B. Brunetti et V. Piacente, Sublimation enthalpies study for barbituric, tiobarbituric, and selenobarbituric acids from their vapor pressure measurements, J CHEM EN D, 44(4), 1999, pp. 809-812
The vapor pressures for solid barbituric acid and tiobarbituric acid were m
easured by the torsion method; for selenobarbituric acid the vapor pressure
s were measured in both the solid and liquid phases. The results were fit t
o the following linear equations: barbituric acid (solid), log(p/kPa) = (11
.18 +/- 0.20) - (5920 +/- 200)(K/T) (from 392 to 493 K); tiobarbituric acid
(solid), leg(p/kPa) = (10.78 +/- 0.20) - (5770 +/- 200)(K/T) (from 400 to
461 K); selenobarbituric acid (solid), log(p/kPa) = (12.00 +/- 0.20) - (739
3 +/- 200)(WT) (from 449 to 486 K); selenobarbituric acid (liquid), log(p/k
Pa) = (8.33 +/- 0.20) - (5532 +/- 200)(K/T) (from 490 to 557 K). Knudsen me
asurements of the molecular weight of the vapor show that barbituric and ti
obarbituric acids vaporize predominantly in the monomeric form, while the v
apor above selenobarbituric acid is prevalently a dimer. The sublimation en
thalpies at the middle temperatures [Delta(sub)H degrees(442 K) = (113 +/-
4) kJ.mol(-1), Delta(sub)H degrees(430 K) = (110 +/- 4) kJ.mol(-1), and Del
ta(sub)H degrees(466 K) = (141 +/- 4) kJ mol(-1)] for solid barbituric, tio
barbituric and selenobarbituric acids respectively were derived. The enthal
py of vaporization [Delta(vap)H degrees(523 K) = (106 +/- 4) kJ.mol(-1)] an
d the enthalpy effusion [Delta(fus)H degrees(486 K) = 18 kJ mol(-1)] for se
lenobarbituric acid were also derived.