摘要
We clarify the electrochemical behavior of an organometallic cobalt dithiolene complex (1-NH) with a secondary sulfonyl amide (-NHSO2-) substituted Cp ligand involving proton dynamics. The reductions of 1-NH and its deprotonated derivative (1-N-) are centered on the CpCoS2 moiety. The 2e(-) reduction of 1-NH quantitatively gives 1-N- with hydrogen generation.
- 出版日期2013