Analysis reveals structural accuracy of nucleobase tautomers using computational methods, highlighting their implications for molecular recognition.
Tautomerism in nucleobases is a subtle yet decisive factor in key biological processes, including mutagenesis, enzymatic catalysis, and molecular recognition. Capturing the exact geometry of these fleeting forms is a demanding task, as their small energy differences are highly sensitive to stereoelectronic effects and environmental perturbations. Gas-phase high-resolution spectroscopy provides precise experimental data on individual tautomers, but interpreting these measurements in structural terms requires highly accurate quantum-chemical calculations. Here, we compute benchmark-quality structures for a representative set of canonical and noncanonical nucleobase tautomers with available experimental rotational constants. The approach combines geometry optimizations─based on CCSD(T)-F12 energies with MP2 core–valence corrections─with vibrational corrections from DFT anharmonic force fields within second-order vibrational perturbation theory. The resulting near-spectroscopic accuracy enables an unbiased comparison with experiment and demonstrates the robustness of the protocol in capturing subtle structural features. Building on this, we extend the study to fluorinated and sulfur-containing pyrimidine derivatives for which no gas-phase data are available, providing reference-quality structural parameters to guide and accelerate future high-resolution experimental and theoretical investigations.
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Fiore et al. (2025) studied this question.
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