Photoisomerizable command interfaces

Light-Switchable Activation of Redox Proteins by Means of Photoisomerizable Command Interfaces Associated with Electrodes... 

Another approach to the organization of integrated optoelectronic switches is schematically detailed in Figure 7.13 it involves the organization of a photoisomerizable command interface on a solid support. A com-... 

Fe(CN)6] , electrochemically contacted at a photoisomerizable command interface (lla/llb). Figure 7.15 shows the impedance features (as Nyquist plots) of the nitrospiropyran (11a) and protonated nitromerocyanine (lib) electrodes in the presence of [Fe(CN)6] as a redox probe. The impedance spectra show a larger resistance to interfacial electron transfer when the monolayer is in the neutral dinitrospiropyran state (Ret = 60 kll) than when it is in the positively charged protonated merocyanine state (Ret = 48 kQ) (Figure 7.15, curves b and a). The heterogeneous rate constants for electron transfer between the electrode and the redox probe were calculated to be 0.82 X 10" and 1.1 x 10" cm s" for the 11a and 1 lb-monolayer modified Au-electrodes, respectively. 

Another approach to the organization of integrated optoelectronic switches is schematically detailed in Fig. 23, and involves the organization of a photoisomerizable command interface on the solid support [86]. The command surface controls the interfacial electron transfer to a solution-state redox species. In one photoisomeric state, electron transfer to a redox probe solubilized in the electrolyte solution is prohibited (e.g. by repulsive interactions), whereas in the complementary state of the monolayer the interfacial electron transfer is allowed (e.g. because of associative interactions). Various interactions, such as electrostatic interactions, host-guest or donor-acceptor interactions, contribute to the selective contacting of the redox probe to one state of the photoisomerizable monolayer. 

FIG. 7.19 Electronic transduction of photoswrtehable bloelectrocatalytic functions of enzymes/ proteins by the application of a photoisomerizable command interface that controls the electrical contact between the redox enzyme/protein and the electrode. 

A further approach to controlling electrical communication between redox proteins and their electrode support through a photo-command interface includes photo stimulated electrostatic control over the electrical contact between the redox enzyme and the electrode in the presence of a diffusional electron mediator (Scheme 12).[58] A mixed monolayer, consisting of the photoisomerizable thiolated nitrospiropyran units 30 and the semi-synthetic FAD cofactor 25, was assembled on an Au electrode. Apo-glucose oxidase was reconstituted onto the surface FAD sites to yield an aligned enzyme-layered electrode. The surface-reconstituted enzyme (2 x 10-12 mole cm-2) by itself lacked electrical communication with the electrode. In the presence of the positively charged, protonated diffusional electron mediator l-[l-(dimethylamino)ethyl]ferrocene 29, however, the bioelectrocatalytic functions of the enzyme-layered electrode could be activated and controlled by the photoisomerizable component co-immobilized in the monolayer assembly (Figure 12). In the... 

In another example, a mixed monolayer composed of a photoisomerizable component and an electrochemical catalyst was applied to switch the electrocatalytic properties of a modified electrode between ON - and OFF -states. A gold electrode surface functionalized with a spiropyran-monolayer and pyrroloquinoline quinone (PQQ) moieties incorporated into the mono-layer was applied to control the electrocatalytic oxidation of NADH by light [92]. The positively charged merocyanine-state interface resulted in the repulsion of Ca2+ cations (promoters for the NADH oxidation by the PQQ), thus resulting in the inhibition of the electrocatalytic process. In the nitrospiropyran-state the monolayer does not prevent association of the PQQ-catalyst and Ca2+-promoter, so provides efficient electrocatalytic oxidation of NADH. Similar results have been achieved by a combination of the photo- and thermal effects resulting in the isomerization of the spiropyran-monolayer with the incorporated PQQ-catalyst [93], Other photoisomerizable materials such as an azobenzenealkanethiol derivative mixed with a ferrocene-redox component have also been used to control the electrocatalyzed electron transfer process between a command interface and a dissolved redox probe [94]. 

Photonic control over electroactivated bio-catalytic processes can also be achieved by the use of electrode surfaces that are modified by photoisomerizable units. These interfaces, whose state controls the ability of a substrate to interact with them, are known as command surfaces [382, 386-390]. In one example, a... 

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