The goal of this work is to provide regional T(1) and T(2) values at a field strength of 7 T for the normal mouse brain at 6 weeks and 1 year old. A novel segmented snapshot FLASH sequence was used to measure T(1) in the hippocampus, corpus callosum, and the retrosplenial granular (RSG) cortex; T(2)
Measurement of solute proton spin-lattice relaxation times in water using the 1,3,3,1 sequence
✍ Scribed by S. S. Sankar; P. A. Molé; R. L. Coulson
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 257 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
1H NMR spin-lattice relaxation times (T1) of the N-CH3 proton resonances of phosphocreatine (PCr) and creatine (Cr) in water solutions were obtained using the 1,3,3,1 pulse sequence. These T1 values were equivalent to those obtained in D2O and water using either the conventional inversion-recovery experiment or the 1,3,3,1 pulse sequence. Thus, the 1,3,3,1 sequence of proton NMR can provide an independent means along with phosphorous NMR for assess PCr and for the study of the creatine kinase reaction (PCr + ADP in equilibrium ATP + Cr) in aqueous solutions and perhaps in biological preparations.
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## 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 90° pulses. The use of the sequence is illustrated for a cross‐linked polymeric system which contains composite peaks having bot
## Abstract A new method for measuring spin‐lattice relaxation times and chemical exchange (CE) rate constants in multiple‐site exchanging systems is described. The method, chemical exchange and __T__~1~ measurement using progressive saturation (CUPS), was applied to determine __T__~1~s and analyze