Marinas V, Platzer B, Labella J, Caroleo F, Nardis S, Paolesse R, Guldi DM, Torres T (2022)
Publication Type: Journal article
Publication year: 2022
Porphyrinoids are considered perfect candidates for their incorporation into electron donor-acceptor (D-A) arrays due to their remarkable optoelectronic properties and low reorganization energies. For the first time, a series of subphthalocyanine (SubPc) and corrole (Cor) were covalently connected through a short-range linkage. SubPc axial substitution strategies were employed, which allowed the synthesis of the target molecules in decent yields. In this context, a qualitative synthetic approach was performed to reverse the expected direction of the different electronic events. Consequently, in-depth absorption, fluorescence, and electrochemical assays enabled the study of electronic and photophysical properties. Charge separation was observed in cases of electron-donating Cors, whereas a quantitative energy transfer from the Cor to the SubPc was detected in the case of electron accepting Cors.
APA:
Marinas, V., Platzer, B., Labella, J., Caroleo, F., Nardis, S., Paolesse, R.,... Torres, T. (2022). Controlling Electronic Events Through Rational Structural Design in Subphthalocyanine-Corrole Dyads: Synthesis, Characterization, and Photophysical Properties. Chemistry - A European Journal. https://doi.org/10.1002/chem.202201552
MLA:
Marinas, Victor, et al. "Controlling Electronic Events Through Rational Structural Design in Subphthalocyanine-Corrole Dyads: Synthesis, Characterization, and Photophysical Properties." Chemistry - A European Journal (2022).
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