Abstract
In this paper, we present a new dinuclear triazenido‑copper(I) complex, [Cu2(L)2] 1, formed by the reaction of the triazenido ligand, 1,3-bis[(2-bromo)benzene]triazene (HL) with CuCl. At room temperature, this copper complex shows photoluminescence at 667nm. Additionally, electrochemical investigations reveal that the electrocatalytic systems based on this copper complex can afford 91.23 and 582.2mol of hydrogen per mole of catalyst per hour (mol H2/mol catalyst/h) from acetic acid at an overpotential (OP) of 991.6mV and an aqueous buffer at an OP of 837.6mV, respectively. The findings show that transition metal complexes may exhibit various functions in different directions.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
