Stability and Reactivity of Alternative Nucleobases in Concentrated Sulfuric Acid

Recent findings demonstrate that concentrated sulfuric acid supports rich organic chemistry, including the stability of the canonical DNA bases adenine, thymine, guanine and cytosine. Yet, due to full protonation in concentrated sulfuric acid, these bases may not pair as effectively as they do in water. We are therefore motivated to study nucleic acid bases that pair via hydrophobic and van der Waals interactions instead of canonical hydrogen bonding. Here, we investigate the stability of 14 selected, commercially available alternative nucleobases in concentrated sulfuric acid to evaluate their potential for forming DNA-like polymers in this solvent. The reactivity of compounds <b>1</b>-<b>14</b> have not been previously investigated in concentrated sulfuric acid. We incubate the selected compounds in 98% and 81% <i>w</i>/<i>w</i> sulfuric acid and monitor their stability using <sup>1</sup>H and <sup>13</sup>C NMR spectroscopy over 3 weeks at room temperature. In 98% <i>w</i>/<i>w</i> sulfuric acid, six bases-benzo[c][1,2,5]thiadiazole (<b>1</b>), 2,2'-bipyridine (<b>2</b>), 1,1'-biphenyl (<b>3</b>), 1-methoxy-3-methylbenzene (MMO2) (<b>7</b>) and 1-chloro-3-methoxybenzene (ClMO) (<b>13</b>), and 2,4-difluorotoluene (<b>14</b>)-remain soluble and stable with no detectable degradation. A few compounds show non-destructive reactivity, like sulfonation (compound <b>3</b>) or H/D exchange (compounds <b>7</b>, <b>13</b>, <b>14</b>). The other compounds react rapidly or are insoluble in 98% <i>w</i>/<i>w</i> sulfuric acid. In 81% <i>w</i>/<i>w</i> sulfuric acid, only compounds <b>1</b> and <b>2</b> remain stable and soluble, while other selected compounds are insoluble or unstable. Our findings identify a subset of alternative bases stable in concentrated sulfuric acid, advancing efforts towards the design of an example genetic-like polymer in this unusual solvent. Our work further highlights sulfuric acid's potential for supporting complex organic chemistry, with implications for astrobiology, planetary science of Venus and synthetic biology.

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Journal
Molecules
Published
2026-03-03
DOI
https://doi.org/10.3390/molecules31050845
Citations
1
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
Field-Weighted Citation Impact
22.24
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article

Stability and Reactivity of Alternative Nucleobases in Concentrated Sulfuric Acid

Jingyi Huang, Janusz J. Petkowski, Maxwell D. Seager
1 citations
Molecules
DNA and Nucleic Acid Chemistry
22.24
article

Stability and Reactivity of Alternative Nucleobases in Concentrated Sulfuric Acid

Jingyi Huang, Janusz J. Petkowski, Maxwell D. Seager
article en
1 citations

Abstract

Recent findings demonstrate that concentrated sulfuric acid supports rich organic chemistry, including the stability of the canonical DNA bases adenine, thymine, guanine and cytosine. Yet, due to full protonation in concentrated sulfuric acid, these bases may not pair as effectively as they do in water. We are therefore motivated to study nucleic acid bases that pair via hydrophobic and van der Waals interactions instead of canonical hydrogen bonding. Here, we investigate the stability of 14 selected, commercially available alternative nucleobases in concentrated sulfuric acid to evaluate their potential for forming DNA-like polymers in this solvent. The reactivity of compounds <b>1</b>-<b>14</b> have not been previously investigated in concentrated sulfuric acid. We incubate the selected compounds in 98% and 81% <i>w</i>/<i>w</i> sulfuric acid and monitor their stability using <sup>1</sup>H and <sup>13</sup>C NMR spectroscopy over 3 weeks at room temperature. In 98% <i>w</i>/<i>w</i> sulfuric acid, six bases-benzo[c][1,2,5]thiadiazole (<b>1</b>), 2,2'-bipyridine (<b>2</b>), 1,1'-biphenyl (<b>3</b>), 1-methoxy-3-methylbenzene (MMO2) (<b>7</b>) and 1-chloro-3-methoxybenzene (ClMO) (<b>13</b>), and 2,4-difluorotoluene (<b>14</b>)-remain soluble and stable with no detectable degradation. A few compounds show non-destructive reactivity, like sulfonation (compound <b>3</b>) or H/D exchange (compounds <b>7</b>, <b>13</b>, <b>14</b>). The other compounds react rapidly or are insoluble in 98% <i>w</i>/<i>w</i> sulfuric acid. In 81% <i>w</i>/<i>w</i> sulfuric acid, only compounds <b>1</b> and <b>2</b> remain stable and soluble, while other selected compounds are insoluble or unstable. Our findings identify a subset of alternative bases stable in concentrated sulfuric acid, advancing efforts towards the design of an example genetic-like polymer in this unusual solvent. Our work further highlights sulfuric acid's potential for supporting complex organic chemistry, with implications for astrobiology, planetary science of Venus and synthetic biology.

MoleculesVol. 31(5)
Worcester Polytechnic Institute (US), Wrocław University of Science and Technology (PL), American Institute of Aeronautics and Astronautics (US), Massachusetts Institute of Technology (US), AGH University of Krakow (PL)
Openalex Percentile: Top 1%
DNA and Nucleic Acid Chemistry
22.24
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