TEOS (tetraethoxysilane)와 CTMS (chlorotrimethylsilane)를 사용하여 물과의 가수분해 및 중축합 반응에 의해 발수 코팅 용액을 합성하였다. 또한 이 용액을 PMMA 시트 위에 도포하고 열처리하여 비불소계 발수 코팅 도막을 제조하였다. 코팅 도막은 수접촉각, UV-Vis 투과율 및 미세구조 관찰에 의해 분석되었다. CTMS/TEOS의 몰비를 0.6~1.0으로 변화시켜 제조 된 코팅 도막은 CTMS/TEOS의 몰 비가 0.8일 때 $107^{\circ}$의 최대 접촉각을 나타내었다. 또한 코팅 도막은 CTMS/TEOS의 몰 비가 0.6~0.8일 때 90%의 높은 가시광선 투과율을 보였다. 그러나 CTMS/TEOS의 몰 비가 0.9~1.0인 경우에는 거친 표면의 불균일한 형상으로 인해 코팅 도막은 70% 이하의 낮은 투과율을 보였다.

• Bulletin of the Korean Chemical Society
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• 제16권4호
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• pp.377-379
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• 1995

• Bulletin of the Korean Chemical Society
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• 제10권5호
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• pp.471-472
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• 1989

• Bulletin of the Korean Chemical Society
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• 제19권12호
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• pp.1303-1305
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• 1998

• Bulletin of the Korean Chemical Society
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• 제23권9호
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• pp.1325-1327
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• 2002

• Bulletin of the Korean Chemical Society
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• 제12권2호
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• pp.149-153
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• 1991

Chlorotrimethylsilane reacts with chromic anhydride to form a very reactive neutral chromium (Ⅵ) oxidizing agent. The active oxidizing species is not trimethylsilyl chlorochromate as was previously reported but chromyl chloride generated in equilibrium concentration. This oxidizing agent was proved very suitable for benzylic oxidations of toluenes and alkylbenzenes to benzaldehydes and aralkyl ketones. Dichlorodimethylsilane and trichlormethylsilane also react with chromic anhydride to form chromyl chloride in an equilibrium concentration.

• Bulletin of the Korean Chemical Society
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• 제16권4호
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• pp.349-355
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• 1995

Bromo-and chlorotrimethylsilane react with selenium dioxide in halocarbon solvents and generate selenium oxybromide and oxychloride, respectively. These in-situ generated oxyhalides turned out to be very efficient for selective bromination and chlorination of aldehydes and ketones. Under carefully controlled reaction conditions, second and third introduction of halogens into carbonyl compounds can be greatly suppressed, and high yields of monohalo compounds were obtained. The product ratios of this halogenation reactions can be best explained if the reactions are assumed to involve intermediate β-ketoselenenyl chlorides.

• Journal of Microbiology and Biotechnology
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• 제8권3호
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• pp.229-236
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• 1998

6-Substituted derivatives of 1-［(2-hydroxyethoxy)methyl］-6-(phenylthio)thymine (HEPT) were synthesized by introducing alkyl groups with the aid of chlorotrimethylsilane, and then purified ranging 40 to 81 % of yield. Because of their peculiar structures, we presumed that HEPT derivatives would contain extra biological activities other than their already known anti-human immunodeficiency viral (HIV -1) activities. In this study, we investigated the possible effects of the HEPT derivatives on bacterial growth and found their selective antibiotic activities against gram-positive strains. We could not observe the corresponding activity from a disc-zone test, but confirmed the activity by liquid cultivation. Since the growth rate of cells was easily recovered, the antibiotic function was suggested to be bacteriostatic. We also suggested that the intracellular fate of HEPT derivatives would be fast. A HEPT derivative f-3 was shown to synergize unidirectionally toward chloramphenicol (Chr). With 0.1 mM f-3, the Chr-directed growth-inhibitory curve appeared 4 hours earlier than found without the additive. Interestingly, from the data of SDS-polyacrylamide gel electrophoresis (PAGE), we found that a membrane-bound protein having a molecular weight of 70-kDa was overexpressed by f-3 in S. aureus.

• Bulletin of the Korean Chemical Society
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• 제19권11호
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• pp.1211-1216
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• 1998

Bis(diethyldithiocarbamato)ioxomolybdenum(VI), cis-MoO2(S2CNEt2)2, 1, reacted with chlorotrimethylsilane (Me33SiCl) to give a seven-coordinate, pentagonal bipyramidal complex MoOC12(S2CN]Et2)2, 3, in which the oxo ligand is trans to the chloride ligand and the two chloride ligands are mutually cis. The monooxo molybdenum complex bis(diethyidithiocarbamato)oxomolybdenum(IV), MoO(S2CNEt2)2, 2, reacted with phenyl isocyanate (PhNCO) to give an Mo dimer MO2{μ-N(CONPh)Ph}(μ-NPh)(NPh)2(S2CNEt2)2, 4, which contains an Mo-Mo bond, two diethyldithiocarbamato ligands, two terminal imido (NPh) ligands, and two bridging hnido (NPh) ligands. One of the two bridging NPh ligands seemed to have been attacked by the electrophilic phenyl isocyanate carbon, which suggests that the bridging imido NPh ligand is more nucleophilic than the terminal one. Crystallographic data for 3: monoclinic space group P21/c, a=8.908(l) Å, b=17.509(3) Å, c=12.683(2) Å, β=110.15(1)°, Z=4, R(wR2)=0.0611(0.1385). Crystallographic data for 4-THF: orthorhombic space group P212121, a=17.932(4) Å, b=22.715(5) Å, c=11.802(3) Å, Z=4, R(wR2)=0.0585(0.1286).