Fourier-transform Raman and infrared spectroscopic analysis of dipyrrinones and mesobilirubins

Spectrochim Acta A Mol Biomol Spectrosc. 2001 Dec;57(14):2737-43. doi: 10.1016/s1386-1425(01)00468-1.

Abstract

The Fourier-transform Raman (FT-Raman), infrared (FT-IR), and UV-visible absorption spectra of four dipyrrinones and two mesobilirubins have been investigated in the solid state and in CH2Cl2 solutions. A detailed spectral analysis, assignment and discussion of these spectra are presented. The bands at 1735-1738, 1691-1707 and 1359-1377 cm(-1) which were assigned to the stretching vibrations of the C-O-C and C-O-H and symmetric deformation of C-H bonds, respectively, can act as a marker to distinguish the compounds of this class. The striking differences between the spectra of the compounds suggest that mesobilirubin XIIIalpha is tending to adopt as ridge-tile conformation, rather than linear conformation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bilirubin / analogs & derivatives*
  • Bilirubin / chemistry*
  • Molecular Structure
  • Pyrroles / chemistry*
  • Spectrophotometry, Ultraviolet
  • Spectroscopy, Fourier Transform Infrared
  • Spectrum Analysis, Raman

Substances

  • 2,7,9-trimethyl-8-ethoxycarbonylethylpyrromethenone
  • Pyrroles
  • kryptopyrrolmethene
  • xanthobilirubic acid
  • Bilirubin