Ru catalyzed cyclodimerization of bis(2‐thienyl)acetylene and bis(3‐thienyl)acetylene. Synthesis properties of 4,5,6‐tris(2‐thienyl)benzo(b)thiophene and 5,6,7‐tris(3‐thienyl)benzo[b]thiophene

Activated dihydridocarbonyltris(triphenylphosphine)ruthenium catalyzes the cyclodimerization of both bis(2‐thienyl)acetylene and bis(3‐thienyl)acetylene to yield, respectively, 4,5,6‐tris(2′‐thienyl)‐benzob]thiophene and 5,6,7‐tris(3′‐thienyl)benzob]thiophene. These fluoresce in the blue. Both undergo irreversible one electron oxidation at & sim1.1 mV versus Ag/Ag⁺ electrode, consistent with oxidation of the benzob]thiophene nuclei rather than the substituent thiophene rings.