A coordinatively saturated nickel complex supported by triazenido ligands: a new electrocatalyst for hydrogen generation via ligand-centered proton-transfer. (20th July 2017)

• Record Type: Journal Article
• Authors: Xue, Dan; Luo, Su-Ping; Zhan, Shu-Zhong
• Is Part Of: New journal of chemistry. Volume 41:Number 16(2017)
• Page Start: 8503
• Page End: 8508
• Publication Date: 2017-07-20
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c7nj01705g
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : The reaction of 1, 3-bis[2-aminobenzothiazole]triazene (HL) with Ni(CH3 CO2 )2 affords a nickel complex, [Ni II (L)2 ]1, an electrocatalyst for hydrogen generation. Abstract : It is regarded that transition metal complexes can catalyze hydrogen production via an unstable metal-hydride species, and the reduction reaction occurs at the metal center. In this paper, we present a new catalytic mechanism via ligand-centered proton-transfer for hydrogen generation catalyzed by a coordinatively saturated nickel complex, [Ni II (L)2 ]1, which is obtained by the reaction of the triazenido ligand, 1, 3-bis[2-aminobenzothiazole]triazene (HL), with Ni(CH3 CO2 )2 . Electrochemical investigations show that the electrocatalytic system based on [Ni II (L)2 ] can afford 76.31 and 685.76 moles of hydrogen per mole of catalyst per hour (mol H2 /mol catalyst/h) from acetic acid at an overpotential (OP) of 991.6 mV and from a neutral aqueous buffer (pH 7.0) at an OP of 837.6 mV, respectively.