“…Different mechanisms to attach redox mediators to electrode surfaces have been tried so far, among which direct adsorption464, 465 or covalent binding466–468 of monolayers of the redox mediator, in situ electropolymerization,469, 470 immobilization in a pre‐cast lipidic film,471, 472 direct mix in a carbon paste,473 and deposition of a polymer bearing redox moieties 474. Examples of catecholic compounds explored as suitable redox shuttles include pyrocatechol,475–478 3,4‐dihydroxybenzaldehyde,479 3,4‐dihydroxybenzylamine,480, 481 dopamine,467, 468, 471, 481, 482 norepinephrine,472, 481 L‐DOPA,483 serotonin,484 several arylalkylcatechols,464, 465 chlorogenic acid,485 caffeic acid,486 nordihydroguaiaretic acid,487 pyrocatechol violet,488 lignosulfonic acid,489 and catecholic flavonoids, such as rutin490 and quercetin 468, 491. A recent study by Bartlett and co‐workers on the reversible catalytic oxidation of NADH systematically screened 13 different dihydroxybenzene derivatives covalently linked to GCEs by means of two different spacers, showing how the substitution pattern of the aryl ring affects both the redox potential and the surface coverage of the electrode 492.…”