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http://hdl.handle.net/1942/13293
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DC Field | Value | Language |
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dc.contributor.author | VAN MIERLOO, Sarah | - |
dc.contributor.author | Liégeois, V. | - |
dc.contributor.author | KUDRJASOVA, Julija | - |
dc.contributor.author | Botek, E. | - |
dc.contributor.author | LUTSEN, Laurence | - |
dc.contributor.author | Champagne, B. | - |
dc.contributor.author | VANDERZANDE, Dirk | - |
dc.contributor.author | ADRIAENSENS, Peter | - |
dc.contributor.author | MAES, Wouter | - |
dc.date.accessioned | 2012-03-02T14:28:45Z | - |
dc.date.available | 2012-03-02T14:28:45Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | MAGNETIC RESONANCE IN CHEMISTRY, 50 (5), p. 379-387 | - |
dc.identifier.issn | 0749-1581 | - |
dc.identifier.uri | http://hdl.handle.net/1942/13293 | - |
dc.description.abstract | Four 2,5-bis(5-aryl-3-hexylthiophen-2-yl)thiazolo[5,4-d]thiazole derivatives have been synthesized and thoroughly characterized. The extended aromatic core of the molecules was designed to enhance the charge transport characteristics, and solubilizing hexyl side chains were introduced on the thiophene subunits to enable possible integration of these semiconducting small molecules in printable electronics. Complete elucidation of the chemical structures Q1 by detailed one-dimensional/two-dimensional NMR spectroscopy is described, providing interesting input for chemical shift prediction software as well, because limited experimental data on these types of compounds are currently available. Furthermore, theoretical calculations have assisted experimental observations — giving support for the chemical shift assignment and providing a springboard for future screening and predictions — demonstrating the benefits of a coordinated theoretical–experimental approach. | - |
dc.language.iso | en | - |
dc.rights | Copyright © 2012 John Wiley & Sons, Ltd. | - |
dc.subject.other | NMR; 1H and 13C NMR chemical shift assignment; density functional theory calculations; thiazolo[5,4-d]thiazoles; chemical shift prediction software; printable electronics | - |
dc.title | Combined experimental–theoretical NMR study on 2,5-bis(5-aryl-3-hexylthiophen-2-yl) thiazolo[5,4-d]thiazole derivatives for printable electronics | - |
dc.type | Journal Contribution | - |
dc.identifier.epage | 387 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 379 | - |
dc.identifier.volume | 50 | - |
local.bibliographicCitation.jcat | A1 | - |
local.type.refereed | Refereed | - |
local.type.specified | Article | - |
dc.bibliographicCitation.oldjcat | A1 | - |
dc.identifier.doi | 10.1002/mrc.3812 | - |
dc.identifier.isi | 000303116200008 | - |
item.fulltext | With Fulltext | - |
item.fullcitation | VAN MIERLOO, Sarah; Liégeois, V.; KUDRJASOVA, Julija; Botek, E.; LUTSEN, Laurence; Champagne, B.; VANDERZANDE, Dirk; ADRIAENSENS, Peter & MAES, Wouter (2012) Combined experimental–theoretical NMR study on 2,5-bis(5-aryl-3-hexylthiophen-2-yl) thiazolo[5,4-d]thiazole derivatives for printable electronics. In: MAGNETIC RESONANCE IN CHEMISTRY, 50 (5), p. 379-387. | - |
item.accessRights | Restricted Access | - |
item.validation | ecoom 2013 | - |
item.contributor | VAN MIERLOO, Sarah | - |
item.contributor | Liégeois, V. | - |
item.contributor | KUDRJASOVA, Julija | - |
item.contributor | Botek, E. | - |
item.contributor | LUTSEN, Laurence | - |
item.contributor | Champagne, B. | - |
item.contributor | VANDERZANDE, Dirk | - |
item.contributor | ADRIAENSENS, Peter | - |
item.contributor | MAES, Wouter | - |
crisitem.journal.issn | 0749-1581 | - |
crisitem.journal.eissn | 1097-458X | - |
Appears in Collections: | Research publications |
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File | Description | Size | Format | |
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MRC3812.pdf Restricted Access | 822.71 kB | Adobe PDF | View/Open Request a copy |
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