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Rigid Annulated Carbon–Sulfur Structures

2006; Wiley; Volume: 45; Issue: 48 Linguagem: Inglês

10.1002/anie.200603461

1521-3773

Tomás Torroba, María García‐Valverde,

Organic Electronics and Photovoltaics

Angewandte Chemie International EditionVolume 45, Issue 48 p. 8092-8096 Highlight Rigid Annulated Carbon–Sulfur Structures† Tomás Torroba Prof., Tomás Torroba Prof. [email protected] Department of Chemistry, University of Burgos, 09001 Burgos, Spain, Fax: (+34) 947-258087Search for more papers by this authorMaría García-Valverde Dr., María García-Valverde Dr. Department of Chemistry, University of Burgos, 09001 Burgos, Spain, Fax: (+34) 947-258087Search for more papers by this author Tomás Torroba Prof., Tomás Torroba Prof. [email protected] Department of Chemistry, University of Burgos, 09001 Burgos, Spain, Fax: (+34) 947-258087Search for more papers by this authorMaría García-Valverde Dr., María García-Valverde Dr. Department of Chemistry, University of Burgos, 09001 Burgos, Spain, Fax: (+34) 947-258087Search for more papers by this author First published: 04 December 2006 https://doi.org/10.1002/anie.200603461Citations: 31 † Financial support from the Dirección General de Investigación of Spain (CTQ2006-15456-C04-04/BQU) is gratefully acknowledged. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Graphical Abstract Open or closed? The first heterocyclic circulene, octathio[8]circulene, was recently synthesized through a highly efficient sulfurization and pyrolysis sequence (see picture; S yellow, C gray). This macrocyclic compound as well as chiral, helical oligothiophenes are rigid structures that open fascinating possibilities for applications in molecular electronics. Citing Literature Volume45, Issue48December 11, 2006Pages 8092-8096 RelatedInformation