In the above paper the following was omitted: Acknowledgements: The authors wish to thank the Wellcome Trust (049704) for financial support, and EPSRC Mass Spectrometry Service Swansea for analyses. SJS also thanks EPSRC for a studentship.
A 13C NMR spectral examination of α- and β-carbon signal peak heights in some disubstituted arylporphyrins
✍ Scribed by Susanna J. Shaw; Sakthitharan Shanmugathasan; Oliver J. Clarke; Ross W. Boyle; Alan G. Osborne; Christine Edwards
- Book ID
- 102399773
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 106 KB
- Volume
- 05
- Category
- Article
- ISSN
- 1088-4246
- DOI
- 10.1002/jpp.364
No coin nor oath required. For personal study only.
✦ Synopsis
A ^13^ C NMR spectral study of 29 arylporphyrin derivatives is presented. In all of the tetrasubstituted and trisubstituted compounds examined the α- and β-carbons exhibited the expected broadened signals. In complete contrast, the diphenylporphyrins all showed sharp α- and β-carbon peaks which facilitated structural confirmation. These observations have been correlated with differing tautomeric exchange rates.
📜 SIMILAR VOLUMES
A new 13C N M R method based on solvent effects allows the identification of carbon atoms a to a carbonyl group. With a simple change in solvent from CDCl, to CDC1,-dioxane (1:4), the -C absorption for all carbons except those a to the carbonyl group in the compounds under study were displaced to lo