The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
The excited state antiaromatic benzene ring: a molecular Mr Hyde?
Abstract
Baird's rule tells that benzene is an antiaromatic “Mr Hyde” in its lowest excited states, explaining many photoreactions of benzene derivatives.
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Citations
Cites
Krygowski, T. M. (1993) · Journal of Chemical Information and Computer Sciences · doi:10.1021/ci00011a011 · Cited by 1,320
Baird, N. C. (1972) · Journal of the American Chemical Society · doi:10.1021/ja00769a025 · Cited by 680
Rosenberg, M., Dahlstrand, C., Kilså, K., & Ottosson, H. (2014) · Chemical Reviews · doi:10.1021/cr300471v · Cited by 505
Self-citationGround- and Excited-State Aromaticity and Antiaromaticity in Benzene and Cyclobutadiene
Karadakov, P. B. (2008) · The Journal of Physical Chemistry A · doi:10.1021/jp8037335 · Cited by 250
Aromaticity and Antiaromaticity in the Low-Lying Electronic States of Cyclooctatetraene
Karadakov, P. B. (2008) · The Journal of Physical Chemistry A · doi:10.1021/jp8067365 · Cited by 170
The Strange Case of Dr. Jekyll and Mr. Hyde
OISHI, Y. (2001) · Studies in Regional Science · doi:10.2457/srs.32.139 · Cited by 134
Evaluation of Triplet Aromaticity by the Isomerization Stabilization Energy
Zhu, J., An, K., & Schleyer, P. V. R. (2013) · Organic Letters · doi:10.1021/ol400908z · Cited by 100
Evaluation of Triplet Aromaticity by the Indene–Isoindene Isomerization Stabilization Energy Method
An, K., & Zhu, J. (2014) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201301810 · Cited by 57
Feixas, F., Matito, E., Solà, M., & Poater, J. (2010) · Physical Chemistry Chemical Physics · doi:10.1039/b924972a · Cited by 44
Cited by
Calculations of magnetically induced current densities: theory and applications
Sundholm, D., Fliegl, H., & Berger, R. J. F. (2016) · WIREs Computational Molecular Science · doi:10.1002/wcms.1270 · Cited by 373
Oh, J., Sung, Y. M., Hong, Y., & Kim, D. (2018) · Accounts of Chemical Research · doi:10.1021/acs.accounts.7b00629 · Cited by 123
Ueda, M., Jorner, K., Sung, Y. M., Mori, T., Xiao, Q., Kim, D., Ottosson, H., Aida, T., & Itoh, Y. (2017) · Nature Communications · doi:10.1038/s41467-017-00382-1 · Cited by 115
Self-citationExcited-state proton transfer relieves antiaromaticity in molecules
Wu, C.-H., Karas, L. J., Ottosson, H., & Wu, J. I.-C. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1908516116 · Cited by 110
Self-citationHow do the Hückel and Baird Rules Fade away in Annulenes?
Casademont-Reig, I., Ramos-Cordoba, E., Torrent-Sucarrat, M., & Matito, E. (2020) · Molecules · doi:10.3390/molecules25030711 · Cited by 71
“Both conformers are expected to be antiaromatic, displaying an energy destabilization that is responsible for their prominent photochemical reactivity [79].”
Background
Metadata
- Authors
- Papadakis, R., & Ottosson, H.
- Venue
- Chemical Society Reviews
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2015
- Volume
- 44
- Issue
- 18
- Pages
- 6472-6493
- ISSN
- 0306-0012 (ISSN-L)
- 1460-4744
- OpenAlex
- W1819333446
- Cited by
- 163
- References
- 9
- FWCI
- 0.33
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
