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Chitosan – hydrogen iodide salt supported graphite electrode: A simple and novel electrode for the reduction of nitro group under electrochemical condition

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dc.contributor.author Deena, P. L.
dc.contributor.author Selvaraj, Savariraj Joseph
dc.contributor.author Thomas, K. Joby
dc.date.accessioned 2025-01-28T06:13:20Z
dc.date.available 2025-01-28T06:13:20Z
dc.date.issued 2023-11-01
dc.identifier.citation Current Chemistry Letters Volume 13 Issue 2 en_US
dc.identifier.issn 1927-730x
dc.identifier.uri 10.5267/j.ccl.2023.11.001
dc.identifier.uri http://starc.stthomas.ac.in:8080/xmlui/xmlui/handle/123456789/420
dc.description.abstract The present investigation provides a unique, simple, selective and efficient method for the electrochemical reduction of aromatic nitro groups into amines using chitosan-hydrogen iodide salt supported graphite electrode. 3:1 tetrabutyl ammonium chloride and acetic acid mixture was used as the medium for electrolytic process and a constant voltage of 5 V applied between the modified electrodes. The reaction was found to be selective and further reduction of amines was not observed. The purity of the products was checked with HPLC and characterized using spectroscopic tools. The electrochemical synthesis resulted in moderate to good yields of amino compounds which were higher than the reduction using conventional graphite electrodes. Quaternary ammonium chloride behaved as supporting electrolyte during synthesis and the reaction did not progress in the absence of acetic acid. The redox characteristic of the process was studied by cyclic voltammetry of the reaction mixture. en_US
dc.language.iso en en_US
dc.publisher Growing Science en_US
dc.subject Chemoselective reduction en_US
dc.subject Quaternary ammonium chloride en_US
dc.subject Chitosan en_US
dc.subject Acetic acid en_US
dc.subject Nitro group en_US
dc.title Chitosan – hydrogen iodide salt supported graphite electrode: A simple and novel electrode for the reduction of nitro group under electrochemical condition en_US
dc.type Article en_US


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