Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/11301
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dc.contributor.authorDUCHATEAU, Jan-
dc.contributor.authorLUTSEN, Laurence-
dc.contributor.authorGUEDENS, Wanda-
dc.contributor.authorCLEIJ, Thomas-
dc.contributor.authorVANDERZANDE, Dirk-
dc.date.accessioned2010-11-10T08:08:56Z-
dc.date.availableNO_RESTRICTION-
dc.date.available2010-11-10T08:08:56Z-
dc.date.issued2010-
dc.identifier.citationPOLYMER CHEMISTRY, 1 (8). p. 1313-1322-
dc.identifier.issn1759-9954-
dc.identifier.urihttp://hdl.handle.net/1942/11301-
dc.description.abstractA novel conjugated copolymer of poly(2-methoxy-5-(3,7-dimethyloctyloxy)-1,4-phenylene vinylene) (MDMO-PPV) and poly(1,4-(2-(5-carboxypentyloxy)-5-methoxyphenylene) vinylene) (CPM-PPV), which can be used as a platform for further post-polymerization functionalization, is presented. This copolymer is soluble in common organic solvents, such as CHCl3, CH2Cl2, and THF. Post-polymerization functionalization of the acid-groups of this copolymer has been successfully performed via an optimized DCC/DMAP-procedure with the desired alcohol. Several examples have been prepared to demonstrate the versatility of the developed functionalization methodology. PPV-copolymers have been prepared with vinyl groups, propynylphenyl groups, methacrylate groups, ATRP initiator groups, dithiocarbamate initiator groups and propargyl groups. The latter group can be utilized to do "click" chemistry, which has been demonstrated with an azide-functionalized reagent. In all cases, analytical data are consistent with a quantitative conversion of the functional groups. It is demonstrated that no substantial degradation of the conjugated system occurs even after consecutive post-polymerization functionalization reactions.-
dc.description.sponsorshipThe authors want to thank the Flemish Fund for Scientific Research (FWO) for financial support in the FWO project G.0091.07. Also the financial support by the European Science Foundation (ESF) for the ORGANISOLAR Network Program 'New Generation of Organic based Photovoltaic Devices' and for the EUROCORES (ESF) Program SONS (CRP SOHYDs) that is also supported by funds from the FWO (G.068506), the UHasselt (Research Fund) and the EC Sixth Framework Program under Contract ERAS-CT-2003-980409 is acknowledged.-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleVersatile post-polymerization functionalization of poly(p-phenylene vinylene) copolymers containing carboxylic acid substituents: development of a universal method towards functional conjugated copolymers-
dc.typeJournal Contribution-
dc.identifier.epage1322-
dc.identifier.issue8-
dc.identifier.spage1313-
dc.identifier.volume1-
local.format.pages10-
local.bibliographicCitation.jcatA1-
dc.description.notes[Duchateau, Jan; Guedens, Wanda; Cleij, Thomas J.; Vanderzande, Dirk] Hasselt Univ, Inst Mat Res IMO, B-3590 Diepenbeek, Belgium. [Lutsen, Laurence; Vanderzande, Dirk] IMEC, Div IMOMEC, B-3590 Diepenbeek, Belgium. thomas.cleij@uhasselt.be-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.bibliographicCitation.oldjcatA1-
dc.identifier.doi10.1039/c0py00086h-
dc.identifier.isi000282612700018-
item.fullcitationDUCHATEAU, Jan; LUTSEN, Laurence; GUEDENS, Wanda; CLEIJ, Thomas & VANDERZANDE, Dirk (2010) Versatile post-polymerization functionalization of poly(p-phenylene vinylene) copolymers containing carboxylic acid substituents: development of a universal method towards functional conjugated copolymers. In: POLYMER CHEMISTRY, 1 (8). p. 1313-1322.-
item.contributorDUCHATEAU, Jan-
item.contributorLUTSEN, Laurence-
item.contributorGUEDENS, Wanda-
item.contributorCLEIJ, Thomas-
item.contributorVANDERZANDE, Dirk-
item.validationecoom 2011-
item.accessRightsClosed Access-
item.fulltextNo Fulltext-
crisitem.journal.issn1759-9954-
crisitem.journal.eissn1759-9962-
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