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Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/2426

Title: Synthesis and complete NMR spectral assignment of thiophene-substituted sulfinyl monomers
Authors: HENCKENS, Anja
ADRIAENSENS, Peter
GELAN, Jan
LUTSEN, Laurence
VANDERZANDE, Dirk
Issue Date: 2004
Publisher: JOHN WILEY & SONS LTD
Citation: MAGNETIC RESONANCE IN CHEMISTRY, 42(11). p. 931-937
Abstract: This paper describes the synthesis of thiophene-substituted sulfinyl monomers. It comprises a four-step reaction by which the thiophene unit is built in via Suzuki coupling. These monomers could be used as building blocks for the preparation of conducting polymers via a new concept: the sulfinyl precursor route i.e. via thiophene substituted poly(p-phenylenevinylene) precursors. Furthermore, the complete H-1 and C-13 NMR signal assignment is presented. In addition to being essential for the characterization of the polymers concerned, it offers useful input information for further improvement of chemical shift prediction software. Furthermore, the T-1C relaxation. decay times are demonstrated to have the potential of being a fast and robust criterion for the spectral assignment of analogous monomers.
Notes: Univ Limburg Centrum, Lab Organ & Polymer Chem, Div Chem, B-3590 Diepenbeek, Belgium. IMEC, IMOMEC Div, B-3001 Louvain, Belgium.Gelan, J, Univ Limburg Centrum, Lab Organ & Polymer Chem, Div Chem, Univ Campus, B-3590 Diepenbeek, Belgium.jan.gelan@luc.ac.be
URI: http://hdl.handle.net/1942/2426
DOI: 10.1002/mrc.1455
ISI #: 000224875300004
ISSN: 0749-1581
Category: A1
Type: Journal Contribution
Validation: ecoom, 2005
Appears in Collections: Research publications

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