Synthesis and Molecular Properties of Four Isomeric Dialkylated Angular-Shaped Naphthodithiophenes
| dc.citation.epage | 5341 | en_US |
| dc.citation.issue | 20 | en_US |
| dc.citation.spage | 5338 | en_US |
| dc.citation.volume | 15 | en_US |
| dc.citation.woscount | 12 | |
| 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.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | 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.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.identifier.doi | 10.1021/ol4025953 | en_US |
| dc.identifier.issn | 1523-7060 | en_US |
| dc.identifier.journal | ORGANIC LETTERS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1021/ol4025953 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/22975 | |
| dc.identifier.wosnumber | WOS:000326121700049 | |
| 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 |