[NiFe], [FeFe], and [Fe] hydrogenase models from isomers.

The study of hydrogenase enzymes (H2ases) is necessary because of their importance to a future hydrogen energy economy. These enzymes come in three distinct classes: [NiFe] H2ases, which have a propensity toward H2 oxidation; [FeFe] H2ases, which have a propensity toward H2 evolution; and [Fe] H2ases, which catalyze H- transfer. Modeling these enzymes has so far treated them as different species, which is understandable given the different cores and ligand sets of the natural molecules. Here, we demonstrate, using x-ray analysis and nuclear magnetic resonance, infrared, Mössbauer spectroscopies, and electrochemical measurement, that the catalytic properties of all three enzymes can be mimicked with only three isomers of the same NiFe complex.

Multifunctional Catalysts for H2 O2 -Resistant Hydrogen Fuel Cells.

The development of hydrogen fuel cells is greatly hindered by the unwanted generation of H2 O2 at the cathode. A non-Pt cathode catalyst is now shown to be capable of simultaneously reducing both O2 and H2 O2 , thus rendering H2 O2 a useful part of the feed stream. The applicability of this unique catalyst is demonstrated by employing it in a fuel cell running on H2 /CO and O2 /H2 O2 .

Oxidation of Guanosine Monophosphate with O2 via a Ru-peroxo Complex in Water.

Oxidative damage of DNA by reactive oxygen species (ROS) is responsible for aging and cancer. Although many studies of DNA damage by ROS have been conducted, there have been no reports of the oxidation of RNA components, such as guanosine monophosphate, by metal-based species in water. Here, we report the first case of oxidation of guanosine monophosphate to 8-oxoguanosine monophosphate by a metal-based oxygen bound species, derived from O2 and in water.

A model for the water-oxidation and recovery systems of the oxygen-evolving complex.

We propose a model for the water-oxidation and recovery systems of the oxygen-evolving complex (OEC) of the photosystem II (PSII) enzyme. The whole system is constructed from two catalytic cycles, conducted as a tandem reaction: (i) a water-oxidation loop uses cerium(IV) ammonium nitrate as an oxidant to activate a dimanganese complex for water-oxidation and thereby liberate a molecule of O2 and (ii) a recovery loop begins with photoinhibition of the dimanganese complex but then uses O2 to reactivate the manganese centre. The net result is a catalytic water-oxidation catalyst that can use self-generated O2 for recovery.