Polythiophenes moieties

Mesomeric charge delocalization in O-substituted, doped polythiophene moiety. 

Coated materials are evaluated in S-SBR and in 50 50 blends of S-SBR and EPDM rubbers. In blends, the partitioning of fillers and curatives over the phases depends on differences in surface polarity. In S-SBR, polythiophene-modified silica has a strong positive effect on the mechanical properties because of a synergistic reaction of the sulfur-moieties in the polythiophene coating with the sulfur cure system. In S-SBR/EPDM blends, a coating of polyacetylene is most effective because of the chemical similarity of polyacetylene with EPDM. The effect of... 

In all the cases of poly acetylene, polythiophene, and polypyrrole coating, the amount of plasma-film deposition was different, caused by the difference in the structure of the three different monomers and their reactivity during the plasma process. PPy- and PTh-silica are more hydrophobic than PA-silica, probably due to the presence of different chemical moieties in the complex film structure deposited onto the silica surface. 

For silica in SBR, a polyacetylene coating gives the lowest filler-filler interaction, a good filler-polymer interaction, and the best dispersion compared to untreated and the other plasma-treated samples. However, for the stress-strain properties, the polythiophene-treated sample gives the best results. This shows the importance of sulfur moieties on the surface of the filler, which form a secondary network in the cured materials. In the blend of S-SBR and EPDM rubbers, the situation is less conclusive. The Payne effect, the bound rubber, and... 

The molecular orbital (MO) calculations within the PM3 method, using a MOP AC package, provided an explanation of the advantages of a new redox system, poly(l,4-phenylene-l,2,4-dithiazolium-3, 5 -yl) (PPDTA), as a cathode material for high-capacity lithium secondary batteries in comparison with three typical polymer conductors (poly-/>-phenylene, polypyrrole, and polythiophene). The MO calculation revealed that the S-S bond in the 1,2,4-dithiazo-lium moiety of PPDTA caused gap narrowing and a downshift of HOMO and LUMO levels, which is consistent with the electrochemical experiment (HOMO = highest occupied molecular orbital LUMO = lowest unoccupied molecular orbital) <2001MI2305>. 

Novel hybrid materials have been realized in which fullerenes participate in composite films with 7r-conjugated-polymer electron donors such as oligothio-phenes. Established studies have already shown that the photoinduced electron transfer is rather enhanced between 7r-conjugated polymers and fullerenes, while back electron transfer is considerably slower [145,149,171,172].Electrosynthe-sized polythiophene with pendant fullerene substituents was recently obtained from the corresponding biothiophene-fulleropyrrolidine dyad [173]. The novel material described has the potential of a double-cable polymer, heavily loaded with fullerene electron-conducting moieties. 

A hyperbranched polymer 47 containing Re(bipyridine)(CO)3Cl chromophores (the Re(CO)3Cl+ moiety is denoted as [Re]) linked by bipyridineethylene bridges was deposited with a sulfonated polythiophene to yield a solar energy conversion material. This displayed open-circuit voltages of 1.2 V and photocurrents of 27 iA cm 2 under solar illumination [94]. 

Polythiophenes containing electron withdrawing alkyl carboxylates (35k-351) have also been synthesized.[212] OTFTs fabricated with the regioregular polythiophene (35k) gave mobilities of up to 0.07 cm V s compared to 0.0063 cm V s for the regiorandom polythiophene (351).[212] Another electron-with-drawing moiety, tetrafluorobenzene, has been substituted on the polyalkylthiophene backbone (35m). Spin-cast films of 35m from 0.5 wt % chloroform solution showed a mobility of up to 2 x 10 cm V s. [213]... 

Benincori T, Brenna E, Sannicolo F, Trimarco L, Zotti G and Sozzani P 1996 The first charm bracelet conjugated polymer an electroconducting polythiophene with covalently bound fullerene moieties Angew. Chem. Int. Edn. Engl. 35 648-51... 

---