Abstract
Dinuclear [(TPA)CoII(CA2-)CoII(TPA)] (BF4)2·2MeOH (1) [TPA = tris-(2-pyridylmethyl) amine] and [(TPA)CoII(CA•3-)CoII(TPA)] (BF4)·2Et2O (2) with a bridging chloranilate radical ligand formed by reduction of 1 are crystallographically and magnetically characterized. 1 has shown a weak antiferromagnetic coupling within the CoII dimer [J/kB = -0.65 K (-0.45 cm-1)], while 2 has a 2 orders of magnitude stronger antiferromagnetic interaction between the CoII ion and a radical [J/kB = -75 K (52 cm-1)].
| Original language | English |
|---|---|
| Pages (from-to) | 6135-6137 |
| Number of pages | 3 |
| Journal | Inorganic Chemistry |
| Volume | 45 |
| Issue number | 16 |
| DOIs | |
| State | Published - 7 Aug 2006 |