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Coulomb Pairing and Double Photoionization in Aromatic Hydrocarbons

2014/03/11 by D. L. Hùber, D. L. Huber, Huber, D. L.
Chemistry · Physics and Astronomy · #Advanced Chemical Physics Studies #FOS: Physical sciences #Mesoscale and Nanoscale Physics (cond-mat.mes-hall) #Photochemistry and Electron Transfer Studies #Spectroscopy and Quantum Chemical Studies #Strongly Correlated Electrons (cond-mat.str-el) #cond-mat.mes-hall #cond-mat.str-el

paper · pdf · doi:10.48550/arxiv.1403.2640

6 pages. arXiv admin note: substantial text overlap with arXiv:1312.0495

arxiv created 2014/03/11 · openalex publication_date 2014/03/11 · arxiv updated 2014/03/12 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/28

Abstract

Recently reported anomalies in the double-photonionization spectra of the aromatic molecules partially deuterated benzene, naphthalene, anthracene, pentacene, azulene, phenanthrene, pyrene and coronene are attributed to Coulomb-pair resonances of pi electrons. The properties of the resonance in benzene are investigated in detail. The linear behavior in the 2+/1+ ion ratio above the resonance is attributed to a two-electron transition associated with excitation from the ground state to a two-electron continuum. A similar explanation accounts for the linear behavior seen in the pentagonal rings pyrrole, furan, selenophene and thiophene which do not display resonance peaks.

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