Volatile heterometallics: structural diversity of Pd-Pb β-diketonates and correlation with thermal properties.

Volatile heterobimetallics based on Pb(ii) hexafluoroacetylacetonate as a host material and a range of Pd(ii) complexes containing both various donor atoms and terminal substituents in the β-diketonate ligand have been studied to trace the influence of the nature of the initial monometallic complexes on the structure, composition and thermal properties of heterobimetallic compounds. The structural variety and stoichiometry of the heterobimetallic compounds are caused by various combinations of the competing donor-acceptor interactions between the constituting monometallic moieties. The major structure forming factor is the metallophilic interaction between Pd and Pb atoms resulting in polynuclear structures with a specific topology.

Volatile Heterobimetallic Complexes from Pd and Cu β-Diketonates: Structure, Magnetic Anisotropy, and Thermal Properties Related to the Chemical Vapor Deposition of CuPd Thin Films.

A novel approach for preparing volatile heterometallic complexes for use as precursors for the chemical vapor deposition of various materials is reported. New CuPd complexes based on β-diketonate units were prepared, and their structures and compositions were determined. [PdL *CuL ] (1) and [PdL *Cu(tmhd) ] (2) (L=2-methoxy-2,6,6-trimethylheptane-3,5-dionate; tmhd=2,2,6,6- tetramethylheptane-3,5-dionate) are 1D coordination polymers with alternating metal complexes, which are connected through weak interactions between the Cu atoms and the OCH groups from the ligand of the Pd complexes.

Arrangement of Rh3+ ions in fac-triamminetrichloridorhodium from powder data and in fac-triamminetrinitratorhodium crystals twinned by merohedry.

The rhodium complexes [RhCl3(NH3)3], (I), and [Rh(NO3)3(NH3)3], (II), are built from octahedral RhX3(NH3)3 units; in (I) they are isolated units, while in (II) the units are stacked in columns with partially filled sites for the Rh atoms. The octahedra of monoclinic crystals of (I) are linked by N-H···Cl hydrogen bonds and the Rh(3+) ions are located on the mirror planes. In the trigonal crystals of (II), the discontinuous `columns' along the threefold axis are linked by N-H···O hydrogen bonds.