Molecular Catalysts for H2 Conversion and Production

4 Molecular Concepts of Water Splitting Nature s Approach [Pg.212]

The work on biomimetic models for [NiFe] and [FeFe] hydrogenase has been described in several review articles [15b 158]. In this work, many of the structural features important for proper function found in the native systems have been successfully incorporated for example, the bimetallic Ni-Fe or Fe-Fe core with rather short metal-metal distances and an open coordination site at one metal, the sulfur-rich environment (terminal and bridging thiolate ligands), CO/CN ligation of the iron(s), and the incorporation of a base for acceptance of the proton and, more recently, of hydride bridges. Still-existing problems of many model systems are the O2 sensitivity, the high overpotentials, and lack of activity (low turnover rates). [Pg.212]

Inspiration from the native hydrogenases suggests that catalytic activity might require a bimetallic site. However, a closer look shows that - at least for the [Pg.212]

FeFe-enzyme - proton or hydrogen substrate binding and also the hydride-proton reaction exclusively occurs at the iron distal to the [4Fe-4S] cluster, suggesting that mononuclear iron complexes might also be viable catalysts. Consequently, Ott and coworkers have synthesized and characterized some stable pentacoordinated Fe(II) complexes with five ligands that nicely mimic the native ones and exhibit an open coordination site [163, 164]. This approach avoids the formation of the less reactive bridging hydrides that are found in the dinuclear complexes [153]. Catalytic H2 formation from weak acids at low overpotentials with promising TOF and catalyst stability could be demonstrated [164]. [Pg.213]

During recent years, our understanding of the WOC and the hydrogenase enzymes has made considerable progress. This is due to intensive efforts in these important scientific fields of basic research. The availability and combination of structural [Pg.213]

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