Water Splitting Promoted by a Ruthenium(II) PNN Complex: An Alternate Pathway through a Dihydrogen Complex for Hydrogen Production

• Published in: Organometallics 2011-07, Vol.30 (14), p.3888-3891
• Main Authors: Sandhya, K. S, Suresh, Cherumuttathu H
• Format: Article
• Language: English
• ISSN: 0276-7333; 1520-6041
• DOI: 10.1021/om200046u

A new mechanism involving the formation of a dihydrogen intermediate is described using the TPSS level of the DFT method for the generation of hydrogen from water catalyzed by the PNN Ru(II) pincer complex 4 (Science 2009, 324, 74). The Mulliken charge of the hydride ligand in 4 is highly negative (−1.574) and facilitates a dihydrogen bonding with one of the solvated water molecules to yield 4···H 2 O. In the next step, water coordinates to the metal center by forcing a conformational change in the orientations of the hydride and CO ligands to form a transient intermediate, 4′(H 2 O). The activation free energy, G act for this step is 14.92 kcal/mol. Subsequently, the intermediate liberates the dihydrogen with a G act of 10.47 kcal/mol. With respect to (4 + H 2 O) as reference, the effective G act of the entire mechanism is calculated to be 32.56 kcal/mol. Unlike the previously reported mechanism, the new mechanism operates without the cooperation of the aromatization–dearomatization processes of the pincer ligand and bypasses a highly reversible pathway involving the water-mediated 4 to 1 conversion. Further, a direct pathway for the formation of the cis-dihydroxo intermediate is possible with the new mechanism.