Pauling, Linus (1930) The Rotational Motion of Molecules in Crystals. Physical Review, 36 (3). pp. 430-443. ISSN 0031-899X. http://resolver.caltech.edu/CaltechAUTHORS:PAUpr30
See Usage Policy.
Use this Persistent URL to link to this item: http://resolver.caltech.edu/CaltechAUTHORS:PAUpr30
It is shown by the discussion of the wave equation for a diatomic molecule in a crystal that the motion of the molecule in its dependence on the polar angles θ and φ may approach either one of two limiting cases, oscillation and rotation. If the intermolecular forces are large and the moment of inertia of the molecule is large (as in I2, for example), the eigenfunctions and energy levels approach those corresponding to oscillation about certain equilibrium orientations; if they are small (as in H2), the eigenfunctions and energy levels may approximate those for the free molecule, even in the lowest quantum state. It is found in this way that crystalline hydrogen at temperatures somewhat below the melting point is a nearly perfect solid solution of symmetric and antisymmetric molecules, the latter retaining the quantum weight 3 for the state with j=1 as well as the spin quantum weight 3. This leads to the expression S=-nARlognA-(1-nA)Rlog(1-nA)+nARlog9+Str, in which Str is the translational entropy, for the entropy of the solid at these temperatures. At lower temperatures (around 5°K) the solid solution becomes unstable relative to phases of definite composition, and the entropy falls to S=nARlog3+Str, the entropy of mixing and of the quantum weight 3 for j=1 being lost at the same time. Only at temperatures of about 0.001°K will the spin quantum weight entropy be lost. Gradual transitions covering a range of temperatures and often unaccompanied by a change in crystal structure, reported for CH4, HCl, the ammonium halides, and other substances, are interpreted as changes from the state in which most of the molecules are oscillating to that in which most of them are rotating. The significance of molecular rotation in the interpretation of other phenomena is also discussed.
|Additional Information:||©1930 The American Physical Society Received 7 May 1930 I acknowledge with gratitude the inspiration and assistance received through conversations with Professor W.F. Giauque of the Chemistry Department of the University of California.|
|Usage Policy:||No commercial reproduction, distribution, display or performance rights in this work are provided.|
|Deposited By:||Archive Administrator|
|Deposited On:||04 Jan 2007|
|Last Modified:||26 Dec 2012 09:27|
Repository Staff Only: item control page