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Breakdown of the mirror image symmetry in the optical absorption/emission spectra of oligo(para-phenylene)s -: art. no. 054501
被引:116
作者:
Heimel, G
[1
]
Daghofer, M
Gierschner, J
List, EJW
Grimsdale, AC
Müllen, K
Beljonne, D
Brédas, JL
Zojer, E
机构:
[1] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
[2] Graz Univ Technol, Inst Solid State Phys, Christian Doppler Lab Adv Funct Mat, A-8010 Graz, Austria
[3] Graz Univ Technol, Inst Theoret & Computat Phys, A-8010 Graz, Austria
[4] Univ Tubingen, Inst Phys & Theoret Chem, D-72076 Tubingen, Germany
[5] Inst Nanostruct Mat & Photon, A-8160 Weiz, Austria
[6] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[7] Univ Mons, Serv Chim Mat Nouveaux, Ctr Rech Elect & Photon Mol, B-7000 Mons, Belgium
关键词:
D O I:
10.1063/1.1839574
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The absorption and emission spectra of most luminescent, pi-conjugated, organic molecules are the mirror image of each other. In some cases, however, this symmetry is severely broken. In the present work, the asymmetry between the absorption and fluorescence spectra in molecular systems consisting of para-linked phenyl rings is studied. The vibronic structure of the emission and absorption bands is calculated from ab initio quantum chemical methods and a subsequent, rigorous Franck-Condon treatment. Good agreement with experiment is achieved. A clear relation can be established between the strongly anharmonic double-well potential for the phenylene ring librations around the long molecular axis and the observed deviation from the mirror image symmetry. Consequences for related compounds and temperature dependent optical measurements are also discussed. (C) 2005 American Institute of Physics.
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