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dc.contributor.authorChen, Tse-Anen_US
dc.contributor.authorLee, Te-Juen_US
dc.contributor.authorLin, Ming-Yuanen_US
dc.contributor.authorSohel, Shariar M. A.en_US
dc.contributor.authorDian, Eric Wei-Guangen_US
dc.contributor.authorLush, Shie-Fuen_US
dc.contributor.authorLiu, Rai-Shungen_US
dc.date.accessioned2014-12-08T15:07:50Z-
dc.date.available2014-12-08T15:07:50Z-
dc.date.issued2010-01-01en_US
dc.identifier.issn0947-6539en_US
dc.identifier.urihttp://dx.doi.org/10.1002/chem.200902231en_US
dc.identifier.urihttp://hdl.handle.net/11536/6160-
dc.description.abstractWe report the regiocontrolled syntheses of ethene-bridged para-phenylene oligomers in three distinct classes by using Pt(II)- and Ru(II)-catalyzed aromatization. This synthetic approach has been developed based on twofold aromatization of the 1-aryl-2-alkynyl-benzene functionality, which proceeds by distinct regioselectivity for platinum and ruthenium catalysts. Variable-temperature NMR spectra provide evidence that large arrays of these oligomers are prone to twist from planarity. The UV/Vis and photoluminescence (PL) spectra as well as the band gaps of these regularly growing arrays show a pattern of extensive pi conjugation with increasing array sizes, except for in one instance.en_US
dc.language.isoen_USen_US
dc.titleRegiocontrolled Synthesis of Ethene-Bridged para-Phenylene Oligomers Based on Pt(II)- and Ru(II)-Catalyzed Aromatizationen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/chem.200902231en_US
dc.identifier.journalCHEMISTRY-A EUROPEAN JOURNALen_US
dc.citation.volume16en_US
dc.citation.issue6en_US
dc.citation.spage1826en_US
dc.citation.epage1833en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
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