dc.contributor.author
Echavarren, Antonio M.
dc.contributor.author
Lerena, Laura
dc.contributor.author
Zuzak, Rafal
dc.contributor.author
Godlewski, Szymon
dc.date.accessioned
2024-09-03T06:49:22Z
dc.date.accessioned
2024-12-16T11:52:14Z
dc.date.available
2024-09-03T06:49:22Z
dc.date.available
2024-12-16T11:52:14Z
dc.date.issued
2024-07-30
dc.identifier.uri
http://hdl.handle.net/2072/537788
dc.description.abstract
Acenes, the group of polycyclic aromatic hydrocarbons (PAHs) with linearly fused benzene rings, possess distinctive electronic properties with potential applicability in material science. Hexacene was the largest acene obtained and characterized in the last century, followed by heptacene in 2006. Since then, a race for obtaining the largest acene resulted in the development of several members of this family as well as diverse innovative synthetic strategies, from solid-state chemistry to the promising on-surface chemistry. This last technique allows the obtention of higher acenes, up to tridecacene, the largest acene so far. This review presents the different methodologies employed for the synthesis of acenes, highlighting the newest studies, to provide a much more thorough understanding of the essence of the electronic structure of this captivating group of organic compounds.
eng
dc.publisher
Chemistry Europe
dc.source
RECERCAT (Dipòsit de la Recerca de Catalunya)
dc.title
The Journey for the Synthesis of Large Acenes
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion
dc.subject.udc
54 - Química
dc.relation.projectID
MCIN/AEI/10.13039/501100011033 (PID2022-136623NB-I00, and CEX2019-000925-S)
dc.relation.projectID
the EuropeanResearch Council (Advanced Grant 835080)
dc.relation.projectID
AGAUR (2021SGR 01256)
dc.relation.projectID
CERCA Program/Generalitat de Catalunya
dc.identifier.doi
https://doi.org/10.1002/chem.202402122
dc.rights.accessLevel
info:eu-repo/semantics/openAccess