Naphthalene, octafluoro

Radchenko, L.G. and Kitiagorodskii, A.I. Vapor pressure and heat of sublimation of naphthalene, biphenyl, octafluoro-naphthalene, decafluorobiphenyl, acenaphthene and a-nitronaphthalene, Zhur. Fiz. Khim., 48 2702-2704, 1974. 

OcUfluorona rfithaleiie Hexafluororbeiuite(V). O tafluoronaphthalene (0.42 mmol) was dissolved in dry trichlorofluoromethane (0.5 mL) at 273 K in a fused silica vessel. A slight excess of rhenium hexafluoride was admitted to the reaction vessel, causing the deep green octafluoro-naphthalene hexafluororhenate(V) to precipitate at the vapor-liquid in-... 

Vapour pressure measurements have led to heats of sublimation of octafluoro-naphthalene and decafluorobiphenyl of 79.3 2.4 and 85.2 2.3 kJ mol , respectively, and the enthalpy of fusion and heat capacity of octafluorotoluene have been obtained from adiabatic calorimetry at 10—365 K the last study yields a triple-point temperature of 207.69 K, and the standard entropy of the ideal gas is 462.6 J K mol i at 298.15 K. Adiabatic calorimetry has also been used to obtain the heat capacities of the three tetrafluorobenzenes at 11— 353 K, and the entropies of the liquids at 298.15 K are 256.1,257.3, and 250.4 J mol- for the 1,2,3,4-, 1,2,3,5-, and 1,2,4,5-isomers, respectively 1,2,3-trichlorotrifluorobenzene fcry-stals) has an entropy of 243.3 J mol at 298.15 K. . Liquid densities from 293 to 490 K have been determined for eight polyfluoroarenes (CeFe, CeFsH, 1,2,3,4-F4C H2, CsFsa. l,3.5-F3C6Cl3, CsFs CFa, CeFsMe, and CeFsOH) and densities up to the critical temperatures have been estimated the effects of dissolved... 

Coliings, J.C. Roscoe. K.P. Thomas, R.Ll. Batsanov, A.S. Stimson. L.M. Howard. J.A.K. Marder. T.B. Arene-perfluoroarene interactions in crystal engineering. Part 3. Single-crystal structures of 1 1 complexes of octafluoro-naphthalene with fused-ring polyaromatic hydrocarbons. New J. Chem. 2001, 25. 1410-1417. 

The arynes 4,5-dehydro- and 4,5,15,16-bis(dehydro)octafluoro[2.2]paracycloph anes, 162 and 163 (Figure 12.2), generated from the corresponding aryl iodide [87] or acetamide [88], have been captured in Diels-Alder reachons by Dolbier and coworkers. Aromatics, such as benzene, naphthalene, anthracene and furan... 

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