File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Persistent peri‐Heptacene: Synthesis and In Situ Characterization

TitlePersistent peri‐Heptacene: Synthesis and In Situ Characterization
Authors
KeywordsScholl reaction
acenes
graphene
nanostructures
radicals
Issue Date2021
PublisherWiley-VCH Verlag GmbH & Co. KGaA. The Journal's web site is located at https://onlinelibrary.wiley.com/journal/15213773
Citation
Angewandte Chemie (International Edition), 2021, v. 60 n. 25, p. 13853-13858 How to Cite?
Abstractn-peri-Acenes (n-PAs) have gained interest as model systems of zigzag-edged graphene nanoribbons for potential applications in nanoelectronics and spintronics. However, the synthesis of n-PAs larger than peri-tetracene remains challenging because of their intrinsic open-shell character and high reactivity. Presented here is the synthesis of a hitherto unknown n-PA, that is, peri-heptacene (7-PA), in which the reactive zigzag edges are kinetically protected with eight 4-tBu-C6H4 groups. The formation of 7-PA is validated by high-resolution mass spectrometry and in situ FT-Raman spectroscopy. 7-PA displays a narrow optical energy gap of 1.01 eV and exhibits persistent stability (t1/2≈25 min) under inert conditions. Moreover, electron-spin resonance measurements and theoretical studies reveal that 7-PA exhibits an open-shell feature and a significant tetraradical character. This strategy could be considered a modular approach for the construction of next-generation (3 N+1)-PAs (where N≥3).
DescriptionHybrid open access
Persistent Identifierhttp://hdl.handle.net/10722/306338
ISSN
2023 Impact Factor: 16.1
2023 SCImago Journal Rankings: 5.300
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorAjayakumar, MR-
dc.contributor.authorMa, J-
dc.contributor.authorLucotti, A-
dc.contributor.authorSchellhammer, KS-
dc.contributor.authorSerra, G-
dc.contributor.authorDmitrieva, E-
dc.contributor.authorRosenkranz, M-
dc.contributor.authorKomber, H-
dc.contributor.authorLiu, J-
dc.contributor.authorOrtmann, F-
dc.contributor.authorTommasini, M-
dc.contributor.authorFeng, X-
dc.date.accessioned2021-10-20T10:22:12Z-
dc.date.available2021-10-20T10:22:12Z-
dc.date.issued2021-
dc.identifier.citationAngewandte Chemie (International Edition), 2021, v. 60 n. 25, p. 13853-13858-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10722/306338-
dc.descriptionHybrid open access-
dc.description.abstractn-peri-Acenes (n-PAs) have gained interest as model systems of zigzag-edged graphene nanoribbons for potential applications in nanoelectronics and spintronics. However, the synthesis of n-PAs larger than peri-tetracene remains challenging because of their intrinsic open-shell character and high reactivity. Presented here is the synthesis of a hitherto unknown n-PA, that is, peri-heptacene (7-PA), in which the reactive zigzag edges are kinetically protected with eight 4-tBu-C6H4 groups. The formation of 7-PA is validated by high-resolution mass spectrometry and in situ FT-Raman spectroscopy. 7-PA displays a narrow optical energy gap of 1.01 eV and exhibits persistent stability (t1/2≈25 min) under inert conditions. Moreover, electron-spin resonance measurements and theoretical studies reveal that 7-PA exhibits an open-shell feature and a significant tetraradical character. This strategy could be considered a modular approach for the construction of next-generation (3 N+1)-PAs (where N≥3).-
dc.languageeng-
dc.publisherWiley-VCH Verlag GmbH & Co. KGaA. The Journal's web site is located at https://onlinelibrary.wiley.com/journal/15213773-
dc.relation.ispartofAngewandte Chemie (International Edition)-
dc.rightsSubmitted (preprint) Version This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Accepted (peer-reviewed) Version This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectScholl reaction-
dc.subjectacenes-
dc.subjectgraphene-
dc.subjectnanostructures-
dc.subjectradicals-
dc.titlePersistent peri‐Heptacene: Synthesis and In Situ Characterization-
dc.typeArticle-
dc.identifier.emailLiu, J: juliu@hku.hk-
dc.identifier.authorityLiu, J=rp02584-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1002/anie.202102757-
dc.identifier.pmid33848044-
dc.identifier.pmcidPMC8251907-
dc.identifier.scopuseid_2-s2.0-85105669206-
dc.identifier.hkuros327168-
dc.identifier.volume60-
dc.identifier.issue25-
dc.identifier.spage13853-
dc.identifier.epage13858-
dc.identifier.isiWOS:000649415800001-
dc.publisher.placeGermany-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats