Liquid Ammonia: More than an Innocent Solvent for Zintl Anions

Liquid ammonia as the original solvent for Zintl anions has been replaced by easier to handle or more versatile solvents in most recent Zintl chemistry. However, methodological advances have made it possible to structurally investigate the anions in ammoniate crystals via crystallography or in the solutions themselves via nuclear magnetic resonance. While in some cases liquid ammonia acts as an innocent solvent, it also provides different possibilities of direct involvement in chemical reactions. In addition to simple dissolution without changes to the anions observed in the solid starting materials, protonation of the anion, incongruent dissolution involving redox processes, and further oxidation and reduction products have been observed. The use of the solvent liquid ammonia under ambient pressure is limited to low temperatures, which in turn allows the monitoring of kinetically stabilized species, some of which cannot be accessed at higher temperatures. In this work, the available literature reports are summarized or referenced, and compounds that have been characterized as new ammoniate crystals are presented and contextualized. Innocent dissolution is observed for clusters involved in K<sub>2.9</sub>Rb<sub>5.1</sub>[Si<sub>4</sub>][Si<sub>9</sub>]·15NH<sub>3</sub>, Cs<sub>4</sub>Sn<sub>9</sub>·12NH<sub>3</sub>, Cs<sub>4</sub>Pb<sub>9</sub>·5NH<sub>3</sub>, and [Rb@[18]crown-6]<sub>2</sub>[Rb@[2.2.2]crypt]Rb[Ge<sub>9</sub>]·4NH<sub>3</sub>. Formal protonation of [Ge<sub>4</sub>]<sup>4-</sup> results in the crystallization of [Na@[2.2.2]crypt]<sub>2</sub>[H<sub>2</sub>Ge<sub>4</sub>]·3NH<sub>3</sub>. Tt<sub>5</sub><sup>2-</sup> (Tt = Sn or Pb) and HSi<sub>9</sub><sup>3-</sup> cannot be accessed in a binary solid state material but can be crystallized in co-crystals of PPh<sub>3</sub> in [Rb@[2.2.2]crypt]<sub>2</sub>[Sn<sub>5</sub>][PPh<sub>3</sub>]<sub>2</sub>·NH<sub>3</sub>, [Rb@[2.2.2]crypt]<sub>2</sub>[Pb<sub>5</sub>][PPh<sub>3</sub>]<sub>2</sub>·NH<sub>3</sub>, and [K@[2.2.2]crypt]<sub>3</sub>[HSi<sub>9</sub>][PPh<sub>3</sub>]·5NH<sub>3</sub>.

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Publication Details

Journal
Inorganic Chemistry
Published
2024-08-09
DOI
https://doi.org/10.1021/acs.inorgchem.4c01817
Citations
7
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
1.11

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article

Liquid Ammonia: More than an Innocent Solvent for Zintl Anions

Nikolaus Korber, Michael Witzmann, Stefanie Gärtner, Ruth M. Gschwind et al.
7 citations
Inorganic Chemistry
Radioactive element chemistry and processing
1.11
article

Liquid Ammonia: More than an Innocent Solvent for Zintl Anions

Nikolaus Korber, Michael Witzmann, Stefanie Gärtner, Ruth M. Gschwind, Corinna Lorenz-Fuchs
article en
7 citations

Abstract

Liquid ammonia as the original solvent for Zintl anions has been replaced by easier to handle or more versatile solvents in most recent Zintl chemistry. However, methodological advances have made it possible to structurally investigate the anions in ammoniate crystals via crystallography or in the solutions themselves via nuclear magnetic resonance. While in some cases liquid ammonia acts as an innocent solvent, it also provides different possibilities of direct involvement in chemical reactions. In addition to simple dissolution without changes to the anions observed in the solid starting materials, protonation of the anion, incongruent dissolution involving redox processes, and further oxidation and reduction products have been observed. The use of the solvent liquid ammonia under ambient pressure is limited to low temperatures, which in turn allows the monitoring of kinetically stabilized species, some of which cannot be accessed at higher temperatures. In this work, the available literature reports are summarized or referenced, and compounds that have been characterized as new ammoniate crystals are presented and contextualized. Innocent dissolution is observed for clusters involved in K<sub>2.9</sub>Rb<sub>5.1</sub>[Si<sub>4</sub>][Si<sub>9</sub>]·15NH<sub>3</sub>, Cs<sub>4</sub>Sn<sub>9</sub>·12NH<sub>3</sub>, Cs<sub>4</sub>Pb<sub>9</sub>·5NH<sub>3</sub>, and [Rb@[18]crown-6]<sub>2</sub>[Rb@[2.2.2]crypt]Rb[Ge<sub>9</sub>]·4NH<sub>3</sub>. Formal protonation of [Ge<sub>4</sub>]<sup>4-</sup> results in the crystallization of [Na@[2.2.2]crypt]<sub>2</sub>[H<sub>2</sub>Ge<sub>4</sub>]·3NH<sub>3</sub>. Tt<sub>5</sub><sup>2-</sup> (Tt = Sn or Pb) and HSi<sub>9</sub><sup>3-</sup> cannot be accessed in a binary solid state material but can be crystallized in co-crystals of PPh<sub>3</sub> in [Rb@[2.2.2]crypt]<sub>2</sub>[Sn<sub>5</sub>][PPh<sub>3</sub>]<sub>2</sub>·NH<sub>3</sub>, [Rb@[2.2.2]crypt]<sub>2</sub>[Pb<sub>5</sub>][PPh<sub>3</sub>]<sub>2</sub>·NH<sub>3</sub>, and [K@[2.2.2]crypt]<sub>3</sub>[HSi<sub>9</sub>][PPh<sub>3</sub>]·5NH<sub>3</sub>.

Inorganic ChemistryVol. 63(43)
Institute of Inorganic Chemistry of the Slovak Academy of Sciences (SK), University of Regensburg (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 26%
Radioactive element chemistry and processing
1.11
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