RESUMO
The synthesis of a η5-coordinated LiCp complex by simple addition of a Li-salt in benzene is presented. A strongly zwitterionic fulvalene serves as the Cp-precursor. Evidence for the coordination of Li+ was obtained by the characterisitic 7Li NMR chemical shifts, variable temperature experiments in solution and by X-ray structure analysis in the solid state.
RESUMO
Octahedral tungsten iodide clusters equipped with apical ligands (L) are synthesized to implement substantial photophysical properties. The [W6I8(CF3COO)6]2- cluster reported herein is the first example of a family of ligand substituted [W6I8L6]2- clusters. Such compounds are expected to exhibit a rich photochemistry in which the apical ligands play a crucial role. The versatile solid state and solution phase photophysical properties of (TBA)2[W6I8(CF3COO)6] described herein parallel characteristics obtained in some photophysically active organic compounds, including a broad absorption in the UV/VIS region. Upon irradiation of this compound, a broad red emission is observed in the VIS/NIR region resulting from excited triplet states, and singlet oxygen (a1Δg) is generated in the presence of O2.