The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index.
Expanded porphyrins and aromaticity
Abstract
meso-Aryl-substituted expanded porphyrins that are porphyrin homologues consisting of more than five pyrrolic units are a nice platform to realize diverse aromatic and antiaromatic species as well as stable radical species. They are also an ideal series to realize topologically twisted molecules with distinct Möbius aromaticity and antiaromaticity.
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Cites
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
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Krygowski, T. M. (1993) · Journal of Chemical Information and Computer Sciences · doi:10.1021/ci00011a011 · Cited by 1,320
Synthetic Expanded Porphyrin Chemistry
Sessler, J. L., & Seidel, D. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200200561 · Cited by 924
Nonplanar porphyrins and their significance in proteins
A. Shelnutt, J., Song, X.-Z., Ma, J.-G., Jia, S.-L., Jentzen, W., J. Medforth, C., & J. Medforth, C. (1998) · Chemical Society Reviews · doi:10.1039/a827031z · Cited by 829
Schleyer, P. V. R. (2001) · Chemical Reviews · doi:10.1021/cr0103221 · Cited by 783
Investigation of the synthesis of ortho-substituted tetraphenylporphyrins
Lindsey, J. S., & Wagner, R. W. (1989) · The Journal of Organic Chemistry · doi:10.1021/jo00265a021 · Cited by 707
Expanded Porphyrins and Their Heterologs
Jasat, A., & Dolphin, D. (1997) · Chemical Reviews · doi:10.1021/cr950078b · Cited by 572
Hűckel molecular orbitals of Mőbius-type conformations of annulenes
Heilbronner, E. (1964) · Tetrahedron Letters · doi:10.1016/s0040-4039(01)89474-0 · Cited by 537
A new definition of Dewar-type resonance energies
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Cited by
Conjugated porphyrin arrays: synthesis, properties and applications for functional materials
Tanaka, T., & Osuka, A. (2015) · Chemical Society Reviews · doi:10.1039/c3cs60443h · Cited by 699
Self-citationChemistry 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-citationAn electronic aromaticity index for large rings
Matito, E. (2016) · Physical Chemistry Chemical Physics · doi:10.1039/c6cp00636a · Cited by 201
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
“Since the studies of Hückel on organic molecules, the concept of aromaticity has extended importantly including all sorts of new aromatic molecules such as metalloaromatic molecules [4,51,52,60,61], fullerens [62], nanotubes [63], porphyrins [64,65] with a Möbius-like structure [66–73], and all-metal clusters [4,5], a…”
Background
Metadata
- Authors
- Osuka, A., & Saito, S.
- Venue
- Chemical Communications
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2011
- Volume
- 47
- Issue
- 15
- Pages
- 4330
- ISSN
- 1359-7345 (ISSN-L)
- 1364-548X
- OpenAlex
- W2080359804
- Cited by
- 273
- References
- 75
- FWCI
- 13.63
- Type
- journal article
- Language
- en
- Open access
- closed
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Data sources
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.
