Chiang Mai Journal of Science

Print ISSN: 0125-2526 | eISSN : 2465-3845

1,647
Articles
Q3 0.80
Impact Factor
Q3 1.3
CiteScore
7 days
Avg. First Decision

Identification of Three Isomers of BenzyloxyPhenol by their Different Perturbations Behaviors on a Belousov-Zhabotinsky System

Muhammad Yasir Nawabi, Waqar Uddin and Gang Hu
* Author for corresponding; e-mail address: hugang@ustc.edu
Volume: Vol.49 No.2 (March 2022)
Research Article
DOI: https://doi.org/10.12982/CMJS.2022.033
Received: 7 October 2021, Revised: 20 December 2021, Accepted: 30 December 2021, Published: -

Citation: Nawabi M.Y., Uddin W. and Hu G., Identification of Three Isomers of BenzyloxyPhenol by their Different Perturbations Behaviors on a Belousov-Zhabotinsky System, Chiang Mai Journal of Science, 2022; 49(2): 398-408. DOI 10.12982/CMJS.2022.033.

Abstract

      Proposed study described a new approach for the identifi cation of three isomers of benzyloxyphenol (BLP) i.e. 2-BLP, 3-BLP, and 4-BLP on their perturbation effects by using a novel Belousov-Zhabotinsky (BZ) oscillating system. In such a system, typical oscillating profi le was achieved due to the oxidation of malic acid (substrate) by NaBrO3 in the presence of tetra-azamacrocyclic Cu-complex catalyst ([CuL](ClO4)2) in an acidic medium. Ligand “L” in the complex is 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraeazacyclotetradeca-4,11-diene. Perturbation experiments were carried out by adding identical amounts of analytes into the active BZ system. As a result, quite different responses were achieved which can be accredited to propose a new identifi cation technique based on the oscillation system. Concisely, 2-BLP produced a shorter inhibition time (tin) with a small regenerated oscillation amplitude (A) while 3-BLP almost suppressed oscillation (longer tin) with a small regeneration of A. As compared to 2-BLP and 3-BLP, the 4-BLP initiated higher regeneration of A but produce larger tin from 2-BLP and shorter than 3-BLP. Thus, these three isomers were distinguished. Through cyclic voltammetry, redox reactions were confi rmed between the additives and NaBrO3 while the oxidized products (quinones) from these isomers were identifi ed by Ultraviolet (UV) and InfraRed (IR) spectroscopies. The perturbation reaction mechanism is justifi ed on the outcomes of the above-mentioned techniques and the FKN mechanism.

Keywords: Belousov-Zhabotinsky Oscillator, macrocyclic catalyst, isomer identifi cation, benzyloxyphenol, electrode potential
Outline
Figures