Electronically Excited States of Higher Acenes up to Nonacene: A Density Functional Theory/Multireference Configuration Interaction Study

详细信息    查看全文

• 作者：Holger F. Bettinger ; Christina T?nshoff ; Markus Doerr ; Elsa Sanchez-Garcia
• 刊名：Journal of Chemical Theory and Computation
• 出版年：2016
• 出版时间：January 12, 2016
• 年：2016
• 卷：12
• 期：1
• 页码：305-312
• 全文大小：379K
• ISSN：1549-9626

文摘

While the optical spectra of the acene series up to pentacene provide textbook examples for the annulation principle, the spectra of the larger members are much less understood. The present work provides an investigation of the optically allowed excited states of the acene series from pentacene to nonacene, the largest acene observed experimentally, using the density functional based multireference configuration method (DFT/MRCI). For this purpose, the ten lowest energy states of the B_2u and B_3u irreducible representations were computed. In agreement with previous computational investigations, the electronic wave functions of the acenes acquire significant multireference character with increasing acene size. The HOMO → LUMO excitation is the major contributor to the ¹L_a state (p band, B_2u) also for the larger acenes. The oscillator strength decreases with increasing length. The ¹L_b state (α band, B_3u), so far difficult to assign for the larger acenes due to overlap with photoprecursor bands, becomes almost insensitive to acene length. The ¹B_b state (β band, B_3u) also moves only moderately to lower energy with increasing acene size. Excited states of B_3u symmetry that formally result from double excitations involving HOMO, HOMO–1, LUMO, and LUMO+1 decrease in energy much faster with system size. One of them (D1) has very small oscillator strength but becomes almost isoenergetic with the ¹L_a state for nonacene. The other (D2) also has low oscillator strength as long as it is higher in energy than ¹B_b. Once it is lower in energy than the ¹B_b state, both states interact strongly resulting in two states with large oscillator strengths. The emergence of two strongly absorbing states is in agreement with experimental observations. The DFT/MRCI computations reproduce experimental excitation energies very well for pentacene and hexacene (within 0.1 eV). For the larger acenes deviations are larger (up to 0.2 eV), but qualitative agreement is observed.