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Electrosynthesis in systems of two immiscible liquids and phase transfer catalyst. VI: The influence of zinc chloride on the chlorination of naphthalene
The influence of zinc chloride on the chlorination of naphthalene by electrolysis in a water-methylene chloride emulsion and using tetrabutylammonium ion as a phase transfer catalyst is described. It is shown that when the aqueous medium contains both NaCl and ZnCl sub(2) it is the anion ZnCl super(...
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Published in: | Journal of applied electrochemistry 1985-09, Vol.15 (5), p.719-725 |
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container_title | Journal of applied electrochemistry |
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creator | IBRISAGIC, Z PLETCHER, D BROOKS, W. N HEALY, K. P |
description | The influence of zinc chloride on the chlorination of naphthalene by electrolysis in a water-methylene chloride emulsion and using tetrabutylammonium ion as a phase transfer catalyst is described. It is shown that when the aqueous medium contains both NaCl and ZnCl sub(2) it is the anion ZnCl super(2)@)d4 super(-) which transfers into the organic phase and it is confirmed that the presence of ZnCl sub(2) in the electrolyte is, indeed, beneficial. The electrolyses have been carried out in both divided and undivided cells and in both the organic yield of 1-chloronaphthalene can exceed 80% but the former is better from the view-point of speed of electrolysis; in the divided cell, the conversion was 85% (cf. typically 60% in the undivided cell) after the passage of 2.3 F mol super(-1) of naphthalene. |
doi_str_mv | 10.1007/BF00620568 |
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The electrolyses have been carried out in both divided and undivided cells and in both the organic yield of 1-chloronaphthalene can exceed 80% but the former is better from the view-point of speed of electrolysis; in the divided cell, the conversion was 85% (cf. typically 60% in the undivided cell) after the passage of 2.3 F mol super(-1) of naphthalene.</description><identifier>ISSN: 0021-891X</identifier><identifier>EISSN: 1572-8838</identifier><identifier>DOI: 10.1007/BF00620568</identifier><identifier>CODEN: JAELBJ</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Chemistry ; Condensed benzenic and aromatic compounds ; Exact sciences and technology ; Organic chemistry ; Preparations and properties</subject><ispartof>Journal of applied electrochemistry, 1985-09, Vol.15 (5), p.719-725</ispartof><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c204t-943c968fad2fd73df4394e1f8df266e9d3f07622cd2bb7264e3af6b3c3296b313</citedby><cites>FETCH-LOGICAL-c204t-943c968fad2fd73df4394e1f8df266e9d3f07622cd2bb7264e3af6b3c3296b313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8485184$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>IBRISAGIC, Z</creatorcontrib><creatorcontrib>PLETCHER, D</creatorcontrib><creatorcontrib>BROOKS, W. 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The electrolyses have been carried out in both divided and undivided cells and in both the organic yield of 1-chloronaphthalene can exceed 80% but the former is better from the view-point of speed of electrolysis; in the divided cell, the conversion was 85% (cf. typically 60% in the undivided cell) after the passage of 2.3 F mol super(-1) of naphthalene.</description><subject>Chemistry</subject><subject>Condensed benzenic and aromatic compounds</subject><subject>Exact sciences and technology</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><issn>0021-891X</issn><issn>1572-8838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><recordid>eNpFUE1rGzEUFCGFOB-X_AIdSg-BTfW1u1JvbYjbQCAXt_S2yNITqyJrnX0yxf0l-bmRiUlPwxtm5jFDyDVnt5yx_vO3JWOdYG2nT8iCt71otJb6lCwYE7zRhv8-I-eIfxhjRnRqQV7uE7gyT7jPZQSMSGOmuMcCG6RToOXvRONmE9HFdQKa4vMueqQ2e7odLQIts80YYKbOFpuq8Zb-evhCVyPUpJB2kB0cgv7F7Kgb0zRHX4lM67vjnW2JlaiibLdjGW2CDJfkQ7AJ4eqIF-Tn8n5196N5fPr-cPf1sXGCqdIYJZ3pdLBeBN9LH5Q0CnjQPoiuA-NlYH0nhPNive5rZZA2dGvppDAVuLwgn95yt_P0vAMsw6EspGQzTDschGqNaZWowps3oatr4Qxh2M5xY-f9wNlwGH_4P34VfzymWnQ2hTqSi_ju0Eq3XCv5CoGshtU</recordid><startdate>198509</startdate><enddate>198509</enddate><creator>IBRISAGIC, Z</creator><creator>PLETCHER, D</creator><creator>BROOKS, W. 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subjects | Chemistry Condensed benzenic and aromatic compounds Exact sciences and technology Organic chemistry Preparations and properties |
title | Electrosynthesis in systems of two immiscible liquids and phase transfer catalyst. VI: The influence of zinc chloride on the chlorination of naphthalene |
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