Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/61760
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dc.contributor.authorPiched Anuragudomen_US
dc.contributor.authorS. S. Newazen_US
dc.contributor.authorSukon Phanichphanten_US
dc.contributor.authorT. Randall Leeen_US
dc.date.accessioned2018-09-11T08:58:39Z-
dc.date.available2018-09-11T08:58:39Z-
dc.date.issued2006-05-16en_US
dc.identifier.issn00249297en_US
dc.identifier.other2-s2.0-33744481589en_US
dc.identifier.other10.1021/ma060606ten_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33744481589&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/61760-
dc.description.abstractThis paper describes a simple new strategy for preparing poly(9,9-dialkylfluorenyl-2,7-vinylenes) (PFVs) having high molecular weights and no detectable saturated defects along the conjugated backbone. The new route utilizes a modified Horner-Emmons method by coupling suitably designed comonomers to form the targeted conjugated polymers. The newly prepared PFVs were directly compared to PFVs prepared via a previously established Gilch polymerization route. The structure and optical properties of all PFVs were characterized by gel permeation chromatography (GPC), NMR spectroscopy, UV-vis, fluorescence, and photoluminescence spectroscopy. The findings indicate that the modified Horner-Emmons route gave PFVs with lower molecular weights but substantially higher yields and fewer defects than those prepared by using the Gilch route. © 2006 American Chemical Society.en_US
dc.subjectMaterials Scienceen_US
dc.titleFacile Horner-Emmons synthesis of defect-free poly(9,9-dialkylfluorenyl-2, 7-vinylene)en_US
dc.typeJournalen_US
article.title.sourcetitleMacromoleculesen_US
article.volume39en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsPolyorganix Inc.en_US
article.stream.affiliationsUniversity of Houstonen_US
Appears in Collections:CMUL: Journal Articles

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