Eaton's reagent-mediated domino π-cationic arylations of aromatic carboxylic acids to Iasi-red polymethoxylated polycyclic aromatic hydrocarbons: products with unprecedented biological activities as tubulin polymerization inhibitors.

A rapid domino π-cationic arylation of aromatic carboxylic acids, mediated by Eaton's reagent, has been developed for the synthesis of Iasi-red polymethoxylated polycyclic aromatic hydrocarbons (PAHs). This route is currently the easiest method to obtain such popular PAH compounds, which bear in addition numerous methoxy groups. The domino process was generalized, the structure of the obtained red products and the mechanism of their formations were elucidated, and some of their photophysical properties were determined.

Identification of the EPR signal of S₂⁻ in green ultramarine pigments.

Green and blue ultramarine pigments are characterized by the sodalite structure Na(6)(Al(6)Si(6)O(24)) and colored inserted species. These chromophores are sulfur species: S(3)(-) (blue) and S(2)(-) (yellow). Both radicals are encapsulated inside the β-cages.

Occupancy of the sodalite cages in the blue ultramarine pigments.

A quantitative EPR study of blue ultramarine pigments has been performed in order to determine the concentration of the S(3)(-) chromophore. Copper sulfate CuSO(4) x 5H(2)O has been used as a standard, while a ruby crystal was used as an inner standard to take into account the changes of the quality factor of the cavity. These experiments show that, in the most-colored pigments, less than half of the sodalite cages are occupied by a S(3)(-) radical.