N-Phenylmaleimide


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

1,3 Diphenylisobenzofuran + N-Phenylmaleimide = 4,9-Epoxy-1H-benz[f]isoindole-1,3-(2H)-dione, 3a,4,9,9a-tetrahydro-2,4,9-triphenyl-

By formula: C20H14O + C10H7NO2 = C30H21NO3

Quantity Value Units Method Reference Comment
Δr-23.50 ± 0.18kcal/molCmKiselev, Ustyugov, et al., 1977liquid phase; solvent: Dioxane

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: John E. Bartmess

Electron affinity determinations

EA (eV) Method Reference Comment
1.362 ± 0.087IMREPaul and Kebarle, 1989ΔGea(423 K) = -30.0±1 kcal/mol, ΔS = -3±3 eu

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.

Kiselev, Ustyugov, et al., 1977
Kiselev, V.D.; Ustyugov, A.N.; Breus, I.P.; Konovalov, A.I., Kinetic and thermochemical study of the Diels-Alder reaction, Dokl. Phys. Chem. (Engl. Transl.), 1977, 234, 320-322, In original 1089. [all data]

Paul and Kebarle, 1989
Paul, G.; Kebarle, P., Electron Affinities of Cyclic Unsaturated Dicarbonyls: Maleic Anhydrides, Maleimides, and Cyclopentendione, J. Am. Chem. Soc., 1989, 111, 2, 464, https://doi.org/10.1021/ja00184a009 . [all data]


Notes

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