## Abstract Two‐dimensional (2‐D) NMR results are presented for all‐__trans__‐retinal. 2‐D __J__‐resolved ^1^H‐NMR separated the multiplets of the olefinic protons and accurately determined their chemical shifts. 2‐D shift‐correlated ^1^H‐NMR gave the connectivities between scalar coupled protons.
Two-dimensional NMR studies of polyene systems. II. β-carotene
✍ Scribed by Jacques Wernly; JÜRgen Lauterwein
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 705 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Two-dimensional NMR results are presented for B-carotene in chloroform. J-resolved 'H NMR spectroscopy allows the accurate determination of the chemical shifts and coupling constants for the ole6nic protons. In order to obtain su5uent signal intensity in the projection spectrum for the H-C-7, H-C-10 and H-C-14 protons, spin decoupling of the long-range coupled methyl and methylene protons was necessary. 'H,=C chemical shift-correlated NMR spectroscopy gave a relationship between the directly bonded ole6nic CH pairs. Cross-sections through each -C chemical shift allowed the assignment of the carbon resonances. Simulation of the cross-sections was possible when the 180" carbon pulse was removed in the standard pulse sequence. It is shown that, under these conditions, the cross-sections correspond to partial =CH satellite spectra.
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