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dc.contributor.authorCheng, Sheng-Wenen_US
dc.contributor.authorChiou, De-Yangen_US
dc.contributor.authorLai, Yu-Yingen_US
dc.contributor.authorYu, Ruo-Hanen_US
dc.contributor.authorLee, Chia-Haoen_US
dc.contributor.authorCheng, Yen-Juen_US
dc.date.accessioned2014-12-08T15:32:56Z-
dc.date.available2014-12-08T15:32:56Z-
dc.date.issued2013-10-18en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol4025953en_US
dc.identifier.urihttp://hdl.handle.net/11536/22975-
dc.description.abstractA new strategy to synthesize 4,9- and 5,10-dialkylated alpha-aNDTs as well as 4,9- and 5,10-dialkylated beta-aNDTs is described. Four isomeric precursors with different dithienyl-ene-diyne arrangements undergo base-induced double 6 pi-cyclization to construct the central naphthalene cores, leading to the formation of the regiospecific products. These 2,7-distannylated dialkylated aNDT-based monomers can be used for Stille cross-coupling to produce promising conjugated materials for various optoelectronic applications.en_US
dc.language.isoen_USen_US
dc.titleSynthesis and Molecular Properties of Four Isomeric Dialkylated Angular-Shaped Naphthodithiophenesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol4025953en_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume15en_US
dc.citation.issue20en_US
dc.citation.spage5338en_US
dc.citation.epage5341en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000326121700049-
dc.citation.woscount12-
Appears in Collections:Articles


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