Long‐Lived Charge‐Transfer State in Spiro Compact Electron Donor–Acceptor Dyads Based on Pyromellitimide‐Derived Rhodamine: Charge Transfer Dynamics and Electron Spin Polarization. (21st April 2022)

• Record Type: Journal Article
• Authors: Chen, Xi; Sukhanov, Andrey A.; Yan, Yuxin; Bese, Damla; Bese, Cagri; Zhao, Jianzhang; Voronkova, Violeta K.; Barbon, Antonio; Yaglioglu, Halime Gul
• Is Part Of: Angewandte Chemie. Volume 134:Number 33(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-04-21
• Subjects: Charge Transfer -- Charge-Separated State -- Electron Transfer -- Intersystem Crossing -- Triplet State; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.202203758
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: We observed a long‐lived charge transfer (CT) state in a novel orthogonal compact electron donor–acceptor dyads, with closed form of rhodamine (Rho) as electron donor and pyromellitimide (PI), or thionated PI, as electron acceptor. The two parts in the dyads are connected via a spiro quaternary carbon atom, thus the torsion between the donor and acceptor is completely inhibited, which is beneficial to reduce the reorganization energy and to exploit the Marcus inverted region effect to prolong the CT state lifetime. Femtosecond transient absorption spectra show that the charge separation is rather fast, while nanosecond transient absorption spectra confirmed the formation of long‐lived CT state (2.6 μs). Time‐resolved electron paramagnetic resonance (TREPR) spectra determined the spin multiplicity of the long living state and assigned it to a 3 CT state. Replacement of an oxygen atom in the PI part with a sulfur atom favoring classical intersystem crossing processes, causes a consistently shortening of the lifetime of the 3 CT state (0.29 μs). Abstract : A novel fully rigid spiro electron donor–acceptor dyad is prepared by linking the electron donor and acceptor via a spiro quaternary carbon atom, thus the torsion between the electron donor and acceptor is completely inhibited. The dyad shows a long‐lived 3 CT state (2.6 μs) with a high energy level (ca. 2.61 eV), the electron spin multiplicity of the CT state was confirmed with time‐resolved EPR spectra.