Citation:
Cui Xuanxuan, Li Ruifeng, Zhu Yinming, Xiao Xunwen. Synthesies, Structures and Properties of TTF Derivatives with Benzoyloxy[J]. Chemistry,
;2016, 79(3): 272-275.
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Two tetrathiafulvalenes substituted with a phenyl (Ph) (TTF-A) [A=Ph-COOCH3 (7) and A=Ph-COOH (8)] have been synthesized to clear the nature of the donor-acceptor interaction between the TTF unit and the acceptor group. Their structures were characterized by 1H NMR, 13C NMR and mass spectra. The synthesized compounds both display two reversible redox peaks corresponding to the TTF/TTF+· and TTF+·/TTF2+ and show the similar redox potentials comparable to other Ph-substituted TTF derivatives. And the results indicated that compound 7 and 8 are good donor molecules. We also got the crystal of the key intermediate 5 for the synthesis of compound 7 and 8. Compound 5 belongs to monoclinic space group Pc with cell parameters of a=0.3890 (1) nm, b=1.065 (1) nm, c=1.318 (1) nm, Z=2, V=534.5 (2) nm3, Dc=1.542 g·cm-3,F(000)=260,R=0.0467, ωR=0.0739 (I>2σ(I)).
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Keywords:
- TTF,
- Donor-acceptor interaction,
- Redox property,
- Crystal structure
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