N,N-(Dimethyl)thiobenzamide


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
Δfgas136.1 ± 2.8kJ/molCcrRibeiro Da Silva, Souza, et al., 1989 

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
Δfsolid41.3 ± 1.9kJ/molCcrRibeiro Da Silva, Souza, et al., 1989 
Quantity Value Units Method Reference Comment
Δcsolid-5757.0 ± 1.4kJ/molCcrRibeiro Da Silva, Souza, et al., 1989 

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

Quantity Value Units Method Reference Comment
Δvap74. ± 4.kJ/molCBeak, Lee, et al., 1978 
Quantity Value Units Method Reference Comment
Δsub94.8 ± 2.0kJ/molCRibeiro Da Silva, Souza, et al., 1989 

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

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

N,N-(Dimethyl)thiobenzamide = Benzenecarboximidothioic acid, N-methyl-, methyl ester

By formula: C9H11NS = C9H11NS

Quantity Value Units Method Reference Comment
Δr109. ± 0.8kJ/molEqkBeak, Lee, et al., 1978liquid phase

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 as indicated in comments:
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard

Ionization energy determinations

IE (eV) Method Reference Comment
7.70PEBerg, Henriksen, et al., 1982Vertical value; LBLHLM

Mass spectrum (electron ionization)

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Mass spectrum
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Additional Data

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Owner NIST Mass Spectrometry Data Center
Collection (C) 2014 copyright by the U.S. Secretary of Commerce
on behalf of the United States of America. All rights reserved.
Origin F.Larsson ET AL.Acta Chem.Scand.,27,747(1973)
NIST MS number 280178

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References

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, Mass spectrum (electron ionization), Notes

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

Ribeiro Da Silva, Souza, et al., 1989
Ribeiro Da Silva, M.D.M.C.; Souza, P.; Pilcher, G., Enthalpies of combustion of thiobenzamide, N,N-dimethylthiobenzamide, and N,N-diethylthiobenzamide, J. Chem. Thermodyn., 1989, 21, 173-178. [all data]

Beak, Lee, et al., 1978
Beak, P.; Lee, J.-K.; Zeigler, J.M., Equilibration studies: amide-imidate and thioamide-thioimidate functions, J. Org. Chem., 1978, 43, 1536-1538. [all data]

Berg, Henriksen, et al., 1982
Berg, U.; Henriksen, L.; Lerstrup, K.A.; Sandstrom, J., The torsional barrier of the dimethylamino group in N,N-dimethyltellurobenzamide. A comparison with N,N-dimethylbenzamide and its thio and seleno analogues, Acta Chem. Scand., Ser. B, 1982, 36, 19. [all data]


Notes

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