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
Two-Dimensional NMR Studies of Polyene Systems. I. All-trans-Retinal
✍ Scribed by Jacques Wernly; Jürgen Lauterwein
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- German
- Weight
- 663 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
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. From the observed H,H long‐range couplings the assignment of the methyl resonances was possible. 2‐D J‐resolved ^13^C‐NMR separated overlapping C,H‐multiplets and allowed analysis of the C,H long‐range couplings, 2‐D shift‐correlated ^13^C‐NMR related each directly bonded C,H‐pair in this molecule. The potential of 2‐D NMR in resolving and identifying individual resonances in polyene spectra is discussed.
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