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- W2039593178 endingPage "1406" @default.
- W2039593178 startingPage "1392" @default.
- W2039593178 abstract "Optimized geometries and total energies for 3,4-dihydro-1,2-dioxin (1), 3,6-dihydro-1,2-dioxin (2), 4H-1,3-dioxin (1,3-diox-4-ene, 3), and 2,3-dihydro-1,4-dioxin (1,4-dioxene, 4) were calculated using ab initio 3-21G, 6-31G*, and MP2/6-31G*//6-31G* methods. The half-chair conformers of 1 (C1), 2 (C2), 3 (C1), and 4 (C2) are more stable than their respective planar structures [1 (Cs), 2 (C2v), 3 (Cs), and 4 (C2v)]. Among the four isomers 1–4, the half-chair conformer of 3 is the most stable. It is 53.1, 54.6, and 3.4 kcal mol−1 more stable than 1, 2, and 4, respectively. The largest energy difference (19.0 kcal mol−1) is observed between the half-chair and planar conformers of 2. The boat conformers of 2 and 4 are less stable than their respective half-chair conformers, but are more stable than their planar structures. Hyperconjugative orbital interactions (anomeric effects) contribute to the greater stability of 3(nO(3) →σ*C(2)—O(1), nO(3)→σ*,n O(3)→σ*) and of 4 (nO(1)→ σ*). The ab initio calculated structural features of the half-chair conformations of the dihydrodioxins 1–4 are compared with the half-chair conformations of cyclohexene and the chair conformations of cyclohexane, oxacyclohexane (tetrahydropyran), 1,2-dioxacyclohexane (1,2-dioxane), 1,3-dioxacyclohexane (1,3-dioxane), and 1,4-dioxacyclohexane (1,4-dioxane) © 1997 by John Wiley & Sons, Inc. J Comput Chem 18: 1392–1406, 1997" @default.
- W2039593178 created "2016-06-24" @default.
- W2039593178 creator A5025550033 @default.
- W2039593178 creator A5034747948 @default.
- W2039593178 creator A5052626400 @default.
- W2039593178 creator A5081982395 @default.
- W2039593178 date "1997-08-01" @default.
- W2039593178 modified "2023-09-25" @default.
- W2039593178 title "Ab initio molecular orbital calculations of 3,4-dihydro-1,2-dioxin, 3,6-dihydro-1,2-dioxin, 4H-1,3-dioxin (1,3-diox-4-ene), and 2,3-dihydro-1,4-dioxin (1,4-dioxene)" @default.
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