Electrocatalysis aromatics

Pd then plates onto the terrace sites (Fig. 11). On Au(lll), only terrace sites are exposed. In this manner, the surface electrochemical properties of the subject compounds at the steps and on the terraces surfaces can be compared. It should be recalled that aromatic molecules chemisorb only on Pd but not on Au " the expectation is then that the lower the Pd coverage, the lower the amount (and subsequent electrocatalysis) of chemisorbed benzene. 

There are many substances which would appear to be good candidates for LC-EC from a thermodynamic point of view but which do not behave well due to kinetic limitations. Johnson and co-workers at Iowa State University used some fundamental ideas about electrocatalysis to revolutionize the determination of carbohydrates, nearly intractable substances which do not readily lend themselves to ultraviolet absorption (LC-UV), fluorescence (LC-F), or traditional DC amperometry (LC-EC) [2], At the time that this work began, the EC of carbohydrates was more or less relegated to refractive index detection (LC-RI) of microgram amounts. The importance of polysaccharides and glycoproteins, as well as traditional sugars, has focused a lot of attention on pulsed electrochemical detection (FED) methodology. The detection limits are not competitive with DC amperometry of more easily oxidized substances such as phenols and aromatic amines however, they are far superior to optical detection approaches. 

The electrochemical polymerization of Ti-electron-rich aromatics, such as aniline, pyrrole and thiophene, to obtain electrically conducting polymers is well-known. Some reports describe the polymerization of amino-, pyrrolyl- and hydroxy-substituted tetraphenylporphyrins and suitable substituted phthalocyanines (for reviews see [230,231]) (anodic electropolymerization of 2,9,16,23-tetraaminophthalocyanine (M = Co(II), Ni(II)) [231,232] and 2,9,16,23-tetra(l-pyrrolylalkyleneoxy)phthalocyanines (M = 2H, Zn(II), Co(II) [232])) under formation of polymers 53 and 54 shown as idealized structures. Depending on the reaction conditions the film thicknesses are between around 50 nm and several pm. The films remain electroactive at the electrochemical potential so that oxidation or reduction current envelope grows with each successive potential cycle. Electrochromism, redox mediation and electrocatalysis of the electrically conducting films are summarized in [230,231]. 

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