Synthesis, Cyclic Voltammetry and Photophysical Properties of a Bridged o-Phenylenediamine C-60 Dyad.

Diekers M, Hirsch A, Luo C, Guldi DM, Bauer KA, Nickel U (2000)

Publication Type: Journal article, Original article

Publication year: 2000

Journal

Organic Letters American Chemical Society

Original Authors: Dickers M., Hirsch A., Luo C., Guldi D.M., Bauer K., Nickel U.

Publisher: American Chemical Society

Book Volume: 2

Pages Range: 2741-2744

Journal Issue: 18

DOI: 10.1021/ol005992s

Abstract

The synthesis, complete spectroscopic characterization, cyclic voltammetry, and photophysical measurements of a new o-phenylenediamine-C dyad are described. By using a tether strategy, only a single regioisomer was obtained. Cyclic voltammetry measurements indicate that the two electroactive groups do not interact in their singlet ground states. Photophysical investigations reveal a rapid photoinduced electron transfer between the singlet excited state of the fullerene acceptor and the o-phenylenediamine donor, yielding a charge-separated radical pair.

Authors with CRIS profile

Andreas Hirsch Lehrstuhl für Organische Chemie II Dirk Michael Guldi Lehrstuhl für Physikalische Chemie I Ulrich Nickel Lehrstuhl für Physikalische Chemie I

How to cite

APA:

Diekers, M., Hirsch, A., Luo, C., Guldi, D.M., Bauer, K.A., & Nickel, U. (2000). Synthesis, Cyclic Voltammetry and Photophysical Properties of a Bridged o-Phenylenediamine C-60 Dyad. Organic Letters, 2(18), 2741-2744. https://doi.org/10.1021/ol005992s

MLA:

Diekers, Michael, et al. "Synthesis, Cyclic Voltammetry and Photophysical Properties of a Bridged o-Phenylenediamine C-60 Dyad." Organic Letters 2.18 (2000): 2741-2744.

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