Hyperconjugation Controls One-Bond Carbon–Tin Coupling Constants in Anomeric Tin Compounds: A Theoretical Study

One-bond ¹¹⁹Sn-¹³C couplings in organostannanes are sensitive to local stereoelectronic effects, yet quantitative rules linking hyperconjugation to ¹<i>J</i>(Sn-C) remain limited, especially at anomeric centers. We combine DFT studies with NBO analysis across 77 cyclic scaffolds, including matched axial/equatorial (α/β) anomeric pairs, to relate antiperiplanar donor → σ*_(C-_Sn) delocalization to ¹<i>J</i>(Sn-C). Validation against ¹<i>J</i>(C-H) benchmarks reproduces Perlin-type axial/equatorial differences and the classical reversal in 1,3-dithianes. ¹<i>J</i>(Sn-C) scales with the magnitude of donation. Pairwise comparisons are equally diagnostic: across 27 α/β (axial/equatorial) pairs, equatorial isomers show larger couplings in 92% of cases, and Δ<i>J</i> correlates with Δdonation, rationalizing the β > α hierarchy. Ring-size controls reveal a geometric signature consistent with known ring size relationships with coupling constants: as the size of the ring increases, ¹<i>J</i>(C-H) decreases. Incorporation of sulfur in the ring can cause the β > α ¹<i>J</i>(Sn-C) behavior observed in most other cyclic scaffolds to invert with axial ¹<i>J</i>(Sn-C) being greater than equatorial ¹<i>J</i>(Sn-C). A single-parameter empirical scaling (<i>J</i>(corr) = -1.419·<i>J</i>(calc)) improves absolute agreement with experiment without perturbing trends and brings negative calculated ¹<i>J</i>(Sn-C) to the experimentally derived positive ¹<i>J</i>(Sn-C). Collectively, these results deliver a practical, mechanistic framework for predicting tin-carbon coupling constants and assigning the anomeric configuration in anomeric organotin compounds.