2,6-Diphenylthieno[2,3-f][1]benzothiophene
![2,6-Diphenylthieno[2,3-f][1]benzothiophene结构式](https://image.chemsrc.com/caspic/046/219597-02-1.png)
2,6-Diphenylthieno[2,3-f][1]benzothiophene结构式
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常用名 | 2,6-Diphenylthieno[2,3-f][1]benzothiophene | 英文名 | 2,6-Diphenylthieno[2,3-f][1]benzothiophene |
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| CAS号 | 219597-02-1 | 分子量 | 342.477 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 567.4±45.0 °C at 760 mmHg | |
| 分子式 | C22H14S2 | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 226.0±14.9 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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2,6-Diphenylbenzo[1,2-b:4,5-b']dichalcogenophenes: a new class of high-performance semiconductors for organic field-effect transistors.
J. Am. Chem. Soc. 16th ed., 126 , 5084-5085, (2004) 2,6-Diphenylbenzo[1,2-b:4,5-b']dichalcogenophenes including thiophene, selenophene, and tellurophene analogues as organic semiconductors for field-effect transistors were effectively synthesized in three steps from commercially available 1,4-dibromobenzene. A... |
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Hybrid organic semiconductors including chalcogen atoms in pi-conjugated skeletons. Tuning of optical, redox, and vibrational properties by heavy atom conjugation.
J. Phys. Chem. A 23th ed., 110 , 7422-7430, (2006) In this work, the interactions between heteroatoms (S, Se, and Te) and conjugated skeletons are analyzed. The study is carried out by using electronic absorption and fluorescence spectroscopies, electrochemistry, vibrational Raman spectroscopy, and theoretica... |
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