Title
Structural studies of cyclic ureas: 3. Enthalpy of formation of barbital
Date Issued
01 December 2009
Access level
metadata only access
Resource Type
journal article
Author(s)
Ribeiro da Silva M.d.D.M.C.
Ribeiro da Silva M.A.V.
Freitas V.L.S.
Roux M.V.
Jiménez P.
Temprado M.
Cabildo P.
Claramunt R.M.
Elguero J.
Consejo Superior de Investigaciones Científicas
Abstract
A thermochemical and thermophysical study has been carried out for crystalline barbital [5,5′-diethylbarbituric acid]. The thermochemical study was made by static bomb combustion calorimetry, from which the standard (p{ring operator} = 0.1 MPa) molar enthalpy of formation of the crystalline barbital, at T = 298.15 K, was derived as -(753.0 ± 1.8) kJ · mol-1. The thermophysical study was made by differential scanning calorimetry over the temperature interval (265 to 470) K. A solid-solid phase transition was found at T = 413.3 K. The vapour pressures of the crystalline barbital were measured at several temperatures between T = (355 and 377) K, by the Knudsen mass-loss effusion technique, from which the standard molar enthalpy of sublimation, at T = 298.15 K was derived as (117.3 ± 0.6) kJ · mol-1. The combination of the experimental results yielded the standard molar enthalpy of formation of barbital in the gaseous phase, at T = 298.15 K, as -(635.8 ± 1.9) kJ · mol-1. This value is compared and discussed with our theoretical calculations by several methods (Gaussian-n theories G2 and G3, complete basis set CBS-QB3, density functional B3P86 and B3LYP) by means of atomization and isodesmic reaction schemes. © 2009 Elsevier Ltd. All rights reserved.
Start page
1400
End page
1407
Volume
41
Issue
12
Language
English
OCDE Knowledge area
Química
Scopus EID
2-s2.0-69449092476
Source
Journal of Chemical Thermodynamics
ISSN of the container
10963626
Sponsor(s)
Thanks are due to Gabinete de Relações Internacionais da Ciência e do Ensino Superior (GRICES), Lisbon, Portugal, and Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain for a joint research project GRICES/CSIC. Thanks are due to Fundação para a Ciência e a Tecnologia, F.C.T., Lisbon, Portugal, and to FEDER for financial support to Centro de Investigação em Química da Universidade do Porto (CIQ-U.P.). V.L.S.F. thanks Faculdade de Ciências for a research grant. The Spanish co-authors gratefully acknowledged the support of DGES/MEC (CTQ 2006-02586, CTQ 2006-10178/BQU), CTQ2007-60895/BQU.
Sources of information: Directorio de Producción Científica Scopus