Anomeric effect on geminal and vicinal JHH NMR coupling constants

Cláudio F. Tormena, Roberto Rittner, Rubén H. Contreras, Juan E. Peralta

Research output: Contribution to journalArticlepeer-review

33 Scopus citations


Trends for geminal (2JHH) and vicinal ( 3JHH) nuclear magnetic resonance indirect spin-spin coupling constants, SSCCs, for 2-methylthiirane (5) and 2-methyloxirane (6) are studied both from experimental and theoretical points of view to determine the influence of hyperconjugative interactions on these couplings. These two analogous compounds were chosen because it was expected that they exhibit quite different anomeric effects. Hyperconjugative interactions are investigated using the "natural bond orbital" method. Coupling constants are calculated within the density functional theory including all four scalar contributions, that is, the Fermi contact, the spin-dipolar, and the paramagnetic and diamagnetic spin-orbital contributions. Solvent dielectric effects are taken into account using Tomasi's polarizable continuum model. Results for geminal couplings are consistent with linear correlations connecting 2J HH with the coupling pathway occupation numbers taken from the literature. The present analysis suggests that both 2JHH and 3JHH coupling constants are sensitive probes to gauge the anomeric effect, as well as other hyperconjugative interactions.

Original languageEnglish
Pages (from-to)7762-7768
Number of pages7
JournalJournal of Physical Chemistry A
Issue number38
StatePublished - Sep 23 2004


Dive into the research topics of 'Anomeric effect on geminal and vicinal JHH NMR coupling constants'. Together they form a unique fingerprint.

Cite this