Colabello Diane M, Sobalvarro Elizabeth M, Sheckelton John P, Neuefeind Joerg C, McQueen Tyrel M, Khalifah Peter G
Department of Chemistry, Stony Brook University , Stony Brook, New York 11794, United States.
Department of Chemistry, The Johns Hopkins University , Baltimore, Maryland 21218, United States.
Inorg Chem. 2017 Nov 6;56(21):12866-12880. doi: 10.1021/acs.inorgchem.6b02531.
Among oxide compounds with direct metal-metal bonding, the YMoO (ABO) structural family of compounds has a particularly intriguing low-dimensional structure due to the presence of bioctahedral BO dimers arranged in one-dimensional edge-sharing chains along the direction of the metal-metal bonds. Furthermore, these compounds can have a local magnetic moment due to the noninteger oxidation state (+4.5) of the transition metal, in contrast to the conspicuous lack of a local moment that is commonly observed when oxide compounds with direct metal-metal bonding have integer oxidation states resulting from the lifting of orbital degeneracy typically induced by the metal-metal bonding. Although a monoclinic C2/m structure has been previously proposed for LnMoO (Ln = La-Lu and Y) members of this family based on prior single crystal diffraction data, it is found that this structural model misses many important structural features. On the basis of synchrotron powder diffraction data, it is shown that the C2/m monoclinic unit cell represents a superstructure relative to a previously unrecognized orthorhombic Immm subcell and that the superstructure derives from the ordering of interchangeable MoO and LaO building blocks. The superstructure for this reason is typically highly faulted, as evidenced by the increased breadth of superstructure diffraction peaks associated with a coherence length of 1-2 nm in the c* direction. Finally, it is shown that oxygen vacancies can occur when Ln = La, producing an oxygen deficient stoichiometry of LaMoO and an approximately 10-fold reduction in the number of unpaired electrons due to the reduction of the average Mo valence from +4.5 to +4.05, a result confirmed by magnetic susceptibility measurements. This represents the first observation of oxygen vacancies in this family of compounds and provides an important means of continuously tuning the magnetic interactions within the one-dimensional octahedral chains of this system.