![]() 2,2'-双噻吩结构式
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常用名 | 2,2'-双噻吩 | 英文名 | 2,2'-Bithiophene |
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CAS号 | 492-97-7 | 分子量 | 166.263 | |
密度 | 1.2±0.1 g/cm3 | 沸点 | 260.0±0.0 °C at 760 mmHg | |
分子式 | C8H6S2 | 熔点 | 32-33 °C(lit.) | |
MSDS | 美版 | 闪点 | 76.3±6.6 °C |
Length-dependent conductance of oligothiophenes.
J. Am. Chem. Soc. 136(29) , 10486-92, (2014) We have measured the single-molecule conductance of a family of oligothiophenes comprising 1-6 thiophene moieties terminated with methyl-sulfide linkers using the scanning tunneling microscope-based break-junction technique. We find an anomalous behavior: the... |
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Direct C-H arylation of (hetero)arenes with aryl iodides via rhodium catalysis.
J. Am. Chem. Soc. 128 , 11748, (2006) A new method for the catalytic C-H arylation of heteroarenes and arenes that manifests high activity paired with reasonably broad scope was developed. Under the catalytic influence of RhCl(CO){P[OCH(CF3)2]3}2 and Ag2CO3, the direct C-H arylation of heteroaren... |
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Supramolecular luminescence from oligofluorenol-based supramolecular polymer semiconductors.
Int. J. Mol. Sci. 14 , 22368-79, (2013) Supramolecular luminescence stems from non-covalent exciton behaviors of active π-segments in supramolecular entities or aggregates via intermolecular forces. Herein, a π-conjugated oligofluorenol, containing self-complementary double hydrogen bonds, was synt... |
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