The adsorption of 10,15,20-tetrakis(4-N-methylpyridiniumyl)porphyrin (
H(2)TMPyP) from aqueous solutions on silica has been studied by reflec
tometry, while order parameters of the orientation distribution of the
adsorbed porphyrins have been obtained by total internal reflection f
luorescence (TIRF). The initial adsorption rate of the positively char
ged porphyrins on the negative surface is transport-controlled. Subseq
uently, the adsorption continues at a lower rate, leading to significa
ntly higher adsorbed amounts in the presence of electrolyte than from
pure water. From a combination of reflectometer and TIRF results it is
found that ordering in the adsorption layer is primarily determined b
y steric and electrostatic interactions between the adsorbed molecules
and not by charge interactions between the surface and the porphyrin
molecules. In the presence of buffer (screening lateral electrostatic
interactions) the H(2)TMPyP molecules are more or less randomly orient
ed at low surface coverage, while, at higher surface coverage or in th
e absence of background electrolyte, a broad orientation distribution
around an angle of ca. 45 degrees between the porphyrin macrocycle and
the surface is found. From TIRF measurements at various solution visc
osities it is found that the orientation of the adsorbed porphyrins do
es not change on the time scale of fluorescence.