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Möbius aromaticity (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Möbius aromaticity" in English language version.

refsWebsite
Global rank English rank
12doi.org
2nd place
2nd place
8nih.gov
4th place
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1semanticscholar.org
11th place
8th place
1wisc.edu
1,045th place
746th place
1acs.org
1,248th place
1,104th place
1worldcat.org
5th place
5th place
1harvard.edu
18th place
17th place

acs.org

pubs.acs.org

doi.org

  • Rzepa, Henry S. (2005). "Möbius Aromaticity and Delocalization". Chem. Rev. 105 (10): 3697–3715. doi:10.1021/cr030092l. PMID 16218564.
  • Seok Yoon, Zin; Osuka, Atsuhiro; Kim, Dongho (2009). "Möbius aromaticity and antiaromaticity in expanded porphyrins". Nature Chemistry. 1 (2): 113–122. doi:10.1038/nchem.172. PMID 21378823.
  • Heilbronner, E. (1964). "Hückel molecular orbitals of Möbius-type conformations of annulenes". Tetrahedron Letters. 5 (29): 1923–1928. doi:10.1016/S0040-4039(01)89474-0.
  • Ajami, D.; Oeckler, O.; Simon, A.; Herges, R. (December 2003). "Synthesis of a Möbius aromatic hydrocarbon". Nature. 426 (6968): 819–821. doi:10.1038/nature02224. PMID 14685233. S2CID 4383956.
  • Paul; Schleyer, R. (1971). "Thermal bicyclo[6.1.0]nonatrienyl chloride-dihydroindenyl chloride rearrangement". Journal of the American Chemical Society. 93: 279–281. doi:10.1021/ja00730a063.
  • Herges, Rainer (2006). "Topology in Chemistry: Designing Möbius Molecules †". Chemical Reviews. 106 (12): 4820–4842. doi:10.1021/cr0505425. PMID 17165676.
  • Mucke, Eva-Katrin; Köhler, Felix; Herges, Rainer (2010-04-16). "The [13]Annulene Cation Is a Stable Möbius Annulene Cation". Organic Letters. 12 (8): 1708–1711. doi:10.1021/ol1002384. ISSN 1523-7060. PMID 20232816.
  • Castro, Claire (2005). "Investigation of a Putative Möbius Aromatic Hydrocarbon. The Effect of Benzannelation on Möbius [4 n ]Annulene Aromaticity". Journal of the American Chemical Society. 127 (8): 2425–2432. doi:10.1021/ja0458165. PMID 15724997.
  • Stępień, Marcin (2007). "Expanded Porphyrin with a Split Personality: A Hückel–Möbius Aromaticity Switch". Angewandte Chemie International Edition. 46 (41): 7869–7873. doi:10.1002/anie.200700555. PMID 17607678.
  • Zhu, Congqing; Ming Luo; Qin Zhu; Jun Zhu; Paul v. R. Schleyer; Judy I-Chia Wu; Xin Lu; Haiping Xia (25 February 2014). "Planar Möbius aromatic pentalenes incorporating 16 and 18 valence electron osmiums". Nature Communications. 5: 3265. Bibcode:2014NatCo...5.3265Z. doi:10.1038/ncomms4265. PMID 24567039.
  • Zimmerman, H. E (1966). "On Molecular Orbital Correlation Diagrams, the Occurrence of Möbius Systems in Cyclization Reactions, and Factors Controlling Ground and Excited State Reactions. I". J. Am. Chem. Soc. 88 (7): 1564–1565. doi:10.1021/ja00959a052.
  • Zimmerman, H. E (1966). "On Molecular Orbital Correlation Diagrams, Möbius Systems, and Factors Controlling Ground and Excited State Reactions. II". J. Am. Chem. Soc. 88 (7): 1566–1567. doi:10.1021/ja00959a053.

harvard.edu

ui.adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Rzepa, Henry S. (2005). "Möbius Aromaticity and Delocalization". Chem. Rev. 105 (10): 3697–3715. doi:10.1021/cr030092l. PMID 16218564.
  • Seok Yoon, Zin; Osuka, Atsuhiro; Kim, Dongho (2009). "Möbius aromaticity and antiaromaticity in expanded porphyrins". Nature Chemistry. 1 (2): 113–122. doi:10.1038/nchem.172. PMID 21378823.
  • Ajami, D.; Oeckler, O.; Simon, A.; Herges, R. (December 2003). "Synthesis of a Möbius aromatic hydrocarbon". Nature. 426 (6968): 819–821. doi:10.1038/nature02224. PMID 14685233. S2CID 4383956.
  • Herges, Rainer (2006). "Topology in Chemistry: Designing Möbius Molecules †". Chemical Reviews. 106 (12): 4820–4842. doi:10.1021/cr0505425. PMID 17165676.
  • Mucke, Eva-Katrin; Köhler, Felix; Herges, Rainer (2010-04-16). "The [13]Annulene Cation Is a Stable Möbius Annulene Cation". Organic Letters. 12 (8): 1708–1711. doi:10.1021/ol1002384. ISSN 1523-7060. PMID 20232816.
  • Castro, Claire (2005). "Investigation of a Putative Möbius Aromatic Hydrocarbon. The Effect of Benzannelation on Möbius [4 n ]Annulene Aromaticity". Journal of the American Chemical Society. 127 (8): 2425–2432. doi:10.1021/ja0458165. PMID 15724997.
  • Stępień, Marcin (2007). "Expanded Porphyrin with a Split Personality: A Hückel–Möbius Aromaticity Switch". Angewandte Chemie International Edition. 46 (41): 7869–7873. doi:10.1002/anie.200700555. PMID 17607678.
  • Zhu, Congqing; Ming Luo; Qin Zhu; Jun Zhu; Paul v. R. Schleyer; Judy I-Chia Wu; Xin Lu; Haiping Xia (25 February 2014). "Planar Möbius aromatic pentalenes incorporating 16 and 18 valence electron osmiums". Nature Communications. 5: 3265. Bibcode:2014NatCo...5.3265Z. doi:10.1038/ncomms4265. PMID 24567039.

semanticscholar.org

api.semanticscholar.org

wisc.edu

jchemed.chem.wisc.edu

  • The Aromaticity of Pericyclic Reaction Transition States Henry S. Rzepa J. Chem. Educ. 2007, 84, 1535. Abstract

worldcat.org