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Assuming additive energy components are statistically independent invalidates standard quantum chemistry error bars; framing their cumulative error as a sequence of random walks resolves this, yielding calibrated confidence bounds on molecular benchmarks like S66.
Accurate calculations reveal that nitrogen's dispersion coefficients are critical for enhancing the precision of gas thermometry experiments.
The short-range interaction of nitrogen is shown to be pivotal for accurate metrological applications, with implications for understanding temperature-dependent properties.
The theoretical estimates of nitrogen's polarizability reveal discrepancies with experimental data, opening avenues for refining metrological standards.