TY - JOUR
T1 - The use of di-2-pyridyl ketone in manganese(II) benzoate chemistry: Two novel Mn II3 linkage isomers containing the ketone form of the ligand and a neutral MnII4 cubane containing the ligand in its gem-diolate(-1) form
AU - Stoumpos, Constantinos C.
AU - Gass, Ian A.
AU - Milios, Constantinos J.
AU - Kefalloniti, Elena
AU - Raptopoulou, Catherine P.
AU - Terzis, Aris
AU - Lalioti, Nikolia
AU - Brechin, Euan K.
AU - Perlepes, Spyros P.
PY - 2007/12/8
Y1 - 2007/12/8
N2 - The use of di-2-pyridyl ketone, (py)2CO, in manganese(II) benzoate chemistry has yielded two MnII3 linkage isomers containing the ketone form of the ligand and a neutral MnII4 cubane cluster containing the gem-diolate(-1) form of the ligand. The 3:2 Mn(O2CPh)2. 2H2O/(py)2CO reaction system in MeCN gives a mixture of the orange complex [Mn3(O2CPh)6{(py)2CO-κ2N,N'}2] (1) and the yellow compound [Mn3(O2CPh)6{(py)2CO-κ2N,O}2]·2MeCN (2·2MeCN). The known compound [Mn6O2(O2CPh)10(MeCN)4] (3) appears as a by-product when the initial reaction solution, that leads to 1 and 2·2MeCN, is allowed to slowly evaporate in the air. The trinuclear molecules adopt a linear structure in both complexes, with one monoatomically bridging η 1:η1:μ2 and two syn,syn η1:η1:μ2 carboxylate groups spanning each pair of MnII ions. The terminal MnII ions are each capped by one chelating-N,N' (py)2CO ligand in 1 and by one chelating-N,O (py)2CO molecule in 2. The 1:1 reaction of Mn(O2CPh)2·2H2O and (py)2CO in CH2Cl2 results in the isolation of [Mn4(O2CPh)4{(py)2C(OH)O}4] (4). The tetranuclear molecule has a cubane topology with the MnII ions and the deprotonated oxygen atoms from the (py)2C(OH)O− ligands occupying alternate vertices. The IR data are discussed in terms of the nature of the bonding. The magnetic properties of 4 in the 300–5 K range have been modeled with two J values and reveal weak intramolecular antiferromagnetic interactions. The low temperature X-band EPR spectra of 1, 2 and 4 are also discussed.
AB - The use of di-2-pyridyl ketone, (py)2CO, in manganese(II) benzoate chemistry has yielded two MnII3 linkage isomers containing the ketone form of the ligand and a neutral MnII4 cubane cluster containing the gem-diolate(-1) form of the ligand. The 3:2 Mn(O2CPh)2. 2H2O/(py)2CO reaction system in MeCN gives a mixture of the orange complex [Mn3(O2CPh)6{(py)2CO-κ2N,N'}2] (1) and the yellow compound [Mn3(O2CPh)6{(py)2CO-κ2N,O}2]·2MeCN (2·2MeCN). The known compound [Mn6O2(O2CPh)10(MeCN)4] (3) appears as a by-product when the initial reaction solution, that leads to 1 and 2·2MeCN, is allowed to slowly evaporate in the air. The trinuclear molecules adopt a linear structure in both complexes, with one monoatomically bridging η 1:η1:μ2 and two syn,syn η1:η1:μ2 carboxylate groups spanning each pair of MnII ions. The terminal MnII ions are each capped by one chelating-N,N' (py)2CO ligand in 1 and by one chelating-N,O (py)2CO molecule in 2. The 1:1 reaction of Mn(O2CPh)2·2H2O and (py)2CO in CH2Cl2 results in the isolation of [Mn4(O2CPh)4{(py)2C(OH)O}4] (4). The tetranuclear molecule has a cubane topology with the MnII ions and the deprotonated oxygen atoms from the (py)2C(OH)O− ligands occupying alternate vertices. The IR data are discussed in terms of the nature of the bonding. The magnetic properties of 4 in the 300–5 K range have been modeled with two J values and reveal weak intramolecular antiferromagnetic interactions. The low temperature X-band EPR spectra of 1, 2 and 4 are also discussed.
U2 - 10.1016/j.inoche.2007.11.025
DO - 10.1016/j.inoche.2007.11.025
M3 - Article
SN - 1387-7003
VL - 11
SP - 196
EP - 202
JO - Inorganic Chemistry Communications
JF - Inorganic Chemistry Communications
IS - 2
ER -