Heterophenoquinones: Tuning Optoelectronics and Electrochromicity.

We report the synthesis and optoelectronic properties of 16 thiophene-based heterophenoquinones. These compounds were accessed in a convergent and modular approach, allowing for their efficient synthesis. Tuning of the optical band gap was achieved through π-extension by annulation of a benzene or tropone moiety to the thiophene, oxidation, change of the heteroatom or by attachment of a donor substituent to the thiophene core.

Quinoidal Azaacenes: 99 % Diradical Character.

Quinoidal azaacenes with almost pure diradical character (y=0.95 to y=0.99) were synthesized.

True Blue Through Oxidation-A Thiaazulenic Heterophenoquinone as Electrochrome.

A thiaazulenic quinone TAQ was synthesized and its optical and redox properties were investigated. The deep blue-colored compound is readily and reversibly reduced to the colorless anionic state. Electrochromic films were prepared and showed reversible switching behavior for the anodically coloring and NIR electrochromic material.

A modular approach to neutral P,N-ligands: synthesis and coordination chemistry.

We report the modular synthesis of three different types of neutral κ(2)-P,N-ligands comprising an imine and a phosphine binding site. These ligands were reacted with rhodium, iridium and palladium metal precursors and the structures of the resulting complexes were elucidated by means of X-ray crystallography. We observed that subtle changes of the ligand backbone have a significant influence on the binding geometry und coordination properties of these bidentate P,N-donors.

Soluble diazaiptycenes: materials for solution-processed organic electronics.

The synthesis and characterization of soluble azaiptycenes is reported. Optical and physical properties were studied and compared with those of the structurally consanguine azaacenes. Electrochemical experiments and quantum-chemical calculations revealed the electronic structure of the iptycene derivatives.