In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Steric and Electronic Effects in Methyl-Substituted 2,2′-Bipyrroles and Poly(2,2′-Bipyrrole)s: Part I. Synthesis and Characterization of Monomers and Polymers, published in 2000-05-31, which mentions a compound: 616-43-3, mainly applied to electrochem polymerization bipyrrole; methyl substituent polypyrrole elec property, Related Products of 616-43-3.
The effects of N- and C-Me substitution on the elec. and spectral properties of pyrrole, 2,2′-bipyrrole, and the corresponding polymers were investigated. A whole series of monomethyl and N- or Cβ-dimethyl-substituted 2,2′-bipyrroles was synthesized, and the electrochem. and spectral properties of all the compounds were investigated under identical testing conditions. The corresponding polymers were prepared by electrochem. anodic oxidation under comparable exptl. conditions and their spectroscopic and conductivity properties evaluated for comparison. The higher degree of efficiency in transmission of electronic effects associated with Me substitution at Cβ with respect to substitution at N was clearly demonstrated. The influence of the symmetry of the starting monomer (C2v or Cs) on the elec. properties of the resulting polymers is discussed.
If you want to learn more about this compound(3-Methyl-1H-pyrrole)Related Products of 616-43-3, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(616-43-3).
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