The background to recent developments in investigations on coal porphy
rins is reviewed. Essentially all the work of the past ten years has b
een with lignites and coals of the humic series. The concentrations of
porphyrins and metalloporphyrins are low (0-ca. 10 mu g g(-1)), which
makes for difficulties in isolation and analysis. The preferred metho
ds of isolation and analysis are summarised. The coal porphyrins diffe
r from the porphyrins from crude oil, oil shale and related deposits i
n a variety of ways which are discussed. The major differences are the
predominance of the etio series over the cycloetio series (DPEP serie
s), the presence of Fe and Ga porphyrins (rather than Ni and VO porphy
rins), and the presence of mesoporphyrin IX in lignite. Recent results
tend to support Treibs' original idea (1935) that, for the coal porph
yrins, both chlorophyll and iron porphyrin (haem) sources are importan
t. The application of a weighted mean molecular mass of the porphyrins
present as a biological marker in determining coal rank (Porphyrin In
dex of Coalification) is illustrated Current activity is directed to t
he isolation and identification of individual iron complexes, and here
a combination of thin layer chromatography and paramagnetically shift
ed H-1-NMR spectroscopy (of dicyanoferrihaems), together with direct c
omparison with authentic haems especially synthesised for the purpose,
has been rewarding.