A modified long-range heteronuclear chemical shift correlation pulse sequence which eliminates modulations of response intensity due to one-bond proton-carbon I'J(CH)] spin couplings is described. The 'decoupling' of one-bond modulation has been accomplished through the use of a bilinear rotational
Modulation of methylene carbon response intensity in long-range heteronuclear 2D NMR chemical shift correlation spectra
โ Scribed by Miguel Salazar; Andrew S. Zektzer; Gary E. Martin
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 367 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
Several recent papers have dealt with the modulation of protonated carbon response intensities in long-range heteronuclear 2D NMR chemical shift correlation spectra. Expressions describing the one-tend modulation of the response intensity of the C-3 methylene resonance of 6,7dimethoxy-3,4dihydroisoquinoline, and the decoupling of this modulation afforded by a BIRD pulse located midway through the A2 refocusing delay, are presented with experimental confirmation. Long-range response intensities are related to the conventional heteronuclear chemical shift correlation spectrum optimized for transfer from the directly attached proton. KEY WORDS two-dimensional NMR 2D-NMR long-range heteronuclear correlation response intensity modulation modulation decoupling.
๐ SIMILAR VOLUMES
BIRD pulses have been shown to provide an effective means of decoupling ow-bond modulation of long-range response intensity. It is not possible to optimize the BIRD pulse effectively wben tbere is a range of one-bond coupling constants. To examine the effects of misoptimization of the fixed delays (