## Abstract Carbon‐13 NMR spectra of pyridine have been observed by using the slow scan technique in the absorption mode. The long range coupling constants between carbon‐13 and protons have been obtained and assigned by the isotope substitution method.
Long-range proton–carbon coupling constants in conformational analysis of oligosaccharides
✍ Scribed by Torgny Rundlöf; Alexandra Kjellberg; Charlotta Damberg; Toshiaki Nishida; Göran Widmalm
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 269 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Long-range heteronuclear coupling constants, 3J(C,H), were measured across glycosidic linkages in b-linked disaccharides and also for vicinally disubstituted trisaccharides. One-dimensional multiple-site 13C excitation experiments using Hadamard spectroscopy and band-selective 1H decoupling during the acquisition period were used in conjunction with pulsed Ðeld gradients for coherence selection in the 1H detected experiment. For one dihedral angle the 3J(C,H) value could only be unambiguously determined utilizing the band-selective 1H decoupling. The 2D EXSIDE was also used for the measurement of 3J(C,H) values and the results showed excellent agreement with those of the 1D measurements. The inÑuence of solvent, water and waterÈdimethyl sulfoxide (7 : 3), on conformation was investigated, but showed only small changes in 3J(C,H) values. In general, the long-range heteronuclear coupling constants related to the / dihedral angles (3.6È4.3 Hz) were smaller than those of the t dihedral angles (4.3È5.3 Hz). A comparison with 3J(C,H) values from Monte Carlo or Langevin dynamics simulations showed better agreement for the t dihedral angles than for the / dihedral angles as calculated using a Karplus relationship.
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