## Abstract The ^1^H and ^13^C NMR spectra of pentalongin, a physiologically active natural product, were completely assigned. Some previous assignments were revised. All ^13^C^1^H coupling constants, both one‐bond and long‐range, were also measured.
Synthesis and complete NMR spectral assignment of thiophene-substituted sulfinyl monomers
✍ Scribed by Anja Henckens; Peter Adriaensens; Jan Gelan; Laurence Lutsen; Dirk Vanderzande
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 147 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1455
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✦ Synopsis
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 ^1^H and ^13^C 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. Copyright © 2004 John Wiley & Sons, Ltd.
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