期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
New modified multiwalled carbon nanotubes paste electrode for electrocatalytic oxidation and determination of warfarin in biological and pharmaceutical samples 被引量:3
1
作者 Masoumeh Taei Fardin Abedi 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2016年第3期436-445,共10页
A novel sensor for the determination of warfarin based on a simple and sensitive method was developed on multiwalled-carbon-nanotube modified ZnCrFeO4 carbon paste electrodes(MWCNT/ZnCrFeO4/CPEs). Cyclic voltammetry... A novel sensor for the determination of warfarin based on a simple and sensitive method was developed on multiwalled-carbon-nanotube modified ZnCrFeO4 carbon paste electrodes(MWCNT/ZnCrFeO4/CPEs). Cyclic voltammetry, differential pulse voltammetry, chronoamperometry, and electrochemical impedance spectroscopy were used to investigate the electrochemical behavior of warfarin at the chemically modified electrode. According to the results, MWCNT/ZnCrFeO4/CPEs showed high electrocatalytic activity for warfarin oxidation, producing a sharp oxidation peak current at about +0.97 vs Ag/AgCl reference electrode at pH = 4.0. The peak current was linearly dependent on warfarin concentration over the range of 0.02–920.0 μmol/L with a detection limit of 0.003 μmol/L. In addition, chronoamperometry was also used to determine warfarin's catalytic rate constant and diffusion coefficient at MWCNT/ZnCrFeO4/CPEs. 展开更多
关键词 ZnCrFeO4 Multiwalled carbon nanotubes WARFARIN Electrochemical impedance SPECTROSCOPY Paste electrode
下载PDF
An environmentally-friendly base organocatalyzed one-pot strategy for the regioselective synthesis of novel 3,6-diaryl-4-methylpyridazines
2
作者 Mehdi Rimaz Farkhondeh Aali 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2016年第4期517-525,共9页
This report describes a new three‐component strategy for the regioselective synthesis of a series of tri‐substituted pyridazines via a 1,4‐diazabicyclo[2.2.2]octane (DABCO)‐catalyzed condensation of propiophenon... This report describes a new three‐component strategy for the regioselective synthesis of a series of tri‐substituted pyridazines via a 1,4‐diazabicyclo[2.2.2]octane (DABCO)‐catalyzed condensation of propiophenones, arylglyoxalmonohydrates and hydrazine hydrate in water. This method provides a green and convenient one‐pot route toward a diverse set of 3,6‐diaryl‐4‐methylpyridazines bearing various aryl substituents. This procedure is highly regioselective, operationally simple, uses water as a safe, environmentally friendly solvent, and DABCO as a green base‐organocatalyst, and affords good to excellent yields of products. 展开更多
关键词 1 4-Diazabicyclo[2.2.2]octane (DABCO) PROPIOPHENONE Arylglyoxalmonohydrate PYRIDAZINE
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部