Diiron complexes containing pyridyl-phosphine ligands, that is, (mu-pdt)[Fe(2)(CO)(5)L] (pdt = S(CH(2))(3)S, L = Ph(2)PCH(2)Py, Ph(2)PPy, ) and (micro-pdt)[Fe(CO)(2)(PMe(3))][Fe(CO)(2)L] (L = Ph(2)PCH(2)Py, Ph(2)PPy, ) were prepared as model complexes of the [FeFe]-hydrogenase active site. Protonation of and by HOTf afforded the pyridyl-nitrogen protonated products [H(N)][OTf] and [H(N)][OTf], respectively. The molecular structures of, as well as [H(N)][OTf] and [H(N)][OTf] were confirmed by X-ray diffraction studies, which show that the Ph(2)PCH(2)Py ligand occupies the basal position both in and its protonated species [H(N)][OTf], while the Ph(2)PPy ligand prefers the apical position in and [H(N)][OTf]. The double protonation process of complex was monitored by in situ IR, (1)H and (31)P NMR spectroscopy at low temperature. The spectroscopic evidence indicates that the protonation of occurs first at the Fe-Fe bond and then at the pyridyl-nitrogen atom. Cyclic voltammograms reveal that protonation of and results in a considerable decrease in the overpotential for electrocatalytic proton reduction in the presence of HOTf, while the efficiency is not influenced by protonation. The electrocatalytic efficiency of for proton reduction in the presence of HOAc in CH(3)CN-H(2)O (50 : 1, v/v) is 5 times higher than that in pure CH(3)CN.
The pH of mitochondria (pHm) has a close relationship with many biological processes. Here we developed a new indicator Mito-pH-1 for the ratiometric fluorescence detection of the mitochondria pH value, which has excellent tolerance to environmental change. And Mito-pH-1 has been used for the first time to monitor the change of pHm under temperature and H2O2 stimuli in living cells.
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