Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization

Stimulated by recent work showing them to be promising electrolytes in batteries and supercapacitors, and to have useful levels of antibacterial, antifungal, and antiviral activity, there is growing interest in salts of boron-centered cations - boronium ions. However, compared to the number of existing structural variants among molecular cations such as ammonium ions, that of boroniums is minescule. This likely stems from the narrow scope of Lewis base types - largely amines and <i>N</i>-heterocycles - known to stabilize cationic boron centres. We have now determined that ureas, in combination with amines, are effective in stabilizing boronium cations, greatly enhancing the scope of structural-geometric space which can be explored with these compounds. And, depending on the specific urea utilized, ionic liquids based upon the new boroniums are effective H-bond donors despite being 'aprotic' ILs in nature. The new materials have been assessed by a broad array of techniques, including TGA, DSC, CV, NMR, and X-ray crystallography.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra05311k
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization

David P. Durkin, Mat­thias Zeller, Paul C. Trulove, E. Alan Salter et al.
RSC Advances
Organoboron and organosilicon chemistry
article

Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization

David P. Durkin, Mat­thias Zeller, Paul C. Trulove, E. Alan Salter, Christopher D. Stachurski, James H. Davis, Anthony S. Wierzbicki, Margaret E. Crowley, Richard O’Brien, Gabriel A. Merchant, Grace L Kingrey, Edgar E Escalante, Novita M Whillock
article en

Abstract

Stimulated by recent work showing them to be promising electrolytes in batteries and supercapacitors, and to have useful levels of antibacterial, antifungal, and antiviral activity, there is growing interest in salts of boron-centered cations - boronium ions. However, compared to the number of existing structural variants among molecular cations such as ammonium ions, that of boroniums is minescule. This likely stems from the narrow scope of Lewis base types - largely amines and <i>N</i>-heterocycles - known to stabilize cationic boron centres. We have now determined that ureas, in combination with amines, are effective in stabilizing boronium cations, greatly enhancing the scope of structural-geometric space which can be explored with these compounds. And, depending on the specific urea utilized, ionic liquids based upon the new boroniums are effective H-bond donors despite being 'aprotic' ILs in nature. The new materials have been assessed by a broad array of techniques, including TGA, DSC, CV, NMR, and X-ray crystallography.

RSC AdvancesVol. 15(48)
University of Mobile (US), United States Naval Academy (US), Purdue University West Lafayette (US), University of South Alabama (US)
National Science Foundation, U.S. Navy, Division of Chemistry, Army Research Office
Openalex Percentile: Top 76%
Organoboron and organosilicon chemistry
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