Arjomandi, Jalal; Holze, Rudolf published an article about the compound: 3-Methyl-1H-pyrrole( cas:616-43-3,SMILESS:CC1=CNC=C1 ).Formula: C5H7N. 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.
A Electrosynthesis of conducting poly(3-methylpyrrole) (P3MPy) and poly(3-methylpyrrole-2,6-dimethyl-β-cyclodextrin) (poly(3MPy-β-DMCD)) films on a gold electrode in acetonitrile electrolyte solution containing lithium perchlorate has been carried out by potential cycling. Products were characterized with cyclic voltammetry CV, in situ UV-Vis spectroscopy, and in situ resistance measurements. Electrosynthesis of poly(3MPy-β-DMCD) started with a (1:1) (3MPy-β-DMCD) supramol. cyclodextrin CD complex of 3-methylpyrrole characterized with proton NMR spectroscopy. The oxidation peak of poly(3MPy-β-DMCD) in CVs is shifted to more pos. values than P3MPy. In situ resistance measurements show that the resistance of poly(3MPy-β-DMCD) is higher than of P3MPy by approx. an order of magnitude. Min. resistance can be observed for P3MPy and poly(3MPy-β-DMCD) at 0.40 < EAg/AgCl < 1.10 V and 0.60 < EAg/AgCl < 1.10 V, resp. The higher resistance of P3MPy compared with polypyrrole may result from the presence of the Me group substituent resulting in a decreased conjugation length. When CD is present during synthesis, resistance is even higher. In situ UV-Vis spectroelectrochem. data for both films prepared potentiodynamically by cycling the potential in the range - 0.20 < EAg/AgCl < 1.10 V in acetonitrile electrolyte show major effects of CD presence during electrosynthesis. When you point to this article, it is believed that you are also very interested in this compound(616-43-3)Formula: C5H7N and due to space limitations, I can only present the most important information.
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