The energy landscape model of the glass transition has received increasing
attention, due to its potential for providing a thermodynamic interpretatio
n of the dynamics of glass-forming liquids. Herein, the idea that the tempe
rature-dependence of the dynamics near the glass temperature ("fragility")
can be related to thermodynamic properties is tested for polymers. Previous
ly, for several homologous series, we found deviations from a proposed corr
elation between fragility and the heat capacity increment at the glass temp
erature. A survey of 17 polymers likewise indicates no correlation between
these two quantities. More recently, the landscape approach to the dynamics
of glass-formers was extended to a proposal that fragility can be determin
ed a priori from thermodynamic information. However, for the 11 polymers fo
r which sufficient thermodynamic and relaxation data were available, we fin
d that thermodynamic properties bear no relationship to fragility. Thus, it
appears that the status of the glass transition as an important unsolved p
roblem in condensed matter physics remains intact. [S0021-9606(99)51136-7].