• Title/Summary/Keyword: Pyrrole

Search Result 222, Processing Time 0.031 seconds

Block Copolymer Thin Films: Nanotemplates for New Functional Nanomaterials

  • Kim, Jin-Kon;Lee, Jeong-In;Yang, Seung-Yun
    • Proceedings of the Polymer Society of Korea Conference
    • /
    • 2006.10a
    • /
    • pp.81-82
    • /
    • 2006
  • In this study, the applications of the block copolymer thin films are introduced. For this purpose, we first obtained cylindrical nanodomains in polystyrene-block-poly(methyl methacrylate) copolymer perpendicularly oriented to a substrate. Then, nanoporous templates were prepared after removing the PMMA nanodomains by UV treatment. By using electropolymerization, high density nanowire arrays of conducting polymer of poly(pyrrole) and poly( 3-hexyl thiopene) were obtained and their electric properties were measured. Also, these nanoporous thin films were found to be very useful for the separation of human Rhinovirus type 14 (HRV 14), major pathogen of a common cold in humans, from the buffer solution.

  • PDF

Fabrication of Conducting Polymer Nanowires using Block Copolymer Nano-porous Templates for Photovoltaic Device

  • Lee, Jeong-In;Yu Jae-Woong;Kim, Jin-Kon;Russell Thomas P.
    • Proceedings of the Polymer Society of Korea Conference
    • /
    • 2006.10a
    • /
    • pp.312-312
    • /
    • 2006
  • Block copolymers with well-defined nanoscopic structures have recently gained much attention for their potential uses as functional nanostructures. Here, we show that nanoporous templates made from polystyrene-block-poly (methyl methacrylate) (PS-b-PMMA) satisfy a novel design concept. At first, arrays of nanoscopic cylindrical microdomains oriented normal to the surface can easily be prepared. Then, we fabricated ultra high density arrays of conducting polymer as poly(pyrrole) (Ppy) and poly(3,4-ethylenedioxythiophene) (PEDOT) nanowires with diameters of $25{\sim}40\;nm$ on the ITO glass by electropolymerization of the monomers inside nanoholes. These high density arrays of conducting polymer nanowires could be used as P-type materials for photovoltaic devices.

  • PDF

Improvement in ammonia gas sensing behavior by polypyrrole/multi-walled carbon nanotubes composites

  • Jang, Woo-Kyung;Yun, Ju-Mi;Kim, Hyung-Il;Lee, Young-Seak
    • Carbon letters
    • /
    • v.13 no.2
    • /
    • pp.88-93
    • /
    • 2012
  • Polypyrrole (PPy)/multi-walled carbon nanotubes (MWCNTs) composites were prepared by in situ polymerization of pyrrole on the surface of MWCNTs templates to improve the ammonia gas sensing properties. PPy morphologies, formed on the surface of MWCNTs, were investigated by field emission scanning electron microscopy. The thermal stabilities of the PPy/MWCNTs composites were improved as the content of MWCNTs increased due to the higher thermal stability of the MWCNTs. PPy/MWCNTs composites showed synergistic effects in improving the ammonia gas sensing properties, attributed to the combination of efficient electron transfer between PPy/MWCNTs composites and ammonia gas, and the reproducible electrical resistance variation on PPy during the gas sensing process.

Photocleavage of DNA by 4′-Bromoacetophenone- Pyrrole Carboxamides

  • Jeon, Raok
    • Proceedings of the Korean Society of Applied Pharmacology
    • /
    • 2001.11a
    • /
    • pp.79-79
    • /
    • 2001
  • Genotoxic chemotherapeutics are irreversible DNA targeting agents, which can act as anticancer and antiviral drugs. Natural antibacterial and anticancer enediynes function through the formation of free radicals formed by Bergman-type cycloaromatization and being capable of cleavage of DNA strand. They have been focused primarily on the design and syntheses of simple enediyne structures, which can be mimic their mechanistic feature. Recently. I have been reported the possible application of 4'-bromoacetophenone as a simple photoactivatable DNA cleaving agent, which could be readily prepared and exhibit potent and selective DNA cleaving activity. Herein, we further investigated the activity of 4'-bromoacetophenone-pyrrolecarboxamides, which consist of both DNA cleaving element and recognition unit under various conditions in order to get more understanding of the mechanism of the action and find a broad spectrum of application.

  • PDF

Electrochemical Properties of Polypyrrole Enzyme Electrode Immobilized Glucose Oxidase with Different Ligand (포도당 산화효소를 고정화한 Polypyrrole 효소전극의 배위자 변화에 다른 전기화학적 특성)

  • Kim, Hyun-Cheol;Gu, Han-Bon
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
    • /
    • 2001.11b
    • /
    • pp.529-532
    • /
    • 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-TS 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.

  • PDF

Effect of Heat Treatment on CO2 Adsorption of Ammonized Graphite Nanofibers

  • Meng, Long-Yue;Cho, Ki-Sook;Park, Soo-Jin
    • Carbon letters
    • /
    • v.11 no.1
    • /
    • pp.34-37
    • /
    • 2010
  • In this work, graphite nanofibers (GNFs) were prepared by ammonia and heat treatment at temperatures up to $1000^{\circ}C$ to improve its $CO_2$ adsorption capacity. The effects of the heat treatment on the textural properties and surface chemistry of the GNFs were investigated by $N_2$ adsorption isotherms, XRD, and elemental analysis. We found that the chemical properties of GNFs were significantly changed after the ammonia treatment. Mainly amine groups were formed on the GNF surfaces such as lactam groups, pyrrole and pyridines. The GNFs treated at $500^{\circ}C$ showed highest $CO_2$ adsorption capacity of 26.9 mg/g at 273 K in this system.

A New Chemosensing Ensemble for Colorimetric Detection of Oxalate in Water

  • Tang, Li-Jun;Liu, Ming-Hui
    • Bulletin of the Korean Chemical Society
    • /
    • v.31 no.11
    • /
    • pp.3159-3162
    • /
    • 2010
  • To realize highly selective recognition of oxalate in water, a new chemosensing ensemble that behaves highly selective colorimetric recognition of oxalate in water at pH 7.4 has been developed. The ensemble was constructed by a pyrrole containing mononuclear copper complex and chromeazurol S. The ensemble shows a highly selective recognition of oxalate through an obvious color change from blue to yellow upon the addition of oxalate, whereas, other dicarboxylates such as malonate, succinate, fumarate, maleate, glutarate, adipate, phthalate, isophthalate and terephthalate do not induce any noticeable color changes. The oxalate recognition process is not significantly affected by other coexisting dicarboxylate.

Decarbonylation of the 2-Hydroxypyridine Radical Cation: A Computational Study

  • Choe, Joong Chul
    • Bulletin of the Korean Chemical Society
    • /
    • v.35 no.10
    • /
    • pp.3021-3024
    • /
    • 2014
  • The potential energy surface (PES) for the dissociation of the 2-hydroxypyridine (2-HP) radical cation was determined from G3//B3LYP calculations, including the loss of CO, HCN, and HNC. The formation of the 1H-pyrrole radical cation by decarbonylation through a more stable tautomer, the 2-pyridone (2-PY) radical cation, was the most favorable dissociation pathway. Kinetic analysis by the Rice-Ramsperger-Kassel-Marcus model calculations was carried out based on the obtained PES. It is proposed that the dissociation occurs after a rapid tautomerization to 2-$PY^{{\cdot}+}$, and that most of the ions generated by ionization of 2-HP have the structure of 2-$PY^{{\cdot}+}$ at equilibrium above the tautomerization barrier.

Acid and Base Properties of Chemical-Treated Natural Zeolite

  • Lee, Jae-Young;Shim, Mi-Ja;Kim, Sang-Woo
    • Korean Journal of Materials Research
    • /
    • v.5 no.5
    • /
    • pp.620-624
    • /
    • 1995
  • To study the acid and base properties of chemical-treated natural zeolite, FT-IR analysis was performed by the adsorption of pyridne and pyrrole and thermo-gravimetric analysis was done by the adsorption of NH$_{3}$. These solid catalysts have two acid sites, which are related to the Bronsted and Lewis acid sites, respectively. HIC-treatment led to the increased acidity and the maintained basicity.Acidity of NaHO-treatment samples also increased with thr NaOH-treatment but basicity decreased. The p-xylene selectivity on the chemical-treatment zelite was higher than that on the untreated zeolite.

  • PDF

The Electrorheological and Dielectric Behaviors of Conducting Polymer-coated Poly(ethyl methacrylate) Suspensions

  • Kim, Young-Dae;Park, Dong-Hyup;Nam, Suk-Woo;Park, Tae-Jin
    • Macromolecular Research
    • /
    • v.10 no.4
    • /
    • pp.215-220
    • /
    • 2002
  • The electrorheological (ER) and dielectric behaviors of the polypyrrole(PPy)-coated poly(ethyl methacrylate)(PEMA) suspensions in mineral oil were investigated. PPy was coated on PEMA particles to enhance the particle polarization, which would lead to the enhanced ER response. Various PPy-coated PEMA particles were synthesized by controlling the oxidant amount during the pyrrole polymerization, and the ER responses of their suspensions were investigated. The ER response initially increases with the oxidant amount, passes through a maximum, and then decreases with the oxidant amount. The initial increase in the ER response with oxidant amounts is due to the enhanced particle polarization with the increased particle surface conductivity. The dielectric properties of the corresponding suspensions support that the ER enhancement arises from the enhanced particle polarization. The decrease in the ER response at large oxidant amounts seems to arise from the increased conduction between the PPy-coated PEMA particles.