Selenophene
Selenophene structure
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Common Name | Selenophene | ||
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| CAS Number | 288-05-1 | Molecular Weight | 131.035 | |
| Density | 1.423 g/mL at 25 °C(lit.) | Boiling Point | 110.5±9.0 °C at 760 mmHg | |
| Molecular Formula | C4H4Se | Melting Point | -30ºC(lit.) | |
| MSDS | USA | Flash Point | 20.6±18.7 °C | |
| Symbol |
GHS02, GHS06, GHS08, GHS09 |
Signal Word | Danger | |
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Controlling phase separation and optical properties in conjugated polymers through selenophene-thiophene copolymerization.
J. Am. Chem. Soc. 132(25) , 8546-7, (2010) Selenophene-thiophene block copolymers were synthesized and studied. The properties of these novel block copolymers are distinct from those of statistical copolymers prepared from the same monomers with a similar composition. Specifically, the block copolymer... |
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General synthesis of thiophene and selenophene-based heteroacenes.
Org. Lett. 7(23) , 5301-4, (2005) [reaction: see text] A new intramolecular triple cyclization of bis(o-haloaryl)diacetylenes, via dilithiation followed by reaction with chalcogen elements, produces pi-conjugated compounds containing heterole-1,2-dichalcogenin-heterole fused tricyclic skeleto... |
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J. Electrochem. Soc. 137 , 1827, (1990)
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Dye-sensitized solar cells based on organic sensitizers with different conjugated linkers: furan, bifuran, thiophene, bithiophene, selenophene, and biselenophene. Li R, et al.
J. Phys. Chem. C Nanomater. Interfaces 113(17) , 7469-79, (2009)
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Low band gap selenophene-diketopyrrolopyrrole polymers exhibiting high and balanced ambipolar performance in bottom-gate transistors. Shahid M, et al.
Chem. Sci. 3(1) , 181-85, (2012)
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Electron transmission spectra of selenophene and tellurophene and Xa computations of electron affinities for chalcophenes. Modelli A, et al.
Chem. Phys. 88(3) , 181-85, (1984)
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