The present new semiconducting compds. with ≥1 optionally substituted phenazine moiety are phenazine derivs. I [R1 =halo, CN, NO2, R2, -​L-​R3, OH, OR2, OR3, NH2, NHR2, N(R2)​2, NR2R3, etc.; L =divalent C1-​40 alkyl, divalent C2-​40 alkenyl, etc.; R2 =C1-​40 alkyl, C2-​40 alkenyl, etc.; R3 =C3-​10 cycloalkylene, etc.; q =0-​6 int.]​. The compds. disclosed herein can exhibit high carrier mobility and​/or efficient light absorption​/emission characteristics, and can possess certain processing advantages such as soln.-​processability and​/or good stability at ambient conditions.

Papagni, A., Facchetti, A., Chen, Z. (2016)Phenazine-​based molecular and polymeric semiconductors. . Brevetto No. 15/168,026.

Phenazine-​based molecular and polymeric semiconductors

PAPAGNI, ANTONIO
Primo
;
2016

Abstract

The present new semiconducting compds. with ≥1 optionally substituted phenazine moiety are phenazine derivs. I [R1 =halo, CN, NO2, R2, -​L-​R3, OH, OR2, OR3, NH2, NHR2, N(R2)​2, NR2R3, etc.; L =divalent C1-​40 alkyl, divalent C2-​40 alkenyl, etc.; R2 =C1-​40 alkyl, C2-​40 alkenyl, etc.; R3 =C3-​10 cycloalkylene, etc.; q =0-​6 int.]​. The compds. disclosed herein can exhibit high carrier mobility and​/or efficient light absorption​/emission characteristics, and can possess certain processing advantages such as soln.-​processability and​/or good stability at ambient conditions.
Si
organic semiconductor, polymers for phovoltaics
Chemistry, Metallurgy
Rilevanza internazionale
15/168,026
1-dic-2016
US 2016/0351815 Al
Università di Milano Bicocca comproprietaria
Papagni, A; Facchetti, A; Chen, Z
Papagni, A., Facchetti, A., Chen, Z. (2016)Phenazine-​based molecular and polymeric semiconductors. . Brevetto No. 15/168,026.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/149821
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