Structural determination of organic compounds
Description
This paper reports that the current methods available in high-field NMR spectroscopy are such that the tridimensional structure determination of any rigid molecule containing only carbon and hydrogen atoms may be achieved. The connectivities between carbon-carbon, carbon-hydrogen, and hydrogen-hydrogen atoms are determined by multipulse and two-dimensional (2D) experiments. These connectivity patterns or maps allow a step-by-step reconstruction of the molecular structures. From the carbon-carbon connectivity map, the carbon framework of the molecule is obtained, whereas the carbon-hydrogen pattern allows determination of the positions of the hydrogen atoms on their corresponding carbon atoms. High-field spectrometers are then necessary to remove fortuitous degeneracy and to reduce the proton spectra to a nearly first-order one, allowing an easy measurement of the chemical shifts and the coupling constants
Additional details
Publishing Information
- Publisher
- Marcel Dekker Inc.
- Imprint Place
- New York, NY (United States)
- ISBN
- 0-8247-8332-8
- Imprint Title
- Modern NMR techniques and their application in chemistry
- Imprint Pagination
- 654 p.
- Journal Page Range
- p. 371-426.
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 24017930
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CHEMICAL SHIFT; COUPLING CONSTANTS; CRYSTAL STRUCTURE; MHZ RANGE 100-1000; NUCLEAR MAGNETIC RESONANCE; ORGANIC COMPOUNDS; SOLVENTS; STEREOCHEMISTRY; TEMPERATURE DEPENDENCE
- Descriptors DEC
- FREQUENCY RANGE; MAGNETIC RESONANCE; MHZ RANGE; RESONANCE