Amino acid adsorption on tetraphenyl porphyrin films
In this work, metal free, zinc and copper tetraphenyl porphyrin thin films were employed as substrates to study their interaction with glycine, serine, glutamate, lysine and argynine amino acids in order to investigate the effect of the metallic center and the amino acid characteristics in the adsorption phenomena. The amount of amino acid adsorbed on the films was quantified by using the Ruhemann method. Adsorption isotherms were obtained and analyzed in order to predict the adsorption mechanism for each case. In addition, the morphology of the films was investigated before and after the amino acid immersion by using scanning electron and atomic force microscopies. On the other hand, dynamic contact angle measurements were performed to monitor the spreading phenomena and changes in the hydrophobic nature of the surfaces after the amino acid interaction. From the results, it was observed that the largest deposited amino acid on all three surfaces corresponded to the positively charged compounds, while serine was the lowest adsorbed amino acid in all cases. These results can be attributed to electronic interactions between the amino acids’ lateral chains and the electronic [Formula: see text] distribution of the porphyrin macrocycle ring, and they provide important information regarding the amino acid selectivity of adsorption on tetraphenyl porphyrin films.