CV, scan rate 0.1 Vs-1 (top) and DPV (bottom) for (A) 3 and (B) 4 in 0.1 M [n-Bu4N][B(C6F5)4] in CH2Cl2 (CAS 75-09-2) using a glassy carbon working electrode. Potentials are referenced to the internal standard, Cp*2Fe
Ferrocene-based nanoelectronics Regioselective syntheses and electrochemical characterization of α-monothiol and α,ω- dithiol, phenylethynyl-conjugated, 2,5-diethynylpyridyl- And pyridinium-linked diferrocene frameworks having an end-to-end distance of ~4 nm
Figure 3
As shown in Figure 3A, compound 3 displays a single unresolved redox couple for the two ferrocenes, which means that the redox potentials of these two moieties must be within a few tens of millivolts of one another.33 Viewed another way, as previously determined for 43,6 the unsymmetric 2,5-diethyl-nylpyridyl unit of 3 is sufficiently long enough so that the two ferrocene groups of 3 do not experience any significant electrostatic repulsion between one another upon oxidation,34 nor does the unsymmetric nature of this bridging group preferentially perturb the electronic structure of one ferrocene significantly over the other.
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