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Renaissance of Annulene Chemistry
Abstract
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRenaissance of Annulene ChemistryEric L. Spitler, Charles A. Johnson, and Michael M. HaleyView Author Information Department of Chemistry and Materials Science Institute, University of Oregon, Eugene, Oregon 97403-1253 Cite this: Chem. Rev. 2006, 106, 12, 5344–5386Publication Date (Web):September 19, 2006Publication History Received31 March 2006Published online19 September 2006Published inissue 1 December 2006https://pubs.acs.org/doi/10.1021/cr050541chttps://doi.org/10.1021/cr050541cresearch-articleACS PublicationsCopyright © 2006 American Chemical SocietyRequest reuse permissionsArticle Views5753Altmetric-Citations339LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Aromatic compounds,Aromaticity,Chemical structure,Hydrocarbons,Mathematical methods Get e-Alerts
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Citations
Cites
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
Schleyer, P. V. R., Maerker, C., Dransfeld, A., Jiao, H., & van Eikema Hommes, N. J. R. (1996) · Journal of the American Chemical Society · doi:10.1021/ja960582d · Cited by 6,210
Nucleus-Independent Chemical Shifts (NICS) as an Aromaticity Criterion
Chen, Z., Wannere, C. S., Corminboeuf, C., Puchta, R., & Schleyer, P. V. R. (2005) · Chemical Reviews · doi:10.1021/cr030088+ · Cited by 3,847
Tahara, K., & Tobe, Y. (2006) · Chemical Reviews · doi:10.1021/cr050556a · Cited by 373
Sondheimer, F. (1972) · Accounts of Chemical Research · doi:10.1021/ar50051a001 · Cited by 329
Cited by
Graphdiyne and graphyne: from theoretical predictions to practical construction
Li, Y., Xu, L., Liu, H., & Li, Y. (2014) · Chemical Society Reviews · doi:10.1039/c3cs60388a · Cited by 1,162
Two‐Dimensional Polymers: Just a Dream of Synthetic Chemists?
Sakamoto, J., van Heijst, J., Lukin, O., & Schlüter, A. D. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200801863 · Cited by 734
Chemistry of meso-Aryl-Substituted Expanded Porphyrins: Aromaticity and Molecular Twist
Tanaka, T., & Osuka, A. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00371 · Cited by 490
Mechanical properties of graphyne
Cranford, S. W., & Buehler, M. J. (2011) · Carbon · doi:10.1016/j.carbon.2011.05.024 · Cited by 472
Zethrenes, Extended p-Quinodimethanes, and Periacenes with a Singlet Biradical Ground State
Sun, Z., Zeng, Z., & Wu, J. (2014) · Accounts of Chemical Research · doi:10.1021/ar5001692 · Cited by 445
From molecular to supramolecular electronics
Chen, H., & Fraser Stoddart, J. (2021) · Nature Reviews Materials · doi:10.1038/s41578-021-00302-2 · Cited by 380
Explorations of the Indenofluorenes and Expanded Quinoidal Analogues
Frederickson, C. K., Rose, B. D., & Haley, M. M. (2017) · Accounts of Chemical Research · doi:10.1021/acs.accounts.7b00004 · Cited by 300
Self-citationAromatic and antiaromatic ring currents in a molecular nanoring
Peeks, M. D., Claridge, T. D. W., & Anderson, H. L. (2017) · Nature · doi:10.1038/nature20798 · Cited by 277
Global aromaticity at the nanoscale
Rickhaus, M., Jirasek, M., Tejerina, L., Gotfredsen, H., Peeks, M. D., Haver, R., Jiang, H.-W., Claridge, T. D. W., & Anderson, H. L. (2020) · Nature Chemistry · doi:10.1038/s41557-019-0398-3 · Cited by 175
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
How 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
“In this section, we employ quantum chemistry methods to study the geometry of annulenes, which often do not attain a planar conformation in their ground state configuration [77] (see Figure 2).”
MethodEffect of size, charge, and spin state on Hückel and Baird aromaticity in [ N ]annulenes
Van Nyvel, L., Alonso, M., & Solà, M. (2025) · Chemical Science · doi:10.1039/d4sc08225g · Cited by 19
Gribanova, T. N., Minyaev, R. M., & Minkin, V. I. (2016) · Structural Chemistry · doi:10.1007/s11224-016-0748-3 · Cited by 5
Metadata
- Authors
- Spitler, E. L., Johnson, C. A., & Haley, M. M.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2006-09-19
- Volume
- 106
- Issue
- 12
- Pages
- 5344-5386
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W2056137417
- Cited by
- 387
- References
- 4
- FWCI
- 1.04
- Type
- journal article
- Language
- en
- Open access
- closed
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