cis-Stilbene

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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
Δcliquid-7404.05 ± 0.75kJ/molCcbYates and McDonald, 1971Corresponding Δfliquid = 179.9 kJ/mol (simple calculation by NIST; no Washburn corrections)
Δcliquid-7407.6 ± 1.5kJ/molCcbCoops and Hoijtink, 1950Reanalyzed by Cox and Pilcher, 1970, Original value = -7404.1 ± 0.74 kJ/mol; Corresponding Δfliquid = 183.48 kJ/mol (simple calculation by NIST; no Washburn corrections)

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:
BS - Robert L. Brown and Stephen E. Stein
AC - William E. Acree, Jr., James S. Chickos
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Quantity Value Units Method Reference Comment
Δvap70.5 ± 0.4kJ/molGSCammenga, Emel'yanenko, et al., 2009Based on data from 308. to 343. K.; AC
Δvap50.3 ± 1.0kJ/molN/ABrackman and Plesch, 1952Based on data from 276. to 286. K. See also Cammenga, Emel'yanenko, et al., 2009.; AC
Δvap66. ± 1.kJ/molVBrackman and Plesch, 1952, 2ALS

Reduced pressure boiling point

Tboil (K) Pressure (bar) Reference Comment
356.20.0005Aldrich Chemical Company Inc., 1990BS

Enthalpy of vaporization

ΔvapH (kJ/mol) Temperature (K) Method Reference Comment
66.5388.AStephenson and Malanowski, 1987Based on data from 373. to 428. K.; AC

Enthalpy of sublimation

ΔsubH (kJ/mol) Temperature (K) Method Reference Comment
90.8 ± 0.8329.VWolf and Weghofer, 1938ALS

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

Hydrogen + cis-Stilbene = Bibenzyl

By formula: H2 + C14H12 = C14H14

Quantity Value Units Method Reference Comment
Δr-131.5 ± 0.84kJ/molChydWilliams, 1942liquid phase; solvent: Acetic acid; Reanalyzed by Cox and Pilcher, 1970, Original value = -108.0 ± 8.5 kJ/mol; At 302 K

(E)-Stilbene = cis-Stilbene

By formula: C14H12 = C14H12

Quantity Value Units Method Reference Comment
Δr35. ± 23.kJ/molCphaHerman and Goodman, 1989solid phase; solvent: Acetonitrile/water
Δr19.2 ± 0.4kJ/molCisoSaltiel, Ganapathy, et al., 1987gas phase; At 303.2-461.2 K

cis-Stilbene = (E)-Stilbene

By formula: C14H12 = C14H12

Quantity Value Units Method Reference Comment
Δr-5.0 ± 0.4kJ/molCmBastianelli, Caia, et al., 1991liquid phase; Thermal Isomerization
Δr-12. ± 1.kJ/molCisoFischer, Muszkat, et al., 1968solid phase; solvent: Cyclohexane

Gas Chromatography

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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

Kovats' RI, non-polar column, isothermal

View large format table.

Column type Active phase Temperature (C) I Reference Comment
PackedApiezon L185.1570.Kríz, Popl, et al., 1974 

Kovats' RI, polar column, isothermal

View large format table.

Column type Active phase Temperature (C) I Reference Comment
CapillarySP-1000185.2205.Kríz, Popl, et al., 1974N2; Column length: 50. m; Column diameter: 0.25 mm

References

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

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

Yates and McDonald, 1971
Yates, K.; McDonald, R.S., A thermochemical probe into the mechanism of electrophilic addition to olefins, J. Am. Chem. Soc., 1971, 93, 6297-6299. [all data]

Coops and Hoijtink, 1950
Coops, J.; Hoijtink, G.J., Thermochemical investigations on arylethenes. I. Heats of combustion of phenylethenes, Recl. Trav. Chim. Pays-Bas, 1950, 69, 358-367. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]

Cammenga, Emel'yanenko, et al., 2009
Cammenga, Heiko K.; Emel'yanenko, Vladimir N.; Verevkin, Sergey P., Re-investigation and Data Assessment of the Isomerization and 2,2´-Cyclization of Stilbenes and Azobenzenes «8224», Ind. Eng. Chem. Res., 2009, 48, 22, 10120-10128, https://doi.org/10.1021/ie900800q . [all data]

Brackman and Plesch, 1952
Brackman, D.S.; Plesch, P.H., 406. Some physical properties of cis-stilbene, J. Chem. Soc., 1952, 2188, https://doi.org/10.1039/jr9520002188 . [all data]

Brackman and Plesch, 1952, 2
Brackman, D.S.; Plesch, P.H., Some physical properties of cis-stilbene, J. Chem. Soc., 1952, 2188-21. [all data]

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw, Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2 . [all data]

Wolf and Weghofer, 1938
Wolf, K.L.; Weghofer, H., Uber sublimationswarmen, Z. Phys. Chem., 1938, 39, 194-208. [all data]

Williams, 1942
Williams, R.B., Heats of catalytic hydrogenation in solution. I. Apparatus, technique, and the heats of hydrogenation of certain pairs of stereoisomers, J. Am. Chem. Soc., 1942, 64, 1395-1404. [all data]

Herman and Goodman, 1989
Herman, M.S.; Goodman, J.L., Determination of the enthalpy and reaction volume changes of organic photoreactions using photoacoustic calorimetry, J. Am. Chem. Soc., 1989, 111, 1849-1854. [all data]

Saltiel, Ganapathy, et al., 1987
Saltiel, J.; Ganapathy, S.; Werking, C., The ΔH for thermal trans-stilbene/cis-stilbene isomerization. Do S0 and T1 potential energy curves cross?, J. Phys. Chem., 1987, 91, 2755-2758. [all data]

Bastianelli, Caia, et al., 1991
Bastianelli, C.; Caia, V.; Cum, G.; Gallo, R.; Mancini, V., Thermal isomerization of photochemically synthesized (Z)-9-styrylacridines. An unusually high enthalpy of Z->E conversion for stilbene-like compounds, J. Chem. Soc. Perkin Trans. 2, 1991, 679-683. [all data]

Fischer, Muszkat, et al., 1968
Fischer, G.; Muszkat, K.A.; Fischer, E., Thermodynamic equilibrium between cis- and trans-isomers in stilbene and some derivatives, J. Chem. Soc. B, 1968, 1156-1158. [all data]

Kríz, Popl, et al., 1974
Kríz, J.; Popl, M.; Mostecký, J., Retention indices of biphenyls and diphenylalkanes, J. Chromatogr., 1974, 97, 1, 3-13, https://doi.org/10.1016/S0021-9673(01)97577-6 . [all data]


Notes

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