• Journal of Integrative Natural Science
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• v.8 no.4
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• pp.235-243
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• 2015

Rhodium(I)-complex of $[Rh(CO)_2I_2{^-}]$ catalyzed carbonylation of anhydrous-trimethylamine in the presence of methyl iodide to give DMAC (N,N-dimethylacetamide) in no solvent. The catalyst had been reused 20 times, the analyses and distillation of collected products showed that the yields of DMAC, MAA (N-methylacetamide), and DMF (N,N-dimethylformamide) were 82.3%, 12.6%, and 4.4%. The conversion rate of trimethylamine was 99 % and the selectivity of DMAC was 82.3% with TON (Turnover Number) of 700. Stepwise procedure of inner-sphere reductive elimination for the formation of DMAC was suggested instead of acyl iodide intermediate.

• Biotechnology and Bioprocess Engineering:BBE
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• v.11 no.2
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• pp.140-145
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• 2006

The behaviour of alginate immobilized and soluble watermelon (Citrullus vulgaris) urease in water miscible organic solvents like, acetonitrile, dimethylformamide (DMF), ethanol, methanol, and propanol is described. The organic solvents exhibited a concentration dependent inhibitory effect on both the immobilized and the soluble urease in the presence of urea. Pretreatment of soluble enzyme preparations with organic solvents in the absence of substrate for 10 min at $30^{\circ}C$ led to rapid loss in the activity, while similar pretreatment of immobilized urease with 50% (v/v) of ethanol, propanol, and acetonitrile was ineffective. Time-dependent inactivation of immobilized urease, both in the presence and in the absence of urea, revealed stability for longer duration of time even at very high concentration of organic solvents. The soluble enzyme, on the other hand, was rapidly inactivated even at fairly lower concentrations. The results suggest that the immobilization of watermelon urease in calcium alginate make it suitable for its application in organic media. The observations are discussed.

• Textile Coloration and Finishing
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• v.22 no.3
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• pp.246-256
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• 2010

This study studies on the physical property of MWNT/PU composite film for electrostatic dissipation (ESD) function by dispersing multi-wall carbon nanotubes (MWNT) in dimethylformamide (DMF) and by combining it with polyurethane(PU). For this purpose, four kinds of MWNT were selected and the composite films were made by dispersion processing, and their physical properties were measured and investigated in terms of electrical conductivity. For dispersion parameters, four MWNT contents(0.5, 1, 2, 5wt%) and two dispersion times(30min, 120min) were selected. The dispersion property and the electrical conductivity of MWNT/PU film was measured using a UV-Vis spectrometer and conductivity measuring apparatus. Finally, their physical properties according to the dispersion conditions were analyzed and discussed with various processing conditions.

• Applied Science and Convergence Technology
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• v.24 no.6
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• pp.219-223
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• 2015

Enhancement of the surface hydrophobicity of polydimethylsiloxane (PDMS) thin films deposited on substrates covered with titanium dioxide ($TiO_2$) nanospheres was studied. First, a low-temperature solution-phase method using polyvinylpyrrolidone (PVP) as a surface capping agent and a water/dimethylformamide (DMF) mixture as the reaction medium was used to synthesize monodisperse $TiO_2$ nanospheres. It was possible to easily control hydrolysis rate of the Ti-precursors and the size of the synthesized nanospheres by varying the amount of PVP and the volume ratio of the solvent mixture. Spray coating of the synthesized $TiO_2$ nanospheres under the PDMS film increased the water contact angle of the film surface to $150.3^{\circ}$. This simple treatment can modify the surface morphology at a nanometer scale without any long or complicated nanoprocess; hence, the surface enters the superhydrophobic Cassie-Baxter regime.

• Proceedings of the Korean Vacuum Society Conference
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• 2012.02a
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• pp.532-532
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• 2012

탄소 나노튜브(carbon nanotube, CNT)를 사용하여 AC 구동 방식의 organic light emitting devices (OLED)를 만들었다. 이 소자는 ITO가 코팅된 유리 위에 유전체 층, 유기 발광층 그리고 맨 위의 금속 전극 층으로 총 3개의 층으로 구성되어있다. 유전물질로써는 cyanoethyl pullulan (CRS)를 N,N dimethylformamide (DMF) 용매에 녹여 ITO층 위에 코팅하였고, 유기발광 물질로 poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV)를 chloroform (CF)에 녹여 유전체 층 위에 코팅하였다. CNT를 MEH-PPV와 섞어서 유기발광 혼합물을 만들고 난 후, 유전체층 위에 코팅하였다. 마지막으로 알류미늄 전극을 시료 위에 코팅하였다. 소자에서 사용한 MEH-PPV에 의해 나오는 붉은색 발광을 확인 한 결과, CNT를 사용한 OLED 소자가 CNT를 사용하지 않는 소자보다 brightness가 좋았고, 전류도 더 작게 흘렀다. CNT의 농도에 따라 brightness의 변화는 경향을 나타냈다. CNT에 의한 percolation 효과 때문에 이러한 OLED 시료의 성능 향상이 이루어졌음을 입증하는 실험결과를 발표에서 설명할 예정이다.

• Fibers and Polymers
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• v.1 no.2
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• pp.71-75
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• 2000

Intermolecular cyclization of 2-alkylamino-3-chloro-5,6-dicyanopyrazine 2 in the presence of tributylamine in N,N-dimethylformamide (DMF) gave 5,10-disubstituted-2,3,7,8-tetracyano -5,10-dihydrodipyrazino〔2,3-b:2',3'-e]pyrazines 3, which showed strong mesomorphic property and were anticipated as new chromophoric system for functional dye materials. Absorption spectra, fluorescent properties and other physical properties were correlated with their chemical structures. Vanadyl oligomeric porphyrazine with long alkyl groups synthesized from 3 had satisfactory solubility in tetrahydrofuran (THF), diethyl ether and dimethylsulfoxide (DMSO). The syntheses and characterization of vanadyl polymeric porphyrazines derived from 3 with long alkyl groups are reported.

• The Transactions of The Korean Institute of Electrical Engineers
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• v.59 no.2
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• pp.385-389
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• 2010

This paper presents a microfabricated nanowire diluter which dilutes the concentration of nanowires in solution instead of by the conventional centrifuge process. The device has 16 pairs of gold electrodes in a micro channel composed of a glass substrate and PDMS. We prepared nickel nanowires by the template-directed electrodeposition method using nanoporous anodized aluminum template (AAO). We injected the Dimethylformamide (DMF) solution containing nanowires into the inlet of the diluter while applying square wave voltages on the electrodes to trap the nanowires at the subsequent gold electrodes by means of dielectrophoretic attraction forces. The concentration of nanowires at the outlet of the micro channel was changed as we expected, which illustrates that the device can effectively dilute nanowires and can be applied to a controlled assembly of nanowires.

• Macromolecular Research
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• v.12 no.1
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• pp.32-37
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• 2004

The atom transfer radical polymerization (ATRP) of hexadecyl acrylate (HDA) was carried out in Ν,Ν-dimethylformamide (DMF) in the presence of CuSCN/Ν,Ν,Ν′,Ν"Ν"-pentamethyldiethylenetriamine (PMDETA). The results indicate that the polymerization is well-controlled: a linear increase of molecular weights occurs with respect to conversion and the polydispersities are relatively low. In particular, the use of CuSCN as the catalyst resulted in faster polymerization rates for hexadecyl acrylate than did those using either CuBr or CuCl; the polydis-persity, however, was larger than those obtained in the cases when CuBr and CuCl were used. In addition, we report the thermodynamic data and activation parameters for the solution ATRP of hexadecyl acrylate.

• Bulletin of the Korean Chemical Society
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• v.19 no.1
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• pp.110-114
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• 1998

The hydrogen-bonding interactions between thioacetamide (TA) and urea derivatives such as tetramethylurea (TMU) and dimethyldiphenylurea (DMDPU) have been studied using near-infrared absorption spectroscopy. Thermodynamic parameters for the interactions between TA and urea derivatives were determined by analyzing the $v^{as}_{N-H}$+Amide Ⅱ combination band of TA at 1970 nm. The ΔH° values, indicating the intrinsic strength of hydrogen bonding, are - 23.0 kJ/mole and - 19.8 kJ/mol for TMU and DMDPU, respectively. This is well explained by the inductive effects of substituents. Ab initio molecular orbital calculations for the proton affinity of TMU, N,N-dimethylformamide (DMF), and N,N-dimethylacetamide (DMA) in gas phase have been carried out at HF/3-21G ad HF/6-31G(d) levels, showing that the proton affinity of TMU is larger than that of DMA, which agrees well the experimental results.

• Bulletin of the Korean Chemical Society
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• v.19 no.11
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• pp.1165-1168
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• 1998

2-Tetrahydropyranyl methacrylate with a self-crosslinkable moiety was copolymerized with methyl methacrylate and 4-[(2-methacryloxyethyl)methylamino]-4'-nitrostilbene or 4-[(2-methacryloxyethyl)ethylamino]-4'nitroazobenzene to provide second-order nonlinear optical property. Glass transition temperatures (Tg of the copolymers are around 140 ℃. The copolymers were soluble in common organic solvents such as tetrahydrofuran (THF), cyclohexanone, and N,N-dimethylformamide (DMF). Poling was carried out at 140 ℃ for 20 min and identified with UV-Vis spectroscopy. Electro-optic coefficient (r33) of copolymer was 62 pm/V for polymer 2 at 633 nm, and relaxation did not remarkably occur due to the formation of a crosslinked network at 200 ℃ for 15 min.