1292323-26-2Relevant academic research and scientific papers
Electrocatalytic oxidation of formate with nickel diphosphine dipeptide complexes: Effect of ligands modified with amino acids
Galan, Brandon R.,Reback, Matthew L.,Jain, Avijita,Appel, Aaron M.,Shaw, Wendy J.
, p. 5366 - 5371 (2013)
A series of nickel bis(diphosphine) complexes with dipeptides appended to the ligands were investigated for the catalytic oxidation of formate to carbon dioxide, a proton, and two electrons. Typical rates of approximately 7 s -1 were found, similar to that for the parent complex (ca. 8 s -1), with amino acid size and positioning contributing very little to the rate or operating potential. Hydroxy functionalities did result in lower rates, which were recovered by protecting the hydroxy group. The results suggest that the overall dielectric properties introduced by the dipeptides do not play an important role in catalysis, but free hydroxy groups do influence activity, implying contributions from intra- or intermolecular interactions. These observations are important in developing a fundamental understanding of the effect that an enzyme-like outer coordination sphere can have upon molecular catalysts. Electrocatalysts Ni(PR2N R′2)2 substituted with dipeptides were used for the oxidation of formate. Polar substituents resulted in a significant loss in activity, which was recovered upon protection of these groups. This work adds to our growing understanding of the role of the outer coordination sphere in molecular electrocatalysis. Copyright
Incorporating peptides in the outer-coordination sphere of bioinspired electrocatalysts for hydrogen production
Jain, Avijita,Lense, Sheri,Linehan, John C.,Raugei, Simone,Cho, Herman,Dubois, Daniel L.,Shaw, Wendy J.
experimental part, p. 4073 - 4085 (2011/06/19)
Four new cyclic 1,5-diaza-3,7-diphosphacyclooctane ligands have been prepared and used to synthesize [Ni(PPh2NR 2)2]2+ complexes in which R is a mono- or dipeptide. These complexes represen
