Gonzalez-Tejera, M. J.; Garcia, M. V.; Sanchez de la Blanca, E.; Redondo, M. I.; Raso, M. A.; Carrillo, I. published an article about the compound: 3-Methyl-1H-pyrrole( cas:616-43-3,SMILESS:CC1=CNC=C1 ).Product Details of 616-43-3. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:616-43-3) through the article.
Electrochem. copolymerization of 3-methylpyrrole and N-methylpyrrole perchlorate doped was carried out at 2 overpotentials and at different electrodeposition times in MeCN medium. A mixture of instantaneous and progressive nucleation mechanisms was established from the c.d.-time transients. Doping/dedoping reversibility is deduced from the electrochem. study of copolymer films by cyclic voltammetry. FTIR spectrum anal. shows that electropolymerization time has a great influence on the random monomers proportion in the copolymer obtained. Although the copolymer conductivity is in the range of that measured for poly(3-methylpyrrole) and poly(N-methylpyrrole) obtained in similar conditions, it remains conductive for a much longer time than the homopolymers.
The article 《Electrochemical synthesis of N-methyl and 3-methyl pyrrole perchlorate doped copolymer films》 also mentions many details about this compound(616-43-3)Product Details of 616-43-3, you can pay attention to it, because details determine success or failure
Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate