1997
DOI: 10.1039/a606771i
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Synthesis and characterization of poly[3-(butylthio)thiophene]: a regioregular head-to-tail polymer

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Cited by 41 publications
(50 citation statements)
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“…The film absorption spectrum is coincident with the early reported result where a sharp X-ray diffraction (XRD) peak was observed at 2u ¼ 4.88. [26] The optical band-gaps (E opt g ) estimated from the absorption band edge of the polymer films are listed in Table 1, they are 1.85, 1.54, 1.82, and 1.83 eV for P3HT, P3HOT, P3HST, and P3HST-co-Th, respectively.…”
Section: Thermal Stabilitymentioning
confidence: 99%
See 1 more Smart Citation
“…The film absorption spectrum is coincident with the early reported result where a sharp X-ray diffraction (XRD) peak was observed at 2u ¼ 4.88. [26] The optical band-gaps (E opt g ) estimated from the absorption band edge of the polymer films are listed in Table 1, they are 1.85, 1.54, 1.82, and 1.83 eV for P3HT, P3HOT, P3HST, and P3HST-co-Th, respectively.…”
Section: Thermal Stabilitymentioning
confidence: 99%
“…The purpose of this work is to investigate the effect of the sulphur atom with the larger size in the electron-donating alkylthio side chain on the absorption and electronic energy levels of the polythiophene derivatives in comparison with P3HOT and P3HT, since alkylthio groups show the effect of steric hindrance which affects the absorption and electronic properties of conjugated polymers. [23][24][25][26] It was found that the alkylthio substituent red-shifted the absorption of polythiophene and the HOMO energy level of polythiophene decreased. Both the red-shifted absorption and decreased HOMO level is desirable for application as donor materials in PSCs.…”
Section: Introductionmentioning
confidence: 99%
“…PTs hold outstanding thermal and environmental stability and electrical conductivity when doped, but their processability and properties are strongly affected by the structure and chemical modifications . Consequently, materials with tailor‐made properties can be designed by inserting substituents, such as alkyl groups, in the three position of a thiophene ring in order to obtain configurationally regular and soluble polymeric chains . Poly(3‐alkylthiophene)s (P3ATs) and, in particular, regioregular poly(3‐hexylthiophene) (P3HT) have been used in a plethora of electronic and optoelectronic device applications.…”
Section: Introductionmentioning
confidence: 99%
“…The absence of fine structure is sim- ilar to that observed for the PT with an alkylthio side chain. 16 In n-decanol (a poor solvent for the material) a shoulder arises at about 600 nm, similar to the one observed for the PT with an alkylthio side chain. The CD effect of PTTVb in ndecanol is very low in intensity.…”
Section: Uv-vis and CD Spectroscopymentioning
confidence: 58%