• Title/Summary/Keyword: pyrrole

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Syntheses of Metalloporphyrins and Polymer-bonded Metalloporphyrin and Their Catalytic Effects on Benzoquinone Photoreduction (Metalloporphyrins 와 Polymer-bonded Metalloporphyrin 의 합성 및 Benzoquinone 광환원반응의 촉매효과)

  • Kyu-Ja Whang;Hee-Kyung Lee;Yong-Keun Lee
    • Journal of the Korean Chemical Society
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    • v.35 no.5
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    • pp.569-574
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    • 1991
  • Six free base porphyrins were synthesized by reacting pyrrole with benzaldehyde or its derivatives and then reacted with metal chlorides to prepare corresponding metal complexes. In addition, polymer-bonded porphyrins were synthesized by treating chloromethylated styrene-divinyl benzene (1%) copolymer beads with meso-tetra (p-aminophenyl)porphyrin (TNPP) solution and then treated with cupric chloride to obtain Cu(Res-NH-TPP-$NH_2$). The porphyrin compounds were characterized by visible, inffrared and electron spin resonance spectral analyses. The metal contents of metalloporphyrins were determined by atomic adsorption spectrophotometry. The synthesized porphyrin compounds were subsequently examined for their catalytic strength and found the activity to increase in the following order: free base porphyrins; metalloporphyrins; polymer-bonded metalloporphyrin. Among metalloporphyrins, Cu-TNPP showed the greatest catalytic power.

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Thermal Changes of Aroma Components in Soybean Pastes (Doenjang) (된장 가열조리 시 생성되는 향기성분 변화)

  • Lee, Seung-Joo;Ahn, Bo-Mi
    • Korean Journal of Food Science and Technology
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    • v.40 no.3
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    • pp.271-276
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    • 2008
  • In this study, volatile compounds were isolated from traditional and commercial fermented soybean pastes according to different heating temperatures (room temperature, $50^{\circ}C$, $100^{\circ}C$) using headspace-solid phase microextraction (HS-SPME). The compounds were then analyzed by gas chromatography-mass spectrometry (GC-MS). A total of 51 volatile components, including 18 esters, 3 alcohols, 6 acids, 8 pyrazines, 5 volatile phenols, 6 aldehydes, and 5 miscellaneous compounds, were identified. Esters and acids such as ethyl hexadecanoate, acetic acid, and 2/3-methyl butanoic acid were the largest groups among the quantified volatiles. By applying principal component analyses to the GCMS data sets, differences were observed in the volatile components of the soybean pastes as to the different heating temperatures. A large variation was shown between the volatile components of the traditional and commercial soybean pastes by increasing the heating temperature. Commercial samples had significantly higher levels of longer chain ethyl esters, aldehydes, and thermal degradation products such as maltol and 2-acetyl pyrrole, while traditional samples showed higher concentrations of acids and pyrazines.

Increase in Discharge Capacity of Li Battery Assembled with Electrochemically Prepared V2O5/polypyrrole-composite-film Cathode

  • Kim, You-Na;Kim, Joo-Seong;Thieu, Minh-Triet;Dinh, Hung-Cuong;Yeo, In-Hyeong;Cho, Won-Il;Mho, Sun-Il
    • Bulletin of the Korean Chemical Society
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    • v.31 no.11
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    • pp.3109-3114
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    • 2010
  • Flexible composite films of $V_2O_5$ and conductive polypyrrole ($V_2O_5$/PPy) were grown by facile electrochemical polymerization, wherein an anodization potential was applied to the substrate electrode in an electrolyte solution containing pyrrole monomer and dispersed $V_2O_5$ particles. The coating of polypyrrole (PPy) on the surface of $V_2O_5$ particles was induced by the oxidative catalytic action of $V_2O_5$ during the electrochemical polymerization of pyrrole. PPy in the composite film connects the isolated $V_2O_5$ particles. This results in the formation of conductive networks in the composite film cathode, thereby enhancing the Li+ ion diffusion to the surface of the isolated $V_2O_5$ particles and thus increasing the accessibility of the $Li^+$ ions. The specific capacity tests of the Li rechargeable batteries revealed that the discharge capacity of this composite film cathode was higher, i.e., $497\;mAhg^{-1}$, than that of $V_2O_5$/PPy powder or pristine $V_2O_5$.

Kinetic Studies of the Hydrolysis of 1-Arylpyrrole Imine (1-Arylpyrrole Imine의 가수분해 반응의 속도론적 연구)

  • Hak-Soo Lyu;Hee-Ju Chae
    • Journal of the Korean Chemical Society
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    • v.27 no.2
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    • pp.133-141
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    • 1983
  • The kinetics of the acid-catalyzed hydrolysis of a series of 1-aryl-2-pyrrylideneaniline (3) have been studied in 20% MeOH solution using UV spectrophotometer. Substituents in 3 showed a relatively small effect, with hydrolysis facilitated by electron withdrawing group. By obtaing linear plots of $log k_{obs}$ against Hammett ${\sigma}$ constants, it was able to show that substituents had a considerable contribution to the aromaticity of pyrrole compounds. The small positive ${\rho}$ values were consistent with the rate-determining addition of water to the protonated schiff base in the buffer solution of pH 4 to 8, whereas the addition of water to the free imine seemed to be the rate-determining in the solution of acidities greater than pH 8.

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Deposition of Alkali Metal Ions at Polypyrrole Film Electrodes Modified with Fullerene (플러렌으로 수식된 피를 고분자 피막전극에 알카리 금속이온의 포집)

  • Cha Seong-Keuck;Lee Sangchun
    • Journal of the Korean Electrochemical Society
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    • v.7 no.1
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    • pp.16-20
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    • 2004
  • To electropolymerize Polypyrrole(ppy) film modified with fullerene $ions(full^-)$ the cell, Au/5 mM pyrrole, 1mM fullerene, 0.1M $TBABF_4,\;CH_2Cl_2/Pt$, was employed to Prepare the wafer-like type of $electrode/ppy(full^-)ppy(full^-){\ldots}$ electrodes. They were applied to deposit alkali metal ions with the cell of Au(quartz crystal analyzer; QCA)/ppy$(full^-)$, 0.01M metal ion(aq.)/Pt. The depositing rate constant of each ion for $Li^+,\;Na^+,\;K^+,\;Rb^+\;and\;Cs^+$, determined from the first order equation was $1.60\times10^{-8},\;3.13\times10^{-11},\;1.38\times10^{-9},\;2.71\times10^{-11}\;and\;2.98\times10^{-12}mo1.s^{-1}$ respectively. The calculated stoichiometry of the ions determined by quartz crystal microbalance(QCM) at the electrodes was $Li_7C_{60},\;Na_4C_{60},\;K_3C_{60},\;Rb_1C_{60}\;and\;Cs_1C_{60}$ respectively.

Characterization of Conductive Polypyrrole Coated Wool Yarns

  • Kaynak, Akif;Wang, Kijing;Hurren, Chris;Wang, Xungai
    • Fibers and Polymers
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    • v.3 no.1
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    • pp.24-30
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    • 2002
  • Wool yams were coated with conducting Polypyrrole by chemical synthesis methods. Polymerization of pyrrole was caned out in the presence of wool yarn at various concentrations of the monomer and dopant anion. The changes in tensile, moisture absorption, and electrical Properties of the yam upon coating with conductive polypyrrole are Presented. Coating the wool yams with conductive Polypyrrole resulted in higher tenacity, higher breaking strain, and lower initial modulus. The changes in tensile properties are attributed to the changes in surface morphology due to the coating and reinforcing effect of conductive Polypyrrole. The thickness of the coating increased with the concentration of p-toluene sulfonic acid, which in turn caused a reduction in the moisture regain of the wool yin. Reducing the synthesis temperature and replacing p-toluenesulfonic acid by anthraquinone sulfonic acid resulted in a large reduction in the resistance of the yam.

Effect of humidity and operating temperature on sensing characteristics of polypyrrole methanol sensors (습도와 온도에 따른 Polypyrrole 센서의 methanol에 대한 반응특성)

  • ;;;Linsh Jiang
    • Proceedings of the Materials Research Society of Korea Conference
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    • 2003.03a
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    • pp.133-133
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    • 2003
  • 가스센서는 인간의 오감 중에 후각 기능을 대신하는 것으로 사회 여러 분야에 응용범위가 확대되고 있다. 유기화합물(VOC; volatile organic compounds) 가스는 대기환경을 오염시켜 스모그를 발생하며 인체에 발암을 유발하는 물질이기 때문에 많은 문제와 규제가 예상되고 있다. 따라서 VOC를 감지하고 정확히 분석할 수 있는 환경 측정용 센서에 대한 요구가 절실해지고 있다. 최근에는 고온에서 동작하는 산화물 반도체 센서와는 달리 상온에서 유해성 가스를 감지할 수 있는 전도성 고분자의 특성이 알려지면서 센서 물질로 각광을 받고 있으며, 특히 유해성 가스인 VOC 가스를 검지 할 수 있는 센서로서 주목을 받고 있다. 전도성 고분자인 Polypyrrole를 pyrrole monomer, APS, DBSA를 사용하여 $0^{\circ}C$, 1기압에서 화학중합을 하였다. 만들어진 powder를 chloroform과 DBSA를 사용하여 용액을 만들어 전극에 dipping하고 7$0^{\circ}C$, 질소 분위기에서 1시간동안 건조를 하고 methanol에서 1시간동안 soaking 처리를 한 뒤 7$0^{\circ}C$, 질소 분위기에서 4시간동안 열처리 과정을 통해 센서를 제조하였다.

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Electrochemical Properties of Polypyrrole-Glucose Oxidase Enzyme Electrode Depending on Dopant Size (Polypyrrole-Glucose Oxidase 효소전극의 배위자 크기에 따른 전기 화학적 특성)

  • 김현철;구할본;사공건
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2001.07a
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    • pp.745-748
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    • 2001
  • We synthesized polypyrrole (PPy) by electrolysis of the pyrrole monomer solution containing support electrolyte KCl and/or p-toluene sulfonic acid sodium salt (p-TS). The electrochemical behavior was investigated using cyclic voltammetry and AC impedance. In the case of using electrolyte p-TS, the redox potential was about -0.3 V vs. Ag/AgCl reference electrode, while the potential was about 0 V for using electrolyte KCl. It is considered as the backbone forms a queue effectively by doping p-T S. Therefore, it is possible to be arranged regularly. That leads to improvement in the electron hopping. The AC impedance plot gave a hint of betterment of mass transport. PPy doped with p-TS has improved in mass transport, or diffusion. That is because the PPy doped with p-TS has a good orientation, and is more porous than PPy with KCl.

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Cyclic Oligopyrroles as Sensors for Absolute Configuration Determination of Carboxylic Acids

  • Lintuluoto Juha M.;Nakayama Kana;Setsune Jun-Ichiro
    • Proceedings of the Polymer Society of Korea Conference
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    • 2006.10a
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    • pp.241-241
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    • 2006
  • Absolute configuration of carboxylic acids, including amino acids can be determined by circular dichroism (CD) exciton chirality method. This method employs cyclic oligopyrroles able to form stable complexes with carboxylic acids. Addition of carboxylic acids to the oligopyrroles induce CD spectrum at the macrocycle absorption region and in which the sign of the $1^{st}$ Cotton effect is determined solely by the absolute configuration of the carboxylic acid. The basicity of the pyrrole nitrogen can be controlled by macrocycle substitution thus yielding more sensitive chirality sensors.

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