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Abstract Previously, a boronium salt possessing a terminal benzyl group was reported to have greater antibacterial activity than a commercial quaternary ammonium disinfectant solution againstEscherichia coli,Pseudomonas aeruginosa, andStaphylococcus aureus. Results of the current study indicate that the same boronium salt without a benzyl group, exhibited equal or better antifungal activity against actively growingCandida albicansyeast andAspergillus fumigatusmold when compared to the same quat disinfectant. This same compound also displayed antifungal activity against dormantA. fumigatusspores comparable to the quat disinfectant. In contrast, the boronium ion with a benzyl group was 4–16X less effective than either the non‐benzylated form or quat disinfectant for all 3 fungal test conditions. The observation that the boronium salt without a benzyl group exhibited substantial antifungal activity in the current study but did not display any antibacterial activity in the previous study is of particular interest. This finding represents a flip‐flop outcome from the previous bacterial testing. It suggests that the presence of a terminal benzyl group greatly influences the boronium ion's ability to interact with fungal membranes. 

Ionic liquids (ILs) are highly tailorable materials with unique physical and chemical properties that set them apart from conventional organic solvents. As the library of readily accessible ILs continues to grow, so too does their relevance in applications ranging from material processing to electrochemical energy storage as solvents capable of accessing new chemistries disallowed by traditional chemicals. While a great deal of interest has been directed towards imidazolium and quaternary ammonium based ionic liquids, there are other understudied classes of cations which have potentially favorable properties for energy related applications. One such class is that with boronium cations. These cations have a unique structure with a formally negative boron flanked by positive nitrogens. This inherently zwitterionic structure presents interesting possibilities for electrochemical applications. To date only a handful of boronium cation-based ionic liquids have been thoroughly characterized despite exhibiting impressive electrochemical stabilities (> 5.0 V). In the present study we synthesized a series of ILs with novel boronium cations coupled with the bis(trifluoro-methanesulfonyl)imide anion. We then characterized the electrochemical and physical properties of these boronium ionic liquids by techniques such as cyclic voltammetry, broadband dielectric spectroscopy, oscillatory shear rheology, and thermogravimetric analysis. We will discuss how systematic variations in boronium cation structure impacted electrochemical and physical properties. 

Quaternary ammonium compounds (QACs) are routinely used as disinfectants in a variety of settings. They are generally effective against a wide range of microbes but often exhibit undesirable toxicity. Consequently, companies are constantly seeking alternatives to QACs that are just as effective but with reduced health and environmental hazards. Two boronium salt derivatives were tested against influenza A and SARS-CoV-2 viruses. One salt possessed a terminal benzyl group, while the other lacked the same terminal benzyl group. Both salts demonstrated virus inactivation similar to a commercial QAC disinfectant. The non-benzylated form exhibited the same cell toxicity profile as the QAC. However, the benzylated form displayed less cell toxicity than both the non-benzylated form and QAC. These results suggest that the boronium salts may be suitable for use as a disinfecting agent against enveloped viruses in lieu of using a QAC. Continued evaluation of the boronium salts is warranted to determine the lowest effective concentration capable of effectively controlling influenza A and SARS-CoV-2 viruses that also demonstrates low cytotoxicity.