1,3-Dioxane,2,4,6-trimethyl-,(2α,4α,6β)-

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Gas phase thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Quantity Value Units Method Reference Comment
Δfgas-106.8 ± 0.8kcal/molCcbPihlaja and Heikkila, 1967 

Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DRB - Donald R. Burgess, Jr.

Quantity Value Units Method Reference Comment
Δvap10.3 ± 0.3kcal/molVPihlaja and Heikkila, 1967ALS
Δvap10.3kcal/molN/APihlaja and Heikkila, 1967DRB

Gas phase ion energetics data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Appearance energy determinations

Ion AE (eV) Other Products MethodReferenceComment
C6H11O2+9.448 ± 0.002CH3EIPihlaja and Jalonen, 1971 

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Pihlaja and Heikkila, 1967
Pihlaja, K.; Heikkila, J., The configurations of isomeric 2,2,4,6-tetramethyl-1,3-dioxanes, Acta Chem. Scand., 1967, 21, 2430-2434. [all data]

Pihlaja and Jalonen, 1971
Pihlaja, K.; Jalonen, J., Appearance potentials determined by the electron-impact method as an analytical aid in the evaluation of conformational energies and clarification of ring conformation-I: Appearance potentials of the [M-R]+ ions formed in the primary fragmentation of stereoisomeric 1,3-dioxans. A direct route to conformational energies, Org. Mass Spectrom., 1971, 5, 1363. [all data]


Notes

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