Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/18221
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKUDRJASOVA, Julija-
dc.contributor.authorHERCKENS, Roald-
dc.contributor.authorPENXTEN, Huguette-
dc.contributor.authorADRIAENSENS, Peter-
dc.contributor.authorLUTSEN, Laurence-
dc.contributor.authorVANDERZANDE, Dirk-
dc.contributor.authorMAES, Wouter-
dc.date.accessioned2015-02-04T08:02:33Z-
dc.date.available2015-02-04T08:02:33Z-
dc.date.issued2014-
dc.identifier.citationORGANIC & BIOMOLECULAR CHEMISTRY, 12 (26), p. 4663-4672-
dc.identifier.issn1477-0520-
dc.identifier.urihttp://hdl.handle.net/1942/18221-
dc.description.abstractA series of thiazolo[5,4-d]thiazole-based small molecule organic optoelectronic materials is synthesized via a straightforward microwave-activated Pd-catalyzed C–H arylation protocol. The procedure allows us to obtain extended 2,5-dithienylthiazolo[5,4-d]thiazole chromophores with tailor-made energy levels and absorption patterns, depending on the introduced (het)aryl moieties and the molecular (a)symmetry, by shortened sequences without organometallic intermediates. The synthesized materials can be applied as either electron donor or electron acceptor light-harvesting materials in molecular bulk heterojunction organic solar cells.-
dc.description.sponsorshipThe reported work is supported by the Interuniversity Attraction Poles Programme (P7/05), initiated by the Belgian Science Policy Office, and the project ORGANEXT (EMR INT4-1.2-2009-04/054), selected in the frame of the operational program INTERREG IV-A Euregio Maas-Rijn. We also acknowledge Hercules for providing the funding for the LTQ Orbitrap Velos Pro mass spectrometer.-
dc.language.isoen-
dc.rightsThis journal is © The Royal Society of Chemistry 2014.-
dc.titleDirect arylation as a versatile tool towards thiazolo- [5,4-d]thiazole-based semiconducting materials-
dc.typeJournal Contribution-
dc.identifier.epage4672-
dc.identifier.issue26-
dc.identifier.spage4663-
dc.identifier.volume12-
local.bibliographicCitation.jcatA1-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1039/c4ob00360h-
dc.identifier.isi000337139800019-
item.fullcitationKUDRJASOVA, Julija; HERCKENS, Roald; PENXTEN, Huguette; ADRIAENSENS, Peter; LUTSEN, Laurence; VANDERZANDE, Dirk & MAES, Wouter (2014) Direct arylation as a versatile tool towards thiazolo- [5,4-d]thiazole-based semiconducting materials. In: ORGANIC & BIOMOLECULAR CHEMISTRY, 12 (26), p. 4663-4672.-
item.accessRightsRestricted Access-
item.contributorKUDRJASOVA, Julija-
item.contributorHERCKENS, Roald-
item.contributorPENXTEN, Huguette-
item.contributorADRIAENSENS, Peter-
item.contributorLUTSEN, Laurence-
item.contributorVANDERZANDE, Dirk-
item.contributorMAES, Wouter-
item.fulltextWith Fulltext-
item.validationecoom 2015-
crisitem.journal.issn1477-0520-
crisitem.journal.eissn1477-0539-
Appears in Collections:Research publications
Files in This Item:
File Description SizeFormat 
Kudrjasova, OBC 2014, 4663.pdf
  Restricted Access
1.08 MBAdobe PDFView/Open    Request a copy
Show simple item record

SCOPUSTM   
Citations

20
checked on Sep 2, 2020

WEB OF SCIENCETM
Citations

32
checked on Apr 15, 2024

Page view(s)

210
checked on Jun 13, 2022

Download(s)

178
checked on Jun 13, 2022

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.