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Article: Effects of strained bicyclic annelation on the benzene nucleus: The X-ray crystal structures of a triphenylene and two anthracene derivatives

TitleEffects of strained bicyclic annelation on the benzene nucleus: The X-ray crystal structures of a triphenylene and two anthracene derivatives
Authors
Cardullo, FrancescaGiuffrida, DanieleKohnke, Franz H.Raymo, Françisco M.Stoddart, J. FraserWilliams, David J.
KeywordsBond-length alternation
Mills-Nixon effect
Polycycles
Strained rings
Triepoxytriphenylenes
Issue Date1996
Citation
Angewandte Chemie - International Edition, 1996, v. 35, n. 3, p. 339-341 How to Cite?
DOI: http://dx.doi.org/10.1002/anie.199603391
AbstractPronounced bond length alternation in the central aromatic ring is the eye-catching structural feature of triepoxytriphenylene 1. By contrast, no significant bond length alternation is observed in the linearly bisannelated compounds 2 and 3. The key difference is ascribed to the position of annelations with the bicyclic units (Image Presented).
Persistent Identifierhttp://hdl.handle.net/10722/332687
ISSN
1433-7851
2023 Impact Factor: 16.1
2023 SCImago Journal Rankings: 5.300
ISI Accession Number ID
WOS:A1996TX49100022

 

DC FieldValueLanguage
dc.contributor.authorCardullo, Francesca-
dc.contributor.authorGiuffrida, Daniele-
dc.contributor.authorKohnke, Franz H.-
dc.contributor.authorRaymo, Françisco M.-
dc.contributor.authorStoddart, J. Fraser-
dc.contributor.authorWilliams, David J.-
dc.date.accessioned2023-10-06T05:13:30Z-
dc.date.available2023-10-06T05:13:30Z-
dc.date.issued1996-
dc.identifier.citationAngewandte Chemie - International Edition, 1996, v. 35, n. 3, p. 339-341-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10722/332687-
dc.description.abstractPronounced bond length alternation in the central aromatic ring is the eye-catching structural feature of triepoxytriphenylene 1. By contrast, no significant bond length alternation is observed in the linearly bisannelated compounds 2 and 3. The key difference is ascribed to the position of annelations with the bicyclic units (Image Presented).-
dc.languageeng-
dc.relation.ispartofAngewandte Chemie - International Edition-
dc.subjectBond-length alternation-
dc.subjectMills-Nixon effect-
dc.subjectPolycycles-
dc.subjectStrained rings-
dc.subjectTriepoxytriphenylenes-
dc.titleEffects of strained bicyclic annelation on the benzene nucleus: The X-ray crystal structures of a triphenylene and two anthracene derivatives-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/anie.199603391-
dc.identifier.scopuseid_2-s2.0-33748216706-
dc.identifier.volume35-
dc.identifier.issue3-
dc.identifier.spage339-
dc.identifier.epage341-
dc.identifier.eissn1521-3773-
dc.identifier.isiWOS:A1996TX49100022-

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