### Abstract

Intervalence electron transfer spectra in mixed-valence molecules are frequently modeled by an interacting pair of adiabatic potential energy surfaces. The presence or absence of a double minimum in the lower surface is correlated with trapped or delocalized charges, respectively. In the time-dependent picture of the spectroscopy, calculations are conveniently carried out in a diabatic basis. The choice of a diabatic basis for a given adiabatic potential surface is not unique. The appropriateness of a given representation depends on the physical model that is chosen to represent the system. We present three diabatic models that give the same adiabatic potential surface. The first model represents charge transfer between two sites, the second represents a transition between bonding and antibonding molecular orbitals, and the third represents a nonbonding to nonbonding transition. Each of these models gives rise to a different calculated absorption spectrum even though they arise from the same adiabatic picture. A very important consideration after a model is chosen is the selection of the transition dipole moment. We derive and discuss the symmetry of the transition dipole moment for each of the models for the different polarization directions of the incident light and show how the symmetry depends on the choice of the model. Surprisingly, the Condon approximation corresponds to different polarization directions in the different models. We derive the explicit relationships and interconnections between the three models and the adiabatic model.

Original language | English |
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Pages (from-to) | 8712-8721 |

Number of pages | 10 |

Journal | Journal of Physical Chemistry |

Volume | 100 |

Issue number | 21 |

DOIs | |

State | Published - 1 Jan 1996 |

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*Journal of Physical Chemistry*, vol. 100, no. 21, pp. 8712-8721. https://doi.org/10.1021/jp951165a

**Choosing a model and appropriate transition dipole moments for time-dependent calculations of intervalence electronic transitions.** / Talaga, David S.; Zink, Jeffrey I.

Research output: Contribution to journal › Article

TY - JOUR

T1 - Choosing a model and appropriate transition dipole moments for time-dependent calculations of intervalence electronic transitions

AU - Talaga, David S.

AU - Zink, Jeffrey I.

PY - 1996/1/1

Y1 - 1996/1/1

N2 - Intervalence electron transfer spectra in mixed-valence molecules are frequently modeled by an interacting pair of adiabatic potential energy surfaces. The presence or absence of a double minimum in the lower surface is correlated with trapped or delocalized charges, respectively. In the time-dependent picture of the spectroscopy, calculations are conveniently carried out in a diabatic basis. The choice of a diabatic basis for a given adiabatic potential surface is not unique. The appropriateness of a given representation depends on the physical model that is chosen to represent the system. We present three diabatic models that give the same adiabatic potential surface. The first model represents charge transfer between two sites, the second represents a transition between bonding and antibonding molecular orbitals, and the third represents a nonbonding to nonbonding transition. Each of these models gives rise to a different calculated absorption spectrum even though they arise from the same adiabatic picture. A very important consideration after a model is chosen is the selection of the transition dipole moment. We derive and discuss the symmetry of the transition dipole moment for each of the models for the different polarization directions of the incident light and show how the symmetry depends on the choice of the model. Surprisingly, the Condon approximation corresponds to different polarization directions in the different models. We derive the explicit relationships and interconnections between the three models and the adiabatic model.

AB - Intervalence electron transfer spectra in mixed-valence molecules are frequently modeled by an interacting pair of adiabatic potential energy surfaces. The presence or absence of a double minimum in the lower surface is correlated with trapped or delocalized charges, respectively. In the time-dependent picture of the spectroscopy, calculations are conveniently carried out in a diabatic basis. The choice of a diabatic basis for a given adiabatic potential surface is not unique. The appropriateness of a given representation depends on the physical model that is chosen to represent the system. We present three diabatic models that give the same adiabatic potential surface. The first model represents charge transfer between two sites, the second represents a transition between bonding and antibonding molecular orbitals, and the third represents a nonbonding to nonbonding transition. Each of these models gives rise to a different calculated absorption spectrum even though they arise from the same adiabatic picture. A very important consideration after a model is chosen is the selection of the transition dipole moment. We derive and discuss the symmetry of the transition dipole moment for each of the models for the different polarization directions of the incident light and show how the symmetry depends on the choice of the model. Surprisingly, the Condon approximation corresponds to different polarization directions in the different models. We derive the explicit relationships and interconnections between the three models and the adiabatic model.

UR - http://www.scopus.com/inward/record.url?scp=0000951535&partnerID=8YFLogxK

U2 - 10.1021/jp951165a

DO - 10.1021/jp951165a

M3 - Article

AN - SCOPUS:0000951535

VL - 100

SP - 8712

EP - 8721

JO - Journal of Physical Chemistry

JF - Journal of Physical Chemistry

SN - 0022-3654

IS - 21

ER -