Abstract
The electrochemistry of [CuL1] I and [CuL2] 2 [H2L1 = 1,2-bis(pyridine-2-carboxdmido)benzene, H2L2 = 3,4-bis(pyridine-2-carboxamido)toluene] was investigated. Both complexes show a quasi-reversible Cu(II/I) reduction near -1.6 V vs Fc(+)/Fc. Spectroelectrochemistry confirmed that the Cu(III) state is accessible near +0.4 V, and undergoes an EC reaction (k similar or equal to 10 s(-1)) to generate a new Cu(II) species. (C) 2002 Elsevier Science B.V. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 853-855 |
| Number of pages | 3 |
| Journal | Inorganic Chemistry Communications |
| Volume | 5 |
| DOIs | |
| Publication status | Published - Oct 2002 |
Keywords
- copper(II)/(III)/(I)
- tetradentate ligands
- mononuclear
- electrochemistry
- EC reaction
- NICKEL(III)
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