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Nitroazoles: Synthesis, Structure and Applications pp 157–405Cite as

Structure and Physical–Chemical Properties of Nitroazoles

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Part of the book series: Topics in Applied Chemistry ((TAPP))

Abstract

The critical evaluation of a large body of the information on five-membered nitroazoles and nitrobenzazoles study by physical chemical methods – nuclear magnetic resonance (NMR), nuclear quadrupole resonance (NQR), electron spin resonance (ESR), ion-cyclotron resonance, UV and IR- spectroscopy, X-ray analysis, mass spectrometry, polarography, dipole moments, chromatography, luminescence, photolysis, etc. is presented. The extensive investigations of structure, tautomerism, and properties of nitroazoles by multinuclear 1H, 13C, 15N, 19F, 31P, 29Si and two-dimensional NMR spectroscopy are reviewed. A great emphasis is given to tautomerism studies of nitroazoles by multinuclear dynamic NMR because prototropic transformations of almost all azoles in solutions proceed so quickly. The mechanisms of electrochemical reactions and vicarious nucleophilic C-amination of nitroazoles are discussed. Quantum-chemical investigations of nitroazoles are covered in detail.

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Notes

  1. 1.

    *PM3 calculations with geometry optimization (SPARTAN 5.0) have been carried out at Universite L. Pasteur, Chemistry Department, Strasbourg, France (with kind help of Dr. A. Varnek).

  2. 2.

    For electron paramagnetic resonance (EPR) spectroscopy, we prefer to use the title ESR in organic chemistry

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  1. Favorsky Irkutsk Institute of Chemistry, Irkutsk, Russian

    L. Larina & V. Lopyrev

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Larina, L., Lopyrev, V. (2009). Structure and Physical–Chemical Properties of Nitroazoles. In: Nitroazoles: Synthesis, Structure and Applications. Topics in Applied Chemistry. Springer, New York, NY. https://doi.org/10.1007/978-0-387-98070-6_3

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