A study of the eigenvectors of the low-frequency vibrational modes in crystalline adenosine via high pressure Raman spectroscopy

Abstract

High-pressure Raman spectroscopy has been used to study the eigenvectors and eigenvalues of the vibrational modes of crystalline adenosine at 295 K by evaluating the logarithmic derivative of the vibrational frequency with respect to pressure: . Crystalline samples of molecular materials such as adenosine will have vibrational modes that are localized within a molecular unit (“internal” modes) as well as modes in which the molecular units vibrate against each other (“external” modes). The value of the logarithmic derivative is found to be a diagnostic probe of the nature of the eigenvector of the vibrational modes. Stretching modes which are predominantly internal to the molecule have low logarithmic derivatives while external modes have higher logarithmic derivatives. Particular interest is paid to the low-frequency (≤150 cm⁻¹) modes. Based on the pressure dependence of its logarithmic derivative, a mode near 49 cm⁻¹ is identified as internal mode. The other modes below 400 cm⁻¹ have pressure dependences of their logarithmic derivatives consistent with being either (1) modes which are mainly external, meaning that the molecules of the unit cell vibrate against each other in translational or librational motions (or linear combinations thereof), or (2) torsional or bending modes involving a large number of atoms, mainly within a molecule. The modes above 400 cm⁻¹ all have pressure dependences of their logarithmic derivatives consistent with being mainly internal modes.

Keywords:

• high pressure
• adenosine
• nucleosides
• Raman scattering
• low-frequency modes