Elefteria Psillakis, John C. Jeffery, Jon A. McCleverty and Michael D. Ward
Reaction of 3-(2-pyridyl)pyrazole with POBr3 in toluene–NEt3 afforded not the expected tris(pyrazolyl)phosphine oxide but the partially hydrolysed compound bis[3-(2-pyridyl)pyrazol-1-yl]phosphinate (as its triethylammonium salt). This compound has two potentially chelating N,N′-bidentate arms linked by an apical PO2- group. Reaction with AgNO3, Tl(O2CMe), Pb(NO3)2 or Ba(NO3)2 in dry MeCN followed by recrystallisation afforded crystals of the complexes [AgL]·2H2O, [TlL]·MeOH, [PbL2]·H2O and [(BaL2)3]·6MeCN·2H2O respectively, all of which have been crystallographically characterised. The compound [AgL]·2H2O contains infinite helical chains (AgL)∞ in which each ligand donates one N,N′-bidentate arm to each of two metals and each metal ion is four-co-ordinated by two arms from different ligands. The strands are held together in the crystal by a complex network of hydrogen bonds involving lattice water molecules and also by aromatic π-stacking interactions. The compound [TlL]·MeOH is likewise a one-dimensional helical polymer of TlL units, with each ligand bridging two metals and each Tl ion in a ‘2 + 3’ co-ordination geometry with two short bonds to ligands (<2.71 Å) and three longer, weak bonds (>2.87 Å): there is an obvious gap in the co-ordination sphere due to a stereochemically active lone pair. A combination of interstrand aromatic π-stacking interactions and hydrogen-bonding interactions involving the lattice MeOH molecule is present. The compound [PbL2]·H2O is in contrast a discrete mononuclear complex, four-co-ordinated just by one bidentate arm from each of the two ligands with the other bidentate arms pendant: again there is a stereochemically active lone pair. The metal geometry is approximately trigonal bipyramidal with the lone pair in an equatorial position. The lattice water molecule is hydrogen bonded to three different complex units. The compound [(BaL2)3]·6MeCN·2H2O contains mononuclear BaL2 and dinuclear Ba2L4 units: the former is ten-co-ordinate, with each ligand acting as an N4O donor and a phosphinate oxygen atom participating in co-ordination, whereas in the latter each BaII is nine-co-ordinated and two of the ligands are bridging, donating their four N atoms to one metal ion and a phosphinate oxygen atom to the other.