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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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Autores principales: Ryan, Austin J., Ziller, Joseph W., Evans, William J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150099/
https://www.ncbi.nlm.nih.gov/pubmed/34123296
http://dx.doi.org/10.1039/c9sc05794c
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author Ryan, Austin J.
Ziller, Joseph W.
Evans, William J.
author_facet Ryan, Austin J.
Ziller, Joseph W.
Evans, William J.
author_sort Ryan, Austin J.
collection PubMed
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(2))(3) (R = SiMe(3)) with potassium in the presence of 2.2.2-cryptand (crypt) forms the divalent [K(crypt)][Ln(II)(NR(2))(3)] complexes for Ln = Gd, Tb, Dy, and Tm. However, for Ho and Er, the [Ln(NR(2))(3)](1−) anions were only isolable with [Rb(crypt)](1+) counter-cations and isolation of the [Y(II)(NR(2))(3)](1−) 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(2))(3)](1−) 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)(2)](1+), i.e. [K(18-c-6)(2)][Ln(NR(2))(3)]. The [K(18-c-6)(2)](1+) 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(2))(3)](1−) anions that were not obtainable from the [K(crypt)](1+) analogs. Reaction of CO with [K(18-c-6)(2)][Ln(NR(2))(3)], generated in situ, yielded crystals of the ynediolate products, {[(R(2)N)(3)Ln](2)(μ-OC[triple bond, length as m-dash]CO)}(2−), which crystallized with counter-cations possessing 2 : 3 potassium : crown ratios, i.e.{[K(2)(18-c-6)(3)]}(2+), for Gd, Dy, Ho. In contrast, reaction of CO with a solution of isolated [K(18-c-6)(2)][Gd(NR(2))(3)], produced crystals of an enediolate complex isolated with a counter-cation with a 2 : 2 potassium : crown ratio namely [K(18-c-6)](2)(2+) in the complex [K(18-c-6)](2){[(R(2)N)(2)Gd(2)(μ-OCH[double bond, length as m-dash]CHO)(2)]}.
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spelling pubmed-81500992021-06-11 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 Ryan, Austin J. Ziller, Joseph W. Evans, William J. Chem Sci Chemistry 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(2))(3) (R = SiMe(3)) with potassium in the presence of 2.2.2-cryptand (crypt) forms the divalent [K(crypt)][Ln(II)(NR(2))(3)] complexes for Ln = Gd, Tb, Dy, and Tm. However, for Ho and Er, the [Ln(NR(2))(3)](1−) anions were only isolable with [Rb(crypt)](1+) counter-cations and isolation of the [Y(II)(NR(2))(3)](1−) 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(2))(3)](1−) 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)(2)](1+), i.e. [K(18-c-6)(2)][Ln(NR(2))(3)]. The [K(18-c-6)(2)](1+) 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(2))(3)](1−) anions that were not obtainable from the [K(crypt)](1+) analogs. Reaction of CO with [K(18-c-6)(2)][Ln(NR(2))(3)], generated in situ, yielded crystals of the ynediolate products, {[(R(2)N)(3)Ln](2)(μ-OC[triple bond, length as m-dash]CO)}(2−), which crystallized with counter-cations possessing 2 : 3 potassium : crown ratios, i.e.{[K(2)(18-c-6)(3)]}(2+), for Gd, Dy, Ho. In contrast, reaction of CO with a solution of isolated [K(18-c-6)(2)][Gd(NR(2))(3)], produced crystals of an enediolate complex isolated with a counter-cation with a 2 : 2 potassium : crown ratio namely [K(18-c-6)](2)(2+) in the complex [K(18-c-6)](2){[(R(2)N)(2)Gd(2)(μ-OCH[double bond, length as m-dash]CHO)(2)]}. The Royal Society of Chemistry 2020-01-11 /pmc/articles/PMC8150099/ /pubmed/34123296 http://dx.doi.org/10.1039/c9sc05794c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Ryan, Austin J.
Ziller, Joseph W.
Evans, William J.
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 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_full 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_fullStr 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_full_unstemmed 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_short 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_sort 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
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150099/
https://www.ncbi.nlm.nih.gov/pubmed/34123296
http://dx.doi.org/10.1039/c9sc05794c
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