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Issue 19, 2016
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Solution-based intramolecular singlet fission in cross-conjugated pentacene dimers

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Abstract

We show unambiguous and compelling evidence by means of pump–probe experiments, which are complemented by calculations using ab initio multireference perturbation theory, for intramolecular singlet fission (SF) within two synthetically tailored pentacene dimers with cross-conjugation, namely XC1 and XC2. The two pentacene dimers differ in terms of electronic interactions as evidenced by perturbation of the ground state absorption spectra stemming from stronger through-bond contributions in XC1 as confirmed by theory. Multiwavelength analysis, on one hand, and global analysis, on the other hand, confirm that the rapid singlet excited state decay and triplet excited state growth relate to SF. SF rate constants and quantum yields increase with solvent polarity. For example, XC2 reveals triplet quantum yields and rate constants as high as 162 ± 10% and (0.7 ± 0.1) × 1012 s−1, respectively, in room temperature solutions.

Graphical abstract: Solution-based intramolecular singlet fission in cross-conjugated pentacene dimers

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Publication details

The article was received on 25 Mar 2016, accepted on 29 Mar 2016 and first published on 22 Apr 2016


Article type: Paper
DOI: 10.1039/C6NR02493A
Citation: Nanoscale, 2016,8, 10113-10123
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    Solution-based intramolecular singlet fission in cross-conjugated pentacene dimers

    J. Zirzlmeier, R. Casillas, S. R. Reddy, P. B. Coto, D. Lehnherr, E. T. Chernick, I. Papadopoulos, M. Thoss, R. R. Tykwinski and D. M. Guldi, Nanoscale, 2016, 8, 10113
    DOI: 10.1039/C6NR02493A

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