### Abstract

The excited states of chromophore dimers are, in general, delocalized, and the transition energies and transition dipoles are different from those of the monomers. The intermolecular interaction that is responsible for these effects has two contributions: Förster-type Coulomb coupling and a short-range coupling, which depends on the intermolecular overlap of electronic wave functions. The latter contains the Dexter-type exchange coupling and the coupling of excited states to intermolecular charge-transfer (CT) states. Recently, we developed a method (TrEsp) for an accurate and numerically efficient calculation of the Förster-type Coulomb part (Madjet et al. J. Phys. Chem. B 2006, 110, 17268). Here, we combine the latter with quantum chemical calculations to evaluate the short-range contribution, extending a method developed earlier by Scholes et al. (J. Phys. Chem. B 1999, 103, 2543). An effective two-state model is used, which relates the transition energies and transition dipóle moments obtained by quantum chemical calculations of the monomers to those calculated for the dimer. From this relation, the short-range excitonic coupling and effective shifts of the local transition energies due to the coupling to intermolecular CT states can be inferred including a consistency check to evaluate quantum chemical methods that differ in the treatment of electron correlation. The method is applied to the special pairs of the reaction centers of purple bacteria (bRC) and photosystem I (PSI). We find that the short-range coupling represents the dominant contribution to the total excitonic coupling in both special pairs (80% in PSI and 70% in the bRC) and exhibits a monoexponential dependence on the distance between the TT-planes of the pigments with an attenuation factor of 2.8 Å ^{-1}. We obtain significant red-shifts of the local transition energies, which show a biexponential distance dependence with one attenuation factor being 2.8 Å^{-1} and another factor being in the range 0.3-0.7 Å^{-1} for PSI and 0.8-0.9 Å^{-1} for bRC. Both effects of the short-range coupling determine the excitation energy sink in the reaction centers at the special pairs.

Original language | English |
---|---|

Pages (from-to) | 12603-12614 |

Number of pages | 12 |

Journal | Journal of Physical Chemistry B |

Volume | 113 |

Issue number | 37 |

DOIs | |

Publication status | Published - 17 Sep 2009 |

Externally published | Yes |

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### ASJC Scopus subject areas

- Physical and Theoretical Chemistry
- Materials Chemistry
- Surfaces, Coatings and Films

### Cite this

*Journal of Physical Chemistry B*,

*113*(37), 12603-12614. https://doi.org/10.1021/jp906009j

**Deciphering the influence of short-range electronic couplings on optical properties of molecular dimers : Application to "special pairs" in photosynthesis.** / Madjet, Mohamed; Müh, Frank; Renger, Thomas.

Research output: Contribution to journal › Article

*Journal of Physical Chemistry B*, vol. 113, no. 37, pp. 12603-12614. https://doi.org/10.1021/jp906009j

}

TY - JOUR

T1 - Deciphering the influence of short-range electronic couplings on optical properties of molecular dimers

T2 - Application to "special pairs" in photosynthesis

AU - Madjet, Mohamed

AU - Müh, Frank

AU - Renger, Thomas

PY - 2009/9/17

Y1 - 2009/9/17

N2 - The excited states of chromophore dimers are, in general, delocalized, and the transition energies and transition dipoles are different from those of the monomers. The intermolecular interaction that is responsible for these effects has two contributions: Förster-type Coulomb coupling and a short-range coupling, which depends on the intermolecular overlap of electronic wave functions. The latter contains the Dexter-type exchange coupling and the coupling of excited states to intermolecular charge-transfer (CT) states. Recently, we developed a method (TrEsp) for an accurate and numerically efficient calculation of the Förster-type Coulomb part (Madjet et al. J. Phys. Chem. B 2006, 110, 17268). Here, we combine the latter with quantum chemical calculations to evaluate the short-range contribution, extending a method developed earlier by Scholes et al. (J. Phys. Chem. B 1999, 103, 2543). An effective two-state model is used, which relates the transition energies and transition dipóle moments obtained by quantum chemical calculations of the monomers to those calculated for the dimer. From this relation, the short-range excitonic coupling and effective shifts of the local transition energies due to the coupling to intermolecular CT states can be inferred including a consistency check to evaluate quantum chemical methods that differ in the treatment of electron correlation. The method is applied to the special pairs of the reaction centers of purple bacteria (bRC) and photosystem I (PSI). We find that the short-range coupling represents the dominant contribution to the total excitonic coupling in both special pairs (80% in PSI and 70% in the bRC) and exhibits a monoexponential dependence on the distance between the TT-planes of the pigments with an attenuation factor of 2.8 Å -1. We obtain significant red-shifts of the local transition energies, which show a biexponential distance dependence with one attenuation factor being 2.8 Å-1 and another factor being in the range 0.3-0.7 Å-1 for PSI and 0.8-0.9 Å-1 for bRC. Both effects of the short-range coupling determine the excitation energy sink in the reaction centers at the special pairs.

AB - The excited states of chromophore dimers are, in general, delocalized, and the transition energies and transition dipoles are different from those of the monomers. The intermolecular interaction that is responsible for these effects has two contributions: Förster-type Coulomb coupling and a short-range coupling, which depends on the intermolecular overlap of electronic wave functions. The latter contains the Dexter-type exchange coupling and the coupling of excited states to intermolecular charge-transfer (CT) states. Recently, we developed a method (TrEsp) for an accurate and numerically efficient calculation of the Förster-type Coulomb part (Madjet et al. J. Phys. Chem. B 2006, 110, 17268). Here, we combine the latter with quantum chemical calculations to evaluate the short-range contribution, extending a method developed earlier by Scholes et al. (J. Phys. Chem. B 1999, 103, 2543). An effective two-state model is used, which relates the transition energies and transition dipóle moments obtained by quantum chemical calculations of the monomers to those calculated for the dimer. From this relation, the short-range excitonic coupling and effective shifts of the local transition energies due to the coupling to intermolecular CT states can be inferred including a consistency check to evaluate quantum chemical methods that differ in the treatment of electron correlation. The method is applied to the special pairs of the reaction centers of purple bacteria (bRC) and photosystem I (PSI). We find that the short-range coupling represents the dominant contribution to the total excitonic coupling in both special pairs (80% in PSI and 70% in the bRC) and exhibits a monoexponential dependence on the distance between the TT-planes of the pigments with an attenuation factor of 2.8 Å -1. We obtain significant red-shifts of the local transition energies, which show a biexponential distance dependence with one attenuation factor being 2.8 Å-1 and another factor being in the range 0.3-0.7 Å-1 for PSI and 0.8-0.9 Å-1 for bRC. Both effects of the short-range coupling determine the excitation energy sink in the reaction centers at the special pairs.

UR - http://www.scopus.com/inward/record.url?scp=70349156478&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=70349156478&partnerID=8YFLogxK

U2 - 10.1021/jp906009j

DO - 10.1021/jp906009j

M3 - Article

C2 - 19697949

AN - SCOPUS:70349156478

VL - 113

SP - 12603

EP - 12614

JO - Journal of Physical Chemistry B Materials

JF - Journal of Physical Chemistry B Materials

SN - 1520-6106

IS - 37

ER -