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N-Unsubstituted thienoisoindigo (TIIG) and its diphenyl derivative (dph-TIIG) are synthesized by using a tert-butoxy carbonyl (t-Boc) group as a protecting group. TIIG has a stacking structure analogous to isoindigo, and… Click to show full abstract
N-Unsubstituted thienoisoindigo (TIIG) and its diphenyl derivative (dph-TIIG) are synthesized by using a tert-butoxy carbonyl (t-Boc) group as a protecting group. TIIG has a stacking structure analogous to isoindigo, and dph-TIIG is a hybrid of brickwork and herringbone structures. These compounds exhibit ambipolar transistor properties and particularly dph-TIIG shows the maximum hole and electron mobilities greater than 0.1 cm2 V−1 s−1.
Keywords:
unsubstituted thienoisoindigos;
dph tiig;
tiig;
preparation molecular;
thienoisoindigos preparation;
molecular packing
Journal Title: Journal of Materials Chemistry C
Year Published: 2017
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Journal Title: Journal of Materials Chemistry C
Year Published: 2017
Link to full text (if available)
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recommendations!