Journals / Turkish Journal of Chemistry / 2010 / Cilt: 34 - Sayı: 3

Electrochemical properties of 1-(o-, m-, p-nitrophenyl)-3-(m-nitrophenyl)- 5-phenylformazans and their nickel complexes

Pages
565–479
Publication Date
2010-03-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Nicholson and Shain criteria showed that the reaction follows an EC mechanism.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The electrochemical properties of NO2 formazans and their Ni(II) complexes were investigated.
📊
Key Findings & Data:The investigated formazans included a NO2 group at the o-, m-, and p-positions of the 1-phenyl ring and at the m-position of the 3-phenyl ring.
💡
Conclusion & Impact:Nicholson and Shain criteria showed that the reaction follows an EC mechanism.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Formazans · nickel complexes · spectroscopy

Abstract

The electrochemical properties of NO2 formazans and their Ni(II) complexes were investigated. The investigated formazans included a NO2 group at the o-, m-, and p-positions of the 1-phenyl ring and at the m-position of the 3-phenyl ring. The oxidation and reduction peak potentials, number of electrons transferred, diffusion coefficient, heterogeneous rate constant, and possible reaction mechanism of the compounds were determined with the use of cyclic voltammetry (CV), ultramicrodisc electrodes (UMEs), and chronoamperometry (CA). The peak potentials (E}ox1) were observed to shift towards more anodic potentials in formazans and more cathodic potentials in their respective Ni complexes compared to unsubstituted compounds. There was a correlation between their absorption and electrochemical properties. The electrochemical reaction mechanism was observed to be dependent upon the type and position of the substituent in the structure. Nicholson and Shain criteria showed that the reaction follows an EC mechanism.

Özet

The electrochemical properties of NO2 formazans and their Ni(II) complexes were investigated. The investigated formazans included a NO2 group at the o-, m-, and p-positions of the 1-phenyl ring and at the m-position of the 3-phenyl ring. The oxidation and reduction peak potentials, number of electrons transferred, diffusion coefficient, heterogeneous rate constant, and possible reaction mechanism of the compounds were determined with the use of cyclic voltammetry (CV), ultramicrodisc electrodes (UMEs), and chronoamperometry (CA). The peak potentials (E}ox1) were observed to shift towards more anodic potentials in formazans and more cathodic potentials in their respective Ni complexes compared to unsubstituted compounds. There was a correlation between their absorption and electrochemical properties. The electrochemical reaction mechanism was observed to be dependent upon the type and position of the substituent in the structure. Nicholson and Shain criteria showed that the reaction follows an EC mechanism.

🔖

Cite This Article

TEZCAN, H., AKSU, M. L. (2010). Electrochemical properties of 1-(o-, m-, p-nitrophenyl)-3-(m-nitrophenyl)- 5-phenylformazans and their nickel complexes. Turkish Journal of Chemistry, Cilt: 34 - Sayı: 3, 565–479. https://ajindex.com/articles/185252

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...