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Recently the group of Prof. Schubert reported the synthesis of novel redox-active polymer containing π-extended tetrathiafulvalenes systems and its application in a Li-organic battery1. A novel redox-active polymer, poly(2-vinyl(exTTF)), was synthesized from 2-vinyl(exTTF) (V0136) using the free radical polymerization technique with 2,2′-azobis(2-methylpropionitrile) (AIBN) as initiator (Scheme 1). The chemical properties of poly(2-vinyl(exTTF) can be influenced by the choice of the appropriate solvent and the amount of initiator. Due to the low solubility of 2-vinyl(exTTF) (V0136), the polymerization was best performed in DMSO, leading to high conversions, polymers with high molar mass (Mn = 6.02 × 103 g mol −1), and a narrow molar mass distribution (PDI = 2.04). Poly(2-vinyl(exTTF)) is soluble in N,N′-dimethylformamide (DMF), N,N′-dimethylacetamide (DMAc), and dimethylsulfoxide (DMSO), as well as insoluble but swellable in common electrolytes.

Scheme 1.
Poly(2-vinyl(exTTF)) undergoes a redox reaction involving two electrons to form dicationic species in a single step. During the oxidation, the release of the second electron is promoted due to the planar low-energy conformation associated with the re-aromatization of the oxidized dicationic product. Cyclic voltammetry of monomer (V0136) in acetonitrile solution reveals an electrochemical response at ( Epa + Epc ) / 2 = −0.2 V vs Fc / Fc+. The exTTF units have proven to be a promising core structure as an active material unit for organic batteries. The application of poly(2-vinyl(exTTF)) in a Li-organic battery enables charge-storage devices that display a theoretical capacity of 132 mAh g−1, together with a constant cell potential and a long lifetime exceeding 250 cycles.
