Benzene, 1-azido-4-nitro-

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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
Δfgas93.1 ± 1.2kcal/molCcbFinch, Gardner, et al., 1997 

Condensed 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
Δfsolid73.8 ± 1.0kcal/molCcbFinch, Gardner, et al., 1997 
Quantity Value Units Method Reference Comment
Δcsolid-774.7 ± 1.0kcal/molCcbFinch, Gardner, et al., 1997 

Reaction 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

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Individual Reactions

Benzene, 1-azido-4-nitro- + endo-Dicyclopentadiene = C16H16N4O2

By formula: C6H4N4O2 + C10H12 = C16H16N4O2

Quantity Value Units Method Reference Comment
Δr-36.1kcal/molCmSamuilov, Movchan, et al., 1985solid phase; solvent: Chlorobenzene

Pyrrolidine, 1-(1-cyclohexen-1-yl)- + Benzene, 1-azido-4-nitro- = C16H21O2

By formula: C10H17N + C6H4N4O2 = C16H21O2

Quantity Value Units Method Reference Comment
Δr-24.kcal/molCmSamuilov, Movchan, et al., 1985solid phase; solvent: Toluene

References

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Reaction thermochemistry data, Notes

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

Finch, Gardner, et al., 1997
Finch, A.; Gardner, P.J.; Head, A.J.; Xiaoping, W., The enthalpy of formation of 4-nitrophenyl azide, Thermochim. Acta, 1997, 298, 191-194. [all data]

Samuilov, Movchan, et al., 1985
Samuilov, Ya.D.; Movchan, A.I.; Solov'eva, S.E.; Konovalov, A.I., Thermochemical and kinetic study of 1,3-dipolar cycloadditions involving aryl azides and nitrones, Zh. Org. Khim., 1985, 21, 1772-1776. [all data]


Notes

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