Potassium Isopropyl(trimethylsilyl)amide and Potassium <i>tert</i> -Butyl(trimethylsilyl)amide: Solvent-Dependent Solution Structures and Reactivities

Potassium isopropyl(trimethylsilyl)amide (KPTA) and potassium tert-butyl(trimethylsilyl)amide (KBTA) were prepared as stable 1.0 M stock solutions in Et3N or isolable crystalline solids. A combination of the method of continuous variations and a heavy reliance on 29Si NMR spectroscopy revealed solvent-dependent dimers and monomers. DFT computations offered insights into the solvation. Weakly coordinating solvents such as toluene and triethylamine afford dimers. In THF, KPTA is dimeric, whereas KBTA is dimeric at low THF concentration and monomeric in neat THF. Chronic and often poorly understood loss of the 29Si resonance made a broadly based, systematic study difficult and may have obscured deaggregation or ionization. Reactivity was probed using orthometallations by KBTA, which pressed the limits of its basicity and probably impacted the yields in some cases.

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Publication Details

Journal
Organometallics
Published
2025-02-18
DOI
https://doi.org/10.1021/acs.organomet.5c00013
Primary Topic
Inorganic and Organometallic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Potassium Isopropyl(trimethylsilyl)amide and Potassium tert -Butyl(trimethylsilyl)amide: Solvent-Dependent Solution Structures and Reactivities

David B. Collum, Jesse A. Spivey
Organometallics
Inorganic and Organometallic Chemistry
article

Potassium Isopropyl(trimethylsilyl)amide and Potassium tert -Butyl(trimethylsilyl)amide: Solvent-Dependent Solution Structures and Reactivities

David B. Collum, Jesse A. Spivey
article en

Abstract

Potassium isopropyl(trimethylsilyl)amide (KPTA) and potassium tert-butyl(trimethylsilyl)amide (KBTA) were prepared as stable 1.0 M stock solutions in Et3N or isolable crystalline solids. A combination of the method of continuous variations and a heavy reliance on 29Si NMR spectroscopy revealed solvent-dependent dimers and monomers. DFT computations offered insights into the solvation. Weakly coordinating solvents such as toluene and triethylamine afford dimers. In THF, KPTA is dimeric, whereas KBTA is dimeric at low THF concentration and monomeric in neat THF. Chronic and often poorly understood loss of the 29Si resonance made a broadly based, systematic study difficult and may have obscured deaggregation or ionization. Reactivity was probed using orthometallations by KBTA, which pressed the limits of its basicity and probably impacted the yields in some cases.

OrganometallicsVol. 44(5)
Cornell University (US)
National Institute of General Medical Sciences
Openalex Percentile: Top 98%
Inorganic and Organometallic Chemistry
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