Thermochemistry of some alkylsubstituted anthracenes

被引:35
作者
da Silva, MARV [1 ]
Amaral, LMF [1 ]
Santos, AFLOM [1 ]
Gomes, JRB [1 ]
机构
[1] Univ Porto, Ctr Invest Quim, Dept Chem, Fac Sci, P-4169007 Oporto, Portugal
关键词
standard molar enthalpy of formation; standard molar enthalpy of sublimation; combustion calorimetry; Knudsen-effusion technique; vapour pressures; 9-methylanthracene; 2-ethylanthracene; 9,10-dimethylanthracene;
D O I
10.1016/j.jct.2005.06.001
中图分类号
O414.1 [热力学];
学科分类号
摘要
The standard (p(o) = 0.1 MPa) molar enthalpies of combustion, Delta H-c(m)o, for crystalline 9-methylanthracene, 2-ethylanthracene. and 9,10-dimethylanthracene were determined, at the temperature 298.15 K. using a static bomb combustion calorimeter. For these compounds, the standard molar enthalpies of sublimation, Delta(g)(cr) H-m(o), at T = 298.15 K were derived by the Clausius-Clapeyron equation, from the temperature dependence of the vapour pressures of these compounds, measured by the Knudsen-effusion technique. The results were as follows: [GRAPHICS] These values were used to derive the standard molar enthalpies of formation of the compounds in their crystalline and gaseous phases, respectively. The derived standard molar enthalpies of formation, in the gaseous state, are analysed in terms of enthalpic increments and interpreted in terms of molecular structure. Using estimated values for the heat capacity differences between the gas and the crystal phases of the studied compounds, the standard (p(o) = 0.1 MPa) molar enthalpies, entropies, and Gibbs energy of sublimation, at T = 298.15 K, were derived. Additionally, standard enthalpies of formation were estimated by computations based on density-functional theory. The estimated values are in excellent agreement with experimental data. (C) 2005 Elsevier Ltd. All rights reserved.
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页码:367 / 375
页数:9
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