Abstract
The [NiFe]-hydrogenase model complex NiFe(pdt)(dppe)(CO)3 (1) (pdt = 1,3-propanedithiolate) has been efficiently synthesized and found to be robust. This neutral complex sustains protonation to give the first nickel-iron hydride [1H]BF4. One CO ligand in [1H]BF4 is readily substituted by organophosphorus ligands to afford the substituted derivatives [HNiFe(pdt)(dppe)(PR3)(CO)2]BF4, where PR 3 = P(OPh)3 ([2H]BF4); PPh3 ([3H]BF4); PPh2Py ([4H]BF4, where Py = 2-pyridyl). Variable temperature NMR measurements show that the neutral and protonated derivatives are dynamic on the NMR time scale, which partially symmetrizes the phosphine complex. The proposed stereodynamics involve twisting of the Ni(dppe) center, not rotation at the Fe(CO)2(PR3) center. In MeCN solution, 3, which can be prepared by deprotonation of [3H]BF4 with NaOMe, is about 104 stronger base than is 1. X-ray crystallographic analysis of [3H]BF4 revealed a highly unsymmetrical bridging hydride, the Fe-H bond being 0.40 Å shorter than the Ni-H distance. Complexes [2H]BF4, [3H]BF4, and [4H]BF4 undergo reductions near -1.46 V vs Fc0/+. For [2H]BF4, this reduction process is reversible, and we assign it as a one-electron process. In the presence of trifluoroacetic acid, proton reduction catalysis coincides with this reductive event. The dependence of i c/ip on the concentration of the acid indicates that H2 evolution entails protonation of a reduced hydride. For [2H] +, [3H]+, and [4H]+, the acid-independent rate constants are 50-75 s-1. For [2H]+ and [3H]+, the overpotentials for H2 evolution are estimated to be 430 mV, whereas the overpotential for the N-protonated pyridinium complex [4H 2]2+ is estimated to be 260 mV. The mechanism of H 2 evolution is proposed to follow an ECEC sequence, where E and C correspond to one-electron reductions and protonations, respectively. On the basis of their values for its pKa and redox potentials, the room temperature values of ΔGH• and ΔGH- are estimated as respectively as 57 and 79 kcal/mol for [1H]+.
Original language | English (US) |
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Pages (from-to) | 14877-14885 |
Number of pages | 9 |
Journal | Journal of the American Chemical Society |
Volume | 132 |
Issue number | 42 |
DOIs | |
State | Published - Oct 27 2010 |
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Biochemistry
- Colloid and Surface Chemistry