Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study-Reference-Cited by-同舟云学术

Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study

Published:2018-04-10 Issue:17 Volume:122 Page:9346-9355
ISSN:1932-7447
Container-title:The Journal of Physical Chemistry C
language:en
Short-container-title:J. Phys. Chem. C

Author:

Rohwer Egmont J.^ORCID,Akbarimoosavi Maryam,Meckel Steven E.¹,Liu Xunshan,Geng Yan,Lawson Daku Latévi Max²^ORCID,Hauser Andreas²,Cannizzo Andrea,Decurtins Silvio,Stanley Robert J.¹^ORCID,Liu Shi-Xia,Feurer Thomas

Affiliation:

1. Department of Chemistry, Temple University, Philadelphia, Pennsylvania 19122, United States

2. Department of Physical Chemistry, University of Geneva, 1211 Geneva, Switzerland

Funder

Schweizerischer Nationalfonds zur F?rderung der Wissenschaftlichen Forschung

National Aeronautics and Space Administration

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/acs.jpcc.8b02268

Reference37 articles.

1. Tetrathiafulvalenes, Oligoacenenes, and Their Buckminsterfullerene Derivatives: The Brick and Mortar of Organic Electronics

2. Tetrathiafulvalene: the advent of organic metals

3. Imidazole-Annulated Tetrathiafulvalenes Exhibiting pH-Tuneable Intramolecular Charge Transfer and Redox Properties

4. Current advances in fused tetrathiafulvalene donor–acceptor systems

5. New Concepts in Tetrathiafulvalene Chemistry

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