Hexaferrocenylbenzene has been synthesized by six-fold Negishi type ferrocenylation of hexabromo- or hexaiodobenzene.

The self-activated yellow-emitting phosphors of vanadates Ca5M4(VO4)6 (M = Mg, Zn) were synthesized via the solid-state reaction route. The formation of single phase compound with garnet structure was verified through X-ray diffraction (XRD) studies. The excitation and emission spectra and the thermal quenching of luminescence intensities were measured. The different luminescence properties of Ca5Mg4(VO4)6 and Ca5Zn4(VO4)6 phosphors were presented, e.g., the spectra shift, the luminescence lifetimes, the absolute quantum efficiency, the color coordinates and the Stokes shift. This deference was discussed on the base of the relationship between the micro-structure and the charge transfer transitions in [VO4]3- groups in the lattices. Ca5Mg4(VO4)6 could be suggested to be a potential yellow-emitting phosphor for the application on near-UV excited white LEDs.

“Supra”Cp: Fivefold Negishi coupling of pentaiodocymantrene resulted in radial oligocyclopentadienyl metal complexes (see scheme). These complexes show fascinating conformational and chemical behavior, including MM and CpCp bond formation and the liberation of the novel supraligand penta(ferrocenyl)cyclopentadiene. dba=dibenzylideneacetone.

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