Conjugated microporous polymer networks have been prepared from the strong electron donor tetrathiafulvalene (TTF) and 1,3,5-triethynylbenzene (TEB) by using the Sonogashira-Hagihara cross-coupling reaction. Optimization of reaction conditions yields polymers with surface areas of up to 434 m(2) g(-1) . The strong electron-donating properties of the network can be proven by iodine exposure. Structural and electronic changes due to formation of the charge-transfer salt from TTFs in the porous network and iodine within the pores are investigated.
Keywords: donor-acceptor polymers; microporous polymers; organic electronics; post-synthetic modification; tetrathiafulvalene.
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