What Kind of Chemistry Facts Are We Going to Learn About C12H8Br2

SDS of cas: 92-86-4. Bye, fridends, I hope you can learn more about C12H8Br2, If you have any questions, you can browse other blog as well. See you lster.

I found the field of Polymer Science very interesting. Saw the article 2,7-Linked N-methylcarbazole copolymers by combining the macromonomer approach and the oxidative electrochemical polymerization published in 2020. SDS of cas: 92-86-4, Reprint Addresses Soto, JP (corresponding author), Pontificia Univ Catolica Valparaiso, Fac Ciencias, Lab Polimeros, Inst Quim, Ave Brasil 2950, Valparaiso, Chile.; Estrany, F; Aleman, C (corresponding author), Univ Politecn Cataluna, EEBE, Dept Engn Quim, C Eduard Maristany 10-14, Barcelona 08019, Spain.; Estrany, F; Aleman, C (corresponding author), Univ Politecn Cataluna, Barcelona Res Ctr Multiscale Sci & Engn, C Eduard Maristany 10-14, Barcelona 08019, Spain.. The CAS is 92-86-4. Through research, I have a further understanding and discovery of 4,4′-Dibromobiphenyl

The preparation of copolymers bearing N-methylcarbazole and 2,7-linked 3,4-ethylenedioxythiophene units has been carried out using the N-methyl-2,7-di(2-(3,4-ethylenedioxythienyl))carbazole monomer, which has been chemically synthesized through the Stille coupling reaction of 2,7-dibromo-N-methylcarbazole and tributyl-stannylated 3,4-ethylenedioxythiophene. Then, the monomer was electropolymerized by chronoamperometry in acetonitrile with 0.1 M LiClO4 under a constant potential of 0.70 V and using steel AISI 316 electrodes. The electrochemical activity and stability, charge-discharge capacity, charge transfer resistance and surface properties (i.e. morphology, topography and wettability) of the resulting polymer have been characterized and compared with those reported for poly(3,4-ethylenedioxythiophene). Finally, the polymer has been obtained by potentiodynamic sweep, applying around 100 cyclic voltammetry steps to an acetonitrile solution of the N-methyl-2,7-di(2-(3,4-ethylenedioxythienyl))carbazole monomer with 0.1 M LiClO4. Results show that although this technique has been mostly used to electropolymerize diheteroaromatic-subtituted carbazoles, the resulting material presents serious disadvantages with respect to that produced by chronoamperometry under a constant potential.

SDS of cas: 92-86-4. Bye, fridends, I hope you can learn more about C12H8Br2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem