Abstract

Double-charge-transfer spectroscopy has been used to measure the double-ionization energies of acetaldehyde to singlet and triplet electronic states of the dication. The values, measured within the range 30–42 eV, are in good agreement with previously calculated data thus allowing the characteristics of the spectra to be interpreted in terms of specific electronic transitions.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call