Greißel P, Schroeder ZW, Thiel D, Ferguson MJ, Clark T, Guldi DM, Tykwinski RR (2024)
Publication Type: Journal article
Publication year: 2024
DOI: 10.1021/jacs.4c01507
Two isomeric pentacene dimers, each linked by a diamantane spacer, have been synthesized. These dimers are designed to provide experimental evidence to support quantum mechanical calculations, which predict the substitution pattern on the carbon-rich diethynyldiamantane spacer to be decisive in controlling the interpentacene coupling. Intramolecular singlet fission (i-SF) serves as a probe for the existence and strength of the electronic coupling between the two pentacenes, with transient absorption spectroscopy as the method of choice to characterize i-SF. 4,9-Substitution of diamantane provides a pentacene dimer (4,9-dimer) in which the two chromophores are completely decoupled and that, following photoexcitation, deactivates to the ground state analogous to a monomeric pentacene chromophore. Conversely, 1,6-substitution provides a pentacene dimer (1,6-dimer) that exhibits sufficiently strong coupling to drive i-SF, resulting in correlated triplet M(T
APA:
Greißel, P., Schroeder, Z.W., Thiel, D., Ferguson, M.J., Clark, T., Guldi, D.M., & Tykwinski, R.R. (2024). Controlling Interchromophore Coupling in Diamantane-Linked Pentacene Dimers To Create a “Binary” Pair. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.4c01507
MLA:
Greißel, Phillip, et al. "Controlling Interchromophore Coupling in Diamantane-Linked Pentacene Dimers To Create a “Binary” Pair." Journal of the American Chemical Society (2024).
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