## Abstract A method for structure validation based on the simultaneous analysis of a 1D ^1^H NMR and 2D ^1^H^13^C single‐bond correlation spectrum such as HSQC or HMQC is presented here. When compared with the validation of a structure by a 1D ^1^H NMR spectrum alone, the advantage of including a
1D and 2D MAS NMR Spectra of a Dipolar-Coupled Homonuclear Spin-12 Pair
✍ Scribed by Enn Kundla; Ivo Heinmaa; Helgi Kooskora; Endel Lippmaa
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 322 KB
- Volume
- 129
- Category
- Article
- ISSN
- 1090-7807
No coin nor oath required. For personal study only.
✦ Synopsis
An analytical approach based on the average Hamiltonian theory is proposed for efficient calculation of the MAS NMR spectra of a dipolar-coupled homonuclear spin-(1/2) pair. For this purpose a superoperator formalism is developed which allows one to describe the spectra over a broad span of sample spinning rates, including the exact rotational resonances. This formalism can also be applied to the description of 2D polarization exchange spectra, which in many cases turns out to be useful for measuring the coupling strength. The experimental MAS NMR and the 2D spectra of doubly 13C-labeled zinc acetate were found to be in good agreement with the calculated spectra. Copyright 1997 Academic Press. Copyright 1997Academic Press
📜 SIMILAR VOLUMES
## Abstract We report the total assignments of the ^13^C and ^1^H NMR spectra of some 4‐methyl‐2‐oxo‐(2__H__)‐pyrido[1,2‐__a__]pyrimidine and 2‐methyl‐4‐oxo‐(4__H__)‐pyrido[1,2‐__a__]pyrimidine derivatives. The products were characterized by ^1^H and ^13^C NMR and reported data for similar compound
We present novel one-and two-dimensional versions of the 1 -filtered TOCSY experiment. These experiments utilize pulsedfield gradient techniques and INEPT-reverse INEPT magnetization transfer to generate heteronuclear filtering by means of coherence pathway selection. The major advantages of this ap
## Abstract The indirect determination of PP coupling constants and their relative signs in some symmetrical diphosphonates by ^31^P^13^C 2D NMR is introduced. Advantages and disadvantages of this method and others for the determination of the coupling constants of chemically equivalent nuclei ar
## Abstract A combination of solid‐state ^13^C CP/MAS NMR methods was used to study the rates of rotation of the phenyl group in 3,5‐dimethyl‐1‐phenylhex‐1‐yn‐3‐ol. The methods used were __T__~1ρ~ measurements, lineshape analysis and 2D exchange spectroscopy over the temperature range 219–284 K. Th