## Abstract ^13^C NMR spinโlattice relaxation times (__T__~1~) and nuclear Overhauser enhancements (ฮท) were measured for dithiarsolanes. The contributions of dipolar (__T__) and spinโrotation (__T__) mechanisms were determined. The __T__~1~ data were analysed to obtain information on the relative o
Cross-Correlated Quadrupolar Spin Relaxation and Carbon-13 Lineshapes in the 13CD2 Spin Grouping
โ Scribed by L.G. Werbelow; G.A. Morris; P. Kumar; J. Kowalewski
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 104 KB
- Volume
- 140
- Category
- Article
- ISSN
- 1090-7807
No coin nor oath required. For personal study only.
โฆ Synopsis
Lineshape calculations are reported for a spin system consisting of a spin-1 2 nucleus scalar-coupled to two magnetically equivalent spin-1 nuclei, e.g., a CD 2 group. It is found that, because of the differential line broadening, the peak height ratio of the five spin-1 2 nucleus transitions is expected to deviate from the integrated intensity ratio of 1:2:3:2:1. The deviation is dependent on the extent of cross-correlation between the two quadrupolar interactions. The theoretical predictions for peak height ratios and for bandshapes are tested for the carbon-13 spectrum of perdeuterated ethylene glycol, and iterative fitting is used to obtain an estimate of the extent of the correlation between the quadrupolar interactions for the two deuterons.
๐ SIMILAR VOLUMES
details of the approach have been published (15), and an In principle, NMR spectroscopy can provide a wealth of application to the study of the side-chain dynamics of an information about molecular dynamics extending over a SH2 domain from phospholipase C-g1 in the presence and wide range of motiona
We present a simple method for extracting interference effects between chemical shift anisotropy (CSA) and dipolar coupling from spin relaxation measurements in macromolecules, and we apply this method to extracting cross-correlation rates involving interference of amide 15N CSA and 15N-1H dipolar c
## Abstract Carbonโ13 NMR relaxation data obtained for methyl groups in two dicyclohexane compounds were used to compare the Woessner and โmodelโfreeโ approaches. It is shown that the extra flexibility offered by the latter leads to a more successful analysis of the data.
To elucidate chiral recognition difference between pairs of enantiomers which interacted with a cellulosic stationary phase of chiral discrimination high performance liquid chromatography (HPLC), 13C NMR spectroscopy was applied for enantiomers of 1phenylethanol, 1-indanol, 1,2,3,4,-tetrahydro-l-nap
## Abstract A pulse sequence is presented which allows measurement of short __T__~1~ values (< 1 s) in solids, avoiding probe damage by the use of saturating sequences of 90ยฐ pulses. The use of the sequence is illustrated for a crossโlinked polymeric system which contains composite peaks having bot