Carbon‐Based Weakly Coordinating Anions: Molecular Design, Synthesis and Applications
Although carbanions, which are usually regarded as reactive species and powerful metalation reagents, can be stabilized through choice of the substitution pattern, they have rarely been considered for the design of weakly coordinating anions (WCA). Here, we report on an evaluation of the potential o...
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description | Although carbanions, which are usually regarded as reactive species and powerful metalation reagents, can be stabilized through choice of the substitution pattern, they have rarely been considered for the design of weakly coordinating anions (WCA). Here, we report on an evaluation of the potential of a series of differently substituted carbanions to serve as WCA by computational methods. This led us to the synthesis of the water‐ and air‐stable allyl anion 1 with triflyl and 3,5‐bis(trifluoromethyl)phenyl (ArF) moieties, which can be isolated in high yields even on a gram‐scale. Single crystal X‐ray crystallography and NMR studies confirmed the weak coordination ability of the anion by showing negligible or only weak interactions with different cations. This property enabled the application of 1 in the stabilization of reactive group 14 and 15 cations. In addition to the crystallization of a phosphenium cation, the first all‐carbon salt with a non‐aromatic carbanion is reported, which revealed to be a convenient reagent for hydride ion such as from silanes. Overall, this work demonstrates the so far untapped potential of carbanions as WCA, that are accessible with a variety of different cations for various applications.
Based on a systematic, computational evaluation of the potential of differently substituted methanide and propenide anions to serve as as weakly coordinating anion, the mixed 3,5‐bistrifluoromethylphenyl (ArF) and triflyl (Tf) substituted propenide was prepared in gram‐scale and shown to balance proton affinity and coordination ability. The applicability of this weakly coordinating carbanion was demonstrated by the stabilization of p‐block cations. |
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Based on a systematic, computational evaluation of the potential of differently substituted methanide and propenide anions to serve as as weakly coordinating anion, the mixed 3,5‐bistrifluoromethylphenyl (ArF) and triflyl (Tf) substituted propenide was prepared in gram‐scale and shown to balance proton affinity and coordination ability. The applicability of this weakly coordinating carbanion was demonstrated by the stabilization of p‐block cations.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>ISSN: 1521-3773</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202405936</identifier><identifier>PMID: 38877830</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Anions ; Carbanions ; Carbon ; Cations ; Chemical synthesis ; Crystallization ; Crystallography ; NMR ; Nuclear magnetic resonance ; p-block chemistry ; Reagents ; Single crystals ; structure elucidation ; weakly coordination anions</subject><ispartof>Angewandte Chemie International Edition, 2024-09, Vol.63 (37), p.e202405936-n/a</ispartof><rights>2024 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH</rights><rights>2024 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.</rights><rights>2024. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2986-b1f23cab2fa4dd38993311a0028719e1d74a64f80196f072628424fe2e71ab573</cites><orcidid>0000-0001-6557-2366</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.202405936$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.202405936$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38877830$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kelling, Leif</creatorcontrib><creatorcontrib>Eßer, Julian</creatorcontrib><creatorcontrib>Knyszek, Daniel</creatorcontrib><creatorcontrib>Gessner, Viktoria H.</creatorcontrib><title>Carbon‐Based Weakly Coordinating Anions: Molecular Design, Synthesis and Applications</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>Although carbanions, which are usually regarded as reactive species and powerful metalation reagents, can be stabilized through choice of the substitution pattern, they have rarely been considered for the design of weakly coordinating anions (WCA). Here, we report on an evaluation of the potential of a series of differently substituted carbanions to serve as WCA by computational methods. This led us to the synthesis of the water‐ and air‐stable allyl anion 1 with triflyl and 3,5‐bis(trifluoromethyl)phenyl (ArF) moieties, which can be isolated in high yields even on a gram‐scale. Single crystal X‐ray crystallography and NMR studies confirmed the weak coordination ability of the anion by showing negligible or only weak interactions with different cations. This property enabled the application of 1 in the stabilization of reactive group 14 and 15 cations. In addition to the crystallization of a phosphenium cation, the first all‐carbon salt with a non‐aromatic carbanion is reported, which revealed to be a convenient reagent for hydride ion such as from silanes. Overall, this work demonstrates the so far untapped potential of carbanions as WCA, that are accessible with a variety of different cations for various applications.
Based on a systematic, computational evaluation of the potential of differently substituted methanide and propenide anions to serve as as weakly coordinating anion, the mixed 3,5‐bistrifluoromethylphenyl (ArF) and triflyl (Tf) substituted propenide was prepared in gram‐scale and shown to balance proton affinity and coordination ability. The applicability of this weakly coordinating carbanion was demonstrated by the stabilization of p‐block cations.</description><subject>Anions</subject><subject>Carbanions</subject><subject>Carbon</subject><subject>Cations</subject><subject>Chemical synthesis</subject><subject>Crystallization</subject><subject>Crystallography</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>p-block chemistry</subject><subject>Reagents</subject><subject>Single crystals</subject><subject>structure elucidation</subject><subject>weakly coordination anions</subject><issn>1433-7851</issn><issn>1521-3773</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNqF0LtOwzAUBmALgWgprIwoEgsDKb4ktsNWSoFKXAZAHSMncYpLage7EcrGI_CMPAmuWorEwuQzfOf30Q_AIYJ9BCE-E1rJPoY4gnFC6BboohijkDBGtv0cERIyHqMO2HNu5j3nkO6CDuGcMU5gF0yGwmZGf318Xggni2AixWvVBkNjbKG0WCg9DQZaGe3OgztTybyphA0upVNTfRo8tnrx4mcXCF0Eg7quVO53vN4HO6WonDxYvz3wfDV6Gt6Etw_X4-HgNsxxwmmYoRKTXGS4FFFREJ4khCAklpcylEhUsEjQqOQQJbSEDFPMIxyVEkuGRBYz0gMnq9zamrdGukU6Vy6XVSW0NI1LCaScxQxB5OnxHzozjdX-Oq_8x5QRmnjVX6ncGuesLNPaqrmwbYpguqw8XVaebir3C0fr2Caby2LDfzr2IFmBd1XJ9p-4dHA_Hv2GfwN0xoy3</recordid><startdate>20240909</startdate><enddate>20240909</enddate><creator>Kelling, Leif</creator><creator>Eßer, Julian</creator><creator>Knyszek, Daniel</creator><creator>Gessner, Viktoria H.</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6557-2366</orcidid></search><sort><creationdate>20240909</creationdate><title>Carbon‐Based Weakly Coordinating Anions: Molecular Design, Synthesis and Applications</title><author>Kelling, Leif ; Eßer, Julian ; Knyszek, Daniel ; Gessner, Viktoria H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2986-b1f23cab2fa4dd38993311a0028719e1d74a64f80196f072628424fe2e71ab573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Anions</topic><topic>Carbanions</topic><topic>Carbon</topic><topic>Cations</topic><topic>Chemical synthesis</topic><topic>Crystallization</topic><topic>Crystallography</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>p-block chemistry</topic><topic>Reagents</topic><topic>Single crystals</topic><topic>structure elucidation</topic><topic>weakly coordination anions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kelling, Leif</creatorcontrib><creatorcontrib>Eßer, Julian</creatorcontrib><creatorcontrib>Knyszek, Daniel</creatorcontrib><creatorcontrib>Gessner, Viktoria H.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kelling, Leif</au><au>Eßer, Julian</au><au>Knyszek, Daniel</au><au>Gessner, Viktoria H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbon‐Based Weakly Coordinating Anions: Molecular Design, Synthesis and Applications</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2024-09-09</date><risdate>2024</risdate><volume>63</volume><issue>37</issue><spage>e202405936</spage><epage>n/a</epage><pages>e202405936-n/a</pages><issn>1433-7851</issn><issn>1521-3773</issn><eissn>1521-3773</eissn><abstract>Although carbanions, which are usually regarded as reactive species and powerful metalation reagents, can be stabilized through choice of the substitution pattern, they have rarely been considered for the design of weakly coordinating anions (WCA). 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Based on a systematic, computational evaluation of the potential of differently substituted methanide and propenide anions to serve as as weakly coordinating anion, the mixed 3,5‐bistrifluoromethylphenyl (ArF) and triflyl (Tf) substituted propenide was prepared in gram‐scale and shown to balance proton affinity and coordination ability. The applicability of this weakly coordinating carbanion was demonstrated by the stabilization of p‐block cations.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38877830</pmid><doi>10.1002/anie.202405936</doi><tpages>6</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0001-6557-2366</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anions Carbanions Carbon Cations Chemical synthesis Crystallization Crystallography NMR Nuclear magnetic resonance p-block chemistry Reagents Single crystals structure elucidation weakly coordination anions |
title | Carbon‐Based Weakly Coordinating Anions: Molecular Design, Synthesis and Applications |
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