## Abstract ^1^H NMR simultaneous editing of ^13^C‐coupled and ^13^C‐uncoupled methyl protons resonance, using the selection of double quantum coherences by a gradient pulse, was analyzed __in vitro__ and demonstrated __in situ on__ the hindlimb of an exercised rat model postmortem. __In vitro__ ca
Methylene-Only Subspectra in 13C CPMAS Using a New Double Quantum Filtering Sequence
✍ Scribed by Paolo Rossi; Raju Subramanian; Gerard S. Harbison
- Book ID
- 102599325
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 82 KB
- Volume
- 141
- Category
- Article
- ISSN
- 1090-7807
No coin nor oath required. For personal study only.
✦ Synopsis
Methodology for the assignment of 13 C CPMAS spectra is still in its infancy. Previous methods of CPMAS spectral editing have utilized differences in the strength of the 13 C-1 H dipolar interaction or the rate and spin thermodynamics of crosspolarization from protons to carbon, to differentiate between quaternary, tertiary, and methylene carbons. We introduce a different approach, which is based on the fact that double-quantum coherence develops between the protons of a methylene group considerably faster than between most other proton spin pairs in an organic solid. We generate this coherence, filter it, convert it back to single quantum, and then crosspolarize selectively to carbon, followed by a short period of reversed crosspolarization to null out unwanted coherence generated from longer distance spin pairs. The sequence has been named DQCP. While the signal-to-noise of this method is poorer than ordinary CP, it is comparable to previous methods for generating methylene-only spectra, and the technique is straightforward and easy to implement.
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