| 产品描述: | 2,2′:5′,2′′-Terthiophene (TTh) may be prepared by nickel catalysed coupling reaction of grignard′s reagent derived from 2-bromothiophene and magnesium.It generates singlet oxygen. In nature, it is found in the floral extract of Tagetes minuta and Echinops grijisii. It is known to be toxic to mosquitoes.It also exihibits antifungal activity.;2,2′:5′,2′′-Terthiophene (TTh) may be prepared by nickel catalysed coupling reaction of grignard′s reagent derived from 2-bromothiophene and magnesium.It generates singlet oxygen. In nature, it is found in the floral extract of Tagetes minuta and Echinops grijisii. It is known to be toxic to mosquitoes.It also exihibits antifungal activity.Electrochemical copolymerization of carbazole and TTh in sodium perchlorate/acetonitrile was reported.Electrochromic copolymer based on TTh and 3, 4-ethylenedioxythiophene has been reported. TTh acts as a monomer precursor for polythiophene and as a dopant for polycarbonate.It may function as a photosensitizer. |
| 参考文献: |
1. Casado J, et al. Alternated quinoid/aromatic units in terthiophenes building blocks for electroactive narrow band gap polymers. Extended spectroscopic, solid state, electrochemical, and theoretical study. J Phys Chem B. 2005 Sep 8;109(35):16616-27. |
| 保存条件: |
避光,-80℃(运输条件:冰袋低温运输) |
| 配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
| 1 mM |
4.026 ml |
20.13 ml |
40.259 ml |
| 5 mM |
0.805 ml |
4.026 ml |
8.052 ml |
| 10 mM |
0.403 ml |
2.013 ml |
4.026 ml |
| 50 mM |
0.081 ml |
0.403 ml |
0.805 ml |
|
| 注意: |
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