Conformational changes and S1 ← S0 origin transition energies: Polychlorinated biphenyls (PCBs)

Shoji Hirokawa, Tomoko Imasaka, Yoshikazu Oyakawa, Masataka Oishi, Totaro Imasaka

研究成果: Contribution to journalArticle査読

1 被引用数 (Scopus)

抄録

Geometries and S1 ← S0 origin transition energies for biphenyl, deuterated biphenyl, and 24 PCBs were obtained using a Hartree-Fock (HF), a single-excitation configuration interaction (CIS), and a related CI method with doubles correction (CIS(D)). The HF and CIS geometries for biphenyl are in fairly good agreement with those obtained by a complete active space self-consistent field (CASSCF) method. Calculated results show that, in both S0 and S1 states of PCBs, the torsional angles and the inter-ring bond lengths can be classified according to the number of ortho-chlorine atoms, no-Cl. This suggests that the difference in electronic energy between the S0 and the S1 state also can be specified by no-Cl. The HF and CIS energies were corrected for electron correlation on the assumption that the electron correlation energy can be partitioned into constituent contributions. Calculated S1 ← S0 origin transition energies agree with experimental values within an error of 2%. This level of accuracy is comparable to that of the S1 ← S0 origin transition energy for biphenyl calculated using the CASSCF method. The correction for electron correlation energy is largely due to contributions of the parent molecule and ortho-chlorine atoms. The present results will facilitate the analysis of electronic spectra of PCBs.

本文言語英語
ページ(範囲)31-37
ページ数7
ジャーナルJournal of Molecular Structure: THEOCHEM
772
1-3
DOI
出版ステータス出版済み - 10 23 2006

All Science Journal Classification (ASJC) codes

  • 生化学
  • 凝縮系物理学
  • 物理化学および理論化学

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