1,3-Butadiene, 1,4-diphenyl-, (E,E)-

• Formula: C₁₆H₁₄
• Molecular weight: 206.2824
• IUPAC Standard InChI: InChI=1S/C16H14/c1-3-9-15(10-4-1)13-7-8-14-16-11-5-2-6-12-16/h1-14H/b13-7+,14-8+ Copy

  
• IUPAC Standard InChIKey: JFLKFZNIIQFQBS-FNCQTZNRSA-N Copy
• CAS Registry Number: 538-81-8
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • 1,4-Diphenylbutadiene-cis,cis
  • (E,Z)-1,4-diphenyl-1,3-butadiene
  • 1,4-Diphenyl-1,3-butadiene
• Other names: trans,trans-1,4-Diphenyl-1,3-butadiene; (E,E)-(C6H5CH=CH)2; (E,E)-1,4-Diphenyl-1,3-butadiene; trans,trans-1,4-Diphenylbutadiene; Benzene, 1,1'-(1,3-butadiene-1,4-diyl)bis-, (E,E)-; 1,3-Butadiene, 1,4-diphenyl-, trans,trans-; 1,4-Diphenyl-trans-1,trans-3-butadiene; 1,4-Diphenyl-1,3-butadiene, trans,trans-; (E,E)-1,4-Diphenylbutadiene; all-trans-Diphenylbutadiene; [(1E,3E)-4-Phenyl-1,3-butadienyl]benzene; (1E,4E)-1,4-Diphenyl-1,3-butadiene; (E,E)-(c6H5Ch=ch2)2
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• Information on this page:
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • References
  • Notes
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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

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
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Enthalpy of sublimation

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

2 +  =

By formula: 2H₂ + C₁₆H₁₄ = C₁₆H₁₈

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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Additional Data

UV/Visible spectrum

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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: Victor Talrose, Alexander N. Yermakov, Alexy A. Usov, Antonina A. Goncharova, Axlexander N. Leskin, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina

Spectrum

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Additional Data

References

Go To: Top, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Mass spectrum (electron ionization), UV/Visible spectrum, Notes

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

Coops, Hoijtink, et al., 1953
Coops, J.; Hoijtink, G.J.; Kramer, Th.J.E.; Faber, A.C., Thermochemical investigations on arylethenes. II. Heats of combustion of some para and orthotolylethenes and phenylbutadienes, Rec. Trav. Chim. Pays/Bas, 1953, 72, 765. [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]

Coates and Sutton, 1948
Coates, G.E.; Sutton, L.E., The heats of formation of the -N=N- and >C=N- bonds, J. Chem. Soc., 1948, 1187-1196. [all data]

Ott, 1928
Ott, E., Nachtrage zu der Untersuchung uber die Habhydrierung der Acetylen-Binding und die Abhangigkeit der Konfiguration der entstehenden Athylen-Verbin-dungen von der Reaktionsgeschwindigkeit, Ber., 1928, 61, 2119-2123. [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]

Berry, Lipsky, et al., 1956
Berry, P.J.; Lipsky, S.; Burton, M., Radiation-Induced Luminescence Part 2 - The Effect of Oxygen and Bromobenzene, Trans. Faraday Soc., 1956, 52, 311. [all data]

Dombrovsky and Terent'ev, 1956
Dombrovsky, A.V.; Terent'ev, A.P., Haloarylation of Undaturated Compounds with Aromatic Diazo Compounds I. Reaction of Phenyldiazonium Chloride and Bromidw with 1,3-Butadiene and Some Transformations of 4-Chloro-1-phenyl-2-butene, Zh. Obshch. Khim., 1956, 26, 2776-82. [all data]

Cram and Steinberg, 1951
Cram, D.J.; Steinberg, H., J. Am. Chem. Soc., 1951, 73, 5691. [all data]

Hofer and Peebles, 1951
Hofer, L.J.; Peebles, W.C., X-Ray Diffraction Patterns of Solid Aromatic Hydrocarbons, Anal. Chem., 1951, 23, 690. [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]

Timmons, 1966
Timmons, C.J., UV atlas of organic compaunds, 1966, 2, D10/36. [all data]

Notes

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• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point
  ΔcH°solid	Enthalpy of combustion of solid at standard conditions
  ΔrH°	Enthalpy of reaction at standard conditions
  ΔsubH	Enthalpy of sublimation

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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