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  2. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    The reaction with many Lewis acids results in the addition to the nitrogen atom of pyridine, which is similar to the reactivity of tertiary amines. The ability of pyridine and its derivatives to oxidize, forming amine oxides (N-oxides), is also a feature of tertiary amines. [86] The nitrogen center of pyridine features a basic lone pair of ...

  3. Chichibabin reaction - Wikipedia

    en.wikipedia.org/wiki/Chichibabin_reaction

    The rate of amination for three azoles proceeds quickest to slowest as follows: 1-methylbenzimidazole > 1-methylnaphth-[2,3-d]imidazole > 3-methylnaphth[1,2-d]imidazole. [3] Since the addition of the amide ion proceeds quickly with these substrates, the differences in reaction rates is most likely their propensity for hydride elimination and ...

  4. Transition metal complexes of pyridine-N-oxides - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_complexes...

    Pyridine-N-oxides bind to metals through the oxygen. According to X-ray crystallography, the M-O-N angle is approximately 130° in many of these complexes. As reflected by the pKa of 0.79 for C 5 H 5 NOH +, pyridine N-oxides are weakly basic ligands. Their complexes are generally high spin, hence they are kinetically labile.

  5. Heterocyclic compound - Wikipedia

    en.wikipedia.org/wiki/Heterocyclic_compound

    Structures and names of common heterocyclic compounds Pyridine, a heterocyclic compound. A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). [1]

  6. Transition metal imido complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_imido_complex

    Structure of a representative imido complex (py = pyridine, CMe 3 = tert-butyl) [1] In coordination chemistry and organometallic chemistry, transition metal imido complexes is a coordination compound containing an imido ligand.

  7. Simple aromatic ring - Wikipedia

    en.wikipedia.org/wiki/Simple_aromatic_ring

    The nitrogen (N)-containing aromatic rings can be separated into basic aromatic rings that are easily protonated, and form aromatic cations and salts (e.g., pyridinium), and non-basic aromatic rings. In the basic aromatic rings , the lone pair of electrons is not part of the aromatic system and extends in the plane of the ring.

  8. Basic aromatic ring - Wikipedia

    en.wikipedia.org/wiki/Basic_aromatic_ring

    In non-basic aromatic rings the lone pair of electrons of the nitrogen atom is delocalized and contributes to the aromatic pi electron system. In these compounds the nitrogen atom is connected to a hydrogen atom. Examples of non-basic nitrogen-containing aromatic rings are pyrrole and indole. Pyrrole contains a lone pair that is part of the pi ...

  9. Pyridine-N-oxide - Wikipedia

    en.wikipedia.org/wiki/Pyridine-N-oxide

    Pyridine-N-oxide is the heterocyclic compound with the formula C 5 H 5 NO. This colourless, hygroscopic solid is the product of the oxidation of pyridine . It was originally prepared using peroxyacids as the oxidising agent.