Structural features and near infra-red (NIR) luminescence of isomeric Yb( iii ) bipyridyl- N , N ′-dioxide coordination polymers

Gail M. Sequeira, Wayne Y. Tan, Evan G. Moore

The synthesis and structural characterization of a series of lanthanide complexes formed from YbX3 salts (X = NO3(-) or CF3SO3(-)) and the isomeric 4,4'-bipyridine-N,N'-dioxide (4,4'-bpdo) or 3,3'-bipyridine-N,N'-dioxide (3,3'-bpdo) ligands has been undertaken by X-ray crystallography. Depending on the choice of anion, the complexes isolated with L = 4,4'-bpdo yield either an extended 1D linear chain {[Yb(L)(NO3)3(CH3OH)]}∞ or a coordination polymer network {[Yb(L)4](CF3SO3)3}∞ which are isostructural with previously reported compounds using other Ln(iii) metals. The isomeric 3,3'-bpdo ligand yields a similar extended 1D linear chain {[Yb(L)(NO3)3(CH3OH)]}∞ when NO3(-) is used as the anion. However, when substituted by the typically non-coordinating CF3SO3(-) anion, inner sphere coordination yields a coordination polymer {[Yb(L)3(CF3SO3)](CF3SO3)2}∞ with a (2(2)·4(8)·6(5)) network topology. In an effort to rationalize the observed difference in coordinating behavior, DFT calculations of the isomeric bipyridyl-N,N'-dioxide ligands have been undertaken, but revealed no significant differences in the charge distribution of the coordinating N-oxide groups. Lastly, sensitized Yb(iii) emission in the Near Infra-Red (NIR) region operating via the well-known antennae effect has been observed and compared for two of the coordination polymers.