What Is the Structure of the Naphthalene–Benzene Heterodimer Radical Cation? Binding Energy, Charge Delocalization, and Unexpected Charge-Transfer Interaction in Stacked Dimer and Trimer Radical Cations-Reference-Cited by-同舟云学术

What Is the Structure of the Naphthalene–Benzene Heterodimer Radical Cation? Binding Energy, Charge Delocalization, and Unexpected Charge-Transfer Interaction in Stacked Dimer and Trimer Radical Cations

Published:2015-03-13 Issue:7 Volume:6 Page:1111-1118
ISSN:1948-7185
Container-title:The Journal of Physical Chemistry Letters
language:en
Short-container-title:J. Phys. Chem. Lett.

Author:

Attah Isaac K.¹,Platt Sean P.¹,Meot-Ner (Mautner) Michael¹,El-Shall M. Samy¹,Peverati Roberto²³,Head-Gordon Martin²³

Affiliation:

1. Department of Chemistry, Virginia Commonwealth University, Richmond, Virginia 23284-2006, United States

2. Department of Chemistry, University of California, Berkeley, California 94720 United States

3. Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States

Funder

Division of Chemistry

Publisher

American Chemical Society (ACS)

Subject

General Materials Science,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jz502438x

Reference44 articles.

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2. Enkelmann, V.InPolynuclear Aromatic Compounds;Advances in Chemistry Series;Ebert, L. B., Ed.American Chemical Society:Washington, DC, 1987; Vol.217, p177, and references therein.

3. Kinetic Studies on Reversible Dimerization of Thianthrene and 2,3,7,8-Tetramethoxythianthrene Radical Cations

4. New BETS Conductors with Magnetic Anions (BETS = bis(ethylenedithio)tetraselenafulvalene)

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