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 |
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Pages (from-to) | 6135-6137 |
Number of pages | 3 |
Journal | Inorganic Chemistry |
Volume | 45 |
Issue number | 16 |
DOIs | |
State | Published - 7 Aug 2006 |