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Sensory detection of selective substituted acyl chloride and nitrobenzene-sulfonyl chloride by interaction with 1-amino-4-hydroxy-9,10-anthraquinone using spectrophotometry and cyclic voltammetry

Bushra Tariq, Asim Mansha, Sadia Asim, and Sobia Noreen

Department of Chemistry, Government College Women University Faisalabad, Faisalabad, Pakistan

 

E-mail: bushratariq198@gmail.com

Received: 14 February 2024  Accepted: 1 June 2024

Abstract:

Chemical compounds belonging to the quinone class are known for their cyclic diketone structures. Anthraquinone derivatives have been used as sensing materials and dyes or pigments. The spectroscopic and voltammetric sensing capacity of 1-amino-4-hydroxy-9,10-anthraquinone was utilised to sense 2-bromobenzene-sulfonyl chloride, 4-nitrobenzene-sulfonyl chloride, benzoyl chloride, 2-chlorobenzoyl chloride, and 4-bromobenzoyl chloride. These substituted acyl chlorides and nitrobenzene-sulfonyl chloride are important intermediates in various reactions, and the product formation is highly dependent on their concentration. Therefore, it is crucial to take special care as all these compounds are carcinogenic. All studies were carried out in ethanol solvent. Results showed that 1-AHAQ could be effectively used as a UV–visible sensor for sensing 2-bromobenzene-sulfonyl chloride. 1-AHAQ demonstrates good results as a fluorescence sensor for sensing 4-bromobenzene-sulfonyl chloride and behaves as a good voltammetric sensor for sensing 4-nitrobenzene-sulfonyl chloride.

Graphical abstract

Keywords: Absorption and emission spectroscopy; HOMO–LUMO orbitals; Electrostatic interactions; Hydrogen bonding; Bathochromic shift; Hyperchromic shift; Redox potential

Full paper is available at www.springerlink.com.

DOI: 10.1007/s11696-024-03546-8

 

Chemical Papers 78 (11) 6431–6455 (2024)

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