Synthesis and Molecular Properties of Four Isomeric Dialkylated Angular-Shaped Naphthodithiophenes

doi:10.1021/ol4025953

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DC 欄位	值	語言
dc.contributor.author	Cheng, Sheng-Wen	en_US
dc.contributor.author	Chiou, De-Yang	en_US
dc.contributor.author	Lai, Yu-Ying	en_US
dc.contributor.author	Yu, Ruo-Han	en_US
dc.contributor.author	Lee, Chia-Hao	en_US
dc.contributor.author	Cheng, Yen-Ju	en_US
dc.date.accessioned	2014-12-08T15:32:56Z	-
dc.date.available	2014-12-08T15:32:56Z	-
dc.date.issued	2013-10-18	en_US
dc.identifier.issn	1523-7060	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/ol4025953	en_US
dc.identifier.uri	http://hdl.handle.net/11536/22975	-
dc.description.abstract	A 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.iso	en_US	en_US
dc.title	Synthesis and Molecular Properties of Four Isomeric Dialkylated Angular-Shaped Naphthodithiophenes	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1021/ol4025953	en_US
dc.identifier.journal	ORGANIC LETTERS	en_US
dc.citation.volume	15	en_US
dc.citation.issue	20	en_US
dc.citation.spage	5338	en_US
dc.citation.epage	5341	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000326121700049	-
dc.citation.woscount	12	-
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