The DOI matches its Crossref record; 57 of the 57 references it cites were found in a registry or an index.
Expanded Porphyrins and Their Heterologs
Abstract
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTExpanded Porphyrins and Their HeterologsAyub Jasat and David DolphinView Author Information Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, B.C., Canada V6T 1Z1 Cite this: Chem. Rev. 1997, 97, 6, 2267–2340Publication Date (Web):October 1, 1997Publication History Received5 March 1997Revised20 May 1997Published online1 October 1997Published inissue 1 October 1997https://pubs.acs.org/doi/10.1021/cr950078bhttps://doi.org/10.1021/cr950078bresearch-articleACS PublicationsCopyright © 1997 American Chemical SocietyRequest reuse permissionsArticle Views4061Altmetric-Citations514LEARN 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:Absorption,Anions,Aromatic compounds,Macrocycles,Pyrroles Get e-Alerts
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Shannon, R. D. (1976) · Acta Crystallographica Section A · doi:10.1107/s0567739476001551 · Cited by 66,145
Porphyrins and metalloporphyrins
Gray, C. H. (1976) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(76)90037-2 · Cited by 1,941
Emsley, J. (1980) · Chemical Society Reviews · doi:10.1039/cs9800900091 · Cited by 1,124
Carbonyl-coupling reactions using low-valent titanium
McMurry, J. E. (1989) · Chemical Reviews · doi:10.1021/cr00097a007 · Cited by 1,064
"N-Confused Porphyrin": A New Isomer of Tetraphenylporphyrin
Furuta, H., Asano, T., & Ogawa, T. (1994) · Journal of the American Chemical Society · doi:10.1021/ja00081a047 · Cited by 698
Tetra‐p‐tolylporphyrin with an Inverted Pyrrole Ring: A Novel Isomer of Porphyrin
Chmielewski, P. J., Latos‐Grażyński, L., Rachlewicz, K., & Glowiak, T. (1994) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199407791 · Cited by 641
Catalyzed Addition of Aldehydes to Activated Double Bonds—A New Synthetic Approach
Stetter, H. (1976) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197606391 · Cited by 622
Pyrromethanes and Porphyrins Therefrom1
Arsenault, G. P., Bullock, E., & MacDonald, S. F. (1960) · Journal of the American Chemical Society · doi:10.1021/ja01501a066 · Cited by 347
Sondheimer, F. (1972) · Accounts of Chemical Research · doi:10.1021/ar50051a001 · Cited by 329
Synthetic and structural studies of sapphyrin, a 22-.pi.-electron pentapyrrolic "expanded porphyrin"
Sessler, J. L., Cyr, M. J., Lynch, V., McGhee, E., & Ibers, J. A. (1990) · Journal of the American Chemical Society · doi:10.1021/ja00163a059 · Cited by 278
Sapphyrins: novel aromatic pentapyrrolic macrocycles
Bauer, V. J., Clive, D. L. J., Dolphin, D., Paine, J. B., Harris, F. L., King, M. M., Loder, J., Wang, S. W. C., & Woodward, R. B. (1983) · Journal of the American Chemical Society · doi:10.1021/ja00359a012 · Cited by 276
Self-citation306. Corroles. Part I. Synthesis
Johnson, A. W., & Kay, I. T. (1965) · Journal of the Chemical Society (Resumed) · doi:10.1039/jr9650001620 · Cited by 274
Texaphyrins: Synthesis and Applications
Sessler, J. L., Hemmi, G., Mody, T. D., Murai, T., Burrell, A., & Young, S. W. (1994) · Accounts of Chemical Research · doi:10.1021/ar00038a002 · Cited by 260
Diprotonated sapphyrin: a fluoride selective halide anion receptor
Shionoya, M., Furuta, H., Lynch, V., Harriman, A., & Sessler, J. L. (1992) · Journal of the American Chemical Society · doi:10.1021/ja00040a034 · Cited by 227
The porphyrins from the 'annulene chemist's' perspective
Vogel, E. (1993) · Pure and Applied Chemistry · doi:10.1351/pac199365010143 · Cited by 224
Macrocyclic Schiff base complexes of lanthanides and actinides
Fenton, D. E., & Vigato, P. A. (1988) · Chemical Society Reviews · doi:10.1039/cs9881700069 · Cited by 220
DISTRIBUTION AND ELIMINATION OF PHOTOFRIN II IN MICE
Bellnier, D. A., Ho, Y., Pandey, R. K., Missert, J. R., & Dougherty, T. J. (1989) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1989.tb04152.x · Cited by 200
Hexaalkyl Terpyrrole: A New Building Block for the Preparation of Expanded Porphyrins
Sessler, J. L., Weghorn, S. J., Hiseada, Y., & Lynch, V. (1995) · Chemistry – A European Journal · doi:10.1002/chem.19950010110 · Cited by 195
Turcasarin, the Largest Expanded Porphyrin to Date
Sessler, J. L., Weghorn, S. J., Lynch, V., & Johnson, M. R. (1994) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199415091 · Cited by 179
From Porphyrin Isomers to Octapyrrolic “Figure Eight” Macrocycles
Vogel, E., Bröring, M., Fink, J., Rosen, D., Schmickler, H., Lex, J., Chan, K. W. K., Wu, Y., Plattner, D. A., Nendel, M., et al. (1995) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199525111 · Cited by 176
Synthesis and crystal structure of a novel tripyrrane-containing porphyrinogen-like macrocycle
Sessler, J. L., Johnson, M. R., & Lynch, V. (1987) · The Journal of Organic Chemistry · doi:10.1021/jo00228a048 · Cited by 170
Chmielewski, P. J., Latos‐Grażyński, L., & Rachlewicz, K. (1995) · Chemistry – A European Journal · doi:10.1002/chem.19950010111 · Cited by 162
Haddon, R. C. (1979) · Journal of the American Chemical Society · doi:10.1021/ja00501a013 · Cited by 146
Benziporphyrin, a Benzene‐Containing, Nonaromatic Porphyrin Analogue
Berlin, K., & Breitmaier, E. (1994) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199412461 · Cited by 145
Reduction and oxidation of annulenes
Muellen, K. (1984) · Chemical Reviews · doi:10.1021/cr00064a006 · Cited by 140
Ground States of Conjugated Molecules. III. Classical Polyenes1
Dewar, M. J. S., & Gleicher, G. J. (1965) · Journal of the American Chemical Society · doi:10.1021/ja01082a002 · Cited by 138
McCall, H. C., & Grondahl, P. (2022) · State University of New York Press eBooks · doi:10.1515/9781438489643-020 · Cited by 138
Rubyrin: A New Hexapyrrolic Expanded Porphyrin
Sessler, J. L., Morishima, T., & Lynch, V. M. (1991) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199109771 · Cited by 137
Recent advances in the chemistry of large-ring conjugated systems
Sondheimer, F. (1963) · Pure and Applied Chemistry · doi:10.1351/pac196307020363 · Cited by 133
Sessler, J. L., & Burrell, A. K. (1992) · Topics in current chemistry · doi:10.1007/3-540-54348-1_10 · Cited by 124
A Simple Route to Sulfur Bridged Annulenes
Hu, Z., Atwood, J. L., & Cava, M. P. (1994) · The Journal of Organic Chemistry · doi:10.1021/jo00105a025 · Cited by 121
Synthesis of a Fourfold Enlarged Porphyrin with an Extremely Large, Diamagnetic Ring‐Current Effect
Gosmann, M., & Franck, B. (1986) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198611001 · Cited by 121
Bröring, M., Jendrny, J., Zander, L., et al. (1995) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199525151 · Cited by 119
Rosarin: a new, easily prepared hexapyrrolic expanded porphyrin
Sessler, J. L., Weghorn, S. J., Morishima, T., Rosingana, M., Lynch, V. M., & LEE, V. J. (1992) · Journal of the American Chemical Society · doi:10.1021/ja00047a061 · Cited by 115
Uranylpentaphyrin: an actinide complex of an expanded porphyrin
Burrell, A. K., Hemmi, G. W., Lynch, V., et al. (1991) · Journal of the American Chemical Society · doi:10.1021/ja00012a053 · Cited by 110
Schaverien, C. J., & Orpen, A. G. (1991) · Inorganic Chemistry · doi:10.1021/ic00026a023 · Cited by 107
The synthesis of 22 π-electron macrocycles. Sapphyrins and related compounds
Broadhurst, M. J., Grigg, R., & Johnson, A. W. (1972) · Journal of the Chemical Society Perkin Transactions 1 · doi:10.1039/p19720002111 · Cited by 106
The synthesis of a new 22 π-electron macrocycle: pentaphyrin
Rexhausen, H., & Gossauer, A. (1983) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39830000275 · Cited by 100
Topical Problems in the Biosynthesis of Red Blood Pigment
Franck, B. (1982) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198203431 · Cited by 88
Johnson, A. W., Kay, I. T., Markham, E. C., Price, R., & Shaw, K. B. (1959) · Journal of the Chemical Society (Resumed) · doi:10.1039/jr9590003416 · Cited by 86
Sapphyrins and heterosapphyrins.
Sessler, J. L., Cyr, M., & Burrell, A. K. (1992) · Tetrahedron · doi:10.1016/s0040-4020(01)81183-2 · Cited by 85
The Chemistry of Polyphyrins 2. Synthesis of Hexaphyrins and Their Metal Complexes
Gossauer, A., Charriere, R., Jenny, T. A., et al. (1993) · Heterocycles · doi:10.3987/com-93-6339 · Cited by 79
Synthesis and characterization of a new 26.pi.-aromatic thiophene-containing macrocyclic ligand
Johnson, M. R., Miller, D. C., Bush, K. A., et al. (1992) · The Journal of Organic Chemistry · doi:10.1021/jo00042a019 · Cited by 73
Biomimetic Synthesis of an Octavinylogous Porphyrin with an Aromatic [34]Annulene System
Knübel, G., & Franck, B. (1988) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198811701 · Cited by 70
Porphyries with Aromatic 26π‐Electron Systems
Wessel, T., Franck, B., Möller, M., Rodewald, U. C., & Läge, M. (1993) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199311481 · Cited by 53
Vogel, E., Dörr, J., Herrmann, A., Lex, J., Schmickler, H., Walgenbach, P., Gisselbrecht, J. P., & Gross, M. (1993) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199315971 · Cited by 50
New Thiophene−Pyrrole-Derived Annulenes Containing 6 and 10 Heterocyclic Units
Kozaki, M., Parakka, J. P., & Cava, M. P. (1996) · The Journal of Organic Chemistry · doi:10.1021/jo960214s · Cited by 48
Synthesis and x-ray Structure of Selenasapphyrin
Lisowski, J., Sessler, J. L., & Lynch, V. (1995) · Inorganic Chemistry · doi:10.1021/ic00117a032 · Cited by 48
Syntheses of Some Unusual Polypyrrole Macrocycles
Gossauer, A. (1983) · Bulletin des Sociétés Chimiques Belges · doi:10.1002/bscb.19830920905 · Cited by 47
Nakagawa, M. (1979) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197902021 · Cited by 44
Synthesis of new torands and new uses for old torands
Bell, T. W., Cragg, P. J., Drew, M. G. B., Firestone, A., KWOK, A. D. ‐., Liu, J., Ludwig, R. T., & Papoulis, A. T. (1993) · Pure and Applied Chemistry · doi:10.1351/pac199365030361 · Cited by 43
A N,N′,N″,N‴—Tetramethylporphyrinogen
Franck, B., & Wegner, C. (1975) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197504241 · Cited by 42
The synthesis of a 22π-electron tetrapyrrolic macrocycle, [1,3,1,3] platyrin
Berger, R. A., & Legoff, E. (1978) · Tetrahedron Letters · doi:10.1016/s0040-4039(01)95187-1 · Cited by 42
Enhanced transport of fluoride anion effected using protonated sapphyrin as a carrier
Sessler, J. L., Ford, D. A., Cyr, M. J., & Furuta, H. (1991) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39910001733 · Cited by 38
The University of British Columbia
Hardy, C. (1996) · McGill-Queen's University Press eBooks · doi:10.1515/9780773565708-008 · Cited by 30
New porphyrinoids, 9. Synthesis of a bisvinylogous porphyrin with a [22] annulene system
Gosmann, M., Vogt, A., & Franck, B. (1990) · Liebigs Annalen der Chemie · doi:10.1002/jlac.199019900128 · Cited by 20
Two observations on a model of the biosynthesis of uroporphyrinogen III
WHITLOCK, H. W. J., & Buchanan, D. H. (1969) · Tetrahedron Letters · doi:10.1016/s0040-4039(01)88494-x · Cited by 8
Cited by
Sapphyrins: Versatile Anion Binding Agents
Sessler, J. L., & Davis, J. M. (2001) · Accounts of Chemical Research · doi:10.1021/ar980117g · Cited by 578
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
Figure 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
Lang, K., Mosinger, J., & Wagnerová, D. M. (2004) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2004.02.004 · Cited by 431
Metadata
- Authors
- Jasat, A., & Dolphin, D.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 1997-10-01
- Volume
- 97
- Issue
- 6
- Pages
- 2267-2340
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W2036348623
- Cited by
- 572
- References
- 57
- FWCI
- 4.52
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
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.