Benzene, 1,1',1''-(1-ethanyl-2-ylidene)tris-

Data at NIST subscription sites:

NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.


Normal melting point

Go To: Top, References, Notes

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

Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

Tfus (K) Reference Comment
329.3Grovenstein, 1957Uncertainty assigned by TRC = 3. K; TRC
329.Hauser and Hamrick, 1957Uncertainty assigned by TRC = 2. K; TRC
327.Vasil'eva and Tsukervanik, 1957Uncertainty assigned by TRC = 4. K; TRC
324.Zimmerman and Smentowski, 1957Uncertainty assigned by TRC = 3. K; TRC
328.4Hauser, Manyik, et al., 1955Uncertainty assigned by TRC = 2. K; TRC
327.8Coops, Mulder, et al., 1953Uncertainty assigned by TRC = 0.6 K; TRC
327.7Tuot and Guyard, 1947Uncertainty assigned by TRC = 2. K; TRC
328.Zartman and Adkins, 1932Uncertainty assigned by TRC = 4. K; TRC
327.3Smith and Andrews, 1931Uncertainty assigned by TRC = 0.3 K; m.p. with Hg thermometer; TRC
321.15Smith and Andrews, 1931Uncertainty assigned by TRC = 1. K; f.p.with thermocouple; no explanation for low value; TRC

In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products:


References

Go To: Top, Normal melting point, Notes

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

Grovenstein, 1957
Grovenstein, E., J. Am. Chem. Soc., 1957, 79, 4985. [all data]

Hauser and Hamrick, 1957
Hauser, C.R.; Hamrick, P.J., Alkylation of Diphenylmethane with ALkyl Halides by Sodium Amide. Substitution versus β-Elimination. Relative Acidities of Diphenylmethane and Ammonia, J. Am. Chem. Soc., 1957, 79, 3142. [all data]

Vasil'eva and Tsukervanik, 1957
Vasil'eva, N.V.; Tsukervanik, I.P., Condensation of Trichloroethylene with Benzene, Zh. Obshch. Khim., 1957, 27, 1767. [all data]

Zimmerman and Smentowski, 1957
Zimmerman, H.E.; Smentowski, F.J., Carbanion Rearrangements I., J. Am. Chem. Soc., 1957, 79, 5455. [all data]

Hauser, Manyik, et al., 1955
Hauser, C.R.; Manyik, R.; Brasen, W.R.; Bayless, J. Org. Chem., 1955, 20, 1119. [all data]

Coops, Mulder, et al., 1953
Coops, J.; Mulder, D.; Dienske, J.W.; Smittenberg, J., Thermochemical investigations on arylethanes I. Heats of combustion of phenylethanes., Rec. Trav. Chim. Pays/Bas, 1953, 72, 785. [all data]

Tuot and Guyard, 1947
Tuot, M.; Guyard, M., Bull. Soc. Chim. Fr., 1947, 1947, 1086-96. [all data]

Zartman and Adkins, 1932
Zartman, W.H.; Adkins, H., J. Am. Chem. Soc., 1932, 54, 1668. [all data]

Smith and Andrews, 1931
Smith, R.H.; Andrews, D.H., Thermal Energy Studies I. Phenyl Derivatives of Methane, Ethane and Some Related Compounds, J. Am. Chem. Soc., 1931, 53, 3644. [all data]


Notes

Go To: Top, Normal melting point, References