Thienoindolizines and their Benzo‐Fused Derivatives: Synthesis and Physical Properties

A series of thienoindolizine structural isomers have been synthesized in a one‐pot, two‐step procedure starting from easily accessible gem‐difluoroalkene functionalized bromothiophenes. The developed method gives easy access to a range of thienoindolizine products containing thieno[3,2‐g]‐, thieno[3,4‐g]‐ and thieno[2,3‐g]indolizine core structures. The described synthesis strategy consists of a base mediated, transition metal free nucleophilic substitution of fluorine atoms by nitrogen containing heterocycles followed by a Pd catalyzed intramolecular cyclization. A series of 22 final product examples has been obtained with yields ranging from 29 % to 95 %. UV/Vis absorption, fluorescence spectroscopy, fluorescence lifetime measurements and cyclic voltammetry were carried out with selected final products to evaluate structural effects on photophysical and electrochemical properties. (TD)DFT and NICS calculations were performed to provide insight into the electronic properties of the four core molecular structures. Structural isomers of thienoindolizines have been synthesized in a one‐pot, two‐step procedure starting from easily accessible gem‐difluoroalkene functionalized bromothiophenes. The synthesis strategy consists of base mediated nucleophilic substitution followed by Pd catalyzed intramolecular cyclization. Structural effects on the optical and electrochemical properties have been evaluated in selected product examples.