Yamamoto, Takakazu et al. published their research in Journal of the American Chemical Society in 1996 | CAS: 55687-34-8

6-Bromoquinoxalin-2(1H)-one (cas: 55687-34-8) belongs to quinoxaline derivatives. Compounds possessing quinoxaline derivatives were bestowed with a variety of significant biological properties such as antiviral, antimalarial, anticancer, DNA intercalation, DNA duplex stabilization, and many others. Modifying quinoxaline structure it is possible to obtain a wide variety of biomedical applications, namely antimicrobial activities and chronic and metabolic diseases treatment.Related Products of 55687-34-8

Preparation of New Electron-Accepting 蟺-Conjugated Polyquinoxalines. Chemical and Electrochemical Reduction, Electrically Conducting Properties, and Use in Light-Emitting Diodes was written by Yamamoto, Takakazu;Sugiyama, Kiyoshi;Kushida, Takashi;Inoue, Tetsuji;Kanbara, Takaki. And the article was included in Journal of the American Chemical Society in 1996.Related Products of 55687-34-8 This article mentions the following:

Dehalogenation polycondensation of 5,8-dibromoquinoxaline derivatives and 2,6-dibromoquinoxaline with zero-valent Ni complex gives a series of 蟺-conjugated polyquinoxalines with mol. weight of 6 脳 103-260 脳 103. The polymers are electrochem. reduced (or n-doped) with an E掳 value of -1.75 to -2.35 V vs Ag/Ag+ and converted into elec. conducting materials with a conductivity of 1 脳 10-4 to 7 脳 10-3 S cm-1 by chem. reduction Poly(quinoxaline-5,8-diyl)s with aromatic substituents give strong fluorescence with emission peaks at 450-520 nm in solutions as well as in cast films. A light-emitting diode (LED), ITO/polymer/Mg(Ag) (polymer = poly(2,3-diphenylquinoxaline-5,8-diyl)), emits blue-green light (位max at about 500 nm). Introduction of hole-transporting layers such as vacuum-deposited or spin-coated thin layers of poly(thiophene-2,5-diyl), poly(p-phenylene), and poly(N-vinylcarbazole) between ITO and the light-emitting layer enhances electroluminescence efficiency by about 2 orders of magnitude. Polyquinoxalines have an ionization potential of 5.83 卤 0.11 eV and a band gap of 2.56 卤 0.26 eV. In the experiment, the researchers used many compounds, for example, 6-Bromoquinoxalin-2(1H)-one (cas: 55687-34-8Related Products of 55687-34-8).

6-Bromoquinoxalin-2(1H)-one (cas: 55687-34-8) belongs to quinoxaline derivatives. Compounds possessing quinoxaline derivatives were bestowed with a variety of significant biological properties such as antiviral, antimalarial, anticancer, DNA intercalation, DNA duplex stabilization, and many others. Modifying quinoxaline structure it is possible to obtain a wide variety of biomedical applications, namely antimicrobial activities and chronic and metabolic diseases treatment.Related Products of 55687-34-8

Referemce:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider