Photodissociation spectroscopy of (benzene-toluene)+. Charge delocalization in the hetero-dimer ion

Kazuhiko Ohashi, Youko Nakane, Yoshiya Inokuchi, Yasuhiro Nakai, Nobuyuki Nishi

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

The electronic spectrum of the benzene-toluene hetero-dimer ion is measured in the 380-1400 nm region. The spectrum shows intense bands around 1175 and 670 nm and a weaker band around 920 nm, which correspond to charge resonance (CR) bands of homo-dimer ions. The observation indicates that the positive charge stays on the benzene part in some probability, although the ionization potential of benzene is 0.4162 eV higher than that of toluene. A local excitation (LE) band is observed around 420 nm, where a π←π transition is locally excited in the charged benzene or toluene molecule. On the basis of the positions of the CR-like bands, as well as the intensity of the LE band relative to that of homo-dimer ions, the probability of finding the charge on the benzene molecule is analyzed to be approximately 36%.

Original languageEnglish
Pages (from-to)429-436
Number of pages8
JournalChemical Physics
Volume239
Issue number1-3
DOIs
Publication statusPublished - Dec 15 1998

All Science Journal Classification (ASJC) codes

  • Physics and Astronomy(all)
  • Physical and Theoretical Chemistry

Fingerprint Dive into the research topics of 'Photodissociation spectroscopy of (benzene-toluene)<sup>+</sup>. Charge delocalization in the hetero-dimer ion'. Together they form a unique fingerprint.

  • Cite this