The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Metalation of Expanded Porphyrins: A Chemical Trigger Used To Produce Molecular Twisting and Möbius Aromaticity
Open accessAbstract
Round the twist: Metalation of [36]octaphyrin 1 provided the Möbius aromatic Pd2 complex 3 as well as the Hückel antiaromatic Pd2 complex 2. This method can be applied to other expanded porphyrins and Group 10 metal ions. The aromatic/antiaromatic character was supported by NMR spectrscopy, NICS calculation, and two-photon absorption measurements.
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Cites
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Synthetic Expanded Porphyrin Chemistry
Sessler, J. L., & Seidel, D. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200200561 · Cited by 924
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Möbius Aromaticity and Delocalization
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Expanded Porphyrin with a Split Personality: A Hückel–Möbius Aromaticity Switch
Stępień, M., Latos‐Grażyński, L., Sprutta, N., Chwalisz, P., & Szterenberg, L. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200700555 · Cited by 351
meso-Aryl-Substituted Expanded Porphyrins
Shin, J.-Y., Furuta, H., Yoza, K., Igarashi, S., & Osuka, A. (2001) · Journal of the American Chemical Society · doi:10.1021/ja0106624 · Cited by 349
Self-citationSynthesechemie expandierter Porphyrine
Sessler, J. L., & Seidel, D. (2003) · Angewandte Chemie · doi:10.1002/ange.200200561 · Cited by 306
Cited by
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
Self-citationFigure Eights, Möbius Bands, and More: Conformation and Aromaticity of Porphyrinoids
Stępień, M., Sprutta, N., & Latos‐Grażyński, L. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201003353 · Cited by 481
Lu, X., Gopalakrishna, T. Y., Phan, H., Herng, T. S., Jiang, Q., Liu, C., Li, G., Ding, J., & Wu, J. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201807185 · Cited by 76
Two-Photon Absorption: An Open Door to the NIR-II Biological Window?
Shaw, P. A., Forsyth, E., Haseeb, F., Yang, S., Bradley, M., & Klausen, M. (2022) · Frontiers in Chemistry · doi:10.3389/fchem.2022.921354 · Cited by 75
Metadata
- Authors
- Tanaka, Y., Saito, S., Mori, S., Aratani, N., Shinokubo, H., Shibata, N., Higuchi, Y., Yoon, Z. S., Kim, K. S., Noh, S. B., Park, J. K., Kim, D., & Osuka, A.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2008-01-08
- Volume
- 47
- Issue
- 4
- Pages
- 681-684
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2103793155
- Cited by
- 332
- References
- 27
- FWCI
- 15.72
- Type
- journal article
- Language
- en
- Open access
- bronze
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- The paper
- Tanaka, Y., Saito, S., Mori, S., Aratani, N., Shinokubo, H., Shibata, N., Higuchi, Y., Yoon, Z. S., Kim, K. S., Noh, S. B., Park, J. K., Kim, D., & Osuka, A. (2008). Metalation of Expanded Porphyrins: A Chemical Trigger Used To Produce Molecular Twisting and Möbius Aromaticity. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200704407
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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