Vaporization studies on pure (E)-p-dimethylaminoazobenzene (hereafter indicated as DAB) and the DAB-choleic acid (DCADAB) were accomplished by means of the torsion effusion method. The pressure of the vapour in equilibrium with the solid phase was determined for DAB as log P (kPa) = (15.05±0.18)−(6887±500)/T and by the second-law treatment of the vapour pressure data a ΔH°381 = 132±8 kJ mol−1 was obtained for DAB vaporization from the pure compound. Since the tensimetric data of DCADAB lie at the limit of the instrument's working range only a rough value of ΔH°435 = 138 kJ mol−1 was obtained for DAB vaporization from DCADAB. This finding agrees with the strong DAB-DCA interactions found in the DCADAB crystal structure.
Study of the 4:1 inclusion compound between deoxycholic acid and (E)-p-dimethylaminoazobenzene by vapour pressure measurements / Campanelli, Anna Rita; D., Ferro; Pavel, Nicolae Viorel. - In: THERMOCHIMICA ACTA. - ISSN 0040-6031. - STAMPA. - 87:(1985), pp. 231-238. [10.1016/0040-6031(85)85340-5]
Study of the 4:1 inclusion compound between deoxycholic acid and (E)-p-dimethylaminoazobenzene by vapour pressure measurements
CAMPANELLI, Anna Rita;PAVEL, Nicolae Viorel
1985
Abstract
Vaporization studies on pure (E)-p-dimethylaminoazobenzene (hereafter indicated as DAB) and the DAB-choleic acid (DCADAB) were accomplished by means of the torsion effusion method. The pressure of the vapour in equilibrium with the solid phase was determined for DAB as log P (kPa) = (15.05±0.18)−(6887±500)/T and by the second-law treatment of the vapour pressure data a ΔH°381 = 132±8 kJ mol−1 was obtained for DAB vaporization from the pure compound. Since the tensimetric data of DCADAB lie at the limit of the instrument's working range only a rough value of ΔH°435 = 138 kJ mol−1 was obtained for DAB vaporization from DCADAB. This finding agrees with the strong DAB-DCA interactions found in the DCADAB crystal structure.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.