Design, synthesis and characterization of fused bithiazole- and dithiophene-based low bandgap thienylenevinylene copolymers

The structural rigidity of fused units in the polymer backbone, in addition to the resulting stabilizing effect of the quinoidal structure, and tunable electronic properties have played a key role in promoting highly-ordered pi-stacking moieties, exhibiting promising charge carrier mobilities. The electron-deficient thiazole moiety shows high planarity and effective pi-pi stacking, which leads to the reduction in the energy levels of the highest occupied and lowest unoccupied molecular orbitals (HOMO/LUMO), and ideally enhances the electron charge mobility. Four heterocycle-based monomers BTzS, BTzSe, DTS, and DTG based on fused bithiazole and dithiophene units incorporated with sulfur, selenium, silicon, and germanium as the bridging atoms were synthesized and characterized. The monomers were copolymerized with the electron-rich alkylated thienylenevinylene (TV) unit to afford copolymers P1-P4. The thermal, optical, and electrochemical properties and crystallinity of the copolymers were thoroughly investigated. Extensive OFET device optimization using different solvents and annealing temperatures resulted in the best charge mobility of 0.09 cm(2) V-1 s(-1) for the electron-deficient bithiazole BTzS copolymer P1 and 0.36 cm(2) V-1 s(-1) for the DTS copolymer P3.

Automated summary

The study focuses on the structural characteristics of polymers based on thiazole units and their impact on charge carrier mobility. The synthesis of four different heterocycle-based monomers and their copolymerization with electron-rich alkylated thienylenevinylene units resulted in copolymers with the best charge mobility.