The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [Y II (NR 2 ) 3 ] 1- and ynediolate and enediolate complexes from CO reactions

The use of 18-crown-6 (18-c-6) in place of 2.2.2-cryptand (crypt) in rare earth amide reduction reactions involving potassium has proven to be crucial in the synthesis of Ln(ii) complexes and isolation of their CO reduction products. The faster speed of crystallization with 18-c-6 appears to be impo...

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Veröffentlicht in:Chemical science (Cambridge) 2020-01, Vol.11 (7), p.2006-2014
Hauptverfasser: Ryan, Austin J, Ziller, Joseph W, Evans, William J
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description The use of 18-crown-6 (18-c-6) in place of 2.2.2-cryptand (crypt) in rare earth amide reduction reactions involving potassium has proven to be crucial in the synthesis of Ln(ii) complexes and isolation of their CO reduction products. The faster speed of crystallization with 18-c-6 appears to be important. Previous studies have shown that reduction of the trivalent amide complexes Ln(NR ) (R = SiMe ) with potassium in the presence of 2.2.2-cryptand (crypt) forms the divalent [K(crypt)][Ln (NR ) ] complexes for Ln = Gd, Tb, Dy, and Tm. However, for Ho and Er, the [Ln(NR ) ] anions were only isolable with [Rb(crypt)] counter-cations and isolation of the [Y (NR ) ] anion was not possible under any of these conditions. We now report that by changing the potassium chelator from crypt to 18-crown-6 (18-c-6), the [Ln(NR ) ] anions can be isolated not only for Ln = Gd, Tb, Dy, and Tm, but also for Ho, Er, and Y. Specifically, these anions are isolated as salts of a 1 : 2 potassium : crown sandwich cation, [K(18-c-6) ] , [K(18-c-6) ][Ln(NR ) ]. The [K(18-c-6) ] counter-cation was superior not only in the synthesis, but it also allowed the isolation of crystallographically-characterizable products from reactions of CO with the [Ln(NR ) ] anions that were not obtainable from the [K(crypt)] analogs. Reaction of CO with [K(18-c-6) ][Ln(NR ) ], generated , yielded crystals of the ynediolate products, {[(R N) Ln] (μ-OC[triple bond, length as m-dash]CO)} , which crystallized with counter-cations possessing 2 : 3 potassium : crown ratios, {[K (18-c-6) ]} , for Gd, Dy, Ho. In contrast, reaction of CO with a solution of isolated [K(18-c-6) ][Gd(NR ) ], produced crystals of an enediolate complex isolated with a counter-cation with a 2 : 2 potassium : crown ratio namely [K(18-c-6)] in the complex [K(18-c-6)] {[(R N) Gd (μ-OCH[double bond, length as m-dash]CHO) ]}.
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The faster speed of crystallization with 18-c-6 appears to be important. Previous studies have shown that reduction of the trivalent amide complexes Ln(NR ) (R = SiMe ) with potassium in the presence of 2.2.2-cryptand (crypt) forms the divalent [K(crypt)][Ln (NR ) ] complexes for Ln = Gd, Tb, Dy, and Tm. However, for Ho and Er, the [Ln(NR ) ] anions were only isolable with [Rb(crypt)] counter-cations and isolation of the [Y (NR ) ] anion was not possible under any of these conditions. We now report that by changing the potassium chelator from crypt to 18-crown-6 (18-c-6), the [Ln(NR ) ] anions can be isolated not only for Ln = Gd, Tb, Dy, and Tm, but also for Ho, Er, and Y. Specifically, these anions are isolated as salts of a 1 : 2 potassium : crown sandwich cation, [K(18-c-6) ] , [K(18-c-6) ][Ln(NR ) ]. The [K(18-c-6) ] counter-cation was superior not only in the synthesis, but it also allowed the isolation of crystallographically-characterizable products from reactions of CO with the [Ln(NR ) ] anions that were not obtainable from the [K(crypt)] analogs. Reaction of CO with [K(18-c-6) ][Ln(NR ) ], generated , yielded crystals of the ynediolate products, {[(R N) Ln] (μ-OC[triple bond, length as m-dash]CO)} , which crystallized with counter-cations possessing 2 : 3 potassium : crown ratios, {[K (18-c-6) ]} , for Gd, Dy, Ho. In contrast, reaction of CO with a solution of isolated [K(18-c-6) ][Gd(NR ) ], produced crystals of an enediolate complex isolated with a counter-cation with a 2 : 2 potassium : crown ratio namely [K(18-c-6)] in the complex [K(18-c-6)] {[(R N) Gd (μ-OCH[double bond, length as m-dash]CHO) ]}.</description><identifier>ISSN: 2041-6520</identifier><identifier>EISSN: 2041-6539</identifier><identifier>DOI: 10.1039/C9SC05794C</identifier><identifier>PMID: 34123296</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Anions ; Cations ; Chemical reduction ; Chemistry ; Crystallization ; Crystallography ; Dysprosium ; Erbium ; Gadolinium ; Organic chemistry ; Potassium ; Rare earth elements ; Terbium ; Yttrium</subject><ispartof>Chemical science (Cambridge), 2020-01, Vol.11 (7), p.2006-2014</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2020</rights><rights>This journal is © The Royal Society of Chemistry 2020 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c251c-783c7d61445bfd4c8580af0082969af2639c8cba15a08625bbf923149b5d82a83</citedby><cites>FETCH-LOGICAL-c251c-783c7d61445bfd4c8580af0082969af2639c8cba15a08625bbf923149b5d82a83</cites><orcidid>0000-0002-0651-418X ; 0000-0001-7404-950X ; 0000-0003-0983-0150</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150099/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150099/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34123296$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ryan, Austin J</creatorcontrib><creatorcontrib>Ziller, Joseph W</creatorcontrib><creatorcontrib>Evans, William J</creatorcontrib><title>The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [Y II (NR 2 ) 3 ] 1- and ynediolate and enediolate complexes from CO reactions</title><title>Chemical science (Cambridge)</title><addtitle>Chem Sci</addtitle><description>The use of 18-crown-6 (18-c-6) in place of 2.2.2-cryptand (crypt) in rare earth amide reduction reactions involving potassium has proven to be crucial in the synthesis of Ln(ii) complexes and isolation of their CO reduction products. The faster speed of crystallization with 18-c-6 appears to be important. Previous studies have shown that reduction of the trivalent amide complexes Ln(NR ) (R = SiMe ) with potassium in the presence of 2.2.2-cryptand (crypt) forms the divalent [K(crypt)][Ln (NR ) ] complexes for Ln = Gd, Tb, Dy, and Tm. However, for Ho and Er, the [Ln(NR ) ] anions were only isolable with [Rb(crypt)] counter-cations and isolation of the [Y (NR ) ] anion was not possible under any of these conditions. We now report that by changing the potassium chelator from crypt to 18-crown-6 (18-c-6), the [Ln(NR ) ] anions can be isolated not only for Ln = Gd, Tb, Dy, and Tm, but also for Ho, Er, and Y. Specifically, these anions are isolated as salts of a 1 : 2 potassium : crown sandwich cation, [K(18-c-6) ] , [K(18-c-6) ][Ln(NR ) ]. The [K(18-c-6) ] counter-cation was superior not only in the synthesis, but it also allowed the isolation of crystallographically-characterizable products from reactions of CO with the [Ln(NR ) ] anions that were not obtainable from the [K(crypt)] analogs. Reaction of CO with [K(18-c-6) ][Ln(NR ) ], generated , yielded crystals of the ynediolate products, {[(R N) Ln] (μ-OC[triple bond, length as m-dash]CO)} , which crystallized with counter-cations possessing 2 : 3 potassium : crown ratios, {[K (18-c-6) ]} , for Gd, Dy, Ho. In contrast, reaction of CO with a solution of isolated [K(18-c-6) ][Gd(NR ) ], produced crystals of an enediolate complex isolated with a counter-cation with a 2 : 2 potassium : crown ratio namely [K(18-c-6)] in the complex [K(18-c-6)] {[(R N) Gd (μ-OCH[double bond, length as m-dash]CHO) ]}.</description><subject>Anions</subject><subject>Cations</subject><subject>Chemical reduction</subject><subject>Chemistry</subject><subject>Crystallization</subject><subject>Crystallography</subject><subject>Dysprosium</subject><subject>Erbium</subject><subject>Gadolinium</subject><subject>Organic chemistry</subject><subject>Potassium</subject><subject>Rare earth elements</subject><subject>Terbium</subject><subject>Yttrium</subject><issn>2041-6520</issn><issn>2041-6539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpdks1u1DAQxyMEolXphQdAI3EpiIA_E7sHJBTxsVJFJSgHhFDkOBM2VRIvttOyD8r74LBlC9gHezy_-Xs8nix7SMlzSrh-UemPFZGlFtWd7JARQfNCcn13v2fkIDsO4ZKkwTmVrLyfHXBBGWe6OMx-XqwR-nHjfDSTRXAdxHRi3TxF9Lk1sXcT9BN4bGcb-ysEbzzmaHxcw4jRDGDXOPYh-u0pUJVb766nvEgxIaJpF0X2LM3k2G7SJS2YYXDXAfrghp18Qr58htUKTt5_AAZPgMNXoDks8HbCtl9A_G3irWnduBnwBwbovBuhOk85GrsIhgfZvc4MAY9v1qPs05vXF9W7_Oz87ap6dZZbJqnNS8Vt2RZUCNl0rbBKKmI6QlQqjTYdK7i2yjaGSkNUwWTTdJpxKnQjW8WM4kfZy53uZm5GbC1O0Zuh3vh-NH5bO9PX_3qmfl1_c1e1opIQrZPAyY2Ad99nDLFOlbQ4DGZCN4eaSUFKqoUoE_r4P_TSzX5Kz6sZl6UoVKlYop7uqPQNIXjs9slQUi8NU982TIIf_Z3-Hv3THvwXSWC66A</recordid><startdate>20200111</startdate><enddate>20200111</enddate><creator>Ryan, Austin J</creator><creator>Ziller, Joseph W</creator><creator>Evans, William J</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0651-418X</orcidid><orcidid>https://orcid.org/0000-0001-7404-950X</orcidid><orcidid>https://orcid.org/0000-0003-0983-0150</orcidid></search><sort><creationdate>20200111</creationdate><title>The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [Y II (NR 2 ) 3 ] 1- and ynediolate and enediolate complexes from CO reactions</title><author>Ryan, Austin J ; Ziller, Joseph W ; Evans, William J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c251c-783c7d61445bfd4c8580af0082969af2639c8cba15a08625bbf923149b5d82a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Anions</topic><topic>Cations</topic><topic>Chemical reduction</topic><topic>Chemistry</topic><topic>Crystallization</topic><topic>Crystallography</topic><topic>Dysprosium</topic><topic>Erbium</topic><topic>Gadolinium</topic><topic>Organic chemistry</topic><topic>Potassium</topic><topic>Rare earth elements</topic><topic>Terbium</topic><topic>Yttrium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ryan, Austin J</creatorcontrib><creatorcontrib>Ziller, Joseph W</creatorcontrib><creatorcontrib>Evans, William J</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemical science (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ryan, Austin J</au><au>Ziller, Joseph W</au><au>Evans, William J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [Y II (NR 2 ) 3 ] 1- and ynediolate and enediolate complexes from CO reactions</atitle><jtitle>Chemical science (Cambridge)</jtitle><addtitle>Chem Sci</addtitle><date>2020-01-11</date><risdate>2020</risdate><volume>11</volume><issue>7</issue><spage>2006</spage><epage>2014</epage><pages>2006-2014</pages><issn>2041-6520</issn><eissn>2041-6539</eissn><abstract>The use of 18-crown-6 (18-c-6) in place of 2.2.2-cryptand (crypt) in rare earth amide reduction reactions involving potassium has proven to be crucial in the synthesis of Ln(ii) complexes and isolation of their CO reduction products. The faster speed of crystallization with 18-c-6 appears to be important. Previous studies have shown that reduction of the trivalent amide complexes Ln(NR ) (R = SiMe ) with potassium in the presence of 2.2.2-cryptand (crypt) forms the divalent [K(crypt)][Ln (NR ) ] complexes for Ln = Gd, Tb, Dy, and Tm. However, for Ho and Er, the [Ln(NR ) ] anions were only isolable with [Rb(crypt)] counter-cations and isolation of the [Y (NR ) ] anion was not possible under any of these conditions. We now report that by changing the potassium chelator from crypt to 18-crown-6 (18-c-6), the [Ln(NR ) ] anions can be isolated not only for Ln = Gd, Tb, Dy, and Tm, but also for Ho, Er, and Y. Specifically, these anions are isolated as salts of a 1 : 2 potassium : crown sandwich cation, [K(18-c-6) ] , [K(18-c-6) ][Ln(NR ) ]. The [K(18-c-6) ] counter-cation was superior not only in the synthesis, but it also allowed the isolation of crystallographically-characterizable products from reactions of CO with the [Ln(NR ) ] anions that were not obtainable from the [K(crypt)] analogs. Reaction of CO with [K(18-c-6) ][Ln(NR ) ], generated , yielded crystals of the ynediolate products, {[(R N) Ln] (μ-OC[triple bond, length as m-dash]CO)} , which crystallized with counter-cations possessing 2 : 3 potassium : crown ratios, {[K (18-c-6) ]} , for Gd, Dy, Ho. In contrast, reaction of CO with a solution of isolated [K(18-c-6) ][Gd(NR ) ], produced crystals of an enediolate complex isolated with a counter-cation with a 2 : 2 potassium : crown ratio namely [K(18-c-6)] in the complex [K(18-c-6)] {[(R N) Gd (μ-OCH[double bond, length as m-dash]CHO) ]}.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>34123296</pmid><doi>10.1039/C9SC05794C</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0651-418X</orcidid><orcidid>https://orcid.org/0000-0001-7404-950X</orcidid><orcidid>https://orcid.org/0000-0003-0983-0150</orcidid><oa>free_for_read</oa></addata></record>
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subjects Anions
Cations
Chemical reduction
Chemistry
Crystallization
Crystallography
Dysprosium
Erbium
Gadolinium
Organic chemistry
Potassium
Rare earth elements
Terbium
Yttrium
title The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [Y II (NR 2 ) 3 ] 1- and ynediolate and enediolate complexes from CO reactions
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