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Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes”
The recently reported electrochemical, organo‐mediator enabled deuteration of styrenes, a reaction referred to as “electrochemical deuterium atom transfer”, differs mechanistically from reported direct electrochemical hydrogenations/deuterations only by a mediated, homogeneous SET to the substrates....
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Published in: | Angewandte Chemie 2024-11, Vol.136 (46), p.n/a |
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creator | Kolb, Simon Werz, Daniel B. |
description | The recently reported electrochemical, organo‐mediator enabled deuteration of styrenes, a reaction referred to as “electrochemical deuterium atom transfer”, differs mechanistically from reported direct electrochemical hydrogenations/deuterations only by a mediated, homogeneous SET to the substrates. By comparing direct vs. mediated processes in general and for styrene reduction, we display that Qiu's work does not change the concept of this chemistry. Experiments with mediators and the direct reduction of examples from the reported scope show that even electron‐rich substrates can be reduced when our direct protocol, published six months before Qiu's work, is applied.
A comparison between the recently reported organo‐mediator enabled deuteration of styrenes and previously published direct methods display that his transformation does not establish a novel concept, but simply an addition to the portfolio of known reactions. Addition of mediators to our established direct electrolysis protocol and direct conversion of reported scope examples serve further to strengthen this statement. |
doi_str_mv | 10.1002/ange.202316037 |
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A comparison between the recently reported organo‐mediator enabled deuteration of styrenes and previously published direct methods display that his transformation does not establish a novel concept, but simply an addition to the portfolio of known reactions. Addition of mediators to our established direct electrolysis protocol and direct conversion of reported scope examples serve further to strengthen this statement.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.202316037</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Deuteration ; Deuterium ; Direct reduction ; Electrochemistry ; hydrogenation ; mediators ; Styrene ; Styrenes ; synthetic electrochemistry</subject><ispartof>Angewandte Chemie, 2024-11, Vol.136 (46), p.n/a</ispartof><rights>2024 Wiley-VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1177-5acbcb76959f58122978f5862eb88fa1f421d86fa5902feec438b7a443058fbe3</cites><orcidid>0000-0002-3973-2212 ; 0000-0001-6352-4619</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kolb, Simon</creatorcontrib><creatorcontrib>Werz, Daniel B.</creatorcontrib><title>Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes”</title><title>Angewandte Chemie</title><description>The recently reported electrochemical, organo‐mediator enabled deuteration of styrenes, a reaction referred to as “electrochemical deuterium atom transfer”, differs mechanistically from reported direct electrochemical hydrogenations/deuterations only by a mediated, homogeneous SET to the substrates. By comparing direct vs. mediated processes in general and for styrene reduction, we display that Qiu's work does not change the concept of this chemistry. Experiments with mediators and the direct reduction of examples from the reported scope show that even electron‐rich substrates can be reduced when our direct protocol, published six months before Qiu's work, is applied.
A comparison between the recently reported organo‐mediator enabled deuteration of styrenes and previously published direct methods display that his transformation does not establish a novel concept, but simply an addition to the portfolio of known reactions. Addition of mediators to our established direct electrolysis protocol and direct conversion of reported scope examples serve further to strengthen this statement.</description><subject>Deuteration</subject><subject>Deuterium</subject><subject>Direct reduction</subject><subject>Electrochemistry</subject><subject>hydrogenation</subject><subject>mediators</subject><subject>Styrene</subject><subject>Styrenes</subject><subject>synthetic electrochemistry</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkL1OwzAQgC0EEqWwMkdiTvFPEttjVUpBKjAAA5PlOOeSKrWLnQp16yPwAPByfRJSFcHIdDd83530IXRO8IBgTC-1m8GAYspIgRk_QD2SU5IynvND1MM4y1JBM3mMTmKcY4wLymUPvYx8CBCX3lXgDCTeJdvN50OYaee3m487qGrd-pCMnS4bqJJxA6YN3rzCoja6Sa5g1ULQbd2J3iaP7TqAg7jdfJ2iI6ubCGc_s4-er8dPo5t0-jC5HQ2nqSGE8zTXpjQlL2QubS4IpZKLbikolEJYTWxGSSUKq3OJqQUwGRMl11nGcC5sCayPLvZ3l8G_rSC2au5XwXUvFSOUFRxTiTtqsKdM8DEGsGoZ6oUOa0Ww2uVTu3zqN18nyL3wXjew_odWw_vJ-M_9Bub-d1M</recordid><startdate>20241111</startdate><enddate>20241111</enddate><creator>Kolb, Simon</creator><creator>Werz, Daniel B.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-3973-2212</orcidid><orcidid>https://orcid.org/0000-0001-6352-4619</orcidid></search><sort><creationdate>20241111</creationdate><title>Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes”</title><author>Kolb, Simon ; Werz, Daniel B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1177-5acbcb76959f58122978f5862eb88fa1f421d86fa5902feec438b7a443058fbe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Deuteration</topic><topic>Deuterium</topic><topic>Direct reduction</topic><topic>Electrochemistry</topic><topic>hydrogenation</topic><topic>mediators</topic><topic>Styrene</topic><topic>Styrenes</topic><topic>synthetic electrochemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kolb, Simon</creatorcontrib><creatorcontrib>Werz, Daniel B.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kolb, Simon</au><au>Werz, Daniel B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes”</atitle><jtitle>Angewandte Chemie</jtitle><date>2024-11-11</date><risdate>2024</risdate><volume>136</volume><issue>46</issue><epage>n/a</epage><issn>0044-8249</issn><eissn>1521-3757</eissn><abstract>The recently reported electrochemical, organo‐mediator enabled deuteration of styrenes, a reaction referred to as “electrochemical deuterium atom transfer”, differs mechanistically from reported direct electrochemical hydrogenations/deuterations only by a mediated, homogeneous SET to the substrates. By comparing direct vs. mediated processes in general and for styrene reduction, we display that Qiu's work does not change the concept of this chemistry. Experiments with mediators and the direct reduction of examples from the reported scope show that even electron‐rich substrates can be reduced when our direct protocol, published six months before Qiu's work, is applied.
A comparison between the recently reported organo‐mediator enabled deuteration of styrenes and previously published direct methods display that his transformation does not establish a novel concept, but simply an addition to the portfolio of known reactions. Addition of mediators to our established direct electrolysis protocol and direct conversion of reported scope examples serve further to strengthen this statement.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ange.202316037</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-3973-2212</orcidid><orcidid>https://orcid.org/0000-0001-6352-4619</orcidid></addata></record> |
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subjects | Deuteration Deuterium Direct reduction Electrochemistry hydrogenation mediators Styrene Styrenes synthetic electrochemistry |
title | Correspondence on “Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes” |
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