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HEATS OF COMBUSTION, FORMATION, AND HYDROGENATION OF 14 SELECTED CYCLOMONOÖLEFIN HYDROCARBONS1

Cite this: J. Phys. Chem. 1961, 65, 3, 476–480
Publication Date (Print):March 1, 1961
https://doi.org/10.1021/j100821a022
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    Cited By

    This article is cited by 28 publications.

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    2. Eugene Paulechka and Andrei Kazakov . Efficient DLPNO–CCSD(T)-Based Estimation of Formation Enthalpies for C-, H-, O-, and N-Containing Closed-Shell Compounds Validated Against Critically Evaluated Experimental Data. The Journal of Physical Chemistry A 2017, 121 (22) , 4379-4387. https://doi.org/10.1021/acs.jpca.7b03195
    3. Julia P. Baker . Combining Molecular Modeling with 13C and DEPT NMR Spectroscopy To Examine the Dehydration of 1-Methylcyclohexanol. 2016, 99-106. https://doi.org/10.1021/bk-2016-1221.ch007
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    5. Ricardo Morales and, Francisco Zaera. Thermal Chemistry of 1-Methyl-1-cyclohexene and Methylene Cyclohexane on Pt(111) Single-Crystal Surfaces. The Journal of Physical Chemistry C 2007, 111 (49) , 18367-18375. https://doi.org/10.1021/jp077240m
    6. Sergey P. Verevkin,, Dirk Wandschneider, and, Andreas Heintz. Determination of Vaporization Enthalpies of Selected Linear and Branched C7, C8, C9, C11, and C12 Monoolefin Hydrocarbons from Transpiration and Correlation Gas-Chromatography Methods. Journal of Chemical & Engineering Data 2000, 45 (4) , 618-625. https://doi.org/10.1021/je990297k
    7. W. V. Steele,, R. D. Chirico,, S. E. Knipmeyer,, A. Nguyen,, N. K. Smith, and, I. R. Tasker. Thermodynamic Properties and Ideal-Gas Enthalpies of Formation for Cyclohexene, Phthalan (2,5-Dihydrobenzo-3,4-furan), Isoxazole, Octylamine, Dioctylamine, Trioctylamine, Phenyl Isocyanate, and 1,4,5,6-Tetrahydropyrimidine. Journal of Chemical & Engineering Data 1996, 41 (6) , 1269-1284. https://doi.org/10.1021/je960093t
    8. Anita Rágyanszki, Béla Fiser, Edward Lee‐Ruff, Joel F. Liebman. Strained Small Nitrogen Heterocycles‐Azabicyclobutanes and Azirines. ChemistrySelect 2023, 8 (26) https://doi.org/10.1002/slct.202301405
    9. Robert J. Meier, Paul R. Rablen. Group Contribution Revisited: The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy” Part IV. Thermo 2023, 3 (2) , 289-308. https://doi.org/10.3390/thermo3020018
    10. Ari F. Fischer, Enrique Iglesia. The nature of “hydrogen spillover”: Site proximity effects and gaseous intermediates in hydrogenation reactions mediated by inhibitor-scavenging mechanisms. Journal of Catalysis 2023, 420 , 68-88. https://doi.org/10.1016/j.jcat.2022.11.013
    11. Detlev Conrad Mielczarek, Chourouk Nait Saidi, Patrice Paricaud, Laurent Catoire. Generalized Prediction of Enthalpies of Formation Using DLPNO‐CCSD(T) Ab Initio Calculations for Molecules Containing the Elements H, C, N, O, F, S, Cl, Br. Journal of Computational Chemistry 2019, 40 (6) , 768-793. https://doi.org/10.1002/jcc.25763
    12. Rui C. Santos, João P. Leal. A Review on Prediction Methods for Molar Enthalpies of Vaporization of Hydrocarbons: The ELBA Method as the Best Answer. Journal of Physical and Chemical Reference Data 2012, 41 (4) https://doi.org/10.1063/1.4754596
    13. Joel F. Liebman, Torkil Holm, Suzanne W. Slayden. The Thermochemistry of Organomagnesium Compounds. 2009https://doi.org/10.1002/9780470682531.pat0401
    14. Frank Schaffer, Sergey P. Verevkin, Hans‐Jürgen Rieger, Hans‐Dieter Beckhaus, Christoph Rüchardt. Geminal Substituent Effects, 15. Enthalpies of Formation of a Series of Fluorinated Hydrocarbons and Strain‐Free Group Increments to Assess Polar and Anomeric Stabilization and Strain. Liebigs Annalen 1997, 1997 (7) , 1333-1344. https://doi.org/10.1002/jlac.199719970709
    15. Nazih A. Noureldin, Donald G. Lee. THE GASIFICATION OF SASKATCHEWAN LIGNITE. Fuel Science and Technology International 1995, 13 (1) , 87-106. https://doi.org/10.1080/08843759508947666
    16. B.V. Lebedev, N.N. Smirnova, V.G. Vasil'ev, Ye.N. Kropacheva, L.A. Myagkova. Thermodynamics of an alternating ethylene-butadiene copolymer in the range of 0–333 K. Polymer Science U.S.S.R. 1990, 32 (5) , 1009-1014. https://doi.org/10.1016/0032-3950(90)90240-7
    17. Boris V. Lebedev, Natal'ya N. Smirnova, Tat'yana G. Kulagina. Enthalpy, entropy and gibbs energy in bulk polymerization of cyclohexene with ring‐opening between 0 and 330 K at standard pressure. Die Makromolekulare Chemie, Rapid Communications 1988, 9 (11) , 781-784. https://doi.org/10.1002/marc.1988.030091111
    18. J.A Draeger, R.H Harrison, W.D Good. Chemical thermodynamic properties of molecules that undergo inversion I. Aniline, methylamine, cyclopropylamine, and cyclopentene. The Journal of Chemical Thermodynamics 1983, 15 (4) , 367-376. https://doi.org/10.1016/0021-9614(83)90066-6
    19. E.Alexander Hill, Marion M. Myers. Cyclization of the Grignard reagent from 5-chloro-3-methyl-1-hexene; a reversible organomagnesium rearrangement. Journal of Organometallic Chemistry 1979, 173 (1) , 1-13. https://doi.org/10.1016/S0022-328X(00)91230-0
    20. James L. Jensen. Heats of Hydrogenation: A Brief Summary. 1976, 189-228. https://doi.org/10.1002/9780470171912.ch7
    21. D. N. Andreevskii, Z. A. Radyuk, A. D. Peshchenko. Method of ?'similar?' structures?' in the thermodynamics of the methylene cycloalkanes C3-C5. Journal of Structural Chemistry 1976, 17 (1) , 40-45. https://doi.org/10.1007/BF00748390
    22. Adulbert Maercker, Reinhart Geuβ. Umlagerung cyclischer Allylcarbinyl‐Anionen: Ringverengung auf Grund von Stabilitätsunterschieden zwischen primären und sekundären Grignard‐Verbindungen. Chemische Berichte 1973, 106 (3) , 773-797. https://doi.org/10.1002/cber.19731060307
    23. Von Dietmar Kranz, Manfred Beck. Polymerisationsenthalpie der ringöffnenden polymerisation von cyclopenten (CPE) zu trans‐polypentenamer (TPR). Die Angewandte Makromolekulare Chemie 1972, 27 (1) , 29-35. https://doi.org/10.1002/apmc.1972.050270102
    24. V.I. Kleiner, B.A. Krentsel, L.L. Stotskaya. On features of ionic coordination polymerization of vinyl cyclohexane. European Polymer Journal 1971, 7 (12) , 1677-1692. https://doi.org/10.1016/0014-3057(71)90070-X
    25. M.P. Kozina, L.P. Timofeeva, S.M. Skuratov, N.A. Belikova, E.M. Milvitskaya, A.F. Platé. The enthalpies of combustion of some bicyclic compounds. The Journal of Chemical Thermodynamics 1971, 3 (4) , 563-570. https://doi.org/10.1016/S0021-9614(71)80040-X
    26. Adalbert Maercker, Reinhart Geuss. Ring Contraction on Rearrangement of 3‐Cyclohexenyl Grignard Compounds. Angewandte Chemie International Edition in English 1970, 9 (11) , 909-909. https://doi.org/10.1002/anie.197009091
    27. Robert E. Winters, Jerome H. Collins. Mass spectrometric studies of structural isomers—II: Mono‐and bicyclic C 6 H 10 molecules. Organic Mass Spectrometry 1969, 2 (3) , 299-308. https://doi.org/10.1002/oms.1210020308
    28. M. Geisel, C. A. Grob, R. A. Wohl. Struktur und Mechanismus bei Fragmentierungsreaktionen 1. Teil. Die stereoisomeren 10‐Chlor‐decahydro‐isochinoline. Fragmentierungsreaktionen, 23. Mitteilung. Helvetica Chimica Acta 1969, 52 (8) , 2206-2215. https://doi.org/10.1002/hlca.19690520804

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