Conformational Mobility and Pendent Base Effects on Electrochemistry of Synthetic Analogues of the [FeFe]-Hydrogenase Active Site

Dynamic
NMR (13C and 1H) studies of (μ-SCH2XCH2S)­[Fe­(CO)3]2 complexes
(X = CR2, NR) were utilized to examine the fluxional processes
that are important in the [FeFe]-hydrogenase active site models, where
an open site for proton/hydrogen binding, achieved by configurational
mobility of the Fe­(CO)3 unit, is required for electrocatalysis
of proton reduction. In order to interrogate the effects of fluxional
mobility on electrochemical response to added acid, energy barriers
for the CO site exchange in Fe­(CO)3 rotors were determined
for nitrogen- and carbon-based bridgehead complexes. The effect of
the methyl substituent in both the NH/NCH3 and CH2/C­(CH3)2 cases is to lower the Fe­(CO)3 rotational activation barrier relative to the NH or CH2 analogues. Although the C­(CH3)2 case has the
lowest Fe­(CO)3 rotational barrier, its performance as a
proton reduction electrocatalyst is 2-fold less than that for the
X = NR species, indicating the proton-directing effect of the pendent
base on catalytic efficiency.