Highly Fluorescent Open-Shell NIR Dyes: The Time-Dependence of Back Electron Transfer in Triarylamine-Perchlorotriphenylmethyl Radicals-Reference-Cited by-同舟云学术

Highly Fluorescent Open-Shell NIR Dyes: The Time-Dependence of Back Electron Transfer in Triarylamine-Perchlorotriphenylmethyl Radicals

Published:2009-10-27 Issue:49 Volume:113 Page:20958-20966
ISSN:1932-7447
Container-title:The Journal of Physical Chemistry C
language:en
Short-container-title:J. Phys. Chem. C

Author:

Heckmann Alexander¹,Dümmler Stefan¹,Pauli Jutta¹,Margraf Markus¹,Köhler Juliane¹,Stich Dominik¹,Lambert Christoph¹,Fischer Ingo¹,Resch-Genger Ute¹

Affiliation:

1. Institut für Organische Chemie, Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany, Institut für Physikalische Chemie, Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany, Bundesanstalt für Materialforschung und -prüfung, Richard-Willstätter-Strasse 11, D-12489 Berlin, Germany, and Wilhelm Conrad Röntgen Research Center for Complex Material Systems, Würzburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Surfaces, Coatings and Films,Physical and Theoretical Chemistry,General Energy,Electronic, Optical and Magnetic Materials

Link

https://pubs.acs.org/doi/pdf/10.1021/jp908425w

Reference53 articles.

1. Neutral Organic Mixed-Valence Compounds: Synthesis and All-Optical Evaluation of Electron-Transfer Parameters

2. Synthesis and Photophysics of a Neutral Organic Mixed-Valence Compound

3. PCTM radicals also form donor−acceptor dyads in combination with ferrocene donors; see refs4and5.

4. A New Valence Tautomerism Example in an Electroactive Ferrocene Substituted Triphenylmethyl Radical

5. Solvent Tuning from Normal to Inverted Marcus Region of Intramolecular Electron Transfer in Ferrocene-Based Organic Radicals

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