Abdusalom Suleymanov1,Timothy Swager1
Massachusetts Institute of Technology1
Abdusalom Suleymanov1,Timothy Swager1
Massachusetts Institute of Technology1
In recent years, there has been significant interest in incorporating heteroatoms into polycyclic aromatic hydrocarbons (PAHs). This exploration of heteroatom-doped variants of extended π-conjugated materials has revealed their distinct and enhanced electronic and photophysical properties. Among the various five-membered aromatic heterocycles, pyrrole stands out as the most electron-rich when compared to its isoelectronic counterparts, furan and thiophene. The synthetic versatility and strong redox activity of pyrrole enable the creation of synthetic frameworks with enhanced p-doping and other desirable material properties.<br/>Our research has focused on the synthesis and characterization of novel chiral pyrrole-based PAHs. These include twisted azacoronenes and helicenes incorporating pyrrole units. We are currently investigating their chiroptical, electrochemical, and magnetooptical properties.