We introduce circular under-threshold RABBITT (cuRABBITT) as a new interferometric method to probe discrete electronic excitations in atoms with attosecond resolution. By combining circularly polarized attosecond pulses with broadband (“rainbow”) spectral analysis, we directly access two-photon ionization amplitudes and their relative phases. Time-dependent Schrödinger simulations, supported by Green’s function theory, reveal strong resonances in helium and argon and a Cooper-like minimum in xenon. These results demonstrate that cuRABBITT provides continuous spectral mapping of bound-state resonances and extends Fano’s propensity rule into the under-threshold regime. Our Letter establishes cuRABBITT as a powerful attosecond metrology technique, opening the way to polarization-resolved studies of resonant dynamics in atoms and molecules.

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• Atomic & molecular processes in external fields
• Electronic excitation & ionization
• Multiphoton or tunneling ionization & excitation